Hemoglobin, Volume 43, Issue 1 (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 1 (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

Review Article

Review Article
Purulent Pericarditis in Sickle Cell Disease Due to Streptococcus agalactiae; a Unique Case Report and Literature Review
Alina Bhat, Elvira Neculiseanu, Eric L. Tam, Adam Gendy, Daniel L. Beckles, Carol Luhrs & Albert Braverman
Pages: 1-3
Published online: 18 Mar 2019
AbstractforPurulent Pericarditis in Sickle Cell Disease Due to Streptococcus agalactiae; a Unique Case Report and Literature Review | Full Text | References | PDF (691.5 KB) | EPUB
  • 126 Views
  • 3 CrossRef citations
  • 0Altmetric

Original Article

Article
Hb Milano [α109(G16)Leu→Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the α1-Globin Gene in an Italian Family
Cristina Curcio, Valentina Giannone, Elena Benzoni, Claudia Cesaretti & Giovanni Ivaldi
Pages: 4-6
Published online: 14 May 2019
AbstractforHb Milano [α109(G16)Leu→Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the α1-Globin Gene in an Italian Family | Full Text | References | PDF (400.9 KB) | EPUB
  • 84 Views
  • 0 CrossRef citations
  • 0Altmetric
Article
Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln; HBB: c.442T>C)] on the β-Globin Gene
Qiong Su, Shiping Chen, Liusong Wu, Runmei Tian, Xiaoqin Yang, Xiaoyan Huang, Yan Chen, Zhiyu Peng & Jindong Chen
Pages: 7-11
Published online: 14 May 2019
AbstractforSevere Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln; HBB: c.442T>C)] on the β-Globin Gene | Full Text | References | PDF (1.3 MB) | EPUB
  • 148 Views
  • 6 CrossRef citations
  • 0Altmetric
Article
Krüppel-Like Factor 1 Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia
Ahmad Tamaddoni, Sahar Khabaz Astaneh, Reza Tabaripour & Haleh Akhavan-Niaki
Pages: 12-17
Published online: 12 Feb 2019
AbstractforKrüppel-Like Factor 1 Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia | Full Text | References | PDF (1.1 MB) | EPUB
  • 152 Views
  • 1 CrossRef citations
  • 0Altmetric
Article
The Spectrum of β-Thalassemia Mutations in Hamadan Province, West Iran
Reza Alibakhshi, Keivan Moradi, Mozaffar Aznab, Azam Azimi, Samaneh Shafieenia & Mostafa Biglari
Pages: 18-22
Published online: 16 May 2019
AbstractforThe Spectrum of β-Thalassemia Mutations in Hamadan Province, West Iran | Full Text | References | PDF (444.1 KB) | EPUB
  • 110 Views
  • 10 CrossRef citations
  • 0Altmetric
Article
Characterization of the IVS-II-821 (A>C) (HBB: c.316-30A>C) Mutation in a β-Thalassemia Phenotype in Iran
Azam Azimi, Parham Nejati, Soosan Tahmasebi, Sasan Alimoradi & Reza Alibakhshi
Pages: 23-26
Published online: 31 May 2019
AbstractforCharacterization of the IVS-II-821 (A>C) (HBB: c.316-30A>C) Mutation in a β-Thalassemia Phenotype in Iran | Full Text | References | PDF (758.9 KB) | EPUB
  • 128 Views
  • 0 CrossRef citations
  • 0Altmetric
Article
Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study
Alexandra Kolliopoulou, Stavroula Siamoglou, Anne John, Argyro Sgourou, Alexandra Kourakli, Argiris Symeonidis, Efthymia Vlachaki, Panagiota Chalkia, Stamatia Theodoridou, Bassam R. Ali, Theodora Katsila, George P. Patrinos & Adamantia Papachatzopoulou
Pages: 27-33
Published online: 30 Apr 2019
AbstractforRole of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study | Full Text | References | PDF (861 KB) | EPUB | Supplemental
  • 213 Views
  • 7 CrossRef citations
  • 0Altmetric
Article
The Role of Exercise Stress Echocardiography for Determination of Subclinical Cardiac Involvement in β-Thalassemia Major
Mozhgan Parsaee, Hamidreza Pouraliakbar, Azita Azarkeivan, Behshid Ghadrdoost & Mohaddeseh Behjati
Pages: 34-37
Published online: 14 May 2019
AbstractforThe Role of Exercise Stress Echocardiography for Determination of Subclinical Cardiac Involvement in β-Thalassemia Major | Full Text | References | PDF (372.4 KB) | EPUB
  • 53 Views
  • 2 CrossRef citations
  • 0Altmetric
Article
Iron Metabolism and Oxidative Status in Patients with Hb H Disease
Xi Yao, Lu-Hong Xu, Hong-Gui Xu, Xin-Yu Li, Yong Liu & Jian-Pei Fang
Pages: 38-41
Published online: 27 Mar 2019
AbstractforIron Metabolism and Oxidative Status in Patients with Hb H Disease | Full Text | References | PDF (763.2 KB) | EPUB
  • 142 Views
  • 2 CrossRef citations
  • 0Altmetric
Article
Insights into the Progression of Labile Hb A1c to Stable Hb A1cvia a Mechanistic Assessment of 2,3-Bisphosphoglycerate Facilitation of the Slow Nonenzymatic Glycation Process
Christina R. Mottishaw, Stephanie Becker, Brandy Smith, Gentry Titus, R.W. Holman & Kenneth J. Rodnick
Pages: 42-49
Published online: 07 May 2019
AbstractforInsights into the Progression of Labile Hb A1c to Stable Hb A1cvia a Mechanistic Assessment of 2,3-Bisphosphoglycerate Facilitation of the Slow Nonenzymatic Glycation Process | Full Text | References | PDF (1 MB) | EPUB | Supplemental
  • 96 Views
  • 0 CrossRef citations
  • 0Altmetric

