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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 5, Issue 1

February 2015 - 6 articles

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Articles (6)

  • Article
  • Open Access
5 Citations
2,217 Views
5 Pages

23 October 2015

Anemia in pregnancy is one of the causes of maternal morbidity and, maternal and fetal mortality in India. Hemoglobin transports oxygen to different parts of the body. Any defect in hemoglobin structure leads to its adverse functions. Screening of pr...

  • Case Report
  • Open Access
1 Citations
931 Views
4 Pages

A Novel Single Gene Deletion (−αMAL3.5) Giving Rise to Silent α Thalassemia Carrier Removing the Entire HBA2 Gene Observed in Two Chinese Patients with Hb H Disease: Case Report of Two Probands

  • Faidatul Syazlin Abdul Hamid,
  • Rahimah Ahmad,
  • Mohamed Saleem,
  • Nur Aisyah Aziz,
  • Syahira Lazira Omar,
  • Siti Hida Hajira Mohamad Arif,
  • Jameela Sathar and
  • Zubaidah Zakaria

We report a novel deletion at the HBA2 presented with Hb H disease in two Malaysian- Chinese patients. The two unrelated probands were diagnosed with Hb H disease in a primary hematological screening for thalassemia. Results from routine molecular an...

  • Article
  • Open Access
2 Citations
1,188 Views
6 Pages

Haplotypes, Sub-Haplotypes and Geographical Distribution in Omani Patients with Sickle Cell Disease

  • Suha Mustafa Hassan,
  • Muhanna Al Muslahi,
  • Muna Al Riyami,
  • Abeer Al Balushi,
  • Egbert Bakker,
  • Cornelis L. Harteveld and
  • Piero C. Giordano

Despite the fact that patients homozygous for the sickle cell disease (SCD) mutation have an identical genotype, the severity of the disease can be extremely variable. The hemoglobin (Hb) S mutation has been described on five different haplotypes wit...

  • Article
  • Open Access
1 Citations
1,031 Views
2 Pages

Screening of β-Thalassemia Trait among Pregnant Women with NESTROFT

  • Hitesh Sarda,
  • Shankaran Rukmini Niveditha and
  • Nirmala Shivlingaiah

The morbidity of β-thalassemia major has forced medical professionals to formulate screening tests to effectively screen β-thalassemia trait (BTT) of which naked eye single tube osmotic fragility test (NESTROFT) is the most cost effective test. Optim...

  • Article
  • Open Access
3 Citations
1,019 Views
3 Pages

Hemoglobin SE Disease in Hatay, in the Southern Part of Turkey

  • Can Acipayam,
  • Gonul Oktay,
  • Gul Ilhan and
  • Mehmet Akif Çürük

24 February 2015

Double heterozygosity for hemoglobin (Hb) E and S, known as HbSE disease, is a rare, clinically benign condition involving mild hemolysis. Only 25 cases have been reported to date. The current literature generally associates HbSE with a benign clinic...

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Thalass. Rep. - ISSN 2039-4365