Hemoglobin, Volume 40, Issue 5 (2016)

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Hemoglobin, Volume 40, Issue 5 (2016)

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Original Article

Article
Renal Failure in Sickle Cell Disease: Prevalence, Predictors of Disease, Mortality and Effect on Length of Hospital Stay
Sri L.H. Yeruva, Yonette Paul, Patricia Oneal & Mehdi Nouraie
Pages: 295-299
Published online: 18 Sep 2016
AbstractforRenal Failure in Sickle Cell Disease: Prevalence, Predictors of Disease, Mortality and Effect on Length of Hospital Stay | Full Text | References | PDF (437.9 KB)
  • 336 Views
  • 30 CrossRef citations
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Article
Hb Midnapore [β53(D4)Ala→Val; HBB: c.161C>T]: A Novel Hemoglobin Variant with a Structural Abnormality Associated with IVS-I-5 (G>C) (HBB: c.92+5G>C) Found in a Bengali Indian Family
Amrita Panja, Prosanto Chowdhury & Anupam Basu
Pages: 300-303
Published online: 08 Nov 2016
AbstractforHb Midnapore [β53(D4)Ala→Val; HBB: c.161C>T]: A Novel Hemoglobin Variant with a Structural Abnormality Associated with IVS-I-5 (G>C) (HBB: c.92+5G>C) Found in a Bengali Indian Family | Full Text | References | PDF (1.1 MB)
  • 117 Views
  • 3 CrossRef citations
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Article
Epidemiology of Hemoglobinopathies in the Huzhou Region, Zhejiang Province, Southeast China
Zhong-Ying Ding, Guo-Song Shen, Su Zhang & Ping-Ya He
Pages: 304-309
Published online: 11 Sep 2016
AbstractforEpidemiology of Hemoglobinopathies in the Huzhou Region, Zhejiang Province, Southeast China | Full Text | References | PDF (732.7 KB)
  • 157 Views
  • 4 CrossRef citations
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Article
Hb E-β-Thalassemia in Five Indian States
Khushnooma Italia, Pooja Dabke, Pratibha Sawant, Anita Nadkarni, Kanjaksha Ghosh & Roshan B. Colah
Pages: 310-315
Published online: 14 Sep 2016
AbstractforHb E-β-Thalassemia in Five Indian States | Full Text | References | PDF (534.6 KB)
  • 134 Views
  • 6 CrossRef citations
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Article
A Number of Cases in Iran Presenting with Coinheritance of Hemoglobin-H Disease and Beta-Thalassemia Minor
Tahereh Zarei, Javad Dehbozorgian, Jaber Imanifard, Fatemehsadat Setoodegan & Mehran Karimi
Pages: 316-318
Published online: 22 Sep 2016
AbstractforA Number of Cases in Iran Presenting with Coinheritance of Hemoglobin-H Disease and Beta-Thalassemia Minor | Full Text | References | PDF (302.5 KB)
  • 100 Views
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Article
Molecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern Iran
Sima M. Derakhshan, Mahmoud S. Khaniani, Fateme Afkhami & Abbasali H. PourFeizi
Pages: 319-322
Published online: 08 Nov 2016
AbstractforMolecular Study of Deletional and Nondeletional Mutations on the α-Globin Locus in the Azeri Population of Northwestern Iran | Full Text | References | PDF (381.7 KB)
  • 148 Views
  • 7 CrossRef citations
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Article
Patient Involvement as Experts in the Development and Assessment of a Smartphone App as a Patient Education Tool for the Management of Thalassemia and Iron Overload Syndromes
Richard Ward & Karim M. Taha
Pages: 323-329
Published online: 22 Sep 2016
AbstractforPatient Involvement as Experts in the Development and Assessment of a Smartphone App as a Patient Education Tool for the Management of Thalassemia and Iron Overload Syndromes | Full Text | References | PDF (1.4 MB)
  • 403 Views
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Article
Comparison of Emergency Department Wait Times in Adults with Sickle Cell Disease Versus Other Painful Etiologies
Dianne Pulte, Paris B. Lovett, David Axelrod, Albert Crawford, John McAna & Rhea Powell
Pages: 330-334
Published online: 28 Sep 2016
AbstractforComparison of Emergency Department Wait Times in Adults with Sickle Cell Disease Versus Other Painful Etiologies | Full Text | References | PDF (433.4 KB)
  • 190 Views
  • 7 CrossRef citations
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Article
Hb A1c Determination by Capillary Electrophoresis is an Efficient Method for Detecting β-Thalassemias and Hemoglobin Variants
Juan A. Orts, Ángel Zúñiga, Yanis Bello, Aleix B. Fabregat & Ana I. Vicente
Pages: 335-340
Published online: 22 Sep 2016
AbstractforHb A1c Determination by Capillary Electrophoresis is an Efficient Method for Detecting β-Thalassemias and Hemoglobin Variants | Full Text | References | PDF (577.7 KB)
  • 228 Views
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Article
Clinical Course of Two Children with Unstable Hemoglobins: The Effect of Hydroxyurea Therapy
Harriët M. Loovers, Nienke Tamminga, André B. Mulder & Rienk Y. J. Tamminga
Pages: 341-344
Published online: 30 Sep 2016
AbstractforClinical Course of Two Children with Unstable Hemoglobins: The Effect of Hydroxyurea Therapy | Full Text | References | PDF (560.1 KB)
  • 1235 Views
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Open Access

