Hemoglobin, Volume 44, Issue 4 (2020)

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Hemoglobin, Volume 44, Issue 4 (2020)

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Original Articles

Article
Two Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population
Mohammad Hamid, Ebtesam Zargan Nezhad, Bijan Keikhaei, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Marziye Mohammadi-Anaei & Gholamreza Shariati
Pages: 225-230
Published online: 16 Jul 2020
AbstractforTwo Novel and Five Rare Mutations in the Non Coding Regions of the β-Globin Gene in the Iranian Population | Full Text | References | PDF (1.3 MB) | EPUB
  • 109 Views
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Article
The Effect of Five Single Nucleotide Polymorphisms on Hb F Variation of β-Thalassemia Traits and Hematologically Normal Individuals in Southeast Turkey
Ahmet Genc, Deniz Tastemir Korkmaz, Suleyman Bayram & Eyyup Rencuzogullari
Pages: 231-239
Published online: 16 Jul 2020
AbstractforThe Effect of Five Single Nucleotide Polymorphisms on Hb F Variation of β-Thalassemia Traits and Hematologically Normal Individuals in Southeast Turkey | Full Text | References | PDF (1.1 MB) | EPUB
  • 208 Views
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Article
Hematological Characteristics of β-Globin Gene Mutation –50 (G>A) (HBB: c.-100G>A) Carriers in Mainland China
Yuan Zhao, Fan Jiang & Dong-Zhi Li
Pages: 240-243
Published online: 16 Jul 2020
AbstractforHematological Characteristics of β-Globin Gene Mutation –50 (G>A) (HBB: c.-100G>A) Carriers in Mainland China | Full Text | References | PDF (501.7 KB) | EPUB
  • 130 Views
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Article
Distribution of HBB Gene Mutations in the Kurdish Population of Ilam Province, West Iran
Keivan Moradi, Mozaffar Aznab, Susan Tahmasebi, Leila Omidniakan, Nushin Bijari & Reza Alibakhshi
Pages: 244-248
Published online: 01 Sep 2020
AbstractforDistribution of HBB Gene Mutations in the Kurdish Population of Ilam Province, West Iran | Full Text | References | PDF (470.7 KB) | EPUB
  • 79 Views
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Article
β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey
Figen Guzelgul, G. Seyda Seydel & Kiymet Aksoy
Pages: 249-253
Published online: 14 Jul 2020
Abstractforβ-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey | Full Text | References | PDF (555.8 KB) | EPUB
  • 280 Views
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Article
Development of the Next Generation Sequencing-Based Diagnostic Test for β-Thalassemia and its Validation in a Pashtun Family
Bibi Sabiha, Syed Adnan Haider, Hanifullah Jan, Yasar Mehmood Yousafzai, Ome Kalsoom Afridi, Abid Ali Khan & Johar Ali
Pages: 254-258
Published online: 20 Jul 2020
AbstractforDevelopment of the Next Generation Sequencing-Based Diagnostic Test for β-Thalassemia and its Validation in a Pashtun Family | Full Text | References | PDF (708.2 KB) | EPUB
  • 146 Views
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Article
Characterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis
Ming-Li Xu, Jia-Chun Qin, Bi-Yan Chen, Xue-Xi Yang, Hai-Ping Liu, Wei-Xi Yuan, Jian-Mei Zhong, Li-Min Huang & Wan-Jun Zhou
Pages: 259-263
Published online: 10 Jul 2020
AbstractforCharacterization of a Novel 71.8 kb α0-Thalassemia Deletion and Subsequent Summary of a Practical Procedure for Thalassemia Molecular Diagnosis | Full Text | References | PDF (1.2 MB) | EPUB
  • 91 Views
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Article
α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [– –SEA (Southeast Asian)] Deletion in Thailand
Sitthichai Panyasai & Amphai Phasit
Pages: 264-271
Published online: 29 Jul 2020
Abstractforα-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [– –SEA (Southeast Asian)] Deletion in Thailand | Full Text | References | PDF (1.3 MB) | EPUB
  • 54 Views
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Article
Evaluation of Erythroferrone, Hepcidin, and Iron Overload Status in Iraqi Transfusion-Dependent β-Thalassemia Major Patients
Hasan N.K. Smesam, Hasan A.Q. Albuthabhak, Sareh Arjmand, Hussein K. Al-Hakeim & Seyed Omid R. Siadat
Pages: 272-277
Published online: 27 Jul 2020
AbstractforEvaluation of Erythroferrone, Hepcidin, and Iron Overload Status in Iraqi Transfusion-Dependent β-Thalassemia Major Patients | Full Text | References | PDF (650.6 KB) | EPUB
  • 81 Views
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Article
A Report on the Education, Employment and Marital Status of Thalassemia Patients from a Tertiary Care Center in the Middle East
Rayan Bou-Fakhredin, Nadim N. Ghanem, Firas Kreidieh, Rami Tabbikha, Hisham Daadaa, Josephine Ajouz, Suzanne Koussa & Ali T. Taher
Pages: 278-283
Published online: 29 Jul 2020
AbstractforA Report on the Education, Employment and Marital Status of Thalassemia Patients from a Tertiary Care Center in the Middle East | Full Text | References | PDF (606.6 KB) | EPUB
  • 94 Views
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Article
Impact of COVID-19 Infection on 24 Patients with Sickle Cell Disease. One Center Urban Experience, Detroit, MI, USA
Nino Balanchivadze, Adam A. Kudirka, Sally Askar, Khaled Almadhoun, Philip Kuriakose, Raef Fadel & Vrushali Dabak
Pages: 284-289
Published online: 28 Jul 2020
AbstractforImpact of COVID-19 Infection on 24 Patients with Sickle Cell Disease. One Center Urban Experience, Detroit, MI, USA | Full Text | References | PDF (500.6 KB) | EPUB
  • 4054 Views
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Brief Report

Brief Report
Hb Manitoba [α102(G9)Ser→Arg] in Pasifika: Tongan Case Report
Beverley M. Pullon & Jordyn A. Moore
Pages: 290-293
Published online: 03 Jul 2020
AbstractforHb Manitoba [α102(G9)Ser→Arg] in Pasifika: Tongan Case Report | Full Text | References | PDF (765.1 KB) | EPUB
  • 136 Views
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Short Communications

Brief Report
Mild Thalassemia Intermedia Due to Interaction of δβ-Thalassemia with Triplicated α-Globin Genes
Salvador Payán-Pernía, Sara Bernal Noguera, Esther Rojas Rodríguez, Marta Serra Ferrer & Ángel F. Remacha Sevilla
Pages: 294-296
Published online: 21 Jul 2020
AbstractforMild Thalassemia Intermedia Due to Interaction of δβ-Thalassemia with Triplicated α-Globin Genes | Full Text | References | PDF (444.5 KB) | EPUB
  • 57 Views
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Brief Report
Novel α0-Thalassemia Deletion Identified in an Indian Infant with Hb H Disease
Jordyn A. Moore, Beverley M. Pullon, Kylie M. Drake & Stephen O. Brennan
Pages: 297-301
Published online: 28 Jul 2020
AbstractforNovel α0-Thalassemia Deletion Identified in an Indian Infant with Hb H Disease | Full Text | References | PDF (985.2 KB) | EPUB
  • 142 Views
  • 3 CrossRef citations
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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
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Brief Report | Published online: 1 May 2024
Sickle Cell Disease in Brazil: Current Management
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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
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Brief Report | Published online: 23 Apr 2024
A New δ-Globin Gene Variant: Hb A2-Yulin [δ46(CD5)Gly→Arg,HBD: C.139G > A]
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