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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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Introduction to the Thalassemia Syndromes: Molecular Medicine's Index Case

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

Benz, Jr, Edward J

2023

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Molecular and phenotype characterization of an elongated β‐globin variant produced by HBB:C.313delA

International journal of laboratory hematology, 2021-12, Vol.43 (6), p.1620-1627

2021

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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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Laboratory diagnosis of thalassemia

International journal of laboratory hematology, 2016-05, Vol.38 (S1), p.32-40

2016

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Beta‐thalassemia and the advent of new interventions beyond transfusion and iron chelation

British journal of clinical pharmacology, 2022-08, Vol.88 (8), p.3610-3626

2022

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The α-globin chain of hemoglobin potentiates tissue plasminogen activator induced hyperfibrinolysis in vitro

The journal of trauma and acute care surgery, 2022-01, Vol.92 (1), p.159

2022

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Hemoglobin β-Globin Variants In Hispanic Patients: An Institutional Experience From Dallas, Texas

Hemoglobin, 2023-07, Vol.47 (4), p.167-171

2023

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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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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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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, 2023-01, Vol.14 (4), p.257-262

2023

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

Hemoglobin, 2021-07, Vol.45 (4), p.254-255

2021

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

Hemoglobin, 2021-03, Vol.45 (2), p.140-141

2021

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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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Hemoglobin Reims—a rare alpha globin chain variant and its interaction with beta thalassemia

Journal of hematopathology, 2022-12, Vol.15 (4), p.265-269

2022

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Evidence for embryonic haemoglobins from Sparus aurata under normal and hypoxic conditions

Fish physiology and biochemistry, 2019-06, Vol.45 (3), p.943-954

2019

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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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Reduction and alkylation of proteins in preparation of two-dimensional map analysis: Why, when, and how?

Electrophoresis, 2001-06, Vol.22 (10), p.2046-2057

2001

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Reverse Phase-high-performance Liquid Chromatography (RP-HPLC) Analysis of Globin Chains from Human Erythroid Cells

Bio-protocol, 2021-01, Vol.11 (2), p.e3899-e3899

2021

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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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Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband

Indian journal of pathology & microbiology, 2019-04, Vol.62 (2), p.323-325

2019

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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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Imbalanced globin chain synthesis determines erythroid cell pathology in thalassemic mice

Haematologica (Roma), 2009-09, Vol.94 (9), p.1211-1219

2009

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Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects

Blood cells, molecules, & diseases, 2015-06, Vol.55 (1), p.62-67

2015

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Introduction to the Thalassemia Syndromes

Introduction to the Thalassemia Syndromes: Molecular Medicine's Index Case

Molecular and phenotype characterization of an elongated β‐globin variant produced by HBB:C.313delA

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

Laboratory diagnosis of thalassemia

Beta‐thalassemia and the advent of new interventions beyond transfusion and iron chelation

The α-globin chain of hemoglobin potentiates tissue plasminogen activator induced hyperfibrinolysis in vitro

Hemoglobin β-Globin Variants In Hispanic Patients: An Institutional Experience From Dallas, Texas

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

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

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

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

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

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

Hemoglobin Reims—a rare alpha globin chain variant and its interaction with beta thalassemia

Evidence for embryonic haemoglobins from Sparus aurata under normal and hypoxic conditions

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

Reduction and alkylation of proteins in preparation of two-dimensional map analysis: Why, when, and how?

Reverse Phase-high-performance Liquid Chromatography (RP-HPLC) Analysis of Globin Chains from Human Erythroid Cells

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

Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband

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

Imbalanced globin chain synthesis determines erythroid cell pathology in thalassemic mice

Development of a capillary zone electrophoresis method for rapid determination of human globin chains in α and β-thalassemia subjects

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