Hemoglobin, Volume 32, Issue 3 (2008)

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Hemoglobin, Volume 32, Issue 3 (2008)

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Original Article

Article
Hb Agrinio [α29(B10)Leu→Pro (α2)] in Combination with – –MED I Results in a Severe Form of Hb H Disease
Xenia Felekis, Marios Phylactides, Anthi Drousiotou, Sotiroulla Christou, Andreani Kyrri, Kyriakos Kyriakou, Eleni Kalogerou, George Christopoulos & Marina Kleanthous
Pages: 237-246
Published online: 07 Jul 2009
AbstractforHb Agrinio [α29(B10)Leu→Pro (α2)] in Combination with – –MED I Results in a Severe Form of Hb H Disease | Full Text | References | PDF (181.5 KB)
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Original

Article
A +8 (C→T) Mutation within the 5′ Untranslated Region of β-Globin Down-Regulates the mRNA Transcription
Neil Van de Water, Tina Tan, George Chan, Nyree Cole & Peter Browett
Pages: 247-253
Published online: 07 Jul 2009
AbstractforA +8 (C→T) Mutation within the 5′ Untranslated Region of β-Globin Down-Regulates the mRNA Transcription | Full Text | References | PDF (222.9 KB)
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Article
Molecular Spectrum of β-Thalassemia Mutations in Northwestern Iran
Mohammad A. Hosseinpour Feizi, Abbas A. Hosseinpour Feizi, Nasser Pouladi, Mehdi Haghi & Parvin Azarfam
Pages: 255-261
Published online: 07 Jul 2009
AbstractforMolecular Spectrum of β-Thalassemia Mutations in Northwestern Iran | Full Text | References | PDF (123.1 KB)
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Article
Results of the National Program for Prevention of β-Thalassemia Major in the Iranian Province of Mazandaran
Ghasemali Khorasani, Mehrnoosh Kosaryan, Koorosh Vahidshahi, Sepideh Shakeri & Mohamad Mehdi Nasehi
Pages: 263-271
Published online: 07 Jul 2009
AbstractforResults of the National Program for Prevention of β-Thalassemia Major in the Iranian Province of Mazandaran | Full Text | References | PDF (101 KB)
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Article
Molecular Basis of α-Thalassemia in Algeria
Hamida Mesbah-Amroun, Fatiha Rouabhi, Rolande Ducrocq & Jacques Elion
Pages: 273-278
Published online: 07 Jul 2009
AbstractforMolecular Basis of α-Thalassemia in Algeria | Full Text | References | PDF (73.6 KB)
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Article
An Estimation of the Incidence and Demographic Picture of the Major Hemoglobinopathies in Belgium (From a Confidential Inquiry)
Béatrice Gulbis, Alice Ferster, Christiane Vermylen, Marie-Françoise Dresse, Anna Vanderfaeillie, André Delannoy, Veerle Labarque, Pierre Philippet, Alain Kentos, Bernard Sztern, Bernard Deprijck & Françoise Vertongen (for the “Red Blood Cell Disorders Subcommittee” of the Belgian Haematological Society)
Pages: 279-285
Published online: 07 Jul 2009
AbstractforAn Estimation of the Incidence and Demographic Picture of the Major Hemoglobinopathies in Belgium (From a Confidential Inquiry) | Full Text | References | PDF (94.4 KB)
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Article
Analyses of Expression of Cytoglobin by Immunohistochemical Studies in Human Tissues
Akio Shigematsu, Yasushi Adachi, Junko Matsubara, Hiromi Mukaide, Naoko Koike-Kiriyama, Keizo Minamino, Ming Shi, Seiji Yanai, Masahiro Imamura, Shigeru Taketani & Susumu Ikehara
Pages: 287-296
Published online: 07 Jul 2009
AbstractforAnalyses of Expression of Cytoglobin by Immunohistochemical Studies in Human Tissues | Full Text | References | PDF (880.7 KB)
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Short Communications

Article
Hb Jeddah [α68(E17)Asn→His (α1)]: A Newly Recognized α Chain Variant, Seen in Combination with Hb S [β6(A3)Glu→Val], and Found in Three Separate Families of Middle Eastern Origin
Karra M. Markley, Mohamed Elkhalifa, Archana Maini & James D. Hoyer
Pages: 297-302
Published online: 07 Jul 2009
AbstractforHb Jeddah [α68(E17)Asn→His (α1)]: A Newly Recognized α Chain Variant, Seen in Combination with Hb S [β6(A3)Glu→Val], and Found in Three Separate Families of Middle Eastern Origin | Full Text | References | PDF (158.1 KB)
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Original

Article
THE Hb S/β+-Thalassemia Phenotype Demonstrates that the IVS-I (−2) (A>C) Mutation is a Mild β-Thalassemia Allele
Markus Schmugge, John S. Waye, Raveen K. Basran, Karin Zurbriggen & Hannes Frischknecht
Pages: 303-307
Published online: 07 Jul 2009
AbstractforTHE Hb S/β+-Thalassemia Phenotype Demonstrates that the IVS-I (−2) (A>C) Mutation is a Mild β-Thalassemia Allele | Full Text | References | PDF (67.2 KB)
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Article
Compound Heterozygosity for Hb S [β6(A3)Glu→Val, GAG→GTG] and a New Thalassemic Mutation [β132(H10)Lys→Term, AAA→TAA] Detected in a Family from West Africa
Hannes Frischknecht, Heinz Troxler, Jeanette Greiner, Heinz Hengartner & Fabrizio Dutly
Pages: 309-313
Published online: 07 Jul 2009
AbstractforCompound Heterozygosity for Hb S [β6(A3)Glu→Val, GAG→GTG] and a New Thalassemic Mutation [β132(H10)Lys→Term, AAA→TAA] Detected in a Family from West Africa | Full Text | References | PDF (184.9 KB)
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Article
Frameshift Mutation in the α2-Globin Gene Causing α+-Thalassemia: Codon 49 (−GC)
Barry Eng & John S. Waye
Pages: 315-317
Published online: 07 Jul 2009
AbstractforFrameshift Mutation in the α2-Globin Gene Causing α+-Thalassemia: Codon 49 (−GC) | Full Text | References | PDF (584.5 KB)
  • 30 Views
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Article
Association of Hb Q-Thailand with Heterozygous Hb E in a Chinese Patient
Dongzhi Li, Can Liao, Jian Li, Xingmei Xie & Huizhu Zhong
Pages: 319-321
Published online: 07 Jul 2009
AbstractforAssociation of Hb Q-Thailand with Heterozygous Hb E in a Chinese Patient | Full Text | References | PDF (455.8 KB)
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Article
Hemoglobinopathies in the Sudan
Abozer Y. Elderdery, Babiker A. Mohamed, Mubarak E. Karsani, Mohamed H. Ahmed, Gavin Knight & Alan J. Cooper
Pages: 323-326
Published online: 07 Jul 2009
AbstractforHemoglobinopathies in the Sudan | Full Text | References | PDF (56.6 KB)
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