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Introduction to the Thalassemia Syndromes

Hematology/oncology clinics of North America, 2023-04, Vol.37 (2), p.245-259

Benz, Edward J.

2023

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Evaluation of the level of liver enzymes and its relationship with ferritin and the frequency of blood transfusion in patients with thalassemia

Cellular, Molecular and Biomedical Reports, 2024-06, Vol.4 (2), p.100-110

2024

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Production and characterization of monoclonal antibodies against α-globin chain-containing human hemoglobins for detecting α-thalassemia disease

Journal of immunoassay & immunochemistry, 2016-11, Vol.37 (6), p.564-571

2016

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Hb Nivaria: A New Hemoglobin Variant with a Shortened α -Globin Chain [ α 139(HC1)Lys → Stop; HBA1 : c.418A>T]

Hemoglobin, 2022-11, Vol.46 (6), p.344-346

2022

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The Effect of Ferritin Level and Gene Expression of β-globin Promoter with β-thalassemia Patients in Al-Qadisiyah Governorate, Iraq

Journal of applied hematology, 2023-10, Vol.14 (4), p.257-262

2023

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Hb Hubei [α114(GH2)Pro→His, HBA1: c.344C>A]: A Novel Hemoglobin Variant of the α1-Globin Chain

Hemoglobin, 2018-05, Vol.42 (3), p.206-208

2018

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Rapid determination of globin chains in red blood cells by capillary electrophoresis using INSTCoated fused‐silica capillary

Journal of separation science, 2014-04, Vol.37 (8), p.1026-1032

TUMA, Petr

2014

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Detection of Compound Heterozygous Sickle Cell-b+ Thalassaemia in a Patient with Extreme Weakness, Mild Jaundice and Moderate Anaemia - A Case Report

Journal of clinical and diagnostic research, 2017-05, Vol.11 (5), p.ED07-ED08

Chandra, Subhash

2017

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α-globin Alteration in α-thalassemia Disorder: Prediction and Interaction Defect

Pakistan journal of biological sciences, 2017, Vol.20 (7), p.343-349

2017

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A case of beta thalassaemia trait of unusual severity due to co-inheritance of triple alpha mutation

Sri Lanka journal of child health, 2017-03, Vol.46 (1), p.75

2017

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α:Non–α and Gγ:Aγ globin chain ratios in thalassemia intermedia patients treated with hydroxyurea

Asian Pacific journal of tropical biomedicine, 2014-05, Vol.4 (Suppl 1), p.S177-S185

2014

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Haemoglobin Lleida: a new α2‐globin variant (12 bp deletion) with mild thalassaemic phenotype

British journal of haematology, 1996-09, Vol.94 (4), p.639-644

1996

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A SIMPLE AND HIGHLY SENSITIVE ELISA FOR SCREENING OF THE α-THALASSEMIA-1 SOUTHEAST ASIAN-TYPE DELETION

Journal of immunoassay & immunochemistry, 2014-04, Vol.35 (2), p.194-206

2014

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The mammalian α D-globin gene lineage and a new model for the molecular evolution of α-globin gene clusters at the stem of the mammalian radiation

Molecular phylogenetics and evolution, 2006-02, Vol.38 (2), p.439-448

2006

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Two Novel α2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2: c.428A > T) and Severe (HBA2: c.342-345insCC) α-Thalassemia Phenotype

Hemoglobin, 2015-04, Vol.39 (2), p.144-146

2015

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First Description of a Hb A2 Variant in Thailand. Identification of Hb A2-Melbourne [δ43(CD2)Glu→Lys] in Thai Individuals

Hemoglobin, 2012-02, Vol.36 (1), p.80-84

2012

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Description of Two New α Variants: Hb Canuts [α85(F6)Asp→His (α1)] and Hb Ambroise Pare [α117(GH5)Phe→Ile (α2)]; Two New β Variants: Hb Beaujolais [β84(EF8)Thr→Asn] and Hb Monplaisir [β147 (Tyr-Lys-Leu-Ala-Phe-Phe-Leu-Leu-Ser-Asn-Phe-Tyr-158-COOH)] and One New δ Variant: Hb A2-North Africa [δ59(E3)Lys→Met]

Hemoglobin, 2009-01, Vol.33 (3-4), p.196-205

2009

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Hb AHVAZ [α83(F4)Leu→Arg, CTG>CGG (α2); HBA2: c.251T>G],A New Hemoglobin Variant of the α2-Globin Gene

Hemoglobin, 2013, Vol.37 (5), p.477-480

2013

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Long-Standing Microcytic Anemia in a 29-Year-Old Woman

