Hemoglobin, Volume 42, Issue 2 (2018)

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

Hemoglobin, Volume 42, Issue 2 (2018)

See all volumes and issues
Vol 48, 2024 Vol 47, 2023 Vol 46, 2022 Vol 45, 2021 Vol 44, 2020 Vol 43, 2019 Volume 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
Prevalence and Characteristics of Priapism in Sickle Cell Disease
Giovanna A.O. Arduini & Alessandra B. Trovó de Marqui
Pages: 73-77
Published online: 10 May 2018
AbstractforPrevalence and Characteristics of Priapism in Sickle Cell Disease | Full Text | References | PDF (609.2 KB)
  • 390 Views
  • 19 CrossRef citations
  • 0Altmetric

Original Article

Article
Hb Oslo [β42(CD1)Phe→Ile; HBB: c.127T>A]: A Novel Unstable Hemoglobin Variant Found in a Norwegian Patient
Runa M. Grimholt, Anne Vestli, Petter Urdal, Anne Grete Bechensteen, Bente Fjeld, Bjørn Dalhus & Olav Klingenberg
Pages: 78-83
Published online: 23 Jul 2018
AbstractforHb Oslo [β42(CD1)Phe→Ile; HBB: c.127T>A]: A Novel Unstable Hemoglobin Variant Found in a Norwegian Patient | Full Text | References | PDF (1.1 MB)
  • 192 Views
  • 3 CrossRef citations
  • 0Altmetric
Article
Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India
Aditya N. Jha, Hrishikesh Mishra, Henu K. Verma, Isha Pandey & Bhaskar V.K.S. Lakkakula
Pages: 84-90
Published online: 11 Sep 2018
AbstractforCompound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India | Full Text | References | PDF (1.2 MB)
  • 214 Views
  • 7 CrossRef citations
  • 0Altmetric
Article
Molecular Characterization of β-Thalassemia Mutations Via the Amplification Refractory Mutation System-Polymerase Chain Reaction Method at the North Waziristan Agency, Pakistan
Noor M. Khan, Shoaib Ur. Rehman, Muhammad Shakeel, Saadullah Khan, Usman Ahmed, Hazir Rehman, Tabassum Yaseen & Asad Javid
Pages: 91-95
Published online: 11 Sep 2018
AbstractforMolecular Characterization of β-Thalassemia Mutations Via the Amplification Refractory Mutation System-Polymerase Chain Reaction Method at the North Waziristan Agency, Pakistan | Full Text | References | PDF (695.5 KB)
  • 111 Views
  • 2 CrossRef citations
  • 0Altmetric

Articles

Article
Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia
Rim Belhaj Nefissi, Radhouene Doggui, Faida Ouali, Taieb Messaoud & Nasreddine Gritli
Pages: 96-102
Published online: 11 Sep 2018
AbstractforFactor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia | Full Text | References | PDF (587.1 KB)
  • 107 Views
  • 4 CrossRef citations
  • 0Altmetric

Original Article

Article
Study on the Role of Polymorphisms of the SOX-6 and MYB Genes and Fetal Hemoglobin Levels in Sicilian Patients with β-Thalassemia and Sickle Cell Disease
Florinda Listì, Serena Sclafani, Veronica Agrigento, Rita Barone, Aurelio Maggio & Elena D’Alcamo
Pages: 103-107
Published online: 11 Sep 2018
AbstractforStudy on the Role of Polymorphisms of the SOX-6 and MYB Genes and Fetal Hemoglobin Levels in Sicilian Patients with β-Thalassemia and Sickle Cell Disease | Full Text | References | PDF (462.4 KB)
  • 95 Views
  • 2 CrossRef citations
  • 0Altmetric
Article
Relationship of the Interaction Between Two Quantitative Trait Loci with γ-Globin Expression in β-Thalassemia Intermedia Patients
Shiva NickAria, Sezaneh Haghpanah, Mani Ramzi & Mehran Karimi
Pages: 108-112
Published online: 10 May 2018
AbstractforRelationship of the Interaction Between Two Quantitative Trait Loci with γ-Globin Expression in β-Thalassemia Intermedia Patients | Full Text | References | PDF (571.9 KB)
  • 75 Views
  • 1 CrossRef citations
  • 0Altmetric

Articles

Article
Assessment of Peripheral Neuropathy in Patients with β-Thalassemia via Electrophysiological Study: Reevaluation in the Era of Iron Chelators
Turan Bayhan, Şule Ünal, Bahadır Konuşkan, Onur Erdem, Erdem Karabulut & Fatma Gümrük
Pages: 113-116
Published online: 11 Sep 2018
AbstractforAssessment of Peripheral Neuropathy in Patients with β-Thalassemia via Electrophysiological Study: Reevaluation in the Era of Iron Chelators | Full Text | References | PDF (381.1 KB)
  • 146 Views
  • 5 CrossRef citations
  • 0Altmetric

