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Background:
Systematic Review

Parkinson’s Disease in Romania: A Scoping Review

1
Department of Neurology, Victor Babes University of Medicine and Pharmacy of Timisoara, Eftimie Murgu Sq. No. 2, 300041 Timișoara, Romania
2
Department of Neurology, Clinical Emergency County Hospital Timisoara, Bd. Iosif Bulbuca No. 10, 300736 Timisoara, Romania
3
Neuroscience Research Center Timisoara, Clinical Emergency County Hospital Timisoara, Bd. Iosif Bulbuca No. 10, 300736 Timisoara, Romania
*
Author to whom correspondence should be addressed.
Brain Sci. 2021, 11(6), 709; https://doi.org/10.3390/brainsci11060709
Submission received: 29 April 2021 / Revised: 16 May 2021 / Accepted: 25 May 2021 / Published: 27 May 2021
(This article belongs to the Special Issue At the Frontiers in Movement Disorders: In Romania)

Abstract

:
Parkinson’s disease (PD) is a significant cause of disability, with a fast-growing prevalence. This review summarizes the epidemiological and clinical data, research on the diagnostic approaches and the interventions available in the Eastern European country of Romania. This scoping review follows the recommendations on the scoping review methodology by Joanna Briggs Institute. We searched four databases (up to 27 January 2021). The data of eligible studies were extracted in standardized forms. We identified 149 unique studies from 1133 records, with 11 epidemiological studies, 52 studies investigating clinical aspects of PD, 35 studies on diagnostic tools, and 51 intervention studies. A narrative synthesis is provided and placed in a historical context. Our review revealed a considerable increase in the Romanian research on PD in the latest 15 years, which largely follows international trends. However, we also identified several research gaps that provide useful information for policymakers, public health specialists, and clinicians.

1. Introduction

Parkinson’s disease (PD) is a neurodegenerative disorder reported to be a leading global cause of disability. Among the neurological disorders, it was found to present the fastest growth in prevalence, disability, and deaths [1]. Namely, in 2016, the overall worldwide number of individuals with PD was 2.4 times higher than in 1990. A systematic analysis of epidemiological studies estimated that 6.1 million people worldwide had PD; the disease caused 211,296 deaths and 3.2 million disability-adjusted life-years (DALYs). Furthermore, it is estimated that the number of PD cases will double in the coming generation due to increasing life expectancy.
To understand the current situation of PD in Romania, it is essential to identify all the available data and map the severity of the problem accurately. A clear presentation of the research results and trends provides useful insight into the country’s context, assisting researchers, healthcare professionals, and policymakers in decision-making. In addition, it will guide the development of future research strategies, and it will help the design and implementation of programs to reduce the burden of PD in Romania [2].
Consequently, to address this burden, there is a need for effective treatment and care strategies. In addition, data on the incidence and prevalence of the disease, especially in regions in which little data are available, are essential [1].
Romania is a middle-income, formerly socialist Eastern European country, with approximately 19 million people, 17.8% over 65 years old. The patient’s association, a non-governmental organization, estimates there are over 72,000 patients with PD in Romania [3]. This estimation is based on the number of PD medication prescriptions reported by the National Health Insurance House. Nonetheless, some patients with Parkinsonian syndromes may also respond to the PD medication; therefore, this report probably overestimates the number of PD patients in Romania. Furthermore, a systematic review estimating global, regional, and country-specific data on PD reports that in Romania, in 2016, there were 40,517 (95% uncertainty interval UI 31,427 to 50,995) patients with PD, with 23,144 (95% UI 17,467 to 30,057) disability-adjusted life-years (DALY’s) [1].
A study estimating the cost of disorders of the brain in Europe [4] reported that in Romania, in 2010, there were 43,841 individuals with PD; the costs per person for these patients was 3933 Euros purchasing power parities (PPPs). The highest costs in Europe were reported in Luxembourg and United Kingdom, with 21,475 Euros PPP, respectively 21,500 Euros PPP per PD patient. The lowest costs were reported in Bulgaria, with 3143 Euros PPP per PD patient, followed by Romania [4]. These total costs include direct costs (healthcare costs and non-medical costs) and indirect costs associated with patients’ production losses. All the costs are expressed in PPPs adjusted real EUR. The estimates presented in the review were converted to real EUR, using nominal exchange rates from the European central bank (ECB), adjusted for comparative price levels (CPL) for 2009 from Eurostat. The CPL was defined as the ratio of purchasing power parities to exchange rates. The selected CPLs were based on the total consumption in each country (GDP). For example, they were not limited to price differences in healthcare goods [4].
The data from Eurostat show that in 2018, Romania had a physician/inhabitant ratio of 254.99/100,000 and a hospital bed/inhabitant ratio of 669.83/100,000. The Romanian Society of Neurology estimates that currently, there are approximately 750 practicing neurologists.
The present scoping review aims to assess the current situation of PD in Romania by reviewing all the Romanian published studies to provide a thorough understanding of existing literature. Unlike classic systematic reviews, addressing relatively precise questions, scoping reviews offer a much larger perspective on a subject, mapping and examining emerging evidence when it is still unclear what other, more specific research questions can be posed and valuably addressed [5].
Our objective is to report data on PD epidemiology, clinical characteristics, interventions, and diagnostic challenges in Romania [2], with a large perspective on Romania’s PD research gaps [2].

2. Materials and Methods

The detailed protocol for the present review is published elsewhere [2]. In brief, based on the population, concept, and context (PCC) mnemonics, we performed a scoping review to answer the following research questions [6]:
  • What data are published on the epidemiology of PD in Romania?
  • What clinical aspects have been investigated in Romanian PD patients?
  • What are the interventions introduced in Romania to reduce the burden of PD and improve the patient’s care and quality of life?
  • Which are the diagnostic tests used in PD patients in Romania?
We performed a computerized bibliographic search for the following databases: MEDLINE/PubMed, EMBASE, Scopus, and Web of Sciences (up to 27 January 2021). In addition, we checked reference lists of all relevant research papers to identify possible additional studies. For the database search, we used the keywords: “Parkinson’s disease” [MeSH] AND “Romania.” These search terms were for PubMed. Searches in other data sources used similar versions of these terms, appropriate for each database. We did not apply any search filters, as we aimed to generate a broad list of studies that would be suitable for inclusion. In addition, we did not apply language restrictions.
We included all human studies reporting research on adults (over 18 years old), with at least 10 participants (P), investigating the epidemiology, clinical characteristics, interventions, or diagnostic tests in PD patients (C), conducted in Romania (C) [2].
We did not set limits on publication date, study design, or setting. We included in our scoping review published articles and also conference abstracts. Two essential factors were found to increase the probability that a study presented in an abstract will subsequently be published in full: the presence of positive or statistically significant results in the abstract and whether the authors were from an English-speaking country, who wrote their report in English. The consequence is that systematic reviews relying on fully published research may provide inaccurate or biased findings because of an over-reliance on studies with positive results or from English-speaking countries [7]. If a study was reported as a conference abstract and later in a full-text article, we did not exclude from our synthesis the abstracts. A recent systematic review assessing inconsistency between conference abstracts and full papers found that the abstract reports were frequently different from their corresponding full reports. There was a high level of inconsistency, especially concerning sample sizes, outcome measures, result presentation, interpretation, and conclusions or recommendations [8]. Nonetheless, we did not include qualitative studies because exploring barriers and facilitators for interventions was not an aim of our research. We excluded studies with individuals with secondary Parkinsonism (e.g., vascular, toxic, drug-induced, or post-infectious) or atypical Parkinsonism (e.g., corticobasal degeneration, Lewy body dementia, progressive supranuclear palsy, or multiple system atrophy). In addition, we excluded the articles where the full-text was not available and the very concise conference abstracts that did not provide data for extraction.
Two authors reviewed the title and abstract of all identified papers independently to assess the study’s eligibility. After the abstract screening, two authors independently studied the full text of the selected articles in the second stage. Disagreements were solved by a third reviewer with expertise in the domain.
To provide readers with a logical descriptive summary of the results, we charted the studies separately based on the research questions (Supplementary Materials). The results were classified under the main conceptual categories, such as: “epidemiology,” “clinical characteristics,” “interventions,” and “diagnostic tests.” Two independent reviewers extracted data. A third reviewer solved any discrepancies.
As explained in the protocol [2], we did not perform a formal assessment of the methodological quality of the included studies.

3. Results

Our search resulted in 1133 titles. We evaluated in full text 276 research papers and included in the present review 149 studies. The PRISMA diagram is presented in Figure 1.
We identified 52 studies on clinical aspects of PD [9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59], 35 studies investigating diagnostic tools [60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87,88,89,90,91,92,93,94], 51 studies on different pharmacological and non-pharmacological interventions [95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140,141,142,143], and only eleven epidemiological studies [1,144,145,146,147,148,149,150,151,152,153]. Some research was based in a single center, but most the university centers also participated in multicenter, international research [16,26,39,47,49,60,61,62,63,64,77,79,80,88,90,92,93,94,101,102,103,104,105,106,107,109,110,115,116,117,119,123,124,125,126,127,129,132,141,143,144,145,146].
The different categories of studies are presented in Figure 2.
The year of publication ranged from 1973 to 2020. A considerable increase in the Romanian research on PD was observed in the latest 15 years, which largely follows international trends (Figure 3). For example, a comparative search in the PubMed database on the international publications on PD revealed that the number of articles increased each year, with a steady, global rise of research in this domain.
The distribution of the different types of studies (excluding the international multicenter studies) by region is presented in Figure 4.

