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  • Thalassemia Reports is published by MDPI from Volume 12 Issue 1 (2022). Previous articles were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence, and they are hosted by MDPI on mdpi.com as a courtesy and upon agreement with PAGEPress.

Thalassemia Reports, Volume 7, Issue 1

December 2017 - 11 articles

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Articles (11)

  • Article
  • Open Access
894 Views
4 Pages

Spontaneous Fertility in a Male Thalassemic Patient after Allogeneic Hematopoietic Cell Transplantation

  • Nicoletta Iacovidou,
  • Maria Kollia,
  • Emmeleia Nana,
  • Theodora Boutsikou,
  • Christos Savvidis,
  • Antonis Kattamis,
  • Dimitra Kyriakopoulou and
  • Vassilis Ladis

3 November 2017

Patients with thalassemia major who received allogeneic hematopoietic cell transplantation are at increased risk of gonadal insufficiency and reduced fertility due to the toxicity of both the transfusional iron overload and the gonadotoxic effects of...

  • Article
  • Open Access
1 Citations
947 Views
2 Pages

Improving Transfusion Practice in Transfusion Dependent Thalassaemia Patients

  • Chathupa Wickremaarachchi,
  • Elizabeth McGill,
  • Annmarie Bosco and
  • Giselee Kidson-Gerber

5 October 2017

The aim of this study was to improve current transfusion practice in transfusiondependent thalassaemia patients by determining whether safe transition from triplewashed red cells (TWRC) to leucodepleted red cells (LDRC), increasing transfusion rates,...

  • Article
  • Open Access
1,022 Views
4 Pages

Fast-Track Strategy for the Prevention of Hb Bart’s Hydrops Fetalis Syndrome

  • Narutchala Suwannakhon,
  • Khajohnsilp Pongsawatkul,
  • Teerapat Seeratanachot,
  • Wirawan Rasri,
  • Khwanruedee Mahingsa,
  • Arunee Pingyod,
  • Wanwipa Bumrungpakdee and
  • Torpong Sanguansermsri

2 October 2017

We propose a fast-track strategy [direct blood DNA analysis using a quantitative real-time polymerase chain reaction (PCR) technique] for the early risk detection and prenatal diagnosis of α(0)-thalassemia (SEA and Thai deletion). Blood DNA samples w...

  • Article
  • Open Access
3 Citations
1,754 Views
4 Pages

Fertility Assessment in Thalassemic Men

  • Shahla Ansari,
  • Azadeh Kiumarsi,
  • Azita Azarkeivan,
  • Mohammad Mahdi Allameh,
  • Davood Amir kashani and
  • Maryam Razaghi Azar

Male infertility in β-thalassemia patients is typically considered to be the consequence of iron deposition in the endocrine glands. Adult male patients with β-thalassemia, on regular blood transfusions, are prone to developing acquired hypogonadism....

  • Article
  • Open Access
2 Citations
1,083 Views
3 Pages

Thalassemias and hemoglobinopathies are the most common hemolytic congenital disorders in Bangladesh as in many parts of the world. This study was done to find the common types of thalassemias and abnormal hemoglobin variants seen in Bangladeshi popu...

  • Article
  • Open Access
1 Citations
1,094 Views
7 Pages

Granulocyte–Colony Stimulating Factor plus Plerixafor in Patients with β-thalassemia Major Results in the Effective Mobilization of Primitive CD34+ Cells with Specific Gene Expression Profile

  • Elena Baiamonte,
  • Rita Barone,
  • Flavia Contino,
  • Rosalia Di Stefano,
  • Anna Marfia,
  • Aldo Filosa,
  • Emanuela D'Angelo,
  • Salvatore Feo,
  • Santina Acuto and
  • Aurelio Maggio

Successful gene therapy for β-thalassemia requires optimal numbers of autologous gene-transduced hematopoietic stem and progenitor cells (HSPCs) with high repopulating capacity. Previous studies suggested superior mobilization in these patients by th...

  • Case Report
  • Open Access
997 Views
3 Pages

We report a second occurrence of hemoglobin (Hb) Tyne, [β5 (A2) Pro>Ser] HBB:c.16C>T(p.Pro6Ser), which like the first case was associated with normal hematology. We verified the variant was mildly unstable by showing it was greatly enriched in...

  • Case Report
  • Open Access
1 Citations
871 Views
2 Pages

No Transfusion is the Best Transfusion: A Rare Case

  • Dibyajyoti Sahoo,
  • Smita Mahapatra,
  • Rajeev Kumar Nayak and
  • Debasish Mishra

Presence of antibodies against red cell antigens remains a major problem in thalassemia patients. β-thalassemia major patients do commonly suffer from alloimmunization, which is rarely seen in thalassemia intermedia patients. Association of multiple...

  • Case Report
  • Open Access
1 Citations
907 Views
2 Pages

26 January 2017

Glycosylated hemoglobin (GHb) is routinely used to monitor glycemic control over past 2–3 months in diabetics. As per the recommendations of the American Association of Clinical Endocrinologist, 2007 values should be maintained below 7% to prevent th...

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