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.

Tallennettuna:
Bibliografiset tiedot
Päätekijät: V V Fomin, A A Pulin, N A Mukhin
Aineistotyyppi: Artigo
Kieli:Russo
Julkaistu: "Consilium Medicum" Publishing house 2013-06-01
Sarja:Терапевтический архив
Aiheet:
fabry disease
orphan disease
lysosomal storage disease
α-galactosidase a
glycosphingolipids
globotriaosylceramide
nephropathy
chronic kidney disease
enzyme replacement therapy
Linkit:https://ter-arkhiv.ru/0040-3660/article/view/31258
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