Hemoglobin, Volume 36, Issue 5 (2012)

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

Hemoglobin, Volume 36, Issue 5 (2012)

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 Vol 39, 2015 Vol 38, 2014 Vol 37, 2013 Volume 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

Original Article

Article
Low Dose Hydroxyurea is Effective in Reducing the Incidence of Painful Crisis and Frequency of Blood Transfusion in Sickle Cell Anemia Patients from Eastern India
Dilip K. Patel, Ranjeet S. Mashon, Siris Patel, Bhabani S. Das, Prasanta Purohit & Subasa C. Bishwal
Pages: 409-420
Published online: 19 Sep 2012
AbstractforLow Dose Hydroxyurea is Effective in Reducing the Incidence of Painful Crisis and Frequency of Blood Transfusion in Sickle Cell Anemia Patients from Eastern India | Full Text | References | PDF (397.6 KB)
  • 347 Views
  • 31 CrossRef citations
  • 0Altmetric
Article
Identification and Characterization of Two Novel and Differentially Expressed Isoforms of Human α2- and α1-Globin Genes
Reza Ghassemifar, Luke Forster, Talal Qadah & Jill Finlayson
Pages: 421-432
Published online: 19 Sep 2012
AbstractforIdentification and Characterization of Two Novel and Differentially Expressed Isoforms of Human α2- and α1-Globin Genes | Full Text | References | PDF (852.2 KB)
  • 156 Views
  • 2 CrossRef citations
  • 0Altmetric
Article
A Single Nucleotide Polymorphism in the HBBP1 Gene in the Human β-Globin Locus is Associated with a Mild β-Thalassemia Disease Phenotype
Emily Giannopoulou, Marina Bartsakoulia, Christina Tafrali, Alexandra Kourakli, Konstantinos Poulas, Eleana F. Stavrou, Adamantia Papachatzopoulou, Marianthi Georgitsi & George P. Patrinos
Pages: 433-445
Published online: 19 Sep 2012
AbstractforA Single Nucleotide Polymorphism in the HBBP1 Gene in the Human β-Globin Locus is Associated with a Mild β-Thalassemia Disease Phenotype | Full Text | References | PDF (463.3 KB)
  • 360 Views
  • 18 CrossRef citations
  • 0Altmetric
Article
A 25-Year Observation of a Japanese Female Patient with Hb Nottingham who has Two Children with the Same Disorder
Yuko Cho, Susumu Iizuka, Yoshio Hatae, Kunihiko Kobayashi, Yukio Hattori, Yasuhiro Yamashiro & Tadashi Ariga
Pages: 446-455
Published online: 19 Sep 2012
AbstractforA 25-Year Observation of a Japanese Female Patient with Hb Nottingham who has Two Children with the Same Disorder | Full Text | References | PDF (379.3 KB)
  • 77 Views
  • 1 CrossRef citations
  • 0Altmetric
Article
Profile of β-Thalassemia and its Prenatal Diagnosis in Khorasan-E-Jonobi Province, Iran
Ebrahim Miri-Moghaddam & Azita Zadeh-Vakili
Pages: 456-463
Published online: 19 Sep 2012
AbstractforProfile of β-Thalassemia and its Prenatal Diagnosis in Khorasan-E-Jonobi Province, Iran | Full Text | References | PDF (133.5 KB)
  • 87 Views
  • 1 CrossRef citations
  • 0Altmetric
Article
The Spectrum of α- And β-Thalassemia Mutations in Yunnan Province of Southwestern China
Jie Zhang, Bao-Sheng Zhu, Jing He, Xiao-Hong Zeng, Jie Su, Xiang-Hu Xu, Su-Yun Li, Hong Chen & Ying-Hong Zhang
Pages: 464-473
Published online: 19 Sep 2012
AbstractforThe Spectrum of α- And β-Thalassemia Mutations in Yunnan Province of Southwestern China | Full Text | References | PDF (236.7 KB)
  • 290 Views
  • 35 CrossRef citations
  • 0Altmetric

