Cargando…
P1551: CONFORMATIONAL STUDY OF PYRUVATE KINASE DEFICIENT VARIANTS WITH HEMOLYTIC ANEMIA. THE RELATIONSHIPS BETWEEN THE LOSS OF ENZYME FUNCTION AND STRUCTURAL DISRUPTION
Autores principales: | Jorda, L., Montllor, L., Krisnevskaya, E., Leguizamón, V., Hernandez, I., Gelpi, J. L., Vives Corrons, J.-L. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9430620/ http://dx.doi.org/10.1097/01.HS9.0000849060.64856.dd |
Ejemplares similares
-
PB2248: CONCOMITANT HEREDITARY SPHEROCYTOSIS AND PYRUVATE KINASE DEFICIENCY IN A SPANISH FAMILY WITH CHRONIC HEMOLYTIC ANEMIA. CONTRIBUTION OF LASER EKTACYTOMETRY TO CLINICAL DIAGNOSIS
por: Vives Corrons, J.-L., et al.
Publicado: (2022) -
Concomitant Hereditary Spherocytosis and Pyruvate Kinase Deficiency in a Spanish Family with Chronic Hemolytic Anemia: Contribution of Laser Ektacytometry to Clinical Diagnosis
por: Vives Corrons, Joan-Lluis, et al.
Publicado: (2022) -
Mitapivat, a novel pyruvate kinase activator, for the treatment of hereditary hemolytic anemias
por: Al-Samkari, Hanny, et al.
Publicado: (2021) -
Recommendations regarding splenectomy in hereditary hemolytic anemias
por: Iolascon, Achille, et al.
Publicado: (2017) -
Rare anemias in adolescents
por: Vives Corrons, Joan-Lluis, et al.
Publicado: (2021)