Adherence to cysteamine in nephropathic cystinosis: A unique electronic monitoring experience for a better understanding. A prospective cohort study: CrYSTobs-Reference-Cited by-同舟云学术

Adherence to cysteamine in nephropathic cystinosis: A unique electronic monitoring experience for a better understanding. A prospective cohort study: CrYSTobs

Published:2020-09-09 Issue:3 Volume:36 Page:581-589
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Gaillard Segolene^ORCID,Roche Laurent,Lemoine Sandrine,Deschênes Georges,Morin Denis,Vianey-Saban Christine,Acquaviva-Bourdain Cécile,Ranchin Bruno,Bacchetta Justine,Kassai Behrouz,Nony Patrice,Bodénan Eurielle,Laudy Valérie,Rouges Cécile,Zarrabian Setareh,Subtil Fabien,Mercier Catherine,Cochat Pierre,Bertholet-Thomas Aurélia

Funder

PHRC 2009

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology, and Child Health

Link

https://link.springer.com/content/pdf/10.1007/s00467-020-04722-0.pdf

Reference27 articles.

1. Gahl WA, Thoene JG, Schneider JA (2002) Cystinosis. N Engl J Med 347:111–121

2. Town M, Jean G, Cherqui S, Attard M, Forestier L, Whitmore SA, Callen DF, Gribouval O, Broyer M, Bates GP, van't Hoff W, Antignac C (1998) A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis. Nat Genet 18:319–324

3. Kalatzis V, Cherqui S, Antignac C, Gasnier B (2001) Cystinosin, the protein defective in cystinosis, is a H(+)-driven lysosomal cystine transporter. EMBO J 20:5940–5949