Hemoglobin, Volume 39, Issue 2 (2015)

Browse this journal
Sample our Medicine, Dentistry, Nursing & Allied Health journals, sign in here to start your FREE access for 14 days

Hemoglobin, Volume 39, Issue 2 (2015)

See all volumes and issues
Vol 48, 2024 Vol 47, 2023 Vol 46, 2022 Vol 45, 2021 Vol 44, 2020 Vol 43, 2019 Vol 42, 2018 Vol 41, 2017 Vol 40, 2016 Volume 39, 2015 Vol 38, 2014 Vol 37, 2013 Vol 36, 2012 Vol 35, 2011 Vol 34, 2010 Vol 33, 2009 Vol 32, 2008 Vol 31, 2007 Vol 30, 2006 Vol 29, 2005 Vol 28, 2004 Vol 27, 2003 Vol 26, 2002 Vol 25, 2001 Vol 24, 2000 Vol 23, 1999 Vol 22, 1998 Vol 21, 1997 Vol 20, 1996 Vol 19, 1995 Vol 18, 1994 Vol 17, 1993 Vol 16, 1992 Vol 15, 1991 Vol 14, 1990 Vol 13, 1989 Vol 12, 1988 Vol 11, 1987 Vol 10, 1986 Vol 9, 1985 Vol 8, 1984 Vol 7, 1983 Vol 6, 1982 Vol 5, 1981 Vol 4, 1980 Vol 3, 1979 Vol 2, 1978 Vol 1, 1976-1977
Download citations Download PDFs Download issue

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)
  • 263 Views
  • 21 CrossRef citations
  • 0Altmetric

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)
  • 130 Views
  • 3 CrossRef citations
  • 0Altmetric
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)
  • 122 Views
  • 2 CrossRef citations
  • 0Altmetric
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
  • 164 Views
  • 5 CrossRef citations
  • 0Altmetric
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
  • 15 CrossRef citations
  • 0Altmetric
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)
  • 150 Views
  • 4 CrossRef citations
  • 0Altmetric
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
  • 2 CrossRef citations
  • 0Altmetric
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
  • 3 CrossRef citations
  • 0Altmetric
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)
  • 219 Views
  • 8 CrossRef citations
  • 0Altmetric

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)
  • 104 Views
  • 5 CrossRef citations
  • 0Altmetric
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)
  • 174 Views
  • 3 CrossRef citations
  • 0Altmetric
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
  • 3 CrossRef citations
  • 0Altmetric
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
  • 10 CrossRef citations
  • 0Altmetric
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
  • 8 CrossRef citations
  • 0Altmetric
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
  • 2 CrossRef citations
  • 0Altmetric

Explore articles

Explore the most recently published articles

Sickle Cell Disease in Brazil: Current Management
Aderson da Silva Araújo et al.
Review Article | Published online: 25 Apr 2024
A Novel Frameshift Mutation(HBA2:C.337delC) Associated With α-Thalassemia Trait Detected by Next-Generation Sequencing in Southern China
Lei Pan et al.
Brief Report | Published online: 23 Apr 2024
A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg,HBD: C.139G > A]
Hui-Ming Lin et al.
Brief Report | Published online: 7 Mar 2024
Noninvasive Prenatal Diagnosis of SEA-Thalassemia by Combining 1000 Genomes Database and Relative Haplotype Dosage
Dewen Liu et al.
Article | Published online: 18 Apr 2024
View all latest articles