Hemoglobin, Volume 39, Issue 2 (2015)

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Hemoglobin, Volume 39, Issue 2 (2015)

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Review Article

Review Article
Evaluating the Safety and Efficacy of Silymarin in β-Thalassemia Patients: A Review
Behjat Al-Sadat Moayedi Esfahani, Nahid Reisi & Milad Mirmoghtadaei
Pages: 75-80
Published online: 03 Feb 2015
AbstractforEvaluating the Safety and Efficacy of Silymarin in β-Thalassemia Patients: A Review | Full Text | References | PDF (150.2 KB)
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Original Article

Article
A Novel Hemoglobin Variant Found on the α1 Chain: Hb KSVGH (HBA1: p.Lys57_Gly58insSerHisGlySerAlaGlnValLys)
Mei-Chun Wang, Kuo-Wang Tsai, Chih-Hsun Chu, Ming-Sun Yu & Hing-Chung Lam
Pages: 81-87
Published online: 11 Feb 2015
AbstractforA Novel Hemoglobin Variant Found on the α1 Chain: Hb KSVGH (HBA1: p.Lys57_Gly58insSerHisGlySerAlaGlnValLys) | Full Text | References | PDF (1.5 MB)
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Article
Molecular Characterization of Hb Hamilton Hill (HBA2: c.388delC), a Novel HBA2 Variant Generating a Premature Termination Codon and Truncated HBA2 Chain
Talal Qadah, Jill Finlayson, Emma North & Reza Ghassemifar
Pages: 88-94
Published online: 20 Mar 2015
AbstractforMolecular Characterization of Hb Hamilton Hill (HBA2: c.388delC), a Novel HBA2 Variant Generating a Premature Termination Codon and Truncated HBA2 Chain | Full Text | References | PDF (1.5 MB)
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Article
Genetic Determinants of β-Thalassemia Intermedia in Pakistan
Jabbar Khan, Nafees Ahmad, Sami Siraj & Naseruddin Hoti
Pages: 95-101
Published online: 24 Feb 2015
AbstractforGenetic Determinants of β-Thalassemia Intermedia in Pakistan | Full Text | References | PDF (149.2 KB) | Supplemental
  • 166 Views
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Article
Association of an α-Globin Gene Cluster Duplication and Heterozygous β-Thalassemia in a Patient with a Severe Thalassemia Syndrome
Hua Jiang, Sha Liu, Yong-Ling Zhang, Jun-Hui Wan, Ru Li & Dong-Zhi Li
Pages: 102-106
Published online: 18 Feb 2015
AbstractforAssociation of an α-Globin Gene Cluster Duplication and Heterozygous β-Thalassemia in a Patient with a Severe Thalassemia Syndrome | Full Text | References | PDF (726.5 KB)
  • 273 Views
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Article
Broader Spectrum of β-Thalassemia Mutations in Oman: Regional Distribution and Comparison with Neighboring Countries
Suha M. Hassan, Cornelis L. Harteveld, Egbert Bakker & Piero C. Giordano
Pages: 107-110
Published online: 13 Feb 2015
AbstractforBroader Spectrum of β-Thalassemia Mutations in Oman: Regional Distribution and Comparison with Neighboring Countries | Full Text | References | PDF (120.6 KB)
  • 151 Views
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Article
Hb Lansing (HBA2: c.264C > G) and a New β Promoter Transversion [−52 (G > T)]: An Attempt to Define the Phenotype of Two Mutations Found in the Omani Population
Suha M. Hassan, Cornelis L. Harteveld, Engbert Bakker & Piero C. Giordano
Pages: 111-114
Published online: 31 Mar 2015
AbstractforHb Lansing (HBA2: c.264C > G) and a New β Promoter Transversion [−52 (G > T)]: An Attempt to Define the Phenotype of Two Mutations Found in the Omani Population | Full Text | References | PDF (204.6 KB)
  • 150 Views
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Article
A Novel Promoter Mutation (HBB: c.-75G>T) Was Identified as a Cause of β+-Thalassemia
Zeyong Li, Lei Li, Yachao Yao, Nan Li, Yahong Li, Zhen Zhang, Fang Yan, Houkuang Qiu, Chunyan Wu & Zhi Zhang
Pages: 115-120
Published online: 06 Feb 2015
AbstractforA Novel Promoter Mutation (HBB: c.-75G>T) Was Identified as a Cause of β+-Thalassemia | Full Text | References | PDF (743 KB)
  • 203 Views
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Article
A New Krüppel-Like Factor 1 Mutation (c.947G > A or p.C316Y) in Humans Causes β-Thalassemia Minor
Takenori Nitta, Fumio Kawano, Yasuhiro Yamashiro, Fumiya Takagi, Tomoaki Murata, Tatehiko Tanaka, Mella Ferania, Chris Adhiyanto & Yukio Hattori
Pages: 121-126
Published online: 18 Feb 2015
AbstractforA New Krüppel-Like Factor 1 Mutation (c.947G > A or p.C316Y) in Humans Causes β-Thalassemia Minor | Full Text | References | PDF (508.7 KB)
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Short Communication

