Hemoglobin, Volume 43, Issue 2 (2019)

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Hemoglobin, Volume 43, Issue 2 (2019)

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Original Articles

Article
A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia
Thomas R. L. Klei, Sima Kheradmand Kia, Martijn Veldthuis, Javad Dehbozorgian, Mehran Karimi, Judy Geissler, Erica Sellink, Marijke Thiel-Valkhof, Patrick Burger, Floris van Alphen, Alexander B. Meijer, Robin van Bruggen & Rob van Zwieten
Pages: 77-82
Published online: 13 Jun 2019
AbstractforA Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia | Full Text | References | PDF (1.7 MB) | EPUB
  • 81 Views
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Article
The Sub-Phenotypes of Sickle Cell Disease in Kuwait
Adekunle D. Adekile, Sondus Al-Sherida, Rajaa Marouf, Nada Mustafa & Diana Thomas
Pages: 83-87
Published online: 30 May 2019
AbstractforThe Sub-Phenotypes of Sickle Cell Disease in Kuwait | Full Text | References | PDF (497.8 KB) | EPUB
  • 214 Views
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Article
Erythrocyte cAMP in Determining Frequency of Acute Pain Episodes in Sickle Cell Disease Patients from Odisha State, India
Bimal P. Jit, Pradeep K. Mohanty, Avinash Pradhan, Prasanta Purohit, Kishalaya Das, Siris Patel, Satyabrata Meher, Shalini Sinha, Jyoti R. Mohanty, Rajendra Kumar Behera & Padmalaya Das
Pages: 88-94
Published online: 10 Jul 2019
AbstractforErythrocyte cAMP in Determining Frequency of Acute Pain Episodes in Sickle Cell Disease Patients from Odisha State, India | Full Text | References | PDF (842.1 KB) | EPUB
  • 93 Views
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Article
Prevalence and Risk Factors for Cardiac and Liver Iron Overload in Adults with Thalassemia in Malaysia
Chin F. Ngim, Mei Y. Lee, Norliza Othman, Soo M. Lim, Chen S. Ng & Amutha Ramadas
Pages: 95-100
Published online: 10 Jun 2019
AbstractforPrevalence and Risk Factors for Cardiac and Liver Iron Overload in Adults with Thalassemia in Malaysia | Full Text | References | PDF (509.9 KB) | EPUB
  • 214 Views
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Article
Polymorphisms of α-Globin Genes Compromise Polymerase Chain Reaction-Based α-Thalassemia Genotyping in Three Chinese Families
Manna Sun, Jiwu Lou, Ying Zhag, Youqing Fu, Yunshi Dai & Yanhui Liu
Pages: 101-106
Published online: 21 May 2019
AbstractforPolymorphisms of α-Globin Genes Compromise Polymerase Chain Reaction-Based α-Thalassemia Genotyping in Three Chinese Families | Full Text | References | PDF (1.4 MB) | EPUB
  • 90 Views
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Article
The Spectrum of α-Thalassemia Mutations in the Lak Population of Iran
Keivan Moradi, Mozaffar Aznab, Susan Tahmasebi, Zahra Dastafkan, Leila Omidniakan, Mahsa Ahmadi & Reza Alibakhshi
Pages: 107-111
Published online: 14 Jul 2019
AbstractforThe Spectrum of α-Thalassemia Mutations in the Lak Population of Iran | Full Text | References | PDF (549 KB) | EPUB
  • 117 Views
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Article
Detection of a Large Novel α-Thalassemia Deletion in an Autochthonous Belgian Family
Laura Heireman, Ariane Luyckx, Katrien De Schynkel, Annelies Dheedene, Mélanie Delaunoy, Anne-Sophie Adam, Béatrice Gulbis & Johan Dierick
Pages: 112-115
Published online: 21 Jun 2019
AbstractforDetection of a Large Novel α-Thalassemia Deletion in an Autochthonous Belgian Family | Full Text | References | PDF (476.4 KB) | EPUB
  • 166 Views
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Article
MS-275 Chemical Analogues Promote Hemoglobin Production and Erythroid Differentiation of K562 Cells
Stella Voskou, Marios Phylactides, Andreas Afantitis, Georgia Melagraki, Andreas Tsoumanis, Panayotis A. Koutentis, Tina Mitsidi, Styliana I. Mirallai & Marina Kleanthous
Pages: 116-121
Published online: 07 Jul 2019
AbstractforMS-275 Chemical Analogues Promote Hemoglobin Production and Erythroid Differentiation of K562 Cells | Full Text | References | PDF (925.5 KB) | EPUB | Supplemental
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Open Access

