Hb J-Lome or alpha 2 beta 259(E3)Lys----Asn in a Vietnamese 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

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

Uncovering the True Genotype: Unusually Severe Sickle Cell Disease in a Child with an Initial HbSC Diagnosis.

Hemoglobin·2026

Psychosocial and Cultural Correlates of Four-Dimensional Geriatric Depression Scale in Chinese and Korean Community-Dwelling Older Adults.

Journal of transcultural nursing : official journal of the Transcultural Nursing Society·2026

Cultural adaptation and preliminary psychometric evaluation of the Japanese CSBS-DP-ITC: An initial investigation.

Early human development·2026

Age-Related Increase in Skull Vibration-Induced Nystagmus Slow-Phase Velocity in a Clinical Population with Normal vHIT and VEMP: A Retrospective Cross-Sectional Analysis.

Audiology research·2026

Standing Long-Leg Radiographs Underestimate Varus Alignment and Joint Line Obliquity Compared With Computed Tomography in Japanese Patients.

Cureus·2026

Predictors of chronic arthralgia following chikungunya virus infection.

GMS hygiene and infection control·2026

Detection of toxigenic Vibrio cholerae in a traveler with diarrhea lacking classic features, returning from Delhi, India.

IDCases·2026

Related Experiment Videos

Hb J-Lome or alpha 2 beta 259(E3)Lys----Asn in a Vietnamese 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.

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.

Uncovering the True Genotype: Unusually Severe Sickle Cell Disease in a Child with an Initial HbSC Diagnosis.

Psychosocial and Cultural Correlates of Four-Dimensional Geriatric Depression Scale in Chinese and Korean Community-Dwelling Older Adults.

Cultural adaptation and preliminary psychometric evaluation of the Japanese CSBS-DP-ITC: An initial investigation.

Age-Related Increase in Skull Vibration-Induced Nystagmus Slow-Phase Velocity in a Clinical Population with Normal vHIT and VEMP: A Retrospective Cross-Sectional Analysis.

Standing Long-Leg Radiographs Underestimate Varus Alignment and Joint Line Obliquity Compared With Computed Tomography in Japanese Patients.

Predictors of chronic arthralgia following chikungunya virus infection.

Detection of toxigenic Vibrio cholerae in a traveler with diarrhea lacking classic features, returning from Delhi, India.

Related Experiment Videos

Hb J-Lome or alpha 2 beta 259(E3)Lys----Asn in a Vietnamese family

Related Concept Videos

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