Short Communication

Rapid Communication
Hb Kalavasos [HBA2: c.275T > A; p.Leu92His]: a Novel α Chain Hemoglobin Variant
Mai Kelany, John S. Pickersgill, Namir Al Hasso, Adie Viljoen, Nancy van Bijlen & Martin W. Besser
Pages: 345-348
Published online: 14 Sep 2016
AbstractforHb Kalavasos [HBA2: c.275T > A; p.Leu92His]: a Novel α Chain Hemoglobin Variant | Full Text | References | PDF (1 MB)
  • 81 Views
  • 3 CrossRef citations
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Rapid Communication
Hb Olivet (HBA1: C.40G > A; p.Ala14Thr), a Novel Silent Hemoglobin Variant in Two Families of Distinct Origin
Cornelis L. Harteveld, Serge Pissard, Anna M. H. Korver, Jean Riou, Eric Legac, Gideon Lansbergen, Inge L. Pardijs, Piero C. Giordano & Florens G. A. Versteegh
Pages: 349-352
Published online: 14 Sep 2016
AbstractforHb Olivet (HBA1: C.40G > A; p.Ala14Thr), a Novel Silent Hemoglobin Variant in Two Families of Distinct Origin | Full Text | References | PDF (887.6 KB)
  • 757 Views
  • 1 CrossRef citations
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Open Access
Rapid Communication
Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (– –SEA/) Deletion
Xin Yang, Jin-Mei Yan, Jian Li, Xing-Mei Xie, Jian-Ying Zhou, Yan Li & Dong-Zhi Li
Pages: 353-355
Published online: 30 Sep 2016
AbstractforHydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (– –SEA/) Deletion | Full Text | References | PDF (806.8 KB)
  • 187 Views
  • 7 CrossRef citations
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Rapid Communication
Phenotypic Diversity of Sickle Cell Disease in Patients with a Double Heterozygosity for Hb S and Hb D-Punjab
Lidiane S. Torres, Jéssika V. Okumura, Édis Belini-Júnior, Renan G. Oliveira, Patrícia P. Nascimento, Danilo G.H. Silva, Clarisse L.C. Lobo, Sonia M. Oliani & Claudia R. Bonini-Domingos
Pages: 356-358
Published online: 03 Oct 2016
AbstractforPhenotypic Diversity of Sickle Cell Disease in Patients with a Double Heterozygosity for Hb S and Hb D-Punjab | Full Text | References | PDF (310 KB)
  • 176 Views
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Rapid Communication
A Patient with β-Thalassemia Intermedia Secondary to Homozygosity for a Polyadenylation Signal Mutation (AATAAA > AATAGA) (HBB: C.*112A > G) on the β-Globin Gene
Yen-Chian Lim, Karen M.L. Tan, Samuel S. Chong, Joseph Rajendran & Venkatasreekanth Sampath
Pages: 359-360
Published online: 08 Nov 2016
AbstractforA Patient with β-Thalassemia Intermedia Secondary to Homozygosity for a Polyadenylation Signal Mutation (AATAAA > AATAGA) (HBB: C.*112A > G) on the β-Globin Gene | Full Text | References | PDF (447.2 KB)
  • 165 Views
  • 2 CrossRef citations
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Rapid Communication
Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype
Patrick G. Gallagher, Yelena Maksimova, Vincent P. Schulz & Bernard G. Forget
Pages: 361-364
Published online: 22 Sep 2016
AbstractforMutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype | Full Text | References | PDF (925.9 KB)
  • 133 Views
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Rapid Communication
A novel 6.3 kb deletion and the Rare 27.6 kb Deletion Causing α+-Thalassemia in two Chinese Patients
Xian-Yao Wang, Ming-Xiang Lin & Min Lin
Pages: 365-368
Published online: 22 Sep 2016
AbstractforA novel 6.3 kb deletion and the Rare 27.6 kb Deletion Causing α+-Thalassemia in two Chinese Patients | Full Text | References | PDF (1.3 MB)
  • 126 Views
  • 3 CrossRef citations
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Rapid Communication
Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A)
John S. Waye, Barry Eng, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura & Lynda Walker
Pages: 369-370
Published online: 08 Nov 2016
AbstractforNovel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A) | Full Text | References | PDF (353.7 KB)
  • 145 Views
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