Cargando…
Coagulation Parameters in Adult Patients With Type-1 Gaucher Disease
BACKGROUND: Gaucher disease is a rare inborn error of lysosomal metabolism, characterized by lysosomal storage of the β-glucosylceramide. Bleedings observed in type-1 Gaucher disease (GD1) are commonly attributed to a low platelet count, but they can also occur when the platelet count is normal or s...
Autores principales: | Serratrice, Christine, Cherin, Patrick, Lidove, Olivier, Noel, Esther, Masseau, Agathe, Leguy-Seguin, Vanessa, Jaussaud, Roland, Marie, Isabelle, Lavigne, Christian, Maillot, Francois |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153659/ https://www.ncbi.nlm.nih.gov/pubmed/32300455 http://dx.doi.org/10.14740/jh543 |
Ejemplares similares
-
Impact of imiglucerase supply constraint on the therapeutic management and course of disease in French patients with Gaucher disease type 1
por: Stirnemann, Jérôme, et al.
Publicado: (2015) -
Immunoglobulin Abnormalities in Gaucher Disease: an Analysis of 278 Patients Included in the French Gaucher Disease Registry
por: Nguyen, Yann, et al.
Publicado: (2020) -
Splenic Artery Aneurysms, a Rare Complication of Type 1 Gaucher Disease: Report of Five Cases
por: Serratrice, Christine, et al.
Publicado: (2019) -
Cornea verticillata and acroparesthesia efficiently discriminate clusters of severity in Fabry disease
por: Mauhin, Wladimir, et al.
Publicado: (2020) -
Sphingosine-1-Phosphate Levels Are Higher in Male Patients with Non-Classic Fabry Disease
por: Mauhin, Wladimir, et al.
Publicado: (2022)