Hemoglobin, Volume 44, Issue 1 (2020)

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Hemoglobin, Volume 44, Issue 1 (2020)

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Original Articles

Article
Hb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics
André R. Belisário, Anna B. Carneiro-Proietti, Ester Cerdeira Sabino, Aderson Araújo, Paula Loureiro, Cláudia Máximo, Miriam V. Flor-Park, Daniela D.O.W. Rodrigues, Mina Cintho Ozahata, Christopher McClure, Rosimere Afonso Mota, Isabel C. Gomes Moura, Brian Custer, Shannon Kelly & for the Recipient Epidemiology and Donor Evaluation Study (REDS-III) International Component Brazil
Pages: 1-9
Published online: 16 Mar 2020
AbstractforHb S/β-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics | Full Text | References | PDF (2.3 MB) | EPUB | Supplemental
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Article
Novel High Oxygen Affinity Hemoglobin Variant in a Patient with Polycythemia: Hb Kennisis [β85(F1)Phe→Leu (TTT>TTG); HBB: c.258T>G]
Ibrahim Al Nabhani, John C. Aneke, Madeleine Verhovsek, Barry Eng, Kevin H.M. Kuo, Leona C. Rudinskas & John S. Waye
Pages: 10-12
Published online: 09 Mar 2020
AbstractforNovel High Oxygen Affinity Hemoglobin Variant in a Patient with Polycythemia: Hb Kennisis [β85(F1)Phe→Leu (TTT>TTG); HBB: c.258T>G] | Full Text | References | PDF (427.4 KB) | EPUB
  • 122 Views
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Short Communication

Rapid Communication
The Importance of Characterizing the Hemoglobin Instability of New Variants: The Case of Hb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C]
Etienne Mondesert, Muriel Giansily Blaizot, Olivier Tournilhac, Anne François Serre Sapin, Bernard Aubin, Jean-Luc Pellequer & Patricia Aguilar Martinez
Pages: 13-16
Published online: 03 Feb 2020
AbstractforThe Importance of Characterizing the Hemoglobin Instability of New Variants: The Case of Hb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C] | Full Text | References | PDF (593.5 KB) | EPUB
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Original Articles

Article
Nondeletional α-Thalassemia: Two New Mutations on the α2 Gene
Paloma Ropero, Jaime Arbeteta, Jorge M. Nieto, Fernando A. González, Beatriz González, Ana Villegas & Celina Benavente
Pages: 17-19
Published online: 31 Jan 2020
AbstractforNondeletional α-Thalassemia: Two New Mutations on the α2 Gene | Full Text | References | PDF (574.1 KB) | EPUB
  • 85 Views
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Article
α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region
Arwa Z. Al-Riyami, Shahina Daar, Salam Al Kindi, Ali Al Madhani, Yasser Wali, Mohammed Al Rawahi & Shoaib Al Zadjali
Pages: 20-26
Published online: 05 Feb 2020
Abstractforα-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region | Full Text | References | PDF (819.7 KB) | EPUB
  • 120 Views
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Article
Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran
Zahra Sajadpour, Zeinab Amini-Farsani, Majid Motovali-Bashi, Mitra Yadollahi & Nariman Khosravi-Farsani
Pages: 27-30
Published online: 03 Jan 2020
AbstractforAssociation between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran | Full Text | References | PDF (384.9 KB) | EPUB
  • 84 Views
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Article
Distribution of Red Blood Cell Alloantibodies Among Transfusion-Dependent β-Thalassemia Patients in Different Population of Iran: Effect of Ethnicity
Reyhaneh Sarihi, Naser Amirizadeh, Arezoo Oodi & Azita Azarkeivan
Pages: 31-36
Published online: 13 May 2020
AbstractforDistribution of Red Blood Cell Alloantibodies Among Transfusion-Dependent β-Thalassemia Patients in Different Population of Iran: Effect of Ethnicity | Full Text | References | PDF (768.2 KB) | EPUB
  • 72 Views
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Article
Molecular Heterogeneity of β-Thalassemia in the Kohat Region, Khyber Pakhtunkhwa Province, Pakistan
Suraiya Naz, Shoaib Ur Rehman, Muhammad Shakeel, Hazir Rehman, Masroor Hussain & Ayesha Haider
Pages: 37-41
Published online: 21 Feb 2020
AbstractforMolecular Heterogeneity of β-Thalassemia in the Kohat Region, Khyber Pakhtunkhwa Province, Pakistan | Full Text | References | PDF (837.9 KB) | EPUB
  • 98 Views
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Article
Genotype/Phenotype Correlation of β-Thalassemia in Syrian Patients: A Cross-Sectional Study
Ahmad Shoujaa, Faten Moasses, Yasser Mukhalalaty, Hossam Murad & Faizeh Al-Quobaili
Pages: 42-46
Published online: 06 Jan 2020
AbstractforGenotype/Phenotype Correlation of β-Thalassemia in Syrian Patients: A Cross-Sectional Study | Full Text | References | PDF (556.8 KB) | EPUB
  • 140 Views
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Article
Prevalence of Hemoglobinopathies (β-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma’ah, Saudi Arabia
Shabir A. Mir, Bader M. Alshehri, Mohammed Alaidarous, Saeed S. Banawas, Abdul Aziz A. Bin Dukhyil & Mohammad K. Alturki
Pages: 47-50
Published online: 24 Feb 2020
AbstractforPrevalence of Hemoglobinopathies (β-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma’ah, Saudi Arabia | Full Text | References | PDF (566.9 KB) | EPUB
  • 182 Views
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Article
Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene HBA2: c.1A>G Mutation
Xingyuan Chen, Shiqiang Luo, Jun Huang, Dejian Yuan, Tizhen Yan, Ren Cai & Ning Tang
Pages: 51-54
Published online: 14 Jan 2020
AbstractforDiagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene HBA2: c.1A>G Mutation | Full Text | References | PDF (607 KB) | EPUB
  • 113 Views
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Article
A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), HBB: c.92+6T>G] in a Chinese Family
Haiyan Luo, Yongyi Zou & Yanqiu Liu
Pages: 55-57
Published online: 15 Jan 2020
AbstractforA Novel β-Thalassemia Mutation [IVS-I-6 (T>G), HBB: c.92+6T>G] in a Chinese Family | Full Text | References | PDF (426.1 KB) | EPUB
  • 114 Views
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Short Communications