3.1. Studies Investigating Clinical Aspects of Parkinson’s Disease

Among the 52 clinical studies (Supplemental Material: Table S1), 47 studies were done in a single national center, and 5 were multicenter, international studies [16,26,39,47,49]. Among the international studies, four were published as original papers [26,39,47,49], and one as a conference abstract [16]. The research on the clinical aspects of PD focused on a wide range of symptoms, including cognitive impairment (n = 8), depression and anxiety (n = 7), non-motor symptoms (n = 6), sleep disturbances (n = 6), pain (n = 4), and polyneuropathy (n = 4). The detailed distribution of research based on the clinical signs that were investigated is presented in Figure 5.

3.2. Studies on Diagnostic Tests in Parkinson’s Disease

Our systematic review identified 35 studies investigating different diagnostic tools (Supplemental Material: Table S2). Among them, 13 were international multicenter studies [60,61,62,63,64,77,79,80,88,90,92,93,94]; 9 were published as original papers [61,64,77,79,80,87,88,90,92], and four were abstracts of research presented at international conferences [60,62,63,93]. The rest of 41 studies were performed in national settings. A large part of the research focused on modeling studies (n = 12). The detailed presentation on the areas of research included in the diagnostic studies is presented in Figure 6.

3.3. Studies on Pharmacological and Non-Pharmacological Interventions in Parkinson’s Disease

We identified 51 intervention studies (Supplemental Material: Table S3), ranging from phase II to phase III post hoc analysis and post-marketing studies. Twenty-nine trials were national studies. In 22 studies, the Romanian participants were part of international, multicenter studies [101,102,103,104,105,106,107,109,110,115,116,117,119,123,124,125,126,127,129,132,141,143]. In the last category, 11 studies were published as original articles [101,102,115,116,117,119,124,125,129,132,141], and 11 were abstracts presented at international conferences [103,104,105,106,107,109,110,123,126,127,143].
Forty-six studies investigated pharmacological interventions, one study reported on surgical procedures [95], and four studies assessed the effect of non-pharmacological interventions [112,122,130,133]. The different types of investigated interventions are presented in Figure 7.

3.4. Epidemiological Studies

We found eleven epidemiological studies (Supplemental Material: Table S4), including one study on gene-environment interactions [145], one exploring the environmental risk factors for PD [146], one study on tobacco use [144]. In addition, we found seven international studies on the global, regional, and national burden of diseases [1,147,148,149,150,151,152,153] that also presented some data on Romania. However, in the studies on the burden of the diseases, no specific data on the Romanian PD patients were presented except in one study [1]. The data on the epidemiological studies are presented in Figure 8.

4. Discussion

The present scoping review provides a descriptive mapping of the literature body on PD in Romania. We identified 149 studies that assessed the different aspects of PD in Romania.
The studies on clinical aspects of PD (n = 52) constitute most of the research (34.89%) (see Table S1). The authors mainly investigated non-motor aspects of the disease. In addition, some studies also investigated some of the most common adverse effects of L-dopa therapy, like polyneuropathy (Table S1). One reason for the predominance of clinical studies could be that this type of observational study presents fewer technical challenges. It is less complex and less expensive than studies on diagnostic tests or interventions.
Regarding the cognitive impairment from PD, although many researchers focused on the neuropsychological aspects of the disease (Table S1), most studies used an MDS Level I assessment [9,18,39,40,45,46,138] that requires an abbreviated cognitive evaluation, either with a global scale or a limited range of neuropsychological tests [154,155]. The level II definition is based on an extensive assessment of each of the five cognitive domains (i.e., attention, working memory, executive functions, memory, visuospatial skills, and language) [154,155]. This later cognitive assessment is more expensive, time-consuming, requires highly trained personnel, and necessitates tests adapted and validated for Romanian Population. Therefore, a Level II assessment is not readily available in Romania, with implications for further research on cognitive impairment in PD.
The studies investigating different diagnostic tools for PD patients (n = 35) contributed to 23.48% of the research. The Romanian researchers participated in developing various clinical scales, including the non-motor symptoms scale (NMSS) [60,61], scales for outcomes in Parkinson’s disease-cognition (SCOPA-COG) [62], King’s Parkinson’s disease scale [77] and King Parkinson’s disease questionnaire [87], Parkinson’s disease composite scale (PDCS) [90,92], and the “5-2-1” screening criteria for advanced PD [93]. Nonetheless, the number of neuroimaging studies is low (n = 3), and there is a lack of studies on other more expensive diagnostic tools (e.g., dopamine transporters imaging, DaTscan).
From a diagnostic perspective, differential diagnoses of PD necessitate a brain MRI or, sometimes, DaTscan. Patient access to the required diagnostic tools like MRI was limited for many years due to a lack of funding. In addition, DaTscan is not available in Romania. As a result, patients with atypical Parkinsonian syndromes or genetic diseases with Parkinsonism may experience significant delays in diagnosis.
The relatively large number of modeling studies (n = 12) indicates a growing interest in interdisciplinary research, with possible further advancements in the field. The Romanian researchers investigated different tools for early-stage detection of PD, such as nonlinear dynamics, artificial neural networks, and neuro-fuzzy classifiers. In addition, they studied intelligent systems that could be applied to PD patients to predict the evolution of the disease over time and the possible implementation of a high-definition video system in the early management of PD (Table S2).
The studies on different interventions for PD (n = 51) accounted for 34.22% of publications. Most studies focused on pharmacological interventions (n = 46). In 22 studies, the Romanian patients were part of large, multicenter, international cohorts (Table S3). Unfortunately, none of the international studies reported any specific data for Romanian patients. Nonetheless, some researchers also focused on data solely from Romanian patients. Of note, most of the later research was retrospective, observational (Table S3).
The pharmacological studies included research on various therapeutic options, including L-dopa, dopamine agonists, and selective monoamine oxidase B inhibitors. Among the therapeutic options for advanced PD, only Levodopa–carbidopa intestinal gel (LCIG) and deep brain stimulation (DBS) are currently available in Romania. The LCIG has gained increased attention from the Romanian researchers, with the publication of 11 studies [114,118,120,125,126,132,138,139,140,142,143]. However, no studies on DBS were published in Romania, possibly due to the limited availability of the procedure. While in the western countries, there is ample knowledge and experience with managing advanced PD, in Romania, access to some therapies like apomorphine, for example, is limited; therefore, the Romanian neurologists are restricted in their management strategies when faced with a patient with advanced PD.
The number of studies on the non-pharmacological treatment of PD is limited (n = 4). Although globally, the research on non-pharmacological interventions is less extensive than pharmacological treatment, it has been documented to be beneficial for PD patients [156]. Therefore, developing Romanian research in this domain would be beneficial. Contextualization to the Romanian society and the low resource context, focusing on specific demographic features (i.e., multimorbidity), activity limitations, and participation restrictions, may increase Romanian PD patients’ quality of management and care.
The present systematic review revealed only eleven epidemiological studies (7.38%), with three studies focusing on genetic and environmental factors [144,145,146]. The rest of the eight papers communicate research on the global burden of diseases and are based on statistical modeling. To date, data on the number of Romanian PD patients are lacking, with only some estimative numbers. In addition, there is no study on genetic forms of PD.
Internationally, there is growing evidence of the benefits of precision medicine in PD. A personalized approach, tailoring PD treatments based on the patient’s individual genotype, may help reach disease modification [157]. Clinical trials targeting genetic forms of PD, like GBA-associated and LRRK2-associated PD, are timely and of great interest.
Therefore, well-designed large-scale epidemiological, genetic studies are much needed in Romania. In addition, a potential future action could be the initiation of a national registry of PD patients. Nonetheless, the implementation of such a registry may prove to be challenging. For example, such a registry may include non-PD Parkinsonism cases due to a lack of movement disorders specialists and potential PD overdiagnosis [158].
The present scoping review identified several gaps in research in PD research in Romania, providing details on key implications for research and further need for primary studies [6,159]. These gaps could be partially explained by the relatively reduced number of neurologists specializing in movement disorders. For example, in Romania, there are 12 medical universities; however, we found publications only from 10 centers. In addition, there is a limited number of PD nurses and occupational therapy specialists. Therefore, training young specialists with a special interest in movement disorders would be of many benefits.
Other identified gaps comprise limited access to some treatments (e.g., apomorphine infusion, DBS) or some diagnostic investigations (e.g., DaTscan). In addition, increasing the involvement of healthcare policymakers and public awareness on PD would enable further research in movement disorders in this Eastern European country. Specialist medical training on movement disorders, educational activities, research methodology, and support for grant writing initiatives would also help to increase the PD research and care in Romania.
The main identified gaps, possible causes for these gaps, and suggested actions are presented in Supplemental Material Table S5. Therefore, the present scoping review provides implications for research and indicates areas of primary research where future studies are needed. In addition, we provide a basis for further qualitative studies, exploring barriers and facilitators for different actions and interventions that can contribute to a comprehensive understanding of people’s values, attitudes, and beliefs across PD patient populations and healthcare contexts to inform patient-centered practice and policy [160].

5. Conclusions

To our knowledge, this is the first scoping review dedicated to the PD literature in Romania. Overall, we found a steady increase in the number of published studies, reflecting a positive change in the PD research in this region. We provided a complete picture of the current state of knowledge, research, and practices. Furthermore, we identified several gaps in this area. Therefore, a joint effort of local neurologists, healthcare providers, public health specialists, policymakers, and international PD and movement disorders organizations will help overcome the current challenges and provide better research, management, and care of PD patients from Romania.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/brainsci11060709/s1, Table S1: Clinical studies; Table S2: Diagnostic test accuracy studies; Table S3: Intervention Studies; Table S4: Epidemiological studies. doi:10.6084/m9.figshare.14501469.

