Sphingosine-1-Phosphate Levels Are Higher in Male Patients with Non-Classic Fabry Disease

Fabry disease is an X-linked lysosomal disease in which defects in the alpha-galactosidase A enzyme activity lead to the ubiquitous accumulation of glycosphingolipids. Whereas the classic disease is characterized by neuropathic pain, progressive renal failure, white matter lesions, cerebral stroke,...

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Detalles Bibliográficos
Autores principales: Mauhin, Wladimir, Tebani, Abdellah, Amelin, Damien, Abily-Donval, Lenaig, Lamari, Foudil, London, Jonathan, Douillard, Claire, Dussol, Bertrand, Leguy-Seguin, Vanessa, Noel, Esther, Masseau, Agathe, Lacombe, Didier, Maillard, Hélène, Bekri, Soumeya, Lidove, Olivier, Benveniste, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911241/
https://www.ncbi.nlm.nih.gov/pubmed/35268324
http://dx.doi.org/10.3390/jcm11051233

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911241/
https://www.ncbi.nlm.nih.gov/pubmed/35268324
http://dx.doi.org/10.3390/jcm11051233

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