Hb Rio Claro is caused by a mutation at the 33rd position of the beta-globin chain

Hemograms and serial hemogram-derived ratios in survivors and non-survivors of COVID-19 in Campinas, Brazil.

Hematology, transfusion and cell therapy·2022

Effect of hydroxyurea therapy on intravascular hemolysis and endothelial dysfunction markers in sickle cell anemia patients.

Annals of hematology·2021

Alpha thalassemia and alpha-MRE haplotypes in Uruguayan patients with microcytosis and hypochromia without anemia.

Genetics and molecular biology·2021

Serum folate and cytokines in heterozygous β-thalassemia.

International journal of laboratory hematology·2020

Polymorphisms in the heme oxygenase-1 and bone morphogenetic protein receptor type 1b genes and estimated glomerular filtration rate in Brazilian sickle cell anemia patients.

Hematology, transfusion and cell therapy·2020

Rare α0-thalassemia deletions detected by MLPA in five unrelated Brazilian patients.

Genetics and molecular biology·2017

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

Ocular Complications Among Patients with Beta-Thalassaemia Major and Intermedia: A Comparative Study from Pakistan.

Hemoglobin·2026

Psychometric Performance of the Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me) in Jamaicans with Sickle Cell Disease.

Hemoglobin·2026

Unprotected Left Main Disease: Clinical Outcomes Following Deferral, Coronary Artery Bypass Grafting, or Percutaneous Coronary Intervention.

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions·2026

Association Between Coronary Artery Anomalies, Obstructive Coronary Disease, and Procedural Complexity During Coronary Angiography.

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions·2026

Cangrelor in elderly patients undergoing percutaneous coronary intervention: findings from the ICARUS Registry.

Journal of cardiovascular medicine (Hagerstown, Md.)·2026

Machine learning-based assessments of perioperative features in determining long-term conduct block post-transcatheter closure of ventricular septal defect.

Cardiology in the young·2026

Coronary artery bypass grafting outcomes in patients with prior percutaneous coronary intervention: A retrospective cohort study.

Interdisciplinary cardiovascular and thoracic surgery·2026

[Research progress on cerebral hypoperfusion following revascularization for carotid artery stenotic disease].

Zhonghua wai ke za zhi [Chinese journal of surgery]·2026

Related Experiment Videos

Hb Rio Claro is caused by a mutation at the 33rd position of the beta-globin chain

Related Concept Videos

Hemograms and serial hemogram-derived ratios in survivors and non-survivors of COVID-19 in Campinas, Brazil.

Effect of hydroxyurea therapy on intravascular hemolysis and endothelial dysfunction markers in sickle cell anemia patients.

Alpha thalassemia and alpha-MRE haplotypes in Uruguayan patients with microcytosis and hypochromia without anemia.

Serum folate and cytokines in heterozygous β-thalassemia.

Polymorphisms in the heme oxygenase-1 and bone morphogenetic protein receptor type 1b genes and estimated glomerular filtration rate in Brazilian sickle cell anemia patients.

Rare α0-thalassemia deletions detected by MLPA in five unrelated Brazilian patients.

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.

Ocular Complications Among Patients with Beta-Thalassaemia Major and Intermedia: A Comparative Study from Pakistan.

Psychometric Performance of the Adult Sickle Cell Quality-of-Life Measurement Information System (ASCQ-Me) in Jamaicans with Sickle Cell Disease.

Unprotected Left Main Disease: Clinical Outcomes Following Deferral, Coronary Artery Bypass Grafting, or Percutaneous Coronary Intervention.

Association Between Coronary Artery Anomalies, Obstructive Coronary Disease, and Procedural Complexity During Coronary Angiography.

Cangrelor in elderly patients undergoing percutaneous coronary intervention: findings from the ICARUS Registry.

Machine learning-based assessments of perioperative features in determining long-term conduct block post-transcatheter closure of ventricular septal defect.

Coronary artery bypass grafting outcomes in patients with prior percutaneous coronary intervention: A retrospective cohort study.

[Research progress on cerebral hypoperfusion following revascularization for carotid artery stenotic disease].

Related Experiment Videos

Hb Rio Claro is caused by a mutation at the 33rd position of the beta-globin chain

Related Concept Videos

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