Hb F-Cobb or alpha(2)A gamma(2)37(C3)Trp----Gly

Endothelial ENaC as a repressor of oxidative stress and a guardian of lung capillary barrier function in bacterial and viral pneumonia.

Frontiers in physiology·2025

The clinical spectrum of HbSC sickle cell disease-not a benign condition.

British journal of haematology·2024

Evaluating the implementation of a multi-level mHealth study to improve hydroxyurea utilization in sickle cell disease.

Frontiers in health services·2023

A new sickling variant 'Hb S-Wake β[(Glu6Val-Asn139 Ser)]' found in a compound heterozygote with Hb S β(Glu6Val) coinherited with homozygous α-thalassemia-2: phenotype and molecular characteristics.

Acta haematologica·2010

Hb M Dothan [beta 25/26 (B7/B8)/(GGT/GAG-->GAG//Gly/Glu-->Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics.

Blood cells, molecules & diseases·2009

Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.

The pharmacogenomics journal·2007

A Rare Alpha-Globin Mutation: Detailed Analysis of the Hb Rogliano Variant (α1 Cod 108 Thr→Asn).

Hemoglobin·2026

Gender Pattern of Thyroid Dysfunction Among Patients with Beta-Thalassemia Intermedia: A Cross-Sectional Study from Yasuj, Iran.

Hemoglobin·2026

Screening for the 'Silent' Burden of Menstrual and Mental Health Among Women with Sickle Cell Disease: A Prospective Study.

Hemoglobin·2026

Precision Medicine in Transfusion-Dependent and Non-Transfusion-Dependent β-Thalassemia: Toward Personalized Diagnosis and Therapy.

Hemoglobin·2026

The Silent Epidemic: A Scoping Review of Chronic Pain Etiology and Management Strategies in Transfusion-Dependent Thalassemia.

Hemoglobin·2026

Low Prevalence of the HBB c.20A > T (HbS) Allele in a Turkish Cypriot Cohort: A Molecular Screening Study.

Hemoglobin·2026

Tirofiban-Associated Thrombocytopenia: A Case Report.

Cureus·2026

Body weight rather than unfractionated heparin dose predicts periprocedural bleeding during elective PCI.

International journal of cardiology. Cardiovascular risk and prevention·2026

Adjunctive Cerebrolysin therapy following mechanical thrombectomy for acute basilar artery occlusion: a case report.

Journal of medicine and life·2026

Simultaneous detection of thalassemia, hemoglobinopathies, and G6PD variants using long-read nanopore sequencing: genetic complexity and heterogeneity in Thailand.

PeerJ·2026

First Case Report of Triple Recurrent Cholangitis of "Coildocholithiasis," Following Hepatic Artery Pseudoaneurysm Embolization.

DEN open·2026

Preparative leukapheresis impairs autologous donor hemostasis and platelet function.

Research and practice in thrombosis and haemostasis·2026

Related Experiment Videos

Hb F-Cobb or alpha(2)A gamma(2)37(C3)Trp----Gly

Related Concept Videos

Endothelial ENaC as a repressor of oxidative stress and a guardian of lung capillary barrier function in bacterial and viral pneumonia.

The clinical spectrum of HbSC sickle cell disease-not a benign condition.

Evaluating the implementation of a multi-level mHealth study to improve hydroxyurea utilization in sickle cell disease.

A new sickling variant 'Hb S-Wake β[(Glu6Val-Asn139 Ser)]' found in a compound heterozygote with Hb S β(Glu6Val) coinherited with homozygous α-thalassemia-2: phenotype and molecular characteristics.

Hb M Dothan [beta 25/26 (B7/B8)/(GGT/GAG-->GAG//Gly/Glu-->Glu]; a new mechanism of unstable methemoglobin variant and molecular characteristics.

Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea.

A Rare Alpha-Globin Mutation: Detailed Analysis of the Hb Rogliano Variant (α1 Cod 108 Thr→Asn).

Gender Pattern of Thyroid Dysfunction Among Patients with Beta-Thalassemia Intermedia: A Cross-Sectional Study from Yasuj, Iran.

Screening for the 'Silent' Burden of Menstrual and Mental Health Among Women with Sickle Cell Disease: A Prospective Study.

Precision Medicine in Transfusion-Dependent and Non-Transfusion-Dependent β-Thalassemia: Toward Personalized Diagnosis and Therapy.

The Silent Epidemic: A Scoping Review of Chronic Pain Etiology and Management Strategies in Transfusion-Dependent Thalassemia.

Low Prevalence of the HBB c.20A > T (HbS) Allele in a Turkish Cypriot Cohort: A Molecular Screening Study.

Tirofiban-Associated Thrombocytopenia: A Case Report.

Body weight rather than unfractionated heparin dose predicts periprocedural bleeding during elective PCI.

Adjunctive Cerebrolysin therapy following mechanical thrombectomy for acute basilar artery occlusion: a case report.

Simultaneous detection of thalassemia, hemoglobinopathies, and G6PD variants using long-read nanopore sequencing: genetic complexity and heterogeneity in Thailand.

First Case Report of Triple Recurrent Cholangitis of "Coildocholithiasis," Following Hepatic Artery Pseudoaneurysm Embolization.

Preparative leukapheresis impairs autologous donor hemostasis and platelet function.

Related Experiment Videos

Hb F-Cobb or alpha(2)A gamma(2)37(C3)Trp----Gly

Related Concept Videos

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