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4 articles matched your search query. Search Parameters:
Authors = Nassim Kamar ORCID = 0000-0003-1930-8964

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NASSIM (8) , KAMAR (5)

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Open AccessArticle Quantification of HEV RNA by Droplet Digital PCR
Viruses 2016, 8(8), 233; doi:10.3390/v8080233
Received: 17 June 2016 / Revised: 13 August 2016 / Accepted: 16 August 2016 / Published: 19 August 2016
Cited by 3 | Viewed by 727 | PDF Full-text (538 KB) | HTML Full-text | XML Full-text
Abstract
The sensitivity of real-time PCR for hepatitis E virus (HEV) RNA quantification differs greatly among techniques. Standardized tools that measure the real quantity of virus are needed. We assessed the performance of a reverse transcription droplet digital PCR (RT-ddPCR) assay that gives absolute
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The sensitivity of real-time PCR for hepatitis E virus (HEV) RNA quantification differs greatly among techniques. Standardized tools that measure the real quantity of virus are needed. We assessed the performance of a reverse transcription droplet digital PCR (RT-ddPCR) assay that gives absolute quantities of HEV RNA. Analytical and clinical validation was done on HEV genotypes 1, 3 and 4, and was based on open reading frame (ORF)3 amplification. The within-run and between-run reproducibilities were very good, the analytical sensitivity was 80 HEV RNA international units (IU)/mL and linearities of HEV genotype 1, 3 and 4 were very similar. Clinical validation based on 45 samples of genotype 1, 3 or 4 gave results that correlated well with a validated reverse transcription quantitative PCR (RT-qPCR) assay (Spearman rs = 0.89, p < 0.0001). The RT-ddPCR assay is a sensitive method and could be a promising tool for standardizing HEV RNA quantification in various sample types. Full article
(This article belongs to the Special Issue Recent Progress in Hepatitis E Virus Research)
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Open AccessReview Treatment of HEV Infection in Patients with a Solid-Organ Transplant and Chronic Hepatitis
Viruses 2016, 8(8), 222; doi:10.3390/v8080222
Received: 28 June 2016 / Revised: 30 July 2016 / Accepted: 9 August 2016 / Published: 15 August 2016
Cited by 4 | Viewed by 733 | PDF Full-text (667 KB) | HTML Full-text | XML Full-text
Abstract
Hepatitis E virus (HEV) infection can cause hepatic and extra-hepatic manifestations. Treatment of HEV infection has been thoroughly studied in solid-organ-transplant patients who have developed a chronic HEV infection. In this review, we report on our current knowledge regarding treatment of HEV infection.
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Hepatitis E virus (HEV) infection can cause hepatic and extra-hepatic manifestations. Treatment of HEV infection has been thoroughly studied in solid-organ-transplant patients who have developed a chronic HEV infection. In this review, we report on our current knowledge regarding treatment of HEV infection. Full article
(This article belongs to the Special Issue Recent Progress in Hepatitis E Virus Research)
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Open AccessReview Hepatitis E Pathogenesis
Viruses 2016, 8(8), 212; doi:10.3390/v8080212
Received: 30 June 2016 / Revised: 22 July 2016 / Accepted: 27 July 2016 / Published: 5 August 2016
Cited by 6 | Viewed by 999 | PDF Full-text (3435 KB) | HTML Full-text | XML Full-text
Abstract
Although most hepatitis E virus (HEV) infections are asymptomatic, some can be severe, causing fulminant hepatitis and extra-hepatic manifestations, including neurological and kidney injuries. Chronic HEV infections may also occur in immunocompromised patients. This review describes how our understanding of the pathogenesis of
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Although most hepatitis E virus (HEV) infections are asymptomatic, some can be severe, causing fulminant hepatitis and extra-hepatic manifestations, including neurological and kidney injuries. Chronic HEV infections may also occur in immunocompromised patients. This review describes how our understanding of the pathogenesis of HEV infection has progressed in recent years. Full article
(This article belongs to the Special Issue Recent Progress in Hepatitis E Virus Research)
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Open AccessReview Pneumocystis Pneumonia in Solid-Organ Transplant Recipients
J. Fungi 2015, 1(3), 293-331; doi:10.3390/jof1030293
Received: 17 June 2015 / Revised: 1 September 2015 / Accepted: 2 September 2015 / Published: 28 September 2015
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Abstract
Pneumocystis pneumonia (PCP) is well known and described in AIDS patients. Due to the increasing use of cytotoxic and immunosuppressive therapies, the incidence of this infection has dramatically increased in the last years in patients with other predisposing immunodeficiencies and remains an important
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Pneumocystis pneumonia (PCP) is well known and described in AIDS patients. Due to the increasing use of cytotoxic and immunosuppressive therapies, the incidence of this infection has dramatically increased in the last years in patients with other predisposing immunodeficiencies and remains an important cause of morbidity and mortality in solid-organ transplant (SOT) recipients. PCP in HIV-negative patients, such as SOT patients, harbors some specificity compared to AIDS patients, which could change the medical management of these patients. This article summarizes the current knowledge on the epidemiology, risk factors, clinical manifestations, diagnoses, prevention, and treatment of Pneumocystis pneumonia in solid-organ transplant recipients, with a particular focus on the changes caused by the use of post-transplantation prophylaxis. Full article
(This article belongs to the Special Issue Fungal Infections in Transplant Recipients)

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