First Report of Acute Lymphoblastic Leukemia in an Egyptian Child with β-Thalassemia Major
Laila M. Sherief, Naglaa M. Kamal, Hadeel M. Abdelrahman, Besheir Abdalla Hassan & Marwa M. Zakaria
Pages: 127-129
Published online: 24 Feb 2015
AbstractforFirst Report of Acute Lymphoblastic Leukemia in an Egyptian Child with β-Thalassemia Major | Full Text | References | PDF (107.6 KB)
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Is the Medical Home for Adult Patients with Sickle Cell Disease a Reality or an Illusion?
Samir K. Ballas & Elliott P. Vichinsky
Pages: 130-133
Published online: 25 Mar 2015
AbstractforIs the Medical Home for Adult Patients with Sickle Cell Disease a Reality or an Illusion? | Full Text | References | PDF (111 KB)
  • 176 Views
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Prevalence of Hb S (HHB: c.20A > T) in a Honduran Population of African Descent
Brian M. Erazo, Gilberto A. Ramírez, Linda E. Cerrato, Luis J. Pinto, Edder J. Castro, Néstor J. Yanez, Brayan Montoya & Gustavo A. Fontecha
Pages: 134-137
Published online: 24 Feb 2015
AbstractforPrevalence of Hb S (HHB: c.20A > T) in a Honduran Population of African Descent | Full Text | References | PDF (340.5 KB)
  • 114 Views
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Coinheritance of Hb D-Punjab and β-Thalassemia: Diagnosis and Implications in Prenatal Diagnosis
Sheila Das & Ranjeet S. Mashon
Pages: 138-140
Published online: 10 Feb 2015
AbstractforCoinheritance of Hb D-Punjab and β-Thalassemia: Diagnosis and Implications in Prenatal Diagnosis | Full Text | References | PDF (157.1 KB)
  • 344 Views
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Screening for Thalassemia Carriers in Populations with a High Rate of Iron Deficiency: Revisiting the Applicability of the Mentzer Index and the Effect of Iron Deficiency on Hb A2 Levels
Ali Amid, Bahram Haghi-Ashtiani, Melanie Kirby-Allen & Mohammad Taghi Haghi-Ashtiani
Pages: 141-143
Published online: 25 Mar 2015
AbstractforScreening for Thalassemia Carriers in Populations with a High Rate of Iron Deficiency: Revisiting the Applicability of the Mentzer Index and the Effect of Iron Deficiency on Hb A2 Levels | Full Text | References | PDF (344.6 KB)
  • 327 Views
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Two Novel α2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2: c.428A > T) and Severe (HBA2: c.342-345insCC) α-Thalassemia Phenotype
Elisabeth Saller, Fabrizio Dutly & Hannes Frischknecht
Pages: 144-146
Published online: 19 Mar 2015
AbstractforTwo Novel α2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2: c.428A > T) and Severe (HBA2: c.342-345insCC) α-Thalassemia Phenotype | Full Text | References | PDF (268 KB)
  • 111 Views
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