Hemoglobin, Volume 33, Issue 1 (2009)

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Hemoglobin, Volume 33, Issue 1 (2009)

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Review Article

Review Article
Newer Aspects of the Pathophysiology of Sickle Cell Disease Vaso-Occlusion
Nicola Conran, Carla F. Franco-Penteado & Fernando F. Costa
Pages: 1-16
Published online: 07 Jul 2009
AbstractforNewer Aspects of the Pathophysiology of Sickle Cell Disease Vaso-Occlusion | Full Text | References | PDF (738.9 KB)
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Original Article

Article
Prenatal Diagnosis of β-Thalassemia/Hb E by Hemoglobin Typing Compared to DNA Analysis
Supatra Sirichotiyakul, Rattika Saetung & Torpong Sanguansermsri
Pages: 17-23
Published online: 07 Jul 2009
AbstractforPrenatal Diagnosis of β-Thalassemia/Hb E by Hemoglobin Typing Compared to DNA Analysis | Full Text | References | PDF (503.8 KB)
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Article
Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem
Nassima Boudrahem-Addour, Nadia Zidani, Nathalie Carion, Dominique Labie, Meriem Belhani & Cherif Beldjord
Pages: 24-36
Published online: 07 Jul 2009
AbstractforMolecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem | Full Text | References | PDF (130.7 KB)
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Article
Molecular Characterization of α-Thalassemia in the Dohuk Region of Iraq
Nasir A.S. Al-Allawi, Ameer I.A. Badi, Hasham Imanian, Nooshin Nikzat, Jaladet M.S. Jubrael & Hossein Najmabadi
Pages: 37-44
Published online: 07 Jul 2009
AbstractforMolecular Characterization of α-Thalassemia in the Dohuk Region of Iraq | Full Text | References | PDF (103.4 KB)
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Short Communications

Article
Hb Belleville [β10(A7)Ala→Thr] Affects The Determination of Hb A1c by Routine Cation Exchange High Performance Liquid Chromatography
Jonathan P. Williams, Hannah Jackson & Brian N. Green
Pages: 45-50
Published online: 07 Jul 2009
AbstractforHb Belleville [β10(A7)Ala→Thr] Affects The Determination of Hb A1c by Routine Cation Exchange High Performance Liquid Chromatography | Full Text | References | PDF (310 KB)
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Article
Hb North York [β117(G19)His→Asp]: A New β Chain Hemoglobin Variant
John S. Waye, Lynda Walker, Lisa M. Nakamura, Barry Eng & Andrew McFarlane
Pages: 51-53
Published online: 07 Jul 2009
AbstractforHb North York [β117(G19)His→Asp]: A New β Chain Hemoglobin Variant | Full Text | References | PDF (217.1 KB)
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Article
A New α-Globin Variant with Increased Oxygen Affinity in a Swiss Family: Hb Frauenfeld [α138(H21)Ser→Phe, TCC>TTC (α 2)]
Michel Hochuli, Karin Zurbriggen, Marlis Schmid, Oliver Speer, Philippe Rochat, Beat Frauchiger, Peter Kleinert, Markus Schmugge & Heinz Troxler
Pages: 54-58
Published online: 07 Jul 2009
AbstractforA New α-Globin Variant with Increased Oxygen Affinity in a Swiss Family: Hb Frauenfeld [α138(H21)Ser→Phe, TCC>TTC (α 2)] | Full Text | References | PDF (257.3 KB)
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Article
Hematological and Molecular Analysis of Novel and Rare β-Thalassemia Mutations in the Indian Population
Anita Nadkarni, Ajit Gorakshakar, Reema Surve, Pratibha Sawant, Supriya Phanasgaonkar, Sona Nair, Kanjaksha Ghosh & Roshan B. Colah
Pages: 59-65
Published online: 07 Jul 2009
AbstractforHematological and Molecular Analysis of Novel and Rare β-Thalassemia Mutations in the Indian Population | Full Text | References | PDF (340.4 KB)
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Article
Diversity of the 5′ β-Globin Haplotype of Four β-Thalassemia Mutations in the Mexican Population
Karina R. Morales, Maria T. Magaña, Bertha Ibarra & Francisco J. Perea
Pages: 66-71
Published online: 07 Jul 2009
AbstractforDiversity of the 5′ β-Globin Haplotype of Four β-Thalassemia Mutations in the Mexican Population | Full Text | References | PDF (95.5 KB)
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Article
α+-Thalassemia Trait Caused by a Nonsense Mutation in the α2-Globin Gene: Codon 54 (CAG>TAG)
Barry Eng, Lynda Walker & John S. Waye
Pages: 72-74
Published online: 07 Jul 2009
Abstractforα+-Thalassemia Trait Caused by a Nonsense Mutation in the α2-Globin Gene: Codon 54 (CAG>TAG) | Full Text | References | PDF (192.5 KB)
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Article
Homozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family
Mehdi Haghi, Abbas A. Hosseinpour Feizi, Cornelis L. Harteveld, Nasser Pouladi & Mohammad A. Hosseinpour Feizi
Pages: 75-80
Published online: 07 Jul 2009
AbstractforHomozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family | Full Text | References | PDF (147.4 KB)
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