C. Loris

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

V. Álvarez, E. Coto, M. Fischbach, 2004, Kidney international.

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

G. Ariceta, L. Rajmil, C. Loris, 2009, Pediatric Nephrology.

Renin-angiotensin system polymorphisms and renal scarring

V. Álvarez, E. Coto, C. Loris, 2003, Pediatric Nephrology.

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

T. Strom, K. Badenhoop, F. Glorieux, 2006, Nature Genetics.

Towards guidelines for dialysis in children with end-stage renal disease

J. Martín-Govantes, C. Loris, S. Málaga, 2000, Pediatric Nephrology.

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

G. Ariceta, F. Claverie-Martin, F. Santos, 2013, PloS one.

Novel truncating mutations in the ClC-5 chloride channel gene in patients with Dent's disease.

F. Claverie-Martin, V. Garcia-Nieto, C. Loris, 2003, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Predictors of Final Adult Height after Renal Transplantation during Childhood: A Single-Center Study

C. Loris, J. Rodríguez-soriano, S. Málaga, 2000, Nephron.

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

M. Preece, U. Berg, L. Rees, 1991 .

