Results 201 to 210 of about 1,145,402 (246)

Talassemias alfa Alpha thalassemias

Revista Brasileira de Hematologia e Hemoterapia, 2006
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Molecular basis of alpha-thalassemia

, 2018
Farashi, S., Harteveld, C.L.
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Alpha-Thalassemia

Exploration of Host Genetic Factors associated with Malaria, 2021
T. Qidwai
semanticscholar   +2 more sources

The Clinical Phenotypes of Alpha Thalassemia.

Hematology/Oncology Clinics of North America, 2023
Clinical manifestations of α-thalassemia range from no symptoms to severe transfusion-dependent anemia. Alpha thalassemia trait is deletion of 1 to 2 α-globin genes, whereas α-thalassemia major (ATM; Barts hydrops fetalis) is the deletion all 4 α genes.
A. Lal, E. Vichinsky
semanticscholar   +3 more sources

Advancing Alpha-Thalassemia Carrier Screening for Better Predictions Using Explainable AI

2023 4th International Conference on Communication, Computing and Industry 6.0 (C216), 2023
Thalassemia is a category of inherited blood disorders, becoming a primary health threat due to its increased prevalence worldwide. Through examination and testing of Thalassemia is widely accessible to the people.
Aditya H. Meti, B. Maheswari, Aditya Vijjapu   +2 more
semanticscholar   +1 more source

Alpha‐thalassemia

American Journal of Hematology, 1977
AbstractThe current concepts of α‐thalassemia including incidence, genetics, clinical spectrum and diagnosis are reviewed. Speculation concerning clinical application of the molecular biology of α‐thalassemia is also presented.
J G, Adams, M H, Steinberg
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Alpha-Thalassemia Carrier due to –α3.7 Deletion: Not So Silent

Acta Haematologica, 2020
Background/Objective: Alpha-thalassemia is one of the most prevalent genetic diseases, with the –α3.7 deletion being the most common mutation. Molecular studies have suggested mechanisms to explain the mild phenotype of “silent carrier” heterozygotes ...
O. Gilad, O. Steinberg-Shemer, O. Dgany, T. Krasnov, S. Noy-Lotan, H. Tamary, J. Yacobovich   +6 more
semanticscholar   +1 more source

Alpha-Thalassemia in Ashkenazi Jews

Annals of Internal Medicine, 1983
Members of a Jewish family of Polish origin were found to have hypochromic, microcytic erythrocytes. By restriction endonuclease analysis of DNA, the propositus, a brother, and an aunt were found to have a single alpha-globin gene on each chromosome 16. Five family members have one chromosome bearing two alpha-genes (5' and 3') with a single alpha-gene
G B, Sancar, D B, Rausher, R M, Baine, O, Platica, M M, Cedeno, I, Nawabi, R F, Rieder   +6 more
openaire   +3 more sources