Author Contributions

Conceptualization, E.C.R.; R.T.; A.C.; M.S.; methodology, E.C.R.; R.T.; A.C.; M.S.; investigation, E.C.R.; R.T.; A.C. and M.S.; resources, E.C.R.; R.T.; A.C.; M.S.; writing—original draft preparation, E.C.R.; R.T.; writing—review and editing, E.C.R.; R.T.; A.C.; M.S.; supervision, E.C.R.; M.S. The first authorship is shared by E.C.R. and R.T. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Dorsey, E.R.; Elbaz, A.; Nichols, E.; Abd-Allah, F.; Abdelalim, A.; Adsuar, J.C.; Ansha, M.G.; Brayne, C.; Choi, J.-Y.J.; Collado-Mateo, D.; et al. Global, regional, and national burden of Parkinson’s disease, 1990–2016: A systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol. 2018, 17, 939–953. [Google Scholar] [CrossRef] [Green Version]
  2. Rosca, E.C.; Tudor, R.; Cornea, A.; Simu, M. Parkinson’s Disease in Romania: A Scoping Review Protocol. Brain Sci. 2021, 11, 251. [Google Scholar] [CrossRef]
  3. Available online: http://www.asociatia-antiparkinson.ro/ (accessed on 25 January 2021).
  4. Gustavsson, A.; Svensson, M.; Jacobi, F.; Allgulander, C.; Alonso, J.; Beghi, E.; Dodel, R.; Ekman, M.; Faravelli, C.; Fratiglioni, L.; et al. Cost of disorders of the brain in Europe 2010. Eur. Neuropsychopharmacol. 2011, 21, 718–779. [Google Scholar] [CrossRef] [Green Version]
  5. Munn, Z.; Peters, M.D.J.; Stern, C.; Tufanaru, C.; McArthur, A.; Aromataris, E. Systematic review or scoping review? Guidance for authors when choosing between a systematic or scoping review approach. BMC Med. Res. Methodol. 2018, 18, 143. [Google Scholar] [CrossRef] [PubMed]
  6. Peters, M.; Godfrey, C.; McInerney, P.; Munn, Z.; Tricco, A.C.; Khalil, H. Chapter 11: Scoping Reviews (2020 Version). Available online: https://wiki.jbi.global/display/MANUAL/JBI+Manual+for+Evidence+Synthesis (accessed on 16 February 2021).
  7. Scherer, R.W.; Meerpohl, J.J.; Pfeifer, N.; Schmucker, C.; Schwarzer, G.; von Elm, E. Full publication of results initially presented in abstracts. Cochrane Database Syst. Rev. 2018, 11, MR000005. [Google Scholar] [CrossRef] [PubMed]
  8. Li, G.; Abbade, L.P.F.; Nwosu, I.; Jin, Y.; Leenus, A.; Maaz, M.; Wang, M.; Bhatt, M.; Zielinski, L.; Sanger, N.; et al. A scoping review of comparisons between abstracts and full reports in primary biomedical research. BMC Med. Res. Methodol. 2017, 17, 181. [Google Scholar] [CrossRef]
  9. Szocs, I.; Hojda, A.; Szalma, I.; Szasz, J.A.; Szatmari, S.Z. Possible correlation between mental dysfunction and mator performance in Parkinson’s disease patients. Eur. J. Neurol. 2005, 12, 109. [Google Scholar]
  10. Popescu, B.O.; Bajenaru, O.; Obretin, D.; Muresanu, D.F. PDQ 39 correlates with “on” time in patient diaries in fluctuating Parkinson’s disease patients. Eur. J. Neurol. 2007, 14, 205. [Google Scholar]
  11. Reisz, D.; Simu, M.A.; Chirileanu, D.R.; Tamasan, S. Depression and pseudo-depression in Parkinson’s disease. Eur. J. Neurol. 2007, 14, 206. [Google Scholar]
  12. Mihancea, P.; Brisc, C.M.; Havasi, N.; Brisc, C. The non-motor symptoms in Parkinson’s disease. Eur. J. Neurol. 2008, 15, 122. [Google Scholar]
  13. Reisz, D.; Simu, M.A.; Chirileanu, D.R.; Carstina, A.; Bursa, A. Particularities of anxiety, depression and sleep disorder in Parkinson’s disease. Eur. J. Neurol. 2008, 15, 130. [Google Scholar]
  14. Stoian, A.; Barsan, A.O.; Szasz, J.A.; Szatmari, S.; Marusteri, M.; Mihai, A.; Incze, T.; Stoian, M.; Schiopu, A. Repression in Parkinson’s disease. Eur. J. Neurol. 2008, 15, 134. [Google Scholar]
  15. Szocs, I.; Szatmari, S.; Szasz, J.A. Motor fluctuations, depressive symptoms and excessive sleepiness influencing quality of life of Parkinson’s disease patients. Eur. J. Neurol. 2008, 15, 135. [Google Scholar]
  16. Martinez-Martin, P.; Falup-Pecurariu, C.; Rodriguez-Blazquez, C.; van Hilten, B.; Odin, P.; Chaudhuri, K.R.; Grp, E. Gender differences in non-motor symptoms in Parkinson’s disease. Parkinsonism Relat. Disord. 2009, 15, S66–S67. [Google Scholar] [CrossRef]
  17. Muntean, L.; Perju-Dumbrava, L.; Tohanean, N.; Perju-Dumbrava, L. Pain and quality of life in Parkinson’s disease patients. Eur. J. Neurol. 2009, 16, 542. [Google Scholar]
  18. Pirscoveanu, D.; Tudorica, V.; Zaharia, C.; Matcau, D.; Stanca, D.; Trifan, F. One year follow-up study on cognitive performances in patients with Parkinson’s disease. Rom. J. Neurol. Rev. Romana Neurol. 2009, 8, 84–87. [Google Scholar]
  19. Sandulescu, M.C.; Zaharia, C.; Tudorica, V. Study on gait and balance in patients with Parkinson’s disease. Parkinsonism Relat. Disord. 2009, 15, S50. [Google Scholar] [CrossRef]
  20. Tudorica, V.; Zaharia, C.; Pirscoveanu, D.; Stanca, D.; Alexandru, O.; Albu, C. Study on anxiety in patients with Parkinson’s disease. Rom. J. Neurol. Rev. Romana Neurol. 2009, 8, 46–49. [Google Scholar]
  21. Căpuşan, C.; Şerban, A.M.; Cosman, D. The relation between cognitive impairment and clinical presentation in early stages of Parkinson’s disease. Hum. Vet. Med. 2011, 3, 213–219. [Google Scholar]
  22. Căpuşan, C.; Cosman, D.; Rusu, I. The deficit of executive functions in early stages of Parkinson’s disease. Hum. Vet. Med. 2011, 3, 171–177. [Google Scholar]
  23. Georgescu, D.; Georgescu, C.; Simu, M.; Georgescu, L.A. Understanding dyspepsia in patients with Parkinson’s disease. J. Neurol. 2011, 258, 89. [Google Scholar]
  24. Muntean, M.L.; Perju-Dumbrava, L. Night-time sleep disturbances and their impact on the quality of life of parkinson’s disease patients. Eur. J. Neurol. 2011, 18, 494. [Google Scholar]
  25. Tudorica, V.; Zaharia, C.; Pirscoveanu, D.; Pirici, D. Study on factors correlated with pain in patients with parkinson’s disease. Eur. J. Neurol. 2011, 18, 204. [Google Scholar]
  26. Martinez-Martin, P.; Pecurariu, C.F.; Odin, P.; Van Hilten, J.J.; Antonini, A.; Rojo-Abuin, J.M.; Borges, V.; Trenkwalder, C.; Aarsland, D.; Brooks, D.J.; et al. Gender-related differences in the burden of non-motor symptoms in Parkinson’s disease. J. Neurol. 2012, 259, 1639–1647. [Google Scholar] [CrossRef]
  27. Muntean, M.L.; Perju-Dumbrava, L. The impact of non-motor symptoms on the quality of life of Parkinson’s disease patients. Eur. J. Neurol. 2012, 19, 685. [Google Scholar]
  28. Susin, A. Daily living and quality of life in Parkinson’s disease. Philobiblon 2012, 17, 247–257. [Google Scholar]
  29. Tohanean, N.; Dumbrava, L.P. Olfactory dysfunction in Parkinson’ disease diagnosis. Rom. J. Neurol. Rev. Romana Neurol. 2012, 11, 108–114. [Google Scholar]
  30. Dumitru, M. Sleep problems in patients with Parkinson’s disease in a hospital setting from Romania. Sleep Med. 2013, 14, e111. [Google Scholar] [CrossRef]
  31. Dumitru, M.M.; Botezatu, C.; Andrei, R.; Popescu, C.D.; Chirita, V.; Chirita, R. Study on the incidence of depression and apathy in a group of patients diagnosed with parkinson’s disease. Eur. Psychiatry 2013, 28, 1333. [Google Scholar] [CrossRef]
  32. Dumitru, M.M.; Chirita, R.; Chirita, V. Depression and apathy in patients with Parkinson’s disease in a hospital in Romania. Eur. Neuropsychopharmacol. 2013, 23, S322. [Google Scholar] [CrossRef]
  33. Perju-Dumbravă, L.; Muntean, M.L.; Mureşanu, D.F. Cerebrovascular profile assessment in Parkinson’s disease patients. CNS Neurol. Disord. Drug Targets 2014, 13, 712–717. [Google Scholar] [CrossRef]
  34. Vasile, T.M.; Roceanu, A.M.; Antochi, F.; Bajenaru, O.A. Prevalence of non-motor symptoms in Parkinson’s disease—An observational study. Rom. J. Neurol. Rev. Romana Neurol. 2014, 13, 125–132. [Google Scholar]
  35. Baetu, C.; Buraga, I.; Buraga, M.; Petre, V. Polineuropathy and B12 deficiency in levodopa/carbidopa intestinal gel etiology and management -our experience. J. Neurol. Sci. 2015, 357, E255–E256. [Google Scholar] [CrossRef]