Original Article

Article
Molecular Spectrum of α- and β-Thalassemia Mutations in a Large Ethnic Hakka Population in Southern China
Pingsen Zhao, Ruiqiang Weng & Heming Wu
Pages: 117-121
Published online: 23 Jul 2018
AbstractforMolecular Spectrum of α- and β-Thalassemia Mutations in a Large Ethnic Hakka Population in Southern China | Full Text | References | PDF (767.7 KB)
  • 135 Views
  • 11 CrossRef citations
  • 0Altmetric

Original article

Article
Novel α-Globin Splice Site Mutation (HBA2: c.96-5C>A) in Combination with Three-Gene Deletion Hb H Disease
Neil Van de Water, Tina Tan, Megan Crowley, Romy Kerr & Peter Browett
Pages: 122-125
Published online: 11 Sep 2018
AbstractforNovel α-Globin Splice Site Mutation (HBA2: c.96-5C>A) in Combination with Three-Gene Deletion Hb H Disease | Full Text | References | PDF (810.5 KB)
  • 61 Views
  • 0 CrossRef citations
  • 0Altmetric

Short Communication

Rapid Communication
Characterization of Two Deep Intronic Variants on the β-Globin Gene with Inconsistent Interpretations of Clinical Significance
Runa M. Grimholt, Cornelis L. Harteveld, Sandra G. J. Arkesteijn, Bente Fjeld & Olav Klingenberg
Pages: 126-128
Published online: 26 Jul 2018
AbstractforCharacterization of Two Deep Intronic Variants on the β-Globin Gene with Inconsistent Interpretations of Clinical Significance | Full Text | References | PDF (318.2 KB)
  • 177 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
Compound Heterozygosity for Hb Adana (HBA2: c.179G>A) and the –α3.7/αα Thalassemia Deletion in Greece: Clinical Phenotype and Genetic Counseling
Stamatia Theodoridou, Aikaterini Teli, Eleni Yfanti, Timoleon-Achilleas Vyzantiadis, Theodoros Theodoridis & Marina Economou
Pages: 129-131
Published online: 20 Jul 2018
AbstractforCompound Heterozygosity for Hb Adana (HBA2: c.179G>A) and the –α3.7/αα Thalassemia Deletion in Greece: Clinical Phenotype and Genetic Counseling | Full Text | References | PDF (308.2 KB)
  • 109 Views
  • 0 CrossRef citations
  • 0Altmetric
Rapid Communication
Molecular and Hematological Characterization of Two Novel δ-Globin Gene Mutations Found in Chinese Individuals
Manna Sun, Jiwu Lou, Ying Zhao & Yanhui Liu
Pages: 132-134
Published online: 03 May 2018
AbstractforMolecular and Hematological Characterization of Two Novel δ-Globin Gene Mutations Found in Chinese Individuals | Full Text | References | PDF (664.5 KB)
  • 74 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
δ-Thalassemia with Complete Absence of Hb A2 in a Chinese Family
Hai-Shen Tang, De-Gang Wang, Lv-Yin Huang & Dong-Zhi Li
Pages: 135-137
Published online: 08 May 2018
Abstractforδ-Thalassemia with Complete Absence of Hb A2 in a Chinese Family | Full Text | References | PDF (740 KB)
  • 133 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
Fetal Hemoglobin in the Maternal Circulation – Contribution of Fetal Red Blood Cells
Mutaz Dana & Eitan Fibach
Pages: 138-140
Published online: 10 May 2018
AbstractforFetal Hemoglobin in the Maternal Circulation – Contribution of Fetal Red Blood Cells | Full Text | References | PDF (470.5 KB)
  • 381 Views
  • 2 CrossRef citations
  • 0Altmetric
Rapid Communication
Compound Heterozygosity for Hb Alperton (HBB: c.407C>T) and IVS-I-5 (G>C) (HBB: c.92+5G>C) Mutations Presenting as a Moderate Anemia in an Indian Family
Koumudi G. Godbole, Angalena Ramachandran, Ashwini S. Karkamkar & Ashwin B. Dalal
Pages: 141-142
Published online: 13 Apr 2018
AbstractforCompound Heterozygosity for Hb Alperton (HBB: c.407C>T) and IVS-I-5 (G>C) (HBB: c.92+5G>C) Mutations Presenting as a Moderate Anemia in an Indian Family | Full Text | References | PDF (273.7 KB)
  • 113 Views
  • 1 CrossRef citations
  • 0Altmetric

Corrigenda

Correction
Corrigendum
Page: x
Published online: 11 Sep 2018
CitationforCorrigendum | Full Text | PDF (91.5 KB)
  • 398 Views
  • 0 CrossRef citations
  • 0Altmetric
Free Access

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