C Loris

DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis

Bettina Lorenz‐Depiereux, Murat Bastepe, Anna Benet‐Pagès et al. · Nature Genetics · 2006 · 514 citations · Full text

Developmental Biology, Bone Morphogenic Protein, Genetics +9

Quality of life of adolescents with end-stage renal disease and kidney transplant

Isolina Riaño Galán, S Málaga, Luís Rajmil et al. · Pediatric Nephrology · 2009 · 71 citations

Quality Of Life, Hemodialysis, Urology +9

A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies

Eliécer Coto, Julián Rodrı́guez, Nikola Jeck et al. · Kidney International · 2003 · 64 citations · Full text

New Mutation, Allelic Variant, Intron 9 +9

Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

Félix Claverie-Martı́n, Víctor Manuel García Nieto, C Loris et al. · PLoS ONE · 2013 · 60 citations · Full text

Growth Hormone Treatment in Short Children with Chronic Renal Failure and after Renal Transplantation: Combined Data from European Clinical Trials

A. van Es, U. Berg, M. Broycr et al. · Acta Paediatrica · 1991 · 51 citations

Human Growth, Transplantation Medicine, Education +17