  36. Georgescu, D.; Ancusa, O.E.; Georgescu, L.A.; Ionita, I.; Reisz, D. Nonmotor gastrointestinal disorders in older patients with Parkinson’s disease: Is there hope? Clin. Interv. Aging 2016, 11, 1601–1608. [Google Scholar] [CrossRef] [Green Version]
  37. Jurcau, A.; Simion, A. Autonomic dysfunctions and sleep disturbances identify Parkinson’s disease patients at risk for developing dementia. Eur. J. Neurol. 2016, 23, 529. [Google Scholar]
  38. Diaconu, S.; Bucur, B.; Urdea, A.; Farcas, A.; Moarcas, M.; Pecurariu, C.F. Fatigue assessment and risk factors in Parkinson’s disease. Eur. J. Neurol. 2017, 24, 296. [Google Scholar]
  39. Kramberger, M.G.; Auestad, B.; Garcia-Ptacek, S.; Abdelnour, C.; Olmo, J.G.; Walker, Z.; Lemstra, A.W.; Londos, E.; Blanc, F.; Bonanni, L.; et al. Long-Term Cognitive Decline in Dementia with Lewy Bodies in a Large Multicenter, International Cohort. J. Alzheimer Dis. 2017, 57, 787–795. [Google Scholar] [CrossRef] [Green Version]
  40. Davidescu, E.I.; Tanasoiu, E.R. Neurocognitive and mood disorders in Parkinson’s disease. Eur. Psychiatry 2018, 48, S343. [Google Scholar]
  41. Tohanean, N.; Crisan, C.; Perju-Dumbrava, L. Distribution and correlation of psychiatric symptoms in early stages of parkinson’s disease. Rom. J. Neurol. Rev. Romana Neurol. 2018, 17, 78–83. [Google Scholar] [CrossRef]
  42. Criciotoiu, O.; Stanca, D.I.; Bondari, S.; Malin, R.D.; Ciolofan, M.S.; Schenker, M.; Stepan, M.D.; Romanescu, F.M.; Georgescu, O.S.; Dragomir, L.P.; et al. Correlation between the age, motor subtypes and the necessity of advanced therapy in Parkinson disease. Rev. Chim. 2019, 70, 2128–2131. [Google Scholar] [CrossRef]
  43. Criciotoiu, O.; Stanca, D.I.; Glavan, D.G.; Bondari, S.; Malin, R.D.; Ciolofan, M.S.; Bunescu, M.G.; Romanescu, F.M.; Schenker, M.; Georgescu, O.S.; et al. The relations between non-motor symptoms and motor symptoms in Parkinson disease. Rev. Chim. 2019, 70, 2652–2655. [Google Scholar] [CrossRef]
  44. Criciotoiu, O.; Stanca, I.D.; Glavan, D.G.; Latea, R.M.; Mita, A.; Calborean, V.; Gheorman, V.; Udristoiu, I.; Dijmarescu, A.L.; Davitoiu, D.V.; et al. The influence of digestive dysfunctions on quality of life in Parkinson disease. Rev. Chim. 2019, 70, 1667–1670. [Google Scholar] [CrossRef]
  45. Cuciureanu, D.I.; Croitoru, C.G.; Constantinescu, V.; Bolohan, L.; Cuciureanu, T. Neuropsychiatric changes in parkinson’s disease patients: A prospective observational two years study. Rom. J. Neurol. Rev. Romana Neurol. 2019, 18, 161–166. [Google Scholar]
  46. Cuciureanu, D.I.; Cuciureanu, T.; Bolohan, L.; Cuciureanu, A. Psychiatric morbidity in Parkinson’s disease in northeast region of Romania. J. Parkinson Dis. 2019, 9, 110. [Google Scholar]
  47. Fasano, A.; Fung, V.S.C.; Lopiano, L.; Elibol, B.; Smolentseva, I.G.; Seppi, K.; Takáts, A.; Onuk, K.; Parra, J.C.; Bergmann, L.; et al. Characterizing advanced Parkinson’s disease: OBSERVE-PD observational study results of 2615 patients. BMC Neurol. 2019, 19, 50. [Google Scholar] [CrossRef] [Green Version]
  48. Irene, R. Genitourinary Dysfunction Prevalence in Parkinson Disease Patients. ARS Med. Tomitana 2019, 25, 6–10. [Google Scholar] [CrossRef] [Green Version]
  49. Martinez-Martin, P.; Rizos, A.M.; Wetmore, J.B.; Antonini, A.; Odin, P.; Pal, S.; Sophia, R.; Carroll, C.; Martino, D.; Falup-Pecurariu, C.; et al. Relationship of Nocturnal Sleep Dysfunction and Pain Subtypes in Parkinson’s Disease. Mov. Disord. Clin. Pr. 2019, 6, 57–64. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  50. Matei, D.; Luca, C.; Andritoi, D.; Fuior, R.; Zaharia, D.; Onu, I.; Corciova, C. Autonomic dysfunction and peripheral nerve involvement in patients with Parkinson’s disease. Balneo Res. J. 2019, 10, 55–61. [Google Scholar] [CrossRef]
  51. Romosan, A.M.; Dehelean, L.; Romosan, R.S.; Andor, M.; Bredicean, A.C.; Simu, M.A. Affective theory of mind in parkinson’s disease: The effect of cognitive performance. Neuropsychiatr. Dis. Treat. 2019, 15, 2521–2535. [Google Scholar] [CrossRef] [Green Version]
  52. Szász, J.A.; Constantin, V.A.; Orbán-Kis, K.; Rácz, A.; Arianabancu, L.; Georgescu, D.; Szederjesi, J.; Mihály, I.; Fárr, A.M.; Kelemen, K.; et al. Profile of patients with advanced parkinson’s disease suitable for device-aided therapies: Restrospective data of a large cohort of romanian patients. Neuropsychiatr. Dis. Treat. 2019, 15, 3187–3195. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Vanta, O.M.; Pintea, S.; Perju-Dumbrava, L. The impact of associated large-fiber peripheral neuropathy on health-related quality of life in Parkinson’s disease—Results from a romanian cohort. Rom. J. Neurol. Rev. Romana Neurol. 2019, 18, 167–173. [Google Scholar]
  54. Vanta, O.M.; Tohanean, N.; Pintea, S.; Perju-Dumbrava, L. Large-Fiber Neuropathy in Parkinson’s Disease: Clinical, Biological, and Electroneurographic Assessment of a Romanian Cohort. J. Clin. Med. 2019, 8, 1533. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Ciopleias, B.; Al-Masri, N.; Torok, T.; Diaconu, S.; Gioroc, R.; Zosin, R.; Falup-Pecurariu, C.G. Autonomic dysfunctions in males with Parkinson’s disease: Case control study. Eur. J. Neurol. 2020, 27, 534. [Google Scholar]
  56. Diaconu, S.; Maceasa, A.; Ciopleias, B.; Zosin, R.; Falup-Pecurariu, C. Nutrient patterns in Parkinson’s disease: A case-control study. Mov. Disord. 2020, 35, S558. [Google Scholar]
  57. Szász, J.A.; Szatmari, S.; Constantin, V.; Mihaly, I.; Racz, A.; Torok, I.; Nagy, E.; Kelemen, K.; Forro, T.; Baroti, B.; et al. The importance of evaluation of gastrointestinal symptoms in advanced Parkinson’s disease. Orv. Hetil. 2020, 161, 1681–1687. [Google Scholar] [CrossRef]
  58. Muntean, M.L.; Tohanean, N.; Perju-Dumbrava, L. Pain and night time sleep disturbances assessed by bedside questionnaires in Parkinson’s disease patients. Eur. J. Neurol. 2010, 17, 396. [Google Scholar]
  59. Szasz, J.; Constantin, V.; Szatmari, S.; Bancu, L.; Georgescu, D.; Szederjesi, J.; Ciorba, M.; Racz, A.; Mihaly, I.; Orban, K. Possible correlations between symptoms suggesting gastroparesis and dyskinesias in advanced Parkinson’s disease. Mov. Disord. 2020, 35, S353–S354. [Google Scholar]
  60. Martinez-Martin, P.; Falup-Pecurariu, C.; Rodriguez-Blazquez, C.; van Hilten, B.; Odin, P.; Tluk, S.; Naidu, Y.; Chaudhuri, K.R.; Grp, E. Parkinson’s disease staging based of the non-motor symptoms scale. Parkinsonism Relat. Disord. 2009, 15, S66. [Google Scholar] [CrossRef]
  61. Martinez-Martin, P.; Rodriguez-Blazquez, C.; Abe, K.; Bhattacharyya, K.B.; Bloem, B.R.; Carod-Artal, F.J.; Prakash, R.; Esselink, R.A.J.; Falup-Pecurariu, C.; Gallardo, M.; et al. International study on the psychometric attributes of the Non-Motor Symptoms Scale in Parkinson disease. Neurology 2009, 73, 1584–1591. [Google Scholar] [CrossRef]
  62. Martinez-Martin, P.; Rodriguez-Blazquez, C.; Carod-Artal, J.; Falup-Pecurariu, C.; Serrano-Duenas, M. Measuring cognitive deterioration in Parkinson’s disease with the SCOPA-COG. Results of an international study. Eur. J. Neurol. 2009, 16, 521. [Google Scholar]
  63. Kraus, P.H.; Hoffmann, A.; Nirnberger, G.; Ipatov, M.; Schlegelmilch, I. Spiralometry is a valuable technique for control of kinetic tremor in large multicentre studies. Mov. Disord. 2011, 26, S133. [Google Scholar]
  64. Martinez-Martin, P.; Falup-Pecurariu, C.; Rodriguez-Blazquez, C.; Serrano-Dueñas, M.; Carod Artal, F.J.; Rojo Abuin, J.M.; Aarsland, D. Dementia associated with Parkinson’s disease: Applying the Movement Disorder Society Task Force criteria. Parkinsonism Relat. Disord. 2011, 17, 621–624. [Google Scholar] [CrossRef] [PubMed]
  65. Geman, O.; Zamfir, C. Using Wavelet for Early Detection of Pathological Tremor. In Proceedings of the 20th European Signal Processing Conference, EUSIPCO 2012, Bucharest, Romania, 27–31 August 2012; pp. 1723–1727. [Google Scholar]
