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Clinical Nephrology|October 27, 2006
Successful treatment of respiratory dysfunction in cystinosis by nocturnal non-invasive positive pressure ventilationM A Edens, W J van Son, M H G de Greef, et al.Nederlands Tijdschrift Voor Geneeskunde|April 24, 2007
[From gene to disease; 'apparent mineralocorticoid excess' syndrome, a syndrome with an apparent excess of mineral corticoids]E N Levtchenko, J Deinum, N V A M Knoers, et al.Molecular Genetics and Metabolism|January 4, 2011
Elevated concentrations of sedoheptulose in bloodspots of patients with cystinosis caused by the 57-kb deletion: implications for diagnostics and neonatal screeningM M C Wamelink, E A Struys, E E W Jansen, et al.Nederlands Tijdschrift Voor Geneeskunde|August 24, 2005
[A genetic childhood disease with consequences in adult life: the Denys-Drash syndrome]M M Löwik, F W P J van den Berkmortel, C Noordam, et al.Cell Calcium|March 30, 2012
Polycystin-1 and polycystin-2 are both required to amplify inositol-trisphosphate-induced Ca2+ releaseD Mekahli, E Sammels, T Luyten, et al.Molecular Genetics and Metabolism|June 2, 2026
Prevalence and clinical impact of gastrointestinal symptoms in patients with cystinosisA de Vreugd, M L van Campen, E A M Cornelissen, et al.Kidney International|August 24, 2007
Focal segmental glomerulosclerosis in a patient homozygous for a CD2AP mutationM M Löwik, P J T A Groenen, I Pronk, et al.Journal of Inherited Metabolic Disease|September 4, 2010
Neurocognitive functioning in school-aged cystinosis patientsM T P Besouw, G M Hulstijn-Dirkmaat, R E A van der Rijken, et al.Kidney International|September 14, 2007
P-glycoprotein-deficient mice have proximal tubule dysfunction but are protected against ischemic renal injuryM Huls, C Kramers, E N Levtchenko, et al.Pageof 2