Hemoglobin, Volume 32, Issue 4 (2008)

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Hemoglobin, Volume 32, Issue 4 (2008)

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Review Article

Article
Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia
Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, Piero C. Giordano, Cornelis L. Harteveld, Véronique Baudin-Creuza & John Old
Pages: 327-349
Published online: 07 Jul 2009
AbstractforUnstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia | Full Text | References | PDF (501.6 KB)
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Original Article

Article
Hb Montreal II: A Novel Elongated β-Globin Variant Caused by a Frameshift Mutation [β142 (−C)]
Pierre Chagnon, Luigina Mollica, Claude Belisle, Céline Deveaux, Giovanni D. Angelo, Denis-Claude Roy, Denis Soulières & Lambert Busque
Pages: 351-359
Published online: 07 Jul 2009
AbstractforHb Montreal II: A Novel Elongated β-Globin Variant Caused by a Frameshift Mutation [β142 (−C)] | Full Text | References | PDF (225.2 KB)
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Original

Article
A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α+-Thalassemia Deletion: Clinical Aspects in Two Cases
Varvara Douna, Ioannis Papassotiriou, Anastasia Garoufi, Eleni Georgouli, Vassilis Ladis, Alexandra Stamoulakatou, Anna Metaxotou-Mavrommati, Emmanuel Kanavakis & Joanne Traeger-Synodinos
Pages: 361-369
Published online: 07 Jul 2009
AbstractforA Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α+-Thalassemia Deletion: Clinical Aspects in Two Cases | Full Text | References | PDF (85.4 KB)
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Article
First Observation of Hb Taybe [Codons 38/39 (−Acc) Thr→0 (α1)] In Greece: Clinical and Hematological Findings in Patients With Co-Inherited α+-Thalassemia Mutations
Varvara Douna, Dimitra Liapi, Dimitrios Kampourakis, Zoe Repapinou, Ioannis Papassotiriou, Alexandra Stamoulakatou, Christos Poziopoulos, Emmanuel Kanavakis & Joanne Traeger-Synodinos
Pages: 371-378
Published online: 07 Jul 2009
AbstractforFirst Observation of Hb Taybe [Codons 38/39 (−Acc) Thr→0 (α1)] In Greece: Clinical and Hematological Findings in Patients With Co-Inherited α+-Thalassemia Mutations | Full Text | References | PDF (79.6 KB)
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Article
Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (–CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α+-Thalassemia Mutations
Varvara Douna, Ioannis Papassotiriou, Anna Metaxotou-Mavrommati, Alexandra Stamoulakatou, Dimitra Liapi, Dimitrios Kampourakis, Amalia Tsilimigaki, Emmanuel Kanavakis & Joanne Traeger-Synodinos
Pages: 379-385
Published online: 07 Jul 2009
AbstractforFurther Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (–CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α+-Thalassemia Mutations | Full Text | References | PDF (76.5 KB)
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Article
An Unusually Frequent β-Thalassemia Mutation in an Iranian Province
Peyman Eshghi, Azita Zadeh-Vakili, Armin Rashidi & Ebrahim Miri-Moghadam
Pages: 387-392
Published online: 07 Jul 2009
AbstractforAn Unusually Frequent β-Thalassemia Mutation in an Iranian Province | Full Text | References | PDF (67.8 KB)
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Article
Analysis of Real-Time SYBR-Polymerase Chain Reaction Cycle Threshold for Diagnosis of the α-Thalassemia-1 Southeast Asian Type Deletion: Application to Carrier Screening and Prenatal Diagnosis of Hb Bart's Hydrops Fetalis
Sakorn Pornprasert, Kanyakan Sukunthamala, Jittraporn Sacome, Arunee Phusua, Rattika Saetung, Torpong Sanguansermsri & Pranee Leechanachai
Pages: 393-402
Published online: 07 Jul 2009
AbstractforAnalysis of Real-Time SYBR-Polymerase Chain Reaction Cycle Threshold for Diagnosis of the α-Thalassemia-1 Southeast Asian Type Deletion: Application to Carrier Screening and Prenatal Diagnosis of Hb Bart's Hydrops Fetalis | Full Text | References | PDF (755.6 KB)
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Article
Detection of β-Thalassemia Mutations Using a Multiplex Amplification Refractory Mutation System Assay
Saisiri Mirasena, Dawan Shimbhu, Mondhon Sanguansermsri & Torpong Sanguansermsri
Pages: 403-409
Published online: 07 Jul 2009
AbstractforDetection of β-Thalassemia Mutations Using a Multiplex Amplification Refractory Mutation System Assay | Full Text | References | PDF (131.8 KB)
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Short Communication

Article
Two New α-Thalassemia Point Mutations that are Undetectable by Biochemical Techniques
Philippe Joly, Brigitte Pégourié, Stéphane Courby, Claire Barro, Gérard Besson, Laura Cohen, Caroline Garcia & Alain Francina
Pages: 411-417
Published online: 07 Jul 2009
AbstractforTwo New α-Thalassemia Point Mutations that are Undetectable by Biochemical Techniques | Full Text | References | PDF (1.1 MB)
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Original

Article
An α0-Thalassemia-Like Mutation: Hb Suan-Dok [α109(G16)Leu→Arg] Carried by a Recombinant −α3.7 Gene
Kamran Moradkhani, Elodie Mazurier, Piero C. Giordano, Henri Wajcman & Claude Préhu
Pages: 419-424
Published online: 16 Sep 2009
AbstractforAn α0-Thalassemia-Like Mutation: Hb Suan-Dok [α109(G16)Leu→Arg] Carried by a Recombinant −α3.7 Gene | Full Text | References | PDF (282.4 KB)
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