Hemoglobin, Volume 41, Issue 3 (2017)

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

Hemoglobin, Volume 41, Issue 3 (2017)

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 Volume 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 Article

Article
Correlation of Pancreatic Iron Overload Measured by T2*-Weighted Magnetic Resonance Imaging in Diabetic Patients with β-Thalassemia Major
Mehrnoush Kosaryan, Malihe Rahimi, Hadi Darvishi-Khezri, Neda Gholizadeh, Rozita Akbarzadeh & Aily Aliasgharian
Pages: 151-156
Published online: 01 Aug 2017
AbstractforCorrelation of Pancreatic Iron Overload Measured by T2*-Weighted Magnetic Resonance Imaging in Diabetic Patients with β-Thalassemia Major | Full Text | References | PDF (719.8 KB)
  • 161 Views
  • 10 CrossRef citations
  • 0Altmetric
Article
Prevalence of Thalassemia Traits and Iron Deficiency Anemia in Sindh, Pakistan
Abdul H. Kandhro, Virapong Prachayasittikul, Chartchalerm Isarankura Na-Ayudhya & Pornlada Nuchnoi
Pages: 157-163
Published online: 26 Jul 2017
AbstractforPrevalence of Thalassemia Traits and Iron Deficiency Anemia in Sindh, Pakistan | Full Text | References | PDF (1.6 MB)
  • 236 Views
  • 2 CrossRef citations
  • 0Altmetric
Article
Prevalence, Incidence, Trend, and Complications of Thalassemia in Iraq
Kamal A. Kadhim, Kadhim H. Baldawi & Faris H. Lami
Pages: 164-168
Published online: 24 Aug 2017
AbstractforPrevalence, Incidence, Trend, and Complications of Thalassemia in Iraq | Full Text | References | PDF (660.6 KB)
  • 376 Views
  • 34 CrossRef citations
  • 0Altmetric
Article
Comparison of Quality of Life in Patients with β-Thalassemia Intermedia and β-Thalassemia Major in Southern Iran
Sezaneh Haghpanah, Sara Vahdati & Mehran Karimi
Pages: 169-174
Published online: 25 Jul 2017
AbstractforComparison of Quality of Life in Patients with β-Thalassemia Intermedia and β-Thalassemia Major in Southern Iran | Full Text | References | PDF (660.3 KB)
  • 114 Views
  • 6 CrossRef citations
  • 0Altmetric
Article
First Report of a Novel Deletion Due to εγδβ-Thalassemia in a Chinese Family
Annie S. Y. Hui, Patrick K. C. Au, Yuen-Ha Ting, Anita S. Y. Kan, Yvonne K. Y. Cheng, Alex W. K. Leung, Kelvin Y. K. Chan, Chi-Kong Li, Mary H. Y. Tang & Tak-Yeung Leung
Pages: 175-179
Published online: 27 Sep 2017
AbstractforFirst Report of a Novel Deletion Due to εγδβ-Thalassemia in a Chinese Family | Full Text | References | PDF (1.5 MB)
  • 172 Views
  • 8 CrossRef citations
  • 0Altmetric
Article
A Novel 31.1 kb α-Thalassemia Deletion (– –MEX3) Found in a Mexican Family
Víctor M. Rentería-López, Francisco J. Perea-Díaz, Lourdes C. Rizo-delaTorre, Josefina Y. Sánchez-López & Bertha Ibarra-Cortés
Pages: 180-184
Published online: 09 Aug 2017
AbstractforA Novel 31.1 kb α-Thalassemia Deletion (– –MEX3) Found in a Mexican Family | Full Text | References | PDF (1.1 MB)
  • 149 Views
  • 1 CrossRef citations
  • 0Altmetric
Article
α+-Thalassemia Caused by an 811 bp Deletion in Individuals from Nanning, Guangxi: A Report of Two Cases
Qiang Zhang, Mingli Xu, Wanjun Zhou & Xin Fan
Pages: 185-188
Published online: 27 Sep 2017
Abstractforα+-Thalassemia Caused by an 811 bp Deletion in Individuals from Nanning, Guangxi: A Report of Two Cases | Full Text | References | PDF (805.4 KB)
  • 76 Views
  • 1 CrossRef citations
  • 0Altmetric
Article
Hb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and − −SEA/αα
Qiang Zhang, Xin Fan, Mingli Xu, Yijia Zhang, Huiling Xu, Xiaojun Wen & Wanjun Zhou
Pages: 189-192
Published online: 27 Sep 2017
AbstractforHb H Disease Caused by Multiple Mutations in the Polyadenylation Signal Site and − −SEA/αα | Full Text | References | PDF (882 KB)
  • 154 Views
  • 2 CrossRef citations
  • 0Altmetric
Article
A Novel Variant with Positive Natural Selection Influenced Hb A2 Levels in Chinese Individuals with β-Thalassemia
Shanjuan Yu, Yang Chen, Ketong Lai, Roma Kajal Dewan & Yunyan He
Pages: 193-197
Published online: 05 Sep 2017
AbstractforA Novel Variant with Positive Natural Selection Influenced Hb A2 Levels in Chinese Individuals with β-Thalassemia | Full Text | References | PDF (494.3 KB)
  • 76 Views
  • 0 CrossRef citations
  • 0Altmetric
Article
Generation of Induced Pluripotent Stem Cells from Amniotic Fluid Cells of a Fetus with Hb Bart’s Disease
Jin-Mei Yan & Dong-Zhi Li
Pages: 198-202
Published online: 24 Aug 2017
AbstractforGeneration of Induced Pluripotent Stem Cells from Amniotic Fluid Cells of a Fetus with Hb Bart’s Disease | Full Text | References | PDF (1.3 MB)
  • 98 Views
  • 3 CrossRef citations
  • 0Altmetric