Short Communication

Rapid Communication
An Additional Case of Hb Saint Nazaire [β103(G5)Phe→Ile; HBB: c.310T>A] Leading to Moderate Erythrocytosis in a French Family
Victor Bobée, Guillaume Feugray, Valéry Brunel, Philippe Joly & Agnès Lahary
Pages: 50-51
Published online: 30 Jan 2019
AbstractforAn Additional Case of Hb Saint Nazaire [β103(G5)Phe→Ile; HBB: c.310T>A] Leading to Moderate Erythrocytosis in a French Family | Full Text | References | PDF (563.7 KB) | EPUB
  • 64 Views
  • 0 CrossRef citations
  • 0Altmetric
Rapid Communication
Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2
Manit Nuinoon, Orapan Thipthara & Suthat Fucharoen
Pages: 52-55
Published online: 20 May 2019
AbstractforCompound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (HBB: c.364delG) and Hb E (HBB: c.79G>A) with Heterozygous α-Thalassemia-2 | Full Text | References | PDF (980.6 KB) | EPUB
  • 117 Views
  • 1 CrossRef citations
  • 0Altmetric
Rapid Communication
Severe Drug-Induced Hemolysis in a Patient with Compound Heterozygosity for Hb Peterborough (HBB: c.334G>T) and Hb Lepore-Boston-Washington (NG_000007.3: g.63632_71046del)
Charles Agbuduwe, Michelle Rugless, Nigel Asba, Melanie Proven & Muttuswamy Sivakumaran
Pages: 56-59
Published online: 07 May 2019
AbstractforSevere Drug-Induced Hemolysis in a Patient with Compound Heterozygosity for Hb Peterborough (HBB: c.334G>T) and Hb Lepore-Boston-Washington (NG_000007.3: g.63632_71046del) | Full Text | References | PDF (972.4 KB) | EPUB
  • 116 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
Unstable Hemoglobin Variants: The Need for Clinical Vigilance in Infants with Congenital Jaundice
Hua Jiang, Jian-Ying Zhou, Jian Li & Dong-Zhi Li
Pages: 60-62
Published online: 15 May 2019
AbstractforUnstable Hemoglobin Variants: The Need for Clinical Vigilance in Infants with Congenital Jaundice | Full Text | References | PDF (669.6 KB) | EPUB
  • 100 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
A Case Report of Compound Heterozygosity for β0/β+-Thalassemia Resulting from under Diagnosed β-Thalassemia Found in a Hb A'2 Sample
Nutjeera Intasai, Ampai Phasit, Sitthichai Panyasai & Sakorn Pornprasert
Pages: 63-65
Published online: 30 Apr 2019
AbstractforA Case Report of Compound Heterozygosity for β0/β+-Thalassemia Resulting from under Diagnosed β-Thalassemia Found in a Hb A'2 Sample | Full Text | References | PDF (345.6 KB) | EPUB
  • 93 Views
  • 3 CrossRef citations
  • 0Altmetric
Rapid Communication
First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family
Hossam Murad & Faten Moassas
Pages: 66-68
Published online: 07 Mar 2019
AbstractforFirst Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family | Full Text | References | PDF (590.2 KB) | EPUB
  • 110 Views
  • 0 CrossRef citations
  • 0Altmetric
Rapid Communication
Hb H Disease Results from Compound Heterozygosity of – –SEA and –αMAL3.5 in a Chinese Family
Ying Zhao, Jiwu Lou, Manna Sun, Youqing Fu, Wanling Ye, Yanjin Li, Yunshi Dai & Yanhui Liu
Pages: 69-72
Published online: 27 Feb 2019
AbstractforHb H Disease Results from Compound Heterozygosity of – –SEA and –αMAL3.5 in a Chinese Family | Full Text | References | PDF (824.8 KB) | EPUB
  • 87 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
Regulatory Single Nucleotide Polymorphism rs368698783 (G>A): a Genetic Modifier of Hb F Production Only under Erythropoietic Stress Characteristic for β-Globin Chain Deficiency?
Fan Jiang, Jian Li, Jian-Ying Zhou, Can Liao & Dong-Zhi Li
Pages: 73-75
Published online: 20 May 2019
AbstractforRegulatory Single Nucleotide Polymorphism rs368698783 (G>A): a Genetic Modifier of Hb F Production Only under Erythropoietic Stress Characteristic for β-Globin Chain Deficiency? | Full Text | References | PDF (462.7 KB) | EPUB
  • 81 Views
  • 2 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