Laboratory medicine, 2007-04, Vol.38 (4), p.222-226

2007

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Hb Nivaria: A New Hemoglobin Variant with a Shortened α-Globin Chain [α139(HC1)Lys→Stop; HBA1: c.418A>T]

Hemoglobin, 2022, Vol.46 (6), p.344-346

2022

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Removing Peroxide Impurities from Ether Improves the Quality of Globin Chains for Biosynthetic Studies

Hemoglobin, 2005, Vol.29 (2), p.161-164

2005

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Hb Bronte or α93(FG5)Val→Gly: A New Unstable Variant of the α2-Globin Gene, Associated with a Mild α+-Thalassemia Phenotype

Hemoglobin, 2003, Vol.27 (3), p.149-159

2003

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Hb Jeddah [α68(E17)Asn→His (α1)]: A Newly Recognized α Chain Variant, Seen in Combination with Hb S [β6(A3)Glu→Val], and Found in Three Separate Families of Middle Eastern Origin

Hemoglobin, 2008, Vol.32 (3), p.297-302

2008

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A New Hemoglobin Variant: Hb Jiujiang [α18(A16)Gly→Cys, HBA2: c.55G>T]

Hemoglobin, 2021, Vol.45 (4), p.254-255

2021

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Mild α-Thalassemia Caused by a Mosaic α-Globin Gene Mutation

Hemoglobin, 2021, Vol.45 (2), p.140-141

2021

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Introduction to the Thalassemia Syndromes

Evaluation of the level of liver enzymes and its relationship with ferritin and the frequency of blood transfusion in patients with thalassemia

Production and characterization of monoclonal antibodies against α-globin chain-containing human hemoglobins for detecting α-thalassemia disease

Hb Nivaria: A New Hemoglobin Variant with a Shortened α -Globin Chain [ α 139(HC1)Lys → Stop; HBA1 : c.418A>T]

The Effect of Ferritin Level and Gene Expression of β-globin Promoter with β-thalassemia Patients in Al-Qadisiyah Governorate, Iraq

Hb Hubei [α114(GH2)Pro→His, HBA1: c.344C>A]: A Novel Hemoglobin Variant of the α1-Globin Chain

Rapid determination of globin chains in red blood cells by capillary electrophoresis using INSTCoated fused‐silica capillary

Detection of Compound Heterozygous Sickle Cell-b+ Thalassaemia in a Patient with Extreme Weakness, Mild Jaundice and Moderate Anaemia - A Case Report

α-globin Alteration in α-thalassemia Disorder: Prediction and Interaction Defect

A case of beta thalassaemia trait of unusual severity due to co-inheritance of triple alpha mutation

α:Non–α and Gγ:Aγ globin chain ratios in thalassemia intermedia patients treated with hydroxyurea

Haemoglobin Lleida: a new α2‐globin variant (12 bp deletion) with mild thalassaemic phenotype

A SIMPLE AND HIGHLY SENSITIVE ELISA FOR SCREENING OF THE α-THALASSEMIA-1 SOUTHEAST ASIAN-TYPE DELETION

The mammalian α D-globin gene lineage and a new model for the molecular evolution of α-globin gene clusters at the stem of the mammalian radiation

Two Novel α2 Gene Mutations Causing Altered Amino Acid Sequences Produce a Mild (Hb Kinshasa, HBA2: c.428A > T) and Severe (HBA2: c.342-345insCC) α-Thalassemia Phenotype

First Description of a Hb A2 Variant in Thailand. Identification of Hb A2-Melbourne [δ43(CD2)Glu→Lys] in Thai Individuals

Hb AHVAZ [α83(F4)Leu→Arg, CTG>CGG (α2); HBA2: c.251T>G],A New Hemoglobin Variant of the α2-Globin Gene

Long-Standing Microcytic Anemia in a 29-Year-Old Woman

Hb Nivaria: A New Hemoglobin Variant with a Shortened α-Globin Chain [α139(HC1)Lys→Stop; HBA1: c.418A>T]

Removing Peroxide Impurities from Ether Improves the Quality of Globin Chains for Biosynthetic Studies

Hb Bronte or α93(FG5)Val→Gly: A New Unstable Variant of the α2-Globin Gene, Associated with a Mild α+-Thalassemia Phenotype

Hb Jeddah [α68(E17)Asn→His (α1)]: A Newly Recognized α Chain Variant, Seen in Combination with Hb S [β6(A3)Glu→Val], and Found in Three Separate Families of Middle Eastern Origin

A New Hemoglobin Variant: Hb Jiujiang [α18(A16)Gly→Cys, HBA2: c.55G>T]

Mild α-Thalassemia Caused by a Mosaic α-Globin Gene Mutation

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