Hemoglobin, Volume 43, Issue 4-5 (2019)

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Hemoglobin, Volume 43, Issue 4-5 (2019)

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Original Articles

Article
Genetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15)
Wissem Abdaoui, Djamel Eddine Benouareth, Amel Djenouni, Celine Renoux, Fatiha Grifi, Adel Gouri, Fateh Athamnia, Manel Benalioua & Philippe Joly
Pages: 223-228
Published online: 11 Oct 2019
AbstractforGenetic Background of β-Thalassemia in Northeast Algeria with Assessment of the Thalassemia Severity Score and Description of a new β0-Thalassemia Frameshift Mutation (HBB: c.374dup; p.Pro126Thrfs*15) | Full Text | References | PDF (692.8 KB) | EPUB
  • 190 Views
  • 8 CrossRef citations
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Article
Reticulocyte Hemoglobin Equivalent (Ret-He) Combined with Red Blood Cell Distribution Width Has a Differentially Diagnostic Value for Thalassemias
Yu Lian, Jun Shi, Neng Nie, Zhendong Huang, Yingqi Shao, Jing Zhang, Jinbo Huang, Xingxin Li, Meili Ge, Peng Jin, Min Wang & Yizhou Zheng
Pages: 229-235
Published online: 03 Sep 2019
AbstractforReticulocyte Hemoglobin Equivalent (Ret-He) Combined with Red Blood Cell Distribution Width Has a Differentially Diagnostic Value for Thalassemias | Full Text | References | PDF (817.8 KB) | EPUB
  • 297 Views
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Article
Strong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (– –SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart’s Hydrops Fetalis Syndrome in Thailand
Wittaya Jomoui, Wanicha Tepakhan & Rossarin Karnpean
Pages: 236-240
Published online: 21 Oct 2019
AbstractforStrong Linkage of the Single Nucleotide Polymorphism rs77308790 with an α0-Thalassemia (– –SEA deletion) Allele and Application for Double-Check Diagnosis of Hb Bart’s Hydrops Fetalis Syndrome in Thailand | Full Text | References | PDF (740.6 KB) | EPUB
  • 124 Views
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Article
Molecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATC or HBA2: c.3G>C)
Ya-Li Lei, Hong Sui, Yu-Juan Liu, Jun-Jun Pan, Yan-Hui Liu & Ji-Wu Lou
Pages: 241-244
Published online: 05 Nov 2019
AbstractforMolecular and Hematological Characterization of a Novel Translation Initiation Codon Mutation of the α2-Globin Gene (ATG>ATC or HBA2: c.3G>C) | Full Text | References | PDF (801.9 KB) | EPUB
  • 78 Views
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Article
Analysis of Deletional Hb H Diseases in Samples with Hb A2-Hb H and Hb A2-Hb Bart’s on Capillary Electrophoresis
Kunyakan Khongthai, Chedtapak Ruengdit, Sitthichai Panyasai & Sakorn Pornprasert
Pages: 245-248
Published online: 05 Nov 2019
AbstractforAnalysis of Deletional Hb H Diseases in Samples with Hb A2-Hb H and Hb A2-Hb Bart’s on Capillary Electrophoresis | Full Text | References | PDF (693.4 KB) | EPUB
  • 142 Views
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Article
Thalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam
Tuan Mai Anh, Kanokwan Sanchaisuriya, Giang Nguyen Kieu, Dung Nguyen Tien, Huong Bui Thi Thu, Pattara Sanchaisuriya, Supan Fucharoen, Goonnapa Fucharoen & Frank P. Schelp
Pages: 249-253
Published online: 03 Oct 2019
AbstractforThalassemia and Hemoglobinopathies in an Ethnic Minority Group in Northern Vietnam | Full Text | References | PDF (438.3 KB) | EPUB
  • 212 Views
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Article
Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-Thalassemia
Aye Chan Pyae, Hataichanok Srivorakun, Attawut Chaibunruang, Kritsada Singha, Kanchana Tomanakarn, Goonnapa Fucharoen & Supan Fucharoen
Pages: 254-257
Published online: 10 Oct 2019
AbstractforMolecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-Thalassemia | Full Text | References | PDF (381.6 KB) | EPUB
  • 139 Views
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Article
Association of the CCR5Δ32 Mutant Genotype with Sickle Cell Disease in Egyptian Patients
Maha H. El Sissy, Ahmed A. Hafez, Sherif E.A. Moneim & Doaa M. Eldemerdash
Pages: 258-263
Published online: 28 Oct 2019
AbstractforAssociation of the CCR5Δ32 Mutant Genotype with Sickle Cell Disease in Egyptian Patients | Full Text | References | PDF (516.2 KB) | EPUB
  • 58 Views
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Article
The Effect of Blood Transfusion on Growth of Patients with Hb E/β-Thalassemia
Ampaiwan Chuansumrit, Nongnuch Sirachainan, Pimpun Kitpoka, Praguywan Kadegasem, Duantida Songdej, Werasak Sasanakul & Pakawan Wongwerawattanakoon
Pages: 264-272
Published online: 25 Nov 2019
AbstractforThe Effect of Blood Transfusion on Growth of Patients with Hb E/β-Thalassemia | Full Text | References | PDF (1.6 MB) | EPUB
  • 185 Views
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Short Communications

