A further note on the combination of an alpha chain variant with beta-thalassemia

Determination of CEBPA mutations by next generation sequencing in pediatric acute leukemia.

Bratislavske lekarske listy·2018

Multiple Cerebral Emboli in a Homozygous b-Thalassaemia Patient Due to Factor V 1299 (His-Arg) 4070 A-G Mutation.

Turkish journal of haematology : official journal of Turkish Society of Haematology·2016

Hemoglobin Lepore Boston in a Turkish Family.

Turkish journal of haematology : official journal of Turkish Society of Haematology·2016

Frequency of FV 1299 His-Arg (A4070G) in Turkish Cypriots.

Turkish journal of haematology : official journal of Turkish Society of Haematology·2016

Homozygous ß-Thalassemia (FCS8-AA) and Hereditary Spherocytosis in the Same Patient.

Turkish journal of haematology : official journal of Turkish Society of Haematology·2016

p53 Gene Polymorphisms in the Turkish Population.

Turkish journal of haematology : official journal of Turkish Society of Haematology·2016

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

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

Formation and Development of Deep Vein Thrombosis in Hip Fracture Patients With and Without Anticoagulation.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis·2026

EXPRESS: caADAMTS13 reduces neutrophil-mediated vascular inflammation without exacerbating bleeding in experimental intracerebral haemorrhage.

Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism·2026

A Novel Genetic VWF Variant in Siblings with von Willebrand Disease Type 2N: A Case Report.

Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie·2026

Factors Associated With Discordance Between the Activated Partial Thromboplastin Time and Anti-factor Xa Activity During Extracorporeal Membrane Oxygenation: A Retrospective Cohort Study.

Cureus·2026

FOLFOX-HAIC Plus Lenvatinib and Tislelizumab in Advanced Hepatocellular Carcinoma with Arteriovenous Fistulae: A Real-World Study.

Journal of hepatocellular carcinoma·2026

Seeing the Small to Prevent the Big: The Role of Cerebral Microvessels in Ischemic Stroke Etiology and Prevention.

Stroke research and treatment·2026

Related Experiment Videos

A further note on the combination of an alpha chain variant with beta-thalassemia

Related Concept Videos

Determination of CEBPA mutations by next generation sequencing in pediatric acute leukemia.

Multiple Cerebral Emboli in a Homozygous b-Thalassaemia Patient Due to Factor V 1299 (His-Arg) 4070 A-G Mutation.

Hemoglobin Lepore Boston in a Turkish Family.

Frequency of FV 1299 His-Arg (A4070G) in Turkish Cypriots.

Homozygous ß-Thalassemia (FCS8-AA) and Hereditary Spherocytosis in the Same Patient.

p53 Gene Polymorphisms in the Turkish Population.

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.

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?

Formation and Development of Deep Vein Thrombosis in Hip Fracture Patients With and Without Anticoagulation.

EXPRESS: caADAMTS13 reduces neutrophil-mediated vascular inflammation without exacerbating bleeding in experimental intracerebral haemorrhage.

A Novel Genetic VWF Variant in Siblings with von Willebrand Disease Type 2N: A Case Report.

Factors Associated With Discordance Between the Activated Partial Thromboplastin Time and Anti-factor Xa Activity During Extracorporeal Membrane Oxygenation: A Retrospective Cohort Study.

FOLFOX-HAIC Plus Lenvatinib and Tislelizumab in Advanced Hepatocellular Carcinoma with Arteriovenous Fistulae: A Real-World Study.

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Related Experiment Videos

A further note on the combination of an alpha chain variant with beta-thalassemia

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