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Your search keyword '"Moriniere, Vincent"' showing total 17 results

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17 results on '"Moriniere, Vincent"'

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1. Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence

2. The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies

3. A wave of deep intronic mutations in X-linked Alport syndrome

6. School level of children carrying a HNF1B variant or a deletion

9. Corrigendum: Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function

12. NPHS2 p.V290M mutation in late-onset steroid-resistant nephrotic syndrome

14. School level of children carrying a HNF1B variant or a deletion

15. Nphs2 Mutations In Steroid-Resistant Nephrotic Syndrome: A Mutation Update And The Associated Phenotypic Spectrum

16. Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin

17. Prevalence of Mutations in Renal Developmental Genes in Children with Renal Hypodysplasia: Results of the ESCAPE Study

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