Hemoglobin, Volume 29, Issue 3 (2005)

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Hemoglobin, Volume 29, Issue 3 (2005)

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Original Article

Article
Hb Oegstgeest [α104(G11)Cys → Ser (α1)]. A New Hemoglobin Variant Associated with a Mild α-Thalassemia Phenotype
Cornelis L. Harteveld, Lieke Rozendaal, Nico A. Blom, Shirley Lo-A-Njoe, Nicole Akkerman, Sandra Arkestijn, Peter Van Delft & Piero C. Giordano Ph.D.
Pages: 165-169
Published online: 07 Jul 2009
AbstractforHb Oegstgeest [α104(G11)Cys → Ser (α1)]. A New Hemoglobin Variant Associated with a Mild α-Thalassemia Phenotype | Full Text | References | PDF (104.7 KB)
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Article
Clinical and Laboratory Effects of Hydroxyurea in Children and Adolescents with Sickle Cell Anemia: A Portuguese Hospital Study
Lígia Barbosa Braga, Ana Cristina Ferreira, Margarida Guimarães, Carlos Nazário, Paula Pacheco, Armandina Miranda, Isabel Picanço, Teresa Seixas, Lino Rosado & João M. Videira Amaral
Pages: 171-180
Published online: 07 Jul 2009
AbstractforClinical and Laboratory Effects of Hydroxyurea in Children and Adolescents with Sickle Cell Anemia: A Portuguese Hospital Study | Full Text | References | PDF (94.3 KB)
  • 64 Views
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Article
In Vivo Action of Vanillin on Delay Time Determined by Magnetic Relaxation
Adolfo Fernández García, Carlos Cabal, Jorge Losada, Eloy Álvarez, Catalina Soler & Josefina Otero
Pages: 181-187
Published online: 07 Jul 2009
AbstractforIn Vivo Action of Vanillin on Delay Time Determined by Magnetic Relaxation | Full Text | References | PDF (210.1 KB)
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Article
Hyperbilirubinemia in Homozygous HbE Disease Is Associated with the UGT1A1 Gene Polymorphism
Eunice Sindhuvi Edison, Ramachandran V. Shaji, Alok Srivastava & Mammen Chandy F.R.C.P.A.M.D.F.R.A.C.P.
Pages: 189-195
Published online: 07 Jul 2009
AbstractforHyperbilirubinemia in Homozygous HbE Disease Is Associated with the UGT1A1 Gene Polymorphism | Full Text | References | PDF (125.7 KB)
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Article
A Novel GγAγ(δβ)0-Thalassemia with a 27 kb Deletion
Yasuhiro Yamashiro, Yukio Hattori M.D., Naoko Okayama, Emi Shinoda, Naomi Suyama, Tatehiko Tanaka & Shinji Ohi
Pages: 197-208
Published online: 07 Jul 2009
AbstractforA Novel GγAγ(δβ)0-Thalassemia with a 27 kb Deletion | Full Text | References | PDF (417.5 KB)
  • 50 Views
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Article
β-Thalassemia Due to a Novel Nonsense Mutation at Codon 37 (TGG→TAG) Found in an Afghanistani Family
Brian Kornblit, Pia Taaning & Henrik Birgens Dr. Med. Sci.M.D.
Pages: 209-213
Published online: 07 Jul 2009
Abstractforβ-Thalassemia Due to a Novel Nonsense Mutation at Codon 37 (TGG→TAG) Found in an Afghanistani Family | Full Text | References | PDF (161.1 KB)
  • 70 Views
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Short Communication

Article
The First Case of Hb E-Saskatoon Associated with Hb Lepore-Baltimore Found in Spain
Paloma Ropero, Maria José Murga, Fernando A. González, Marta Polo, Celina Benavente, María Salvador & Ana Villegas
Pages: 215-219
Published online: 07 Jul 2009
AbstractforThe First Case of Hb E-Saskatoon Associated with Hb Lepore-Baltimore Found in Spain | Full Text | References | PDF (730.3 KB)
  • 55 Views
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Article
Compound Heterozygosity for Hb E and Hb Lepore-Hollandia in India; First Report and Potential Diagnostic Pitfalls
Eunice Sindhuvi Edison, Ramachandran V. Shaji, Alok Srivastava & Mammen Chandy F.R.C.P.A.M.D.F.R.A.C.P.
Pages: 221-224
Published online: 07 Jul 2009
AbstractforCompound Heterozygosity for Hb E and Hb Lepore-Hollandia in India; First Report and Potential Diagnostic Pitfalls | Full Text | References | PDF (325.7 KB)
  • 80 Views
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Article
A Mutation of the β-Globin Gene Initiation Codon, ATG→AAG, Found in a French Caucasian Man
Philippe Lacan, Martine Aubry, Nicole Couprie & Alain Francina
Pages: 225-228
Published online: 07 Jul 2009
AbstractforA Mutation of the β-Globin Gene Initiation Codon, ATG→AAG, Found in a French Caucasian Man | Full Text | References | PDF (231.1 KB)
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Article
Two French Caucasian Families with Dominant Thalassemia-Like Phenotypes Due to Hyper Unstable Hemoglobin Variants: Hb Sainte Seve [Codon 118 (− T)] and Codon 127 [CAG→TAG (Gln→Stop])
Claude Préhu, Serge Pissard, Maha Al-Sheikh, Catherine Le Niger, Dora Bachir, Fréderic Galactéros & Henri Wajcman
Pages: 229-233
Published online: 07 Jul 2009
AbstractforTwo French Caucasian Families with Dominant Thalassemia-Like Phenotypes Due to Hyper Unstable Hemoglobin Variants: Hb Sainte Seve [Codon 118 (− T)] and Codon 127 [CAG→TAG (Gln→Stop]) | Full Text | References | PDF (223.9 KB)
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Article
A Rare Association of α0-Thalassemia (– –SEA) and an Initiation Codon Mutation (ATG→A-G) of the α2 Gene Causes Hb H Disease in Thailand
Vip Viprakasit D.Phil. (Oxon)M.D., Worrawut Chinchang, Waraporn Glomglao & Voravarn S Tanphaichitr
Pages: 235-240
Published online: 07 Jul 2009
AbstractforA Rare Association of α0-Thalassemia (– –SEA) and an Initiation Codon Mutation (ATG→A-G) of the α2 Gene Causes Hb H Disease in Thailand | Full Text | References | PDF (320.2 KB)
  • 109 Views
  • 6 CrossRef citations
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