Hemoglobin Aichi [alpha 50(CE8)His----Arg] in a French Caucasian patient

Lymphocyte expansion after unrelated cord blood allogeneic stem cell transplantation in adults.

Bone marrow transplantation·2017

Lenalidomide with or without erythropoietin in transfusion-dependent erythropoiesis-stimulating agent-refractory lower-risk MDS without 5q deletion.

Leukemia·2015

Upfront allogeneic stem-cell transplantation for patients with nonlocalized untreated peripheral T-cell lymphoma: an intention-to-treat analysis from a single center.

Annals of oncology : official journal of the European Society for Medical Oncology·2014

Improvements in phenotype studies of hemoglobin disorders brought by advances in reversed-phase chromatography of globin chains.

International journal of laboratory hematology·2014

Stable long-term pulmonary function after fludarabine, antithymocyte globulin and i.v. BU for reduced-intensity conditioning allogeneic SCT.

Bone marrow transplantation·2014

Azacitidine salvage therapy for relapse of myeloid malignancies following allogeneic hematopoietic SCT.

Bone marrow transplantation·2014

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

Co-Heredity of (-α)20.5 Deletion and IVS I-1 G > A (HBB: C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?

Hemoglobin·2026

Hemoglobin E Associated with Hemoglobin Constant Spring: Diagnostic Challenges in Heterozygous and Homozygous States.

Hemoglobin·2026

Experimental characterization of blood rheology and development of a computational rheological Index during progressive hemorrhagic shock.

Clinical hemorheology and microcirculation·2026

Atypical hemolytic uremic syndrome in kidney transplantation.

Journal of nephrology·2026

Late diagnosis of SLC34A3-related hereditary hypophosphatemic osteomalacia following a low-energy proximal humeral 4-part fracture.

JBMR plus·2026

The Association of the Neutrophil-to-Lymphocyte Ratio and the D-dimer-to-Albumin Ratio with Deep Vein Thrombosis in Patients with Spontaneous Intracerebral Hemorrhage.

International journal of general medicine·2026

Trends and forecasting of reported hepatitis B and hepatitis C incidence in Hainan Province, China, 2005-2020.

Frontiers in epidemiology·2026

Precision-guided therapy in dialysis-dependent classic hairy cell leukemia: a case report.

Frontiers in oncology·2026

Related Experiment Videos

Hemoglobin Aichi [alpha 50(CE8)His----Arg] in a French Caucasian patient

Related Concept Videos

Lymphocyte expansion after unrelated cord blood allogeneic stem cell transplantation in adults.

Lenalidomide with or without erythropoietin in transfusion-dependent erythropoiesis-stimulating agent-refractory lower-risk MDS without 5q deletion.

Upfront allogeneic stem-cell transplantation for patients with nonlocalized untreated peripheral T-cell lymphoma: an intention-to-treat analysis from a single center.

Improvements in phenotype studies of hemoglobin disorders brought by advances in reversed-phase chromatography of globin chains.

Stable long-term pulmonary function after fludarabine, antithymocyte globulin and i.v. BU for reduced-intensity conditioning allogeneic SCT.

Azacitidine salvage therapy for relapse of myeloid malignancies following allogeneic hematopoietic SCT.

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.

Co-Heredity of (-α)20.5 Deletion and IVS I-1 G > A (HBB: C.92 + 1 G > A) Mutations in a Pediatric Patient: A Cause of Moderate Anemia Phenotype?

Hemoglobin E Associated with Hemoglobin Constant Spring: Diagnostic Challenges in Heterozygous and Homozygous States.

Experimental characterization of blood rheology and development of a computational rheological Index during progressive hemorrhagic shock.

Atypical hemolytic uremic syndrome in kidney transplantation.

Late diagnosis of SLC34A3-related hereditary hypophosphatemic osteomalacia following a low-energy proximal humeral 4-part fracture.

The Association of the Neutrophil-to-Lymphocyte Ratio and the D-dimer-to-Albumin Ratio with Deep Vein Thrombosis in Patients with Spontaneous Intracerebral Hemorrhage.

Trends and forecasting of reported hepatitis B and hepatitis C incidence in Hainan Province, China, 2005-2020.

Precision-guided therapy in dialysis-dependent classic hairy cell leukemia: a case report.

Related Experiment Videos

Hemoglobin Aichi [alpha 50(CE8)His----Arg] in a French Caucasian patient

Related Concept Videos

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