Results 131 to 140 of about 6,860 (229)

Negligible urinary cysteamine loss in cystinosis patients with Fanconi syndrome.

open access: yes, 2002
Cystinosis is an inborn error of lysosomal cystine transporter, resulting in cystine accumulation in lysosomes of all cells. Renal Fanconi syndrome is an early sign of kidney involvement in cystinosis patients.
Monnens, L.A.H.   +3 more
core  

Molecular characterization of cystinosis patients: predominance of the CTNS c.829dup mutation in Center of Tunisia. [PDF]

open access: yesBMC Genom Data
Sahli C   +10 more
europepmc   +1 more source

Cystinosin regulates Na<sup>+</sup>/H<sup>+</sup> exchanger 3 trafficking and function in kidney proximal tubular cells. [PDF]

open access: yesEMBO Rep
Khare V   +12 more
europepmc   +1 more source

Hematopoietic Stem-Cell Gene Therapy for Cystinosis. [PDF]

open access: yesN Engl J Med
Barshop BA   +19 more
europepmc   +1 more source

Improving Lifelong Comprehensive Care Coordination in Nephropathic Cystinosis: Multidisciplinary Perspectives. [PDF]

open access: yesKidney Int Rep
Golestaneh L   +11 more
europepmc   +1 more source

Cystinosis.

open access: yesProgress in clinical and biological research, 1976
This paper about cystinosis is focused primarily on nosology and genetic heterogeneity, the recurrent themes of these conferences. It briefly discusses cystinosis in relation to other disorders which cause the renal Fanconi syndrome with or without glomerular insufficiency, points out the methods for its reliable diagnosis, and then summarizes evidence
openaire   +2 more sources

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