Hb Himeji or alpha 2 beta 2(140)(H18)Ala----Asp in a Portuguese 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

Morphological and Topographical Characteristics of Parietal Foramen in the Adult Human Skull Bones of North Indian Population and Its Clinical Correlations - A Cross-Sectional Study.

Asian journal of neurosurgery·2026

Genetic diversity and morphology of South Korean Aedes koreicus (Diptera: Culicidae) provide insights into the origin of European populations.

Parasites & vectors·2026

Glasgow Coma Scale in Brazilian Portuguese: foundation translation and cultural adaptation study.

Einstein (Sao Paulo, Brazil)·2026

Intraspecific leaf morphometric diversity in the endangered and narrow endemic Quercus trojana subsp. euboica (Fagaceae): a quantitative dataset from three natural populations in Euboea, Greece.

Biodiversity data journal·2026

First record of Zaitzevia Champion, 1923 (Coleoptera, Elmidae) from Fujian Province, China, with descriptions of two new species.

ZooKeys·2026

A Genetic Method for Distinguishing Cryptic Pocillopora Species in French Polynesia Without Sequencing.

Ecology and evolution·2026

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Hb Himeji or alpha 2 beta 2(140)(H18)Ala----Asp in a Portuguese family

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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.

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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.

Morphological and Topographical Characteristics of Parietal Foramen in the Adult Human Skull Bones of North Indian Population and Its Clinical Correlations - A Cross-Sectional Study.

Genetic diversity and morphology of South Korean Aedes koreicus (Diptera: Culicidae) provide insights into the origin of European populations.

Glasgow Coma Scale in Brazilian Portuguese: foundation translation and cultural adaptation study.

Intraspecific leaf morphometric diversity in the endangered and narrow endemic Quercus trojana subsp. euboica (Fagaceae): a quantitative dataset from three natural populations in Euboea, Greece.

First record of Zaitzevia Champion, 1923 (Coleoptera, Elmidae) from Fujian Province, China, with descriptions of two new species.

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Hb Himeji or alpha 2 beta 2(140)(H18)Ala----Asp in a Portuguese family

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