Hemoglobin, Volume 43, Issue 4-5 (2019)

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

Hemoglobin, Volume 43, Issue 4-5 (2019)

See all volumes and issues
Vol 48, 2024 Vol 47, 2023 Vol 46, 2022 Vol 45, 2021 Vol 44, 2020 Volume 43, 2019 Vol 42, 2018 Vol 41, 2017 Vol 40, 2016 Vol 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

Original Articles

Article
Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15)
Wissem Abdaoui, Djamel Eddine Benouareth, Amel Djenouni, Celine Renoux, Fatiha Grifi, Adel Gouri, Fateh Athamnia, Manel Benalioua & Philippe Joly
Pages: 223-228
Published online: 11 Oct 2019
AbstractforGenetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15) | Full Text | References | PDF (692.8 KB) | EPUB
  • 190 Views
  • 8 CrossRef citations
  • 0Altmetric
Article
Reticulocyte Hemoglobin Equivalent (Ret-He) Combined with Red Blood Cell Distribution Width Has a Differentially Diagnostic Value for Thalassemias
Yu Lian, Jun Shi, Neng Nie, Zhendong Huang, Yingqi Shao, Jing Zhang, Jinbo Huang, Xingxin Li, Meili Ge, Peng Jin, Min Wang & Yizhou Zheng
Pages: 229-235
Published online: 03 Sep 2019
AbstractforReticulocyte Hemoglobin Equivalent (Ret-He) Combined with Red Blood Cell Distribution Width Has a Differentially Diagnostic Value for Thalassemias | Full Text | References | PDF (817.8 KB) | EPUB
  • 295 Views
  • 8 CrossRef citations
  • 0Altmetric
Article
Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (– –SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart’s Hydrops Fetalis Syndrome in Thailand
Wittaya Jomoui, Wanicha Tepakhan & Rossarin Karnpean
Pages: 236-240
Published online: 21 Oct 2019
AbstractforStrong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (– –SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart’s Hydrops Fetalis Syndrome in Thailand | Full Text | References | PDF (740.6 KB) | EPUB
  • 124 Views
  • 2 CrossRef citations
  • 0Altmetric
Article
Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATC or HBA2: c.3G>C)
Ya-Li Lei, Hong Sui, Yu-Juan Liu, Jun-Jun Pan, Yan-Hui Liu & Ji-Wu Lou
Pages: 241-244
Published online: 05 Nov 2019
AbstractforMolecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATC or HBA2: c.3G>C) | Full Text | References | PDF (801.9 KB) | EPUB
  • 78 Views
  • 5 CrossRef citations
  • 0Altmetric
Article
Analysis of Deletional Hb H Diseases in Samples with Hb A2-Hb H and Hb A2-Hb Bart’s on Capillary Electrophoresis
Kunyakan Khongthai, Chedtapak Ruengdit, Sitthichai Panyasai & Sakorn Pornprasert
Pages: 245-248
Published online: 05 Nov 2019
AbstractforAnalysis of Deletional Hb H Diseases in Samples with Hb A2-Hb H and Hb A2-Hb Bart’s on Capillary Electrophoresis | Full Text | References | PDF (693.4 KB) | EPUB
  • 142 Views
  • 3 CrossRef citations
  • 0Altmetric
Article
Thalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam
Tuan Mai Anh, Kanokwan Sanchaisuriya, Giang Nguyen Kieu, Dung Nguyen Tien, Huong Bui Thi Thu, Pattara Sanchaisuriya, Supan Fucharoen, Goonnapa Fucharoen & Frank P. Schelp
Pages: 249-253
Published online: 03 Oct 2019
AbstractforThalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam | Full Text | References | PDF (438.3 KB) | EPUB
  • 212 Views
  • 7 CrossRef citations
  • 0Altmetric
Article
Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-Thalassemia
Aye Chan Pyae, Hataichanok Srivorakun, Attawut Chaibunruang, Kritsada Singha, Kanchana Tomanakarn, Goonnapa Fucharoen & Supan Fucharoen
Pages: 254-257
Published online: 10 Oct 2019
AbstractforMolecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-Thalassemia | Full Text | References | PDF (381.6 KB) | EPUB
  • 138 Views
  • 2 CrossRef citations
  • 0Altmetric
Article
Association of the CCR5Δ32 Mutant Genotype with Sickle Cell Disease in Egyptian Patients
Maha H. El Sissy, Ahmed A. Hafez, Sherif E.A. Moneim & Doaa M. Eldemerdash
Pages: 258-263
Published online: 28 Oct 2019
AbstractforAssociation of the CCR5Δ32 Mutant Genotype with Sickle Cell Disease in Egyptian Patients | Full Text | References | PDF (516.2 KB) | EPUB
  • 56 Views
  • 1 CrossRef citations
  • 0Altmetric
Article
The Effect of Blood Transfusion on Growth of Patients with Hb E/β-Thalassemia
Ampaiwan Chuansumrit, Nongnuch Sirachainan, Pimpun Kitpoka, Praguywan Kadegasem, Duantida Songdej, Werasak Sasanakul & Pakawan Wongwerawattanakoon
Pages: 264-272
Published online: 25 Nov 2019
AbstractforThe Effect of Blood Transfusion on Growth of Patients with Hb E/β-Thalassemia | Full Text | References | PDF (1.6 MB) | EPUB
  • 180 Views
  • 1 CrossRef citations
  • 0Altmetric