  66. Popa, L.; Bolbocean, O.; Ignat, B.; Popescu, C.D. Transcranial magnetic stimulation assessment of functional electrical stimulation effect on Parkinson’s disease patients. Eur. J. Neurol. 2012, 19, 679. [Google Scholar]
  67. Popa, L.; Constantinescu, A.; Popescu, C.D. Differences of cortical excitability between parkinson’s disease patients and healthy subjects. A comparative TMS study. Rom. J. Neurol. Rev. Romana Neurol. 2012, 11, 38–43. [Google Scholar]
  68. Ungurean, I.; Gaitan, N.C. Speech analysis for medical predictions based on Cell Broadband Engine. In Proceedings of the 20th European Signal Processing Conference, EUSIPCO 2012, Bucharest, Romania, 27–31 August 2012; pp. 1733–1736. [Google Scholar]
  69. Alexa, D.; Alexa, L.; Popa, L.; Nicolae Paduraru, D.; Ignat, B.; Constantinescu, A.; Baltag, D.; Rotar, A.; Dinu Popescu, C. Brainstem auditory evoked potentials in Parkinson’s disease. Rom. J. Neurol. Rev. Romana Neurol. 2013, 12, 198–201. [Google Scholar]
  70. Geman, O. Nonlinear dynamics, artificial neural networks and neuro-fuzzy classifier for automatic assessing of tremor severity. In Proceedings of the 4th IEEE International Conference on E-Health and Bioengineering, EHB 2013, Iasi, Romania, 21–23 November 2013. [Google Scholar]
  71. Geman, O.; Costin, H. Parkinson’s disease prediction based on multistate markov models. Int. J. Comput. Commun. Control 2013, 8, 525–537. [Google Scholar]
  72. Geman, O.; Turcu, C.O.; Graur, A. Parkinson’s disease Assessment using Fuzzy Expert System and Nonlinear Dynamics. Adv. Electr. Comput. Eng. 2013, 13, 41–46. [Google Scholar] [CrossRef]
  73. Fazakas, Z.; Tilinca, M.; Nemes-Nagy, E.; Tripon, R.; Kovacs, Z.; Şuş, I.; Kocsis, K.K.; Sǎmǎrghitan, V.B. Arylsulphatase a—A possible important determinant in the pathophysiology of metabolic and neuropsychiatric diseases. Ann. Rom. Soc. Cell Biol. 2013, 18, 80–84. [Google Scholar]
  74. Pohoaţǎ, S.; Graur, A. HDTV system for parkinson’s disease diagnosis. Adv. Electr. Comput. Eng. 2013, 13, 91–96. [Google Scholar] [CrossRef]
  75. Geman, O.; Costin, H. Automatic assessing of tremor severity using nonlinear dynamics, artificial neural networks and neuro-fuzzy classifier. Adv. Electr. Comput. Eng. 2014, 14, 133–138. [Google Scholar] [CrossRef]
  76. Geman, O.; Sanei, S.; Chiuchisan, I.; Graur, A.; Prochazka, A.; Vysata, O. Towards an inclusive Parkinson’s screening system. In Proceedings of the 18th International Conference on System Theory, Control and Computing, ICSTCC 2014, Sinaia, Romania, 17–19 October 2014; pp. 470–475. [Google Scholar]
  77. Chaudhuri, K.R.; Rizos, A.; Trenkwalder, C.; Rascol, O.; Pal, S.; Martino, D.; Carroll, C.; Paviour, D.; Falup-Pecurariu, C.; Kessel, B.; et al. King’s Parkinson’s disease pain scale, the first scale for pain in PD: An international validation. Mov. Disord. 2015, 30, 1623–1631. [Google Scholar] [CrossRef] [Green Version]
  78. Onu, M.; Badea, L.; Roceanu, A.; Tivarus, M.; Bajenaru, O. Increased connectivity between sensorimotor and attentional areas in Parkinson’s disease. Neuroradiology 2015, 57, 957–968. [Google Scholar] [CrossRef] [PubMed]
  79. Biundo, R.; Weis, L.; Bostantjopoulou, S.; Stefanova, E.; Falup-Pecurariu, C.; Kramberger, M.G.; Geurtsen, G.J.; Antonini, A.; Weintraub, D.; Aarsland, D. MMSE and MoCA in Parkinson’s disease and dementia with Lewy bodies: A multicenter 1-year follow-up study. J. Neural Transm. 2016, 123, 431–438. [Google Scholar] [CrossRef] [Green Version]
  80. Fiorenzato, E.; Weis, L.; Falup-Pecurariu, C.; Diaconu, S.; Siri, C.; Reali, E.; Pezzoli, G.; Bisiacchi, P.; Antonini, A.; Biundo, R. Montreal Cognitive Assessment (MoCA) and Mini-Mental State Examination (MMSE) performance in progressive supranuclear palsy and multiple system atrophy. J. Neural Transm. 2016, 123, 1435–1442. [Google Scholar] [CrossRef]
  81. Geman, O.; Chiuchisan, I.; Covasa, M.; Eftaxias, K.; Sanei, S.; Madeira, J.G.F.; Boloy, R.A.M. Joint EEG—EMG signal processing for identification of the mental tasks in patients with neurological diseases. In Proceedings of the 24th European Signal Processing Conference, EUSIPCO 2016, Budapest, Hungary, 28 August–2 September 2016; pp. 1598–1602. [Google Scholar]
  82. Toderean, R.; Geman, O.; Chiuchisan, I.; Lazar, A.M. A Comparison between Healthy and Neurological Disorders Patients using Nonlinear Dynamic Tools. In Proceedings of the 9th International Conference and Exposition on Electrical and Power Engineering (EPE), Iasi, Romania, 20–22 October 2016; pp. 299–303. [Google Scholar]
  83. Tohănean, N.; Perju-Dumbravă, L. The contribution of transcranial sonographic examination to the diagnosis of Parkinson’s disease. Hum. Vet. Med. 2016, 8, 5–9. [Google Scholar]
  84. Badea, L.; Onu, M.; Wu, T.; Roceanu, A.; Bajenaru, O. Exploring the reproducibility of functional connectivity alterations in Parkinson’s disease. PLoS ONE 2017, 12, e0197121. [Google Scholar] [CrossRef] [Green Version]
  85. Bajenaru, O.L.; Ene, A.; Ribigan, A.; Terecoasa, E.; Tiu, C.; Bajenaru, O.A. Study of the role of vitamin d and insulin resistance in patients with parkinson’s disease. Parkinsonism Relat. Disord. 2018, 46, E71. [Google Scholar] [CrossRef]
  86. Geman, O.; Chiuchisan, I. Response Surface Model Prediction of Deep Brain Stimulation Applied in Parkinson’s Disease Tremor. In Proceedings of the 10th International Conference and Expositions on Electrical And Power Engineering, EPE 2018, Iasi, Romania, 18–19 October 2018; pp. 703–707. [Google Scholar]
  87. Martinez-Martin, P.; Rizos, A.M.; Wetmore, J.; Antonini, A.; Odin, P.; Pal, S.; Sophia, R.; Carroll, C.; Martino, D.; Falup-Pecurariu, C.; et al. First comprehensive tool for screening pain in Parkinson’s disease: The King’s Parkinson’s Disease Pain Questionnaire. Eur. J. Neurol. 2018, 25, 1255–1261. [Google Scholar] [CrossRef] [PubMed]
  88. Stocchi, F.; Radicati, F.G.; Chaudhuri, K.R.; Johansson, A.; Padmakumar, C.; Falup-Pecurariu, C.; Martinez-Martin, P. The Parkinson’s Disease Composite Scale: Results of the first validation study. Eur. J. Neurol. 2018, 25, 503–511. [Google Scholar] [CrossRef] [PubMed]
  89. Toderean Aldea, R.; Geman, O.; Chiuchisan, I.; Balas, V.E.; Beiu, V. Novel method for neurodegenerative disorders screening patients using hurst coefficients on EEG delta rhythm. In Proceedings of the 7th International Workshop on Soft Computing Applications, SOFA 2016, Arad, Romania, 24–26 August 2018; pp. 349–358. [Google Scholar]
  90. Balestrino, R.; Hurtado-Gonzalez, C.A.; Stocchi, F.; Radicati, F.G.; Chaudhuri, K.R.; Rodriguez-Blazquez, C.; Martinez-Martin, P.; Adarmes, A.D.; Méndez-del-Barrio, C.; Ariadne, V.; et al. Applications of the European Parkinson’s Disease Association sponsored Parkinson’s Disease Composite Scale (PDCS). NPJ Parkinson Dis. 2019, 5, 26. [Google Scholar] [CrossRef] [PubMed]
  91. Cuciureanu, D.I.; Popescu, R.M.; Cuciureanu, T.; Constantinescu, V.A.; Hodorog, D.N.; Szalontay, A.S. Dopaminergic centers neurodegeneration biochemical and radiologic approach. Rev. Chim. 2019, 70, 1835–1838. [Google Scholar] [CrossRef]
  92. Martinez-Martin, P.; Radicati, F.G.; Rodriguez Blazquez, C.; Wetmore, J.; Kovacs, N.; Ray Chaudhuri, K.; Stocchi, F.; Vuletic, V.; Falup-Pecurariu, C.; Diaconu, Ş.; et al. Extensive validation study of the Parkinson’s Disease Composite Scale. Eur. J. Neurol. 2019, 26, 1281–1288. [Google Scholar] [CrossRef]
  93. Aldred, J.; Anca-Herschkovitsch, M.; Antonini, A.; Bajenaru, O.; Bergmann, L.; Bourgeois, P.; Cubo, E.; Davis, T.L.; Iansek, R.; Kovacs, N.; et al. Application of the ‘5-2-1’ screening criteria in advanced Parkinson’s disease: Interim analysis of DUOGLOBE. Neurodegener. Dis. Manag. 2020, 10, 309–323. [Google Scholar] [CrossRef]