Short Communications

Rapid Communication
Hb Aalesund (HBA2: c.400_406delAGCACCG), an Unstable α-Globin Variant Found in a Norwegian Patient Causing Moderate Hemolytic Anemia and Falsely High Hb A1c Using Ion Exchange High Performance Liquid Chromatography
Runa M. Grimholt, Bente Fjeld, Hilde Selsås, Lutz Schwettmann & Olav Klingenberg
Pages: 122-125
Published online: 30 May 2019
AbstractforHb Aalesund (HBA2: c.400_406delAGCACCG), an Unstable α-Globin Variant Found in a Norwegian Patient Causing Moderate Hemolytic Anemia and Falsely High Hb A1c Using Ion Exchange High Performance Liquid Chromatography | Full Text | References | PDF (880.2 KB) | EPUB
  • 178 Views
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Rapid Communication
First Description of Hb San Diego (HBB: c.328G>A) in a Chinese Family with Congenital Erythrocytosis
Huixia Xiong & Suning Chen
Pages: 126-128
Published online: 14 Jul 2019
AbstractforFirst Description of Hb San Diego (HBB: c.328G>A) in a Chinese Family with Congenital Erythrocytosis | Full Text | References | PDF (509.5 KB) | EPUB | Supplemental
  • 99 Views
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Rapid Communication
A Novel Human β-Globin Gene Variant [Hb London-Ontario, HBB: c.332T>G] is Associated with Transfusion-Dependent Anemia in a Patient with a Hemoglobin Electrophoresis Pattern Consistent with β-Thalassemia Trait
Marc N. Bienz, Cyrus Hsia, John S. Waye, Margo Bode & Ziad Solh
Pages: 129-131
Published online: 27 Jun 2019
AbstractforA Novel Human β-Globin Gene Variant [Hb London-Ontario, HBB: c.332T>G] is Associated with Transfusion-Dependent Anemia in a Patient with a Hemoglobin Electrophoresis Pattern Consistent with β-Thalassemia Trait | Full Text | References | PDF (659.1 KB) | EPUB
  • 107 Views
  • 1 CrossRef citations
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Rapid Communication
Compound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India
Snehadhini Dehury, Satyabrata Meher, Siris Patel, Kishalaya Das, Arpita Jana, Subhra Bhattacharya, Sarmila Sahoo, Biswanath Sarkar & Pradeep K. Mohanty
Pages: 132-136
Published online: 13 Jun 2019
AbstractforCompound Heterozygote of Hb S (HBB: c.20A>T)/Hb Westdale (HBB: c.380_396delTGCAGGCTGCCTATCAG): Report of Four Cases from Odisha State, India | Full Text | References | PDF (961 KB) | EPUB
  • 97 Views
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Rapid Communication
A Krüppel-Like Factor 1 Gene Mutation Ameliorates the Severity of β-Thalassemia: A Case Report
Xing-Mei Xie, Ying-Na Liu, Jian Li, Fan Jiang & Dong-Zhi Li
Pages: 137-139
Published online: 21 May 2019
AbstractforA Krüppel-Like Factor 1 Gene Mutation Ameliorates the Severity of β-Thalassemia: A Case Report | Full Text | References | PDF (728.2 KB) | EPUB
  • 137 Views
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Rapid Communication
A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as β-Thalassemia Intermedia Due to a KLF1 Gene Mutation
Kun Yang, Quan Ren, Yi Wu, Yali Zhou & Xiaolin Yin
Pages: 140-144
Published online: 13 Jun 2019
AbstractforA Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as β-Thalassemia Intermedia Due to a KLF1 Gene Mutation | Full Text | References | PDF (1 MB) | EPUB
  • 168 Views
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Rapid Communication
Coinheritance of Hb City of Hope (HBB: c.208G>A) and β-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (HBB: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization
Jian-Ying Zhou, Fan Jiang, Jian Li, Gui-Lan Chen & Dong-Zhi Li
Pages: 145-147
Published online: 03 Jul 2019
AbstractforCoinheritance of Hb City of Hope (HBB: c.208G>A) and β-Thalassemia: Compromising the Molecular Diagnosis of the Codons 71/72 (+A) (HBB: c.216_217insA) Mutation by Reverse Dot-Blot Hybridization | Full Text | References | PDF (830.4 KB) | EPUB
  • 271 Views
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