Short Communications

Rapid Communication
A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AGT>AGG); HBB: c.270T>G] Resulting in Hemoglobin Vanderbilt
William Shomali, Rondeep Brar, Subramanyeswara R. Arekapudi & Jason R. Gotlib
Pages: 273-276
Published online: 28 Oct 2019
AbstractforA Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AGT>AGG); HBB: c.270T>G] Resulting in Hemoglobin Vanderbilt | Full Text | References | PDF (1 MB) | EPUB
  • 61 Views
  • 0 CrossRef citations
  • 0Altmetric
Rapid Communication
A De Novo Heterozygous Variant (HBB: c.379delG, p.Val127Cysfs*32) Associated with a Mild β-Thalassemia Intermedia Phenotype in a Turkish Child
Dilek Gürlek-Gökçebay, Sibel Akpinar-Tekgunduz, Haktan B. Erdem & Nese Yarali
Pages: 277-279
Published online: 17 Sep 2019
AbstractforA De Novo Heterozygous Variant (HBB: c.379delG, p.Val127Cysfs*32) Associated with a Mild β-Thalassemia Intermedia Phenotype in a Turkish Child | Full Text | References | PDF (836.8 KB) | EPUB
  • 76 Views
  • 0 CrossRef citations
  • 0Altmetric
Rapid Communication
A Novel Frameshift Mutation at Codon 2 (–T) (HBB: c.9delT) and First Report of Three New β-Globin Mutations From Azerbaijan
Bayram Bayramov, Gunay Aliyeva, Chingiz Asadov, Tahira Mammadova, Nigar Karimova, Khagani Eynullazadeh, Surmaya Gafarova, Seymur Akbarov, Sabina Farhadova, Zumrud Safarzadeh & Mehraj Abbasov
Pages: 280-282
Published online: 03 Sep 2019
AbstractforA Novel Frameshift Mutation at Codon 2 (–T) (HBB: c.9delT) and First Report of Three New β-Globin Mutations From Azerbaijan | Full Text | References | PDF (1 MB) | EPUB
  • 245 Views
  • 0 CrossRef citations
  • 0Altmetric
Rapid Communication
Description of a rare β-globin gene mutation, IVS-II-848 (C>A) (HBB: c.316-3C>A) in association with IVS-I-1 (G>A) (HBB: c.92 + 1G>A), observed in a Syrian family: a case report
Ahmad Shoujaa, Yasser Mukhalalaty, Hossam Murad & Faizeh Al-Quobaili
Pages: 283-285
Published online: 12 Nov 2019
AbstractforDescription of a rare β-globin gene mutation, IVS-II-848 (C>A) (HBB: c.316-3C>A) in association with IVS-I-1 (G>A) (HBB: c.92 + 1G>A), observed in a Syrian family: a case report | Full Text | References | PDF (499.5 KB) | EPUB
  • 105 Views
  • 1 CrossRef citations
  • 0Altmetric
Rapid Communication
Compound Heterozygosity for an Unstable Novel Hemoglobin Variant, Hb Dongguan [α52(E1)Ser→Cys (TCT>TGT); HBA1: c.158C>G], and the – –SEA (Southeast Asian) α-Thalassemia Deletion
Wei-Dong Chen, Yu-Xiang Ren, Ya-Jun Wang, Wei-Jie Xie, Jie Li, An-Ping Xu & Ling Ji
Pages: 286-288
Published online: 25 Oct 2019
AbstractforCompound Heterozygosity for an Unstable Novel Hemoglobin Variant, Hb Dongguan [α52(E1)Ser→Cys (TCT>TGT); HBA1: c.158C>G], and the – –SEA (Southeast Asian) α-Thalassemia Deletion | Full Text | References | PDF (724.1 KB) | EPUB
  • 92 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
A β-Thalassemia Trait with Two Mutations in Cis in a Chinese Family
Jian Li, Fan Jiang, Li Zhen, Xue-Wei Tang & Dong-Zhi Li
Pages: 289-291
Published online: 05 Nov 2019
AbstractforA β-Thalassemia Trait with Two Mutations in Cis in a Chinese Family | Full Text | References | PDF (800.6 KB) | EPUB
  • 93 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
Congenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report
Hua Jiang, Fan Jiang, Jian Li, Fang Tang & Dong-Zhi Li
Pages: 292-295
Published online: 23 Oct 2019
AbstractforCongenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report | Full Text | References | PDF (1.1 MB) | EPUB
  • 102 Views
  • 6 CrossRef citations
  • 0Altmetric
Rapid Communication
Use of Direct Oral Anticoagulants in Patients with Sickle Cell Disease and Venous Thromboembolism: A Prospective Cohort Study of 12 Patients
Jacques-Robert Christen, Julien Bertolino, Estelle Jean, Laurence Camoin, Mikael Ebbo, Jean-Robert Harlé, Nicolas Schleinitz, Gabrielle Sarlon & Emmanuelle Bernit
Pages: 296-299
Published online: 14 Nov 2019
AbstractforUse of Direct Oral Anticoagulants in Patients with Sickle Cell Disease and Venous Thromboembolism: A Prospective Cohort Study of 12 Patients | Full Text | References | PDF (376.5 KB) | EPUB
  • 362 Views
  • 15 CrossRef citations
  • 0Altmetric

Explore articles