  94. Geroin, C.; Artusi, C.A.; Gandolfi, M.; Zanolin, E.; Ceravolo, R.; Capecci, M.; Andrenelli, E.; Ceravolo, M.G.; Bonanni, L.; Onofrj, M.; et al. Does the Degree of Trunk Bending Predict Patient Disability, Motor Impairment, Falls, and Back Pain in Parkinson’s Disease? Front. Neurol. 2020, 11, 207. [Google Scholar] [CrossRef]
  95. Arseni, C.; Iacob, M.; Simionescu, M. Stereotaxia in extrapyramidal diseases. Neurologia 1973, 18, 525–538. [Google Scholar]
  96. Pendefunda, G.; Pollingher, B.; Stefanache, F. The treatment of Parkinson’s syndrome with levodopa and amantadine. Neurologia 1973, 18, 559–568. [Google Scholar]
  97. Pendefunda, G.; Pollingher, B.; Stefanache, F. The treatment with l dopa and amantadine in Parkinson’s disease. Ther. Hung. 1975, 23, 12–16. [Google Scholar]
  98. Cinca, I.; Bulandra, R.; Serbanesco, A.; Ninosu, N. Current medical therapy of Parkinsonian syndromes. Rev. Roum. Neurol. 1973, 10, 257–285. [Google Scholar]
  99. Minea, D.; Varga, I.; Falup-Pěcurariu, C.; De Mey, C.; Retzow, A.; Althaus, M. Influence of the dopamine agonist α-dihydroergocryptine on the pharmacokinetics of levodopa in patients with Parkinson’s disease. Clin. Neuropharmacol. 2001, 24, 235–238. [Google Scholar] [CrossRef] [PubMed]
  100. Baltag, D.; Ignat, B.; Manole, O.Z. Secondary effects of chronic treatment with levodopa in Parkinson disease. Rev. Med. Chir. A Soc. Med. Nat. Iasi 2003, 107, 131–135. [Google Scholar]
  101. Olanow, C.W.; Damier, P.; Goetz, C.G.; Mueller, T.; Nutt, J.; Rascol, O.; Serbanescu, A.; Deckers, F.; Russ, H. Multicenter, Open-Label, Trial of Sarizotan in Parkinson Disease Patients with Levodopa-Induced Dyskinesias (the SPLENDID Study). Clin. Neuropharmacol. 2004, 27, 58–62. [Google Scholar] [CrossRef]
  102. Ferreira, J.J.; Almeida, L.; Cunha, L.; Ticmeanu, M.; Rosa, M.M.; Januário, C.; Mitu, C.E.; Coelho, M.; Correia-Guedes, L.; Morgadinho, A.; et al. Effects of nebicapone on levodopa pharmacokinetics, catechol-O- methyltransferase activity, and motor fluctuations in patients with Parkinson disease. Clin. Neuropharmacol. 2008, 31, 2–18. [Google Scholar] [CrossRef] [PubMed]
  103. Borgohain, R.; Szasz, J.; Bhatt, M.; Rossetti, S.; Lucini, V.; Anand, R.; Study, I. Safinamide as an adjunct to levodopa significantly improved motor fluctuations in Parkinson’s disease: A phase III, randomized, double-blind, placebo-controlled study. Parkinsonism Relat. Disord. 2009, 15, S115. [Google Scholar]
  104. Szasz, J.; Borgohain, R.; Bhatt, M.; Rossetti, S.; Lucini, V.; Anand, R.; Study, I. Improvements in symptom severity and daily living with safinamide in Parkinson’s disease: A phase III, randomized, double-blind, placebo-controlled study. Parkinsonism Relat. Disord. 2009, 15, S118. [Google Scholar] [CrossRef]
  105. Bhatt, M.; Chirileanu, D.; Meshram, C.; Stanzione, P.; Forrest, E.C.; Lucini, V.; Study, I. Effect of Safinamide on Dyskinesia in Patients with Mid- to Late-Stage Parkinson’s Disease: Data from a Post Hoc Analysis. Mov. Disord. 2010, 25, S676. [Google Scholar]
  106. Kaufmann, H.; Mathias, C.; Low, P.; Biaggioni, I.; Freeman, R. Experience with droxidopa (NortheraTM) in a phase III multinational, placebo-controlled, parallel group, induction-design study to assess clinical benefit and safety in subjects with neurogenic orthostatic hypotension. Clin. Auton. Res. 2010, 20, 295. [Google Scholar]
  107. Meshram, C.; Bhatt, M.; Chirileanu, D.; Stanzione, P.; Lucini, V.; Rossetti, S.; Anand, R.; Study, I. Safinamide improves motor function without worsening troublesome dyskinesia as add-on therapy in L-DOPA-treated patients with mid- to late-stage Parkinson’s disease (PD). Eur. J. Neurol. 2010, 17, 99. [Google Scholar]
  108. Vasile, D.; Vasiliu, O. Management of Cognitive Symptoms in Dementia Associated with Parkinson’s Disease. In Proceedings of the World Medical Conference, Malta, 15–17 December 2010; pp. 284–286. [Google Scholar]
  109. Borgohain, R.; Szasz, J.; Stanzione, P.; Meshram, C.; Bhatt, M.; Stocchi, F.; Lucini, V.; Anand, R.; Study, I. Results from the first 2-year, controlled study to assess safinamide as add-on to l-dopa in patients with parkinson’s disease and motor fluctuations. Eur. J. Neurol. 2011, 18, 20. [Google Scholar]
  110. Meshram, C.; Borgohain, R.; Bhatt, M.; Chirileanu, D.; Stocchi, F.; Lucini, V.; Giuliani, R.; Anand, R.; Study, I. Two-year, placebo-controlled safety and tolerability data for safinamide as add-on to l-dopa in patients with parkinson’s disease. Eur. J. Neurol. 2011, 18, 232–233. [Google Scholar]
  111. Vasile, D.; Vasiliu, O.; Mangalagiu, A.G.; Blandu, M.; Nanca, A. Comparative efficacy of cholinesterase inhibitors in dementia associated with Parkinson’s disease. Int. J. Neuropsychopharmacol. 2012, 15, 174. [Google Scholar] [CrossRef]
  112. Popa, L.; Constantinescu, A.; Mureşanu, D.F.; Irimie, A.; Bǎlǎnescu, N.R.; Popescu, C.D. Clinical improvement and cortical adaptations after functional electrical stimulation in parkinson’s disease patients. CNS Neurol. Disord. Drug Targets 2013, 12, 265–273. [Google Scholar] [CrossRef] [PubMed]
  113. Vasile, D.; Macovei, R.A.; Vasiliu, O. Efficacy and tolerability of bupropion in major depressive disorder associated with Parkinson’s disease. Eur. Neuropsychopharmacol. 2013, 23, S322. [Google Scholar] [CrossRef]
  114. Baetu, C.; Buraga, I. Levodopa/carbidopa intestinal gel pump treatment in patients with advanced Parkinson’s disease—From Romanian experience. Mov. Disord. 2014, 29, S227. [Google Scholar]
  115. Borgohain, R.; Szasz, J.; Stanzione, P.; Meshram, C.; Bhatt, M.; Chirilineau, D.; Stocchi, F.; Lucini, V.; Giuliani, R.; Forrest, E.; et al. Randomized trial of safinamide add-on to levodopa in Parkinson’s disease with motor fluctuations. Mov. Disord. 2014, 29, 229–237. [Google Scholar] [CrossRef] [PubMed]
  116. Borgohain, R.; Szasz, J.; Stanzione, P.; Meshram, C.; Bhatt, M.H.; Chirilineau, D.; Stocchi, F.; Lucini, V.; Giuliani, R.; Forrest, E.; et al. Two-Year, randomized, controlled study of safinamide as add-on to levodopa in mid to late Parkinson’s disease. Mov. Disord. 2014, 29, 1273–1280. [Google Scholar] [CrossRef] [PubMed]
  117. Hauser, R.A.; Olanow, C.W.; Kieburtz, K.D.; Pourcher, E.; Docu-Axelerad, A.; Lew, M.; Kozyolkin, O.; Neale, A.; Resburg, C.; Meya, U.; et al. Tozadenant (SYN115) in patients with Parkinson’s disease who have motor fluctuations on levodopa: A phase 2b, double-blind, randomised trial. Lancet Neurol. 2014, 13, 767–776. [Google Scholar] [CrossRef]
  118. Baetu, C.; Buraga, I.; Buraga, M.; Mihailescu, G.; Petre, V. Complications related to levodopa/carbidopa intestinal gel treatment colentina hospital experience. J. Neurol. Sci. 2015, 357, E256. [Google Scholar] [CrossRef]
  119. Trenkwalder, C.; Chaudhuri, K.R.; Martinez-Martin, P.; Rascol, O.; Ehret, R.; Vališ, M.; Sátori, M.; Krygowska-Wajs, A.; Marti, M.J.; Reimer, K.; et al. Prolonged-release oxycodone-naloxone for treatment of severe pain in patients with Parkinson’s disease (PANDA): A double-blind, randomised, placebo-controlled trial. Lancet Neurol. 2015, 14, 1161–1170. [Google Scholar] [CrossRef]
  120. Băjenaru, O.; Ene, A.; Popescu, B.O.; Szász, J.A.; Sabău, M.; Mureşan, D.F.; Perju-Dumbrava, L.; Popescu, C.D.; Constantinescu, A.; Buraga, I.; et al. The effect of levodopa–carbidopa intestinal gel infusion long-term therapy on motor complications in advanced Parkinson’s disease: A multicenter Romanian experience. J. Neural Transm. 2016, 123, 407–414. [Google Scholar] [CrossRef] [Green Version]
  121. Crăciun, E.C.; Dronca, E.; Leach, N.V. Antioxidant enzymes activity in subjects with Parkinson’s disease under L-DOPA therapy. Hum. Vet. Med. 2016, 8, 124–127. [Google Scholar]