Rapid Communication
A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AGT>AGG); HBB: c.270T>G] Resulting in Hemoglobin Vanderbilt
William Shomali, Rondeep Brar, Subramanyeswara R. Arekapudi & Jason R. Gotlib
Pages: 273-276
Published online: 28 Oct 2019
AbstractforA Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AGT>AGG); HBB: c.270T>G] Resulting in Hemoglobin Vanderbilt | Full Text | References | PDF (1 MB) | EPUB
  • 61 Views
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Rapid Communication
A De Novo Heterozygous Variant (HBB: c.379delG, p.Val127Cysfs*32) Associated with a Mild β-Thalassemia Intermedia Phenotype in a Turkish Child
Dilek Gürlek-Gökçebay, Sibel Akpinar-Tekgunduz, Haktan B. Erdem & Nese Yarali
Pages: 277-279
Published online: 17 Sep 2019
AbstractforA De Novo Heterozygous Variant (HBB: c.379delG, p.Val127Cysfs*32) Associated with a Mild β-Thalassemia Intermedia Phenotype in a Turkish Child | Full Text | References | PDF (836.8 KB) | EPUB
  • 81 Views
  • 0 CrossRef citations
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Rapid Communication
A Novel Frameshift Mutation at Codon 2 (–T) (HBB: c.9delT) and First Report of Three New β-Globin Mutations From Azerbaijan
Bayram Bayramov, Gunay Aliyeva, Chingiz Asadov, Tahira Mammadova, Nigar Karimova, Khagani Eynullazadeh, Surmaya Gafarova, Seymur Akbarov, Sabina Farhadova, Zumrud Safarzadeh & Mehraj Abbasov
Pages: 280-282
Published online: 03 Sep 2019
AbstractforA Novel Frameshift Mutation at Codon 2 (–T) (HBB: c.9delT) and First Report of Three New β-Globin Mutations From Azerbaijan | Full Text | References | PDF (1 MB) | EPUB
  • 245 Views
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Rapid Communication
Description of a rare β-globin gene mutation, IVS-II-848 (C>A) (HBB: c.316-3C>A) in association with IVS-I-1 (G>A) (HBB: c.92 + 1G>A), observed in a Syrian family: a case report
Ahmad Shoujaa, Yasser Mukhalalaty, Hossam Murad & Faizeh Al-Quobaili
Pages: 283-285
Published online: 12 Nov 2019
AbstractforDescription of a rare β-globin gene mutation, IVS-II-848 (C>A) (HBB: c.316-3C>A) in association with IVS-I-1 (G>A) (HBB: c.92 + 1G>A), observed in a Syrian family: a case report | Full Text | References | PDF (499.5 KB) | EPUB
  • 105 Views
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Rapid Communication
Compound Heterozygosity for an Unstable Novel Hemoglobin Variant, Hb Dongguan [α52(E1)Ser→Cys (TCT>TGT); HBA1: c.158C>G], and the – –SEA (Southeast Asian) α-Thalassemia Deletion
Wei-Dong Chen, Yu-Xiang Ren, Ya-Jun Wang, Wei-Jie Xie, Jie Li, An-Ping Xu & Ling Ji
Pages: 286-288
Published online: 25 Oct 2019
AbstractforCompound Heterozygosity for an Unstable Novel Hemoglobin Variant, Hb Dongguan [α52(E1)Ser→Cys (TCT>TGT); HBA1: c.158C>G], and the – –SEA (Southeast Asian) α-Thalassemia Deletion | Full Text | References | PDF (724.1 KB) | EPUB
  • 92 Views
  • 2 CrossRef citations
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Rapid Communication
A β-Thalassemia Trait with Two Mutations in Cis in a Chinese Family
Jian Li, Fan Jiang, Li Zhen, Xue-Wei Tang & Dong-Zhi Li
Pages: 289-291
Published online: 05 Nov 2019
AbstractforA β-Thalassemia Trait with Two Mutations in Cis in a Chinese Family | Full Text | References | PDF (800.6 KB) | EPUB
  • 93 Views
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Rapid Communication
Congenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report
Hua Jiang, Fan Jiang, Jian Li, Fang Tang & Dong-Zhi Li
Pages: 292-295
Published online: 23 Oct 2019
AbstractforCongenital Nonspherocytic Hemolytic Anemia Caused by Krüppel-Like Factor 1 Gene Variants: Another Case Report | Full Text | References | PDF (1.1 MB) | EPUB
  • 104 Views
  • 6 CrossRef citations
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Rapid Communication
Use of Direct Oral Anticoagulants in Patients with Sickle Cell Disease and Venous Thromboembolism: A Prospective Cohort Study of 12 Patients
Jacques-Robert Christen, Julien Bertolino, Estelle Jean, Laurence Camoin, Mikael Ebbo, Jean-Robert Harlé, Nicolas Schleinitz, Gabrielle Sarlon & Emmanuelle Bernit
Pages: 296-299
Published online: 14 Nov 2019
AbstractforUse of Direct Oral Anticoagulants in Patients with Sickle Cell Disease and Venous Thromboembolism: A Prospective Cohort Study of 12 Patients | Full Text | References | PDF (376.5 KB) | EPUB
  • 365 Views
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