Found: 8
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Case Report: α-Spectrin Mutation Associated with αLELY Polymorphism Responsible for Hereditary Pyropoikilocytosis.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
IMPLEMENTACIÓN DE LA PCR DIGITAL PARA EL DIAGNÓSTICO PRENATAL NO INVASIVO DE LA ENFERMEDAD DE CÉLULAS FALCIFORMES. ESTUDIO PILOTO.
- Published in:
- Anales de la Real Academia Nacional de Medicina, 2024, v. 141, n. 1, p. 21, doi. 10.32440/ar.2024.141.01.rev02
- By:
- Publication type:
- Article
PIROPOIQUILOCITOSIS HEREDITARIA.
- Published in:
- Anales de la Real Academia Nacional de Medicina, 2022, v. 139, n. 1, p. 100, doi. 10.32440/ar.2022.139.01.cc01
- By:
- Publication type:
- Article
β-TALASEMIA INTERMEDIA: TRIPLICACIÓN DE GENES α/β TALASEMIA HETEROCIGOTA EN ESPAÑA.
- Published in:
- Anales de la Real Academia Nacional de Medicina, 2021, v. 138, n. 1, p. 60, doi. 10.32440/ar.2021.138.01.rev07
- By:
- Publication type:
- Article
DIAGNÓSTICO DIFERENCIAL DE LAS ERITROCITOSIS. HEMOGLOBINAS CON ALTA AFINIDAD POR EL OXÍGENO.
- Published in:
- Anales de la Real Academia Nacional de Medicina, 2020, v. 137, n. 1, p. 35, doi. 10.32440/ar.2020.137.01.rev04
- By:
- Publication type:
- Article
Largest comparison between onset and relapses of acquired thrombotic thrombocytopenic purpura reveals severe neurological involvement and worse analytic parameters at debut.
- Published in:
- Annals of Hematology, 2024, v. 103, n. 3, p. 725, doi. 10.1007/s00277-024-05634-x
- By:
- Publication type:
- Article
Pincered red cells in hereditary spherocytosis.
- Published in:
- 2022
- By:
- Publication type:
- Letter
δβ-Thalassemia Trait.
- Published in:
- American Journal of Clinical Pathology, 2014, v. 142, n. 4, p. 567, doi. 10.1309/AJCPPBQ8UB1WHXTS
- By:
- Publication type:
- Article