  122. Dogaru, G.; Muresan, D.; Stanescu, I.; Motricala, M.; Akos, M. The therapeutic benefits of natural therapeutic factors in Baile Tusnad for the rehabilitation of patients with Parkinson’s disease. Balneo Res. J. 2016, 7, 116–124. [Google Scholar] [CrossRef]
  123. Kenney, C.; Kieburtz, K.; Olanow, W.; Bandak, S. Regional differences in the results of a phase 2b study of tozadenant in Parkinson’s disease patients with motor fluctuations. Mov. Disord. 2016, 31 (Suppl. S2), S693. [Google Scholar]
  124. Rizos, A.; Sauerbier, A.; Antonini, A.; Weintraub, D.; Martinez-Martin, P.; Kessel, B.; Henriksen, T.; Falup-Pecurariu, C.; Silverdale, M.; Durner, G.; et al. A European multicentre survey of impulse control behaviours in Parkinson’s disease patients treated with short- and long-acting dopamine agonists. Eur. J. Neurol. 2016, 23, 1255–1261. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  125. Antonini, A.; Poewe, W.; Chaudhuri, K.R.; Jech, R.; Pickut, B.; Pirtošek, Z.; Szasz, J.; Valldeoriola, F.; Winkler, C.; Bergmann, L.; et al. Levodopa-carbidopa intestinal gel in advanced Parkinson’s: Final results of the GLORIA registry. Parkinsonism Relat. Disord. 2017, 45, 13–20. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  126. Chaudhuri, K.R.; Antonini, A.; Poewe, W.; Standaert, D.; Odin, P.; Zamudio, J.; Bergmann, L. A long-term study on effectiveness of levodopa-carbidopa intestinal gel treatment in advanced Parkinson’s disease patients. Mov. Disord. 2017, 32 (Suppl. S2), 952. [Google Scholar]
  127. Muller, T.; Tolosa, E.; Badea, L.; Asgharnejad, M.; Grieger, F.; Markowitz, M.; Nonfondaz, X.; Bauer, L.; Timmermann, L. An observational study of rotigotine transdermal patch and other currently prescribed therapies in patients with Parkinson’s disease. Eur. J. Neurol. 2017, 24, 394–395. Available online: https://apps.webofknowledge.com/full_record.do?product=WOS&search_mode=GeneralSearch&qid=12&SID=5FoVfRjUX9FVKjgvKMl&page=1&doc=1 (accessed on 26 May 2021). [CrossRef] [PubMed]
  128. Szász, J.A.; Constantin, V.; Fazakas, P.A.; Blényesi, E.; Grieb, L.G.; Balla, A.; Sárig, M.; Szegedi, K.; Bartha, E.N.; Szatmári, S. The role of selective monoamine oxidase B inhibitors in the therapeutic strategy of Parkinson’s disease in the neurology clinics of Tirgu Mures County Emergency Clinical Hospital. Orv. Hetil. 2017, 158, 2023–2028. [Google Scholar] [CrossRef]
  129. Müller, T.; Tolosa, E.; Badea, L.; Asgharnejad, M.; Grieger, F.; Markowitz, M.; Nondonfaz, X.; Bauer, L.; Timmermann, L. An observational study of rotigotine transdermal patch and other currently prescribed therapies in patients with Parkinson’s disease. J. Neural Transm. 2018, 125, 953–963. Available online: https://www.scopus.com/record/display.uri?eid=2-s2.0-85042524722&doi=10.1007%2fs00702-018-1860-x&origin=inward&txGid=e695ab90c3ab4d9a10e2b625ad350dd5&featureToggles=FEATURE_NEW_MAIN_SECTION:1,FEATURE_NEW_SOURCE_INFO:1,FEATURE_NEW_REAXYS_SECTION:1,FEATURE_NEW_SCIVAL_TOPICS:1,FEATURE_VIEWS_COUNT:1 (accessed on 26 May 2021). [CrossRef]
  130. Breda, X.M.; Fodor, D.M.; Verdes, R.; Tartamus, D.; Muresan, D.A.; Stanescu, I.C.; Capusan, C.; Dumbrava Perju, L. The Mozart effect combined with specific kinetic treatment in patients with Parkinson’s disease. Balneo Res. J. 2019, 10, 294–299. [Google Scholar] [CrossRef]
  131. Criciotoiu, O.; Stanca, D.I.; Glavan, D.G.; Mirea, C.S.; Mita, A.; Calborean, V.; Gheorman, V.; Udristoiu, I.; Dijmarescu, A.L.; Davitoiu, D.V.; et al. Statistical analysis between the routes of administration of L-DOPA and digestive dysfunctions in Parkinson disease. Rev. Chim. 2019, 70, 1403–1405. [Google Scholar] [CrossRef]
  132. Fasano, A.; Parra, J.C.; Gurevich, T.; Jech, R.; Kovacs, N.; Per, S.; Szasz, J.; Bergmann, L.; Johnson, A.; Sanchez-Solino, O.; et al. Utilization of monotherapy and combination therapies in advanced Parkinson’s disease patients during levodopa-carbidopa intestinal gel treatment from the cosmos study. J. Neurol. Sci. 2019, 405, 104857. [Google Scholar] [CrossRef] [Green Version]
  133. Nemes, B.O.; Pirlog, R.; Tartamus, D.; Capusan, C.; Fodor, D.M. The role of dance therapy in the rehabilitation of Parkinson disease patients. Balneo Res. J. 2019, 10, 300–304. [Google Scholar] [CrossRef]
  134. Petrescu, B.; Vasile, D.; Vasiliu, O.; Mangalagiu, A.; Candea, C.; Riga, D.; Riga, S.; Mitrache, A. Management of psychosis with quetiapine in Alzheimer type dementia and Parkinson type dementia. Eur. Neuropsychopharmacol. 2019, 29, S134–S135. [Google Scholar] [CrossRef]
  135. Szász, J.A.; Orbán-Kis, K.; Constantin, V.A.; Péter, C.; Bíró, I.; Mihály, I.; Szegedi, K.; Balla, A.; Szatmári, S. Therapeutic strategies in the early stages of Parkinson’s disease: A cross-sectional evaluation of 15 years’ experience with a large cohort of Romanian patients. Neuropsychiatr. Dis. Treat. 2019, 15, 831–838. [Google Scholar] [CrossRef] [Green Version]
  136. Szász, J.A.; Szatmári, S.; Constantin, V.; Mihály, I.; Rácz, A.; Domokos, L.C.; Vajda, T.; Orbán-Kis, K. Characteristics of levodopa treatment in advanced Parkinson’s disease in the experiences of the neurology clinics of Târgu Mureș, Romania. Orv. Hetil. 2019, 160, 662–669. [Google Scholar] [CrossRef] [PubMed]
  137. Szász, J.A.; Viorelia, C.; Mihály, I.; Biró, I.; Péter, C.; Orbán-Kis, K.; Szatmári, S. Dopamine agonists in Parkinson’s disease therapy—15 years of experience of the Neurological Clinics from Tîrgu Mureș. A cross-sectional study. Ideggyogy Sz 2019, 72, 187–193. [Google Scholar] [CrossRef] [PubMed]
  138. Constantin, V.A.; Szász, J.A.; Orbán-Kis, K.; Rosca, E.C.; Popovici, M.; Cornea, A.; Bancu, L.A.; Ciorba, M.; Mihály, I.; Nagy, E.; et al. Levodopa-carbidopa intestinal gel infusion therapy discontinuation: A ten-year retrospective analysis of 204 treated patients. Neuropsychiatr. Dis. Treat. 2020, 16, 1835–1844. [Google Scholar] [CrossRef] [PubMed]
  139. Popa, L.C.; Leucuta, D.C.; Tohanean, N.; Popa, S.L.; Perju-Dumbrava, L. Intrajejunal vs oral levodopa-carbidopa therapy in Parkinson disease: A retrospective cohort study. Medicine 2020, 99, e23249. [Google Scholar] [CrossRef]
  140. Popa, L.C.; Leucuta, D.C.; Tohanean, N.; Popa, S.L.; Perju-Dumbrava, L. Levodopa-carbidopa intestinal gel therapy in parkinson’s disease: Procedure complications. Rom. J. Neurol. Rev. Romana Neurol. 2020, 19, 84–88. [Google Scholar] [CrossRef]
  141. Rizos, A.; Sauerbier, A.; Falup-Pecurariu, C.; Odin, P.; Antonini, A.; Martinez-Martin, P.; Kessel, B.; Henriksen, T.; Silverdale, M.; Durner, G.; et al. Tolerability of non-ergot oral and transdermal dopamine agonists in younger and older Parkinson’s disease patients: An European multicentre survey. J. Neural Transm. 2020, 127, 875–879. [Google Scholar] [CrossRef]
  142. Szasz, J.; Simu, M.; Perju-Dumbrava, L.; Antonini, A.; Bergmann, L.; Popescu, D.; Bajenaru, O.A. Efficacy, safety and patient’s quality of life of long-term treatment with levodopa-carbidopa intestinal gel in advanced parkinson’s disease in romania: Results from gloria observational study. Rom. J. Neurol. Rev. Romana Neurol. 2020, 19, 27–35. [Google Scholar] [CrossRef]
  143. Fasano, A.; Parra, J.C.; Gurevich, T.; Jech, R.; Kovacs, N.; Svenningsson, P.; Szasz, J.; Bergmann, L.; Sanchez-Solino, O.; Vela-Desojo, L. Improvements in motor symptoms in patients with advanced Parkinson’s disease on long-term LCIG monotherapy or combination therapy: An analysis of the COSMOS observational study. Eur. J. Neurol. 2020, 27, 662–663. [Google Scholar]
  144. De Palma, G.; Dick, F.D.; Calzetti, S.; Scott, N.W.; Prescott, G.J.; Osborne, A.; Haites, N.; Mozzoni, P.; Negrotti, A.; Scaglioni, A.; et al. A case-control study of Parkinson’s disease and tobacco use: Gene-tobacco interactions. Mov. Disord. 2010, 25, 912–919. [Google Scholar] [CrossRef] [PubMed]