Rapid Communication
A Japanese Family with the Unstable Hb Sydney (HBB: c.203T>C) Variant and Persistent Low Hemoglobin Oxygen Saturation
Atsushi Sakamoto, Hisaya Nakadate, Kinji Tada, Yasuhiro Yamashiro & Akira Ishiguro
Pages: 58-60
Published online: 08 Jan 2020
AbstractforA Japanese Family with the Unstable Hb Sydney (HBB: c.203T>C) Variant and Persistent Low Hemoglobin Oxygen Saturation | Full Text | References | PDF (538.7 KB) | EPUB
  • 101 Views
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Rapid Communication
An Unusual Compound Heterozygosity for Hb O-Arab (HBB: c.364G>A) and Hb D-Los Angeles (HBB: c.364G>C)
Adriaan J. van Gammeren, Leonie Pelkmans, Corné C.W. van Endschot, Roseri J.A.C. Roelofsen-de Beer & Cornelis L. Harteveld
Pages: 61-63
Published online: 23 Jan 2020
AbstractforAn Unusual Compound Heterozygosity for Hb O-Arab (HBB: c.364G>A) and Hb D-Los Angeles (HBB: c.364G>C) | Full Text | References | PDF (490.5 KB) | EPUB
  • 125 Views
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Rapid Communication
Hb Rush (HBB: c.304G>C): A Rare Variant Hemoglobin Mimicking the Hb S (HBB: c.20A>T) Variant on High Performance Liquid Chromatography
Ranjeet S. Mashon, Reena Das, Radhika Dhawan, Naveen Kakkar & Tapasya Dhar
Pages: 64-66
Published online: 03 Mar 2020
AbstractforHb Rush (HBB: c.304G>C): A Rare Variant Hemoglobin Mimicking the Hb S (HBB: c.20A>T) Variant on High Performance Liquid Chromatography | Full Text | References | PDF (664.9 KB) | EPUB
  • 103 Views
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Rapid Communication
Hb F-Wentzville [Gγ24(B6)Gly→Glu; HBG2: c.74G>A, p.Gly25Glu]: An Unstable Gγ-Globin Variant Associated with Neonatal Hemolytic Anemia
Katarina M. Semkiu, Jennifer L. Oliveira, Phuong L. Nguyen, Tavanna R. Porter & David B. Wilson
Pages: 67-69
Published online: 27 Jan 2020
AbstractforHb F-Wentzville [Gγ24(B6)Gly→Glu; HBG2: c.74G>A, p.Gly25Glu]: An Unstable Gγ-Globin Variant Associated with Neonatal Hemolytic Anemia | Full Text | References | PDF (551.1 KB) | EPUB
  • 68 Views
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