Short Communication

Article
A New Hemoglobin Variant: Hb Izmir [β86(F2)Ala→Val, GCC>GTC; HBB:c.260C>T]
Aydan Çelebiler, Derya Aksoy, Serkan Ocakcı & Baysal Karaca
Pages: 474-479
Published online: 19 Sep 2012
AbstractforA New Hemoglobin Variant: Hb Izmir [β86(F2)Ala→Val, GCC>GTC; HBB:c.260C>T] | Full Text | References | PDF (300.6 KB)
  • 119 Views
  • 3 CrossRef citations
  • 0Altmetric
Article
Hb Filottrano [codon 120 (–A)]: A Novel Frameshift Mutation in Exon 3 of the β-Globin Gene Causing Dominantly Inherited β-Thalassemia Intermedia
Antonio Amato, Maria Pia Cappabianca, Maria Perri, Ivo Zaghis, Fabrizio Mastropietro, Donatella Ponzini, Paola Di Biagio & Roberta Piscitelli
Pages: 480-484
Published online: 19 Sep 2012
AbstractforHb Filottrano [codon 120 (–A)]: A Novel Frameshift Mutation in Exon 3 of the β-Globin Gene Causing Dominantly Inherited β-Thalassemia Intermedia | Full Text | References | PDF (354.3 KB)
  • 94 Views
  • 5 CrossRef citations
  • 0Altmetric
Article
Hb E/β-Thalassemia: The Second Most Common Cause of Transfusion-Dependent Thalassemia in the Gwalior-Chambal Region of Central India
Rakesh Kumar, Dharmesh C. Sharma & Purnima Kishor
Pages: 485-490
Published online: 19 Sep 2012
AbstractforHb E/β-Thalassemia: The Second Most Common Cause of Transfusion-Dependent Thalassemia in the Gwalior-Chambal Region of Central India | Full Text | References | PDF (157.4 KB)
  • 116 Views
  • 3 CrossRef citations
  • 0Altmetric
Article
Unmasking Hb Paksé (codon 142, TAA>TAT, α2) and its Combinations in Patients also Carrying Hb Constant Spring (codon 142, TAA>CAA, α2) in Northern Thailand
Sakorn Pornprasert, Sitthichai Panyasai & Kallayanee Treesuwan
Pages: 491-496
Published online: 19 Sep 2012
AbstractforUnmasking Hb Paksé (codon 142, TAA>TAT, α2) and its Combinations in Patients also Carrying Hb Constant Spring (codon 142, TAA>CAA, α2) in Northern Thailand | Full Text | References | PDF (174.4 KB)
  • 222 Views
  • 7 CrossRef citations
  • 0Altmetric
Article
The IVS-II-837 (T>G) Appears to be a Relatively Common 'Rare' β-Globin Gene Mutation in β-Thalassemia Patients in Karnataka State, South India
Murali D. Bashyam, Ajay K. Chaudhary & Vijay Bhat
Pages: 497-503
Published online: 19 Sep 2012
AbstractforThe IVS-II-837 (T>G) Appears to be a Relatively Common 'Rare' β-Globin Gene Mutation in β-Thalassemia Patients in Karnataka State, South India | Full Text | References | PDF (181 KB)
  • 129 Views
  • 2 CrossRef citations
  • 0Altmetric
Article
Identification of a New HBA1 Gene Mutation (HBA1:c.301-2A>T) in Cis with Hb Riccarton (HBA1:c.154G>A) [α51(CE9)Gly→Ser]
Karen G. Scheps, Amanda Binaghi & Viviana Varela
Pages: 504-507
Published online: 19 Sep 2012
AbstractforIdentification of a New HBA1 Gene Mutation (HBA1:c.301-2A>T) in Cis with Hb Riccarton (HBA1:c.154G>A) [α51(CE9)Gly→Ser] | Full Text | References | PDF (257.7 KB)
  • 206 Views
  • 4 CrossRef citations
  • 0Altmetric
Article
A New Frameshift Mutation on the α2-Globin Gene Causing α+-Thalassemia: Codon 43 (TTC>–TC or TTC>T–C)
Philippe Joly, Philippe Lacan, Caroline Garcia, Claire Barro & Alain Francina
Pages: 508-510
Published online: 19 Sep 2012
AbstractforA New Frameshift Mutation on the α2-Globin Gene Causing α+-Thalassemia: Codon 43 (TTC>–TC or TTC>T–C) | Full Text | References | PDF (244.4 KB)
  • 81 Views
  • 1 CrossRef citations
  • 0Altmetric
Article
α-Thalassemia Trait Caused by Frameshift Mutations in Exon 2 of the α2-Globin Gene: HBA2:c.131delT and HBA2:c.143delA
Jill Finlayson, Reza Ghassemifar, Paula Holmes, Dianne Grey, Christopher Newbound, Nicole Pell, Michelle Jennens, Laura Greenwood & John Beilby
Pages: 511-515
Published online: 19 Sep 2012
Abstractforα-Thalassemia Trait Caused by Frameshift Mutations in Exon 2 of the α2-Globin Gene: HBA2:c.131delT and HBA2:c.143delA | Full Text | References | PDF (269.2 KB)
  • 144 Views
  • 1 CrossRef citations
  • 0Altmetric

Explore articles

Explore the most recently published articles

A Novel 165 Kb Duplication Involving the α-Globin Gene Cluster Is Identified by Low-Pass Whole Genome Sequencing in a Chinese Thalassemia Intermedia Patient
Xiaohong He et al.
Brief Report | Published online: 1 May 2024
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
View all latest articles