  145. Dick, F.D.; De Palma, G.; Ahmadi, A.; Osborne, A.; Scott, N.W.; Prescott, G.J.; Bennett, J.; Semple, S.; Dick, S.; Mozzoni, P.; et al. Gene-environment interactions in parkinsonism and Parkinson’s disease: The Geoparkinson study. Occup. Environ. Med. 2007, 64, 673–680. [Google Scholar] [CrossRef] [Green Version]
  146. Dick, F.D.; De Palma, G.; Ahmadi, A.; Scott, N.W.; Prescott, G.J.; Bennett, J.; Semple, S.; Dick, S.; Counsell, C.; Mozzoni, P.; et al. Environmental risk factors for Parkinson’s disease and parkinsonism: The Geoparkinson study. Occup. Environ. Med. 2007, 64, 666–672. [Google Scholar] [CrossRef] [Green Version]
  147. Naghavi, M.; Wang, H.; Lozano, R.; Davis, A.; Liang, X.; Zhou, M.; Vollset, S.E.; Abbasoglu Ozgoren, A.; Abdalla, S.; Abd-Allah, F.; et al. Global, regional, and national age-sex specific all-cause and cause-specific mortality for 240 causes of death, 1990-2013: A systematic analysis for the Global Burden of Disease Study 2013. Lancet 2015, 385, 117–171. [Google Scholar]
  148. Hay, S.I.; Abajobir, A.A.; Abate, K.H.; Abbafati, C.; Abbas, K.M.; Abd-Allah, F.; Abdulle, A.M.; Abebo, T.A.; Abera, S.F.; Aboyans, V.; et al. Global, regional, and national disability-adjusted life-years (DALYs) for 333 diseases and injuries and healthy life expectancy (HALE) for 195 countries and territories, 1990–2016: A systematic analysis for the Global Burden of Disease Study 2016. Lancet 2017, 390, 1260–1344. [Google Scholar] [CrossRef] [Green Version]
  149. Naghavi, M.; Abajobir, A.A.; Abbafati, C.; Abbas, K.M.; Abd-Allah, F.; Abera, S.F.; Aboyans, V.; Adetokunboh, O.; Ärnlöv, J.; Afshin, A.; et al. Global, regional, and national age-sex specifc mortality for 264 causes of death, 1980–2016: A systematic analysis for the Global Burden of Disease Study 2016. Lancet 2017, 390, 1151–1210. [Google Scholar] [CrossRef] [Green Version]
  150. Vos, T.; Abajobir, A.A.; Abbafati, C.; Abbas, K.M.; Abate, K.H.; Abd-Allah, F.; Abdulle, A.M.; Abebo, T.A.; Abera, S.F.; Aboyans, V.; et al. Global, regional, and national incidence, prevalence, and years lived with disability for 328 diseases and injuries for 195 countries, 1990–2016: A systematic analysis for the Global Burden of Disease Study 2016. Lancet 2017, 390, 1211–1259. [Google Scholar] [CrossRef] [Green Version]
  151. Brodszky, V.; Beretzky, Z.; Baji, P.; Rencz, F.; Péntek, M.; Rotar, A.; Tachkov, K.; Mayer, S.; Simon, J.; Niewada, M.; et al. Cost-of-illness studies in nine Central and Eastern European countries. Eur. J. Health Econ. 2019, 20, 155–172. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  152. Canevelli, M.; Bruno, G.; Valletta, M.; Fabbrini, A.; Vanacore, N.; Berardelli, A.; Fabbrini, G. Parkinson’s disease among migrants in Europe: Estimating the magnitude of an emerging phenomenon. J. Neurol. 2019, 266, 1120–1126. [Google Scholar] [CrossRef]
  153. Feigin, V.L.; Nichols, E.; Alam, T.; Bannick, M.S.; Beghi, E.; Blake, N.; Culpepper, W.J.; Dorsey, E.R.; Elbaz, A.; Ellenbogen, R.G.; et al. Global, regional, and national burden of neurological disorders, 1990–2016: A systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol. 2019, 18, 459–480. [Google Scholar] [CrossRef] [Green Version]
  154. Emre, M.; Aarsland, D.; Brown, R.; Burn, D.J.; Duyckaerts, C.; Mizuno, Y.; Broe, G.A.; Cummings, J.; Dickson, D.W.; Gauthier, S.; et al. Clinical diagnostic criteria for dementia associated with Parkinson’s disease. Mov. Disord. 2007, 22, 1689–1707. [Google Scholar] [CrossRef] [PubMed]
  155. Litvan, I.; Goldman, J.G.; Tröster, A.I.; Schmand, B.A.; Weintraub, D.; Petersen, R.C.; Mollenhauer, B.; Adler, C.H.; Marder, K.; Williams-Gray, C.H.; et al. Diagnostic criteria for mild cognitive impairment in Parkinson’s disease: Movement Disorder Society Task Force guidelines. Mov. Disord. 2012, 27, 349–356. [Google Scholar] [CrossRef] [Green Version]
  156. Bloem, B.R.; Okun, M.S.; Klein, C. Parkinson’s disease. Lancet 2021, S0140-6736(21)00218-X, Epub ahead of print. [Google Scholar] [CrossRef]
  157. Schneider, S.A.; Alcalay, R.N. Precision medicine in Parkinson’s disease: Emerging treatments for genetic Parkinson’s disease. J. Neurol. 2020, 267, 860–869. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  158. Kaiyrzhanov, R.; Rizig, M.; Aitkulova, A.; Zharkinbekova, N.; Shashkin, C.; Kaishibayeva, G.; Karimova, A.; Khaibullin, T.; Sadykova, D.; Ganieva, M.; et al. Parkinson’s Disease in Central Asian and Transcaucasian Countries: A Review of Epidemiology, Genetics, Clinical Characteristics, and Access to Care. Parkinsons Dis. 2019, 2019, 2905739. [Google Scholar] [CrossRef] [PubMed]
  159. Khalil, H.; Peters, M.D.J.; Tricco, A.C.; Pollock, D.; Alexander, L.; McInerney, P.; Godfrey, C.M.; Munn, Z. Conducting high quality scoping reviews-challenges and solutions. J. Clin. Epidemiol. 2021, 130, 156–160. [Google Scholar] [CrossRef] [PubMed]
  160. Tong, A.; Palmer, S.; Craig, J.C.; Strippoli, G.F. A guide to reading and using systematic reviews of qualitative research. Nephrol. Dial. Transpl. 2016, 31, 897–903. [Google Scholar] [CrossRef] [Green Version]
Figure 1. PRISMA selection flowchart.
Figure 1. PRISMA selection flowchart.
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Figure 2. Different categories of Romanian studies.
Figure 2. Different categories of Romanian studies.
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Figure 3. Yearly trend (number of articles) in different types of studies.
Figure 3. Yearly trend (number of articles) in different types of studies.
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Figure 4. Number of studies by region.
Figure 4. Number of studies by region.
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Figure 5. Different topics assessed by the clinical research. Some studies investigated multiple clinical aspects. Abbreviations: BMI—body mass index.
Figure 5. Different topics assessed by the clinical research. Some studies investigated multiple clinical aspects. Abbreviations: BMI—body mass index.
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Figure 6. Research areas of the diagnostic studies. Abbreviations: TMS—transcranial magnetic stimulation.
Figure 6. Research areas of the diagnostic studies. Abbreviations: TMS—transcranial magnetic stimulation.
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Figure 7. Different pharmacological and non-pharmacological interventions were investigated in Romanian Parkinson’s disease patients. Abbreviations: LCIG—levodopa-carbidopa intestinal gel; MAO-B inhibitors—monoamine oxidase type B inhibitors.
Figure 7. Different pharmacological and non-pharmacological interventions were investigated in Romanian Parkinson’s disease patients. Abbreviations: LCIG—levodopa-carbidopa intestinal gel; MAO-B inhibitors—monoamine oxidase type B inhibitors.
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Figure 8. Epidemiological studies on Parkinson’s disease.
Figure 8. Epidemiological studies on Parkinson’s disease.
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Rosca, E.C.; Tudor, R.; Cornea, A.; Simu, M. Parkinson’s Disease in Romania: A Scoping Review. Brain Sci. 2021, 11, 709. https://doi.org/10.3390/brainsci11060709

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Rosca EC, Tudor R, Cornea A, Simu M. Parkinson’s Disease in Romania: A Scoping Review. Brain Sciences. 2021; 11(6):709. https://doi.org/10.3390/brainsci11060709

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Rosca, Elena Cecilia, Raluca Tudor, Amalia Cornea, and Mihaela Simu. 2021. "Parkinson’s Disease in Romania: A Scoping Review" Brain Sciences 11, no. 6: 709. https://doi.org/10.3390/brainsci11060709

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