Hemoglobin Daneshgah-Tehran or alpha 2(72) (EF1) His----Arg beta 2 in an Argentinean family

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

Endocrine Complications in Patients with Congenital Dyserythropoietic Anemia: A Single-Center Cohort Study.

Hemoglobin·2026

Metabolomic and Proteomic Profiling of Vaso-Occlusive Crises in Sickle Cell Disease: Current Evidence and Future Perspectives.

Hemoglobin·2026

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

Hemoglobin·2026

CRISPR-Based Mediated Reactivation of Fetal Hemoglobin as a Therapeutic Strategy for Hemoglobinopathies: Evidence from Preclinical to Clinical Trials in Sickle Cell Disease and β-Thalassemia.

Hemoglobin·2026

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Hemoglobin·2026

Mapping the Management-to-Cure Transition in Thalassemia Research: Semantic Topic Modeling of 17,651 Publications Across Three Decades.

Hemoglobin·2026

Isomerization HCN → HNC in the electronic ground state using chirp-optimized mid-IR laser pulses: 4D quantum dynamics.

Physical chemistry chemical physics : PCCP·2026

Association of Thromboelastography With Hematoma Expansion and Disability in Spontaneous Intracerebral Hemorrhage: A Multicenter Study.

Neurology open access·2026

Quantitative assessment of active bleeding on contrast-enhanced computed tomography in primary postpartum hemorrhage.

Diagnostic and interventional radiology (Ankara, Turkey)·2026

The HO-1/bilirubin axis in cardiovascular protection: critical evidence for modulation by plant metabolites and traditional multi-component formulations used in Chinese medicine.

Frontiers in pharmacology·2026

Endovascular management of brachiocephalic vein stenosis and occlusion in hemodialysis patients: Technical outcomes and 6-month dialysis access patency.

Journal of vascular surgery cases and innovative techniques·2026

Factors Associated With 30-Day Functional Outcome and Mortality Following Spontaneous Intracerebral Hemorrhage in Bangladesh: A Prospective Two-Center Cohort Study.

Cureus·2026

Related Experiment Videos

Hemoglobin Daneshgah-Tehran or alpha 2(72) (EF1) His----Arg beta 2 in an Argentinean family

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.

Endocrine Complications in Patients with Congenital Dyserythropoietic Anemia: A Single-Center Cohort Study.

Metabolomic and Proteomic Profiling of Vaso-Occlusive Crises in Sickle Cell Disease: Current Evidence and Future Perspectives.

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

CRISPR-Based Mediated Reactivation of Fetal Hemoglobin as a Therapeutic Strategy for Hemoglobinopathies: Evidence from Preclinical to Clinical Trials in Sickle Cell Disease and β-Thalassemia.

Genotype-Specific Hematologic Signatures Across α-Globin Defect Categories in α-Thalassemia.

Mapping the Management-to-Cure Transition in Thalassemia Research: Semantic Topic Modeling of 17,651 Publications Across Three Decades.

Isomerization HCN → HNC in the electronic ground state using chirp-optimized mid-IR laser pulses: 4D quantum dynamics.

Association of Thromboelastography With Hematoma Expansion and Disability in Spontaneous Intracerebral Hemorrhage: A Multicenter Study.

Quantitative assessment of active bleeding on contrast-enhanced computed tomography in primary postpartum hemorrhage.

The HO-1/bilirubin axis in cardiovascular protection: critical evidence for modulation by plant metabolites and traditional multi-component formulations used in Chinese medicine.

Endovascular management of brachiocephalic vein stenosis and occlusion in hemodialysis patients: Technical outcomes and 6-month dialysis access patency.

Factors Associated With 30-Day Functional Outcome and Mortality Following Spontaneous Intracerebral Hemorrhage in Bangladesh: A Prospective Two-Center Cohort Study.

Related Experiment Videos

Hemoglobin Daneshgah-Tehran or alpha 2(72) (EF1) His----Arg beta 2 in an Argentinean family

Related Concept Videos

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