Short Communication

Rapid Communication
Coinheritance of Hb Bristol-Alesha [β67(E11)Val→Met; HBB: c.202G>A] and the α212 Patchwork Allele in a Brazilian Child with Severe Congenital Hemolytic Anemia
Gisele A. Pedroso, Elza M. Kimura, Magnun N. N. Santos, Dulcinéia M. Albuquerque, Jucilane L. H. Ferruzzi, Susan E. Jorge, Fernando F. Costa, Sara T. O. Saad & Maria F. Sonati
Pages: 203-208
Published online: 03 Jul 2017
AbstractforCoinheritance of Hb Bristol-Alesha [β67(E11)Val→Met; HBB: c.202G>A] and the α212 Patchwork Allele in a Brazilian Child with Severe Congenital Hemolytic Anemia | Full Text | References | PDF (1.2 MB)
  • 146 Views
  • 3 CrossRef citations
  • 0Altmetric
Rapid Communication
Coinheritance of High Oxygen Affinity Hb Helsinki [HBB: c.248A>T; β82(EF6)Lys→Met] with Hb H Disease
Shir-Ying Lee, Jia-Hui Goh, Karen M. L. Tan & Te-Chih Liu
Pages: 209-212
Published online: 09 Aug 2017
AbstractforCoinheritance of High Oxygen Affinity Hb Helsinki [HBB: c.248A>T; β82(EF6)Lys→Met] with Hb H Disease | Full Text | References | PDF (875.6 KB)
  • 118 Views
  • 0 CrossRef citations
  • 0Altmetric
Rapid Communication
Hematological and Molecular Characterization of a Novel Hb A2 Variant with Homozygous α-Thalassemia-2 in a Southern Thai Individual
Manit Nuinoon, Nutjaree Jeenduang, Aumpika Kesornsit, Dararat Horpet & Thunyaluk Plyduang
Pages: 213-215
Published online: 10 Aug 2017
AbstractforHematological and Molecular Characterization of a Novel Hb A2 Variant with Homozygous α-Thalassemia-2 in a Southern Thai Individual | Full Text | References | PDF (702.8 KB)
  • 137 Views
  • 10 CrossRef citations
  • 0Altmetric
Rapid Communication
A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal Hemoglobin
Graham R. Serjeant, Beryl E. Serjeant, Ian R. Hambleton, Matthew Oakley, Swee Lay Thein & Barnaby Clark
Pages: 216-217
Published online: 05 Sep 2017
AbstractforA Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal Hemoglobin | Full Text | References | PDF (242.6 KB)
  • 140 Views
  • 6 CrossRef citations
  • 0Altmetric
Rapid Communication
α0-Thalassemia Due to a 90.7 kb Deletion (– –NFLD)
John S. Waye, Barry Eng, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura & Lynda Walker
Pages: 218-219
Published online: 13 Sep 2017
Abstractforα0-Thalassemia Due to a 90.7 kb Deletion (– –NFLD) | Full Text | References | PDF (473.6 KB)
  • 99 Views
  • 1 CrossRef citations
  • 0Altmetric
Rapid Communication
Phenotypic Evaluation of a Novel Nucleotide Substitution (HBD: c.442T>C) on the δ-Globin Gene
Filippo Cassarà, Margherita Vinciguerra, Monica Cannata, Giorgio Marchese, Cristina Passarello, Filippo Leto, Aurelio Maggio & Antonino Giambona
Pages: 220-222
Published online: 27 Sep 2017
AbstractforPhenotypic Evaluation of a Novel Nucleotide Substitution (HBD: c.442T>C) on the δ-Globin Gene | Full Text | References | PDF (493.1 KB)
  • 59 Views
  • 0 CrossRef citations
  • 0Altmetric
Rapid Communication
Rivaroxaban Use in Patients with Hemoglobinopathies
Chrysoula Apostolou, Philippos Klonizakis, Maria Mainou, Eleni Kapsali, Katerina Kafantari, Aggeliki Kotsiafti, Evaggelia Vetsiou, Sofia Vakalopoulou & Efthymia Vlachaki
Pages: 223-224
Published online: 27 Sep 2017
AbstractforRivaroxaban Use in Patients with Hemoglobinopathies | Full Text | References | PDF (246.6 KB)
  • 291 Views
  • 16 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