Nephropathy in Fabry disease: possibilities for the radical improvement of prognosis for orphan diseases

The paper discusses the specific features of the diagnosis and treatment of kidney involvement in patients with Fabry disease.

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Détails bibliographiques
Auteurs principaux: V V Fomin, A A Pulin, N A Mukhin
Format: Artigo
Langue:Russo
Publié: "Consilium Medicum" Publishing house 2013-06-01
Collection:Терапевтический архив
Sujets:
fabry disease
orphan disease
lysosomal storage disease
α-galactosidase a
glycosphingolipids
globotriaosylceramide
nephropathy
chronic kidney disease
enzyme replacement therapy
Accès en ligne:https://ter-arkhiv.ru/0040-3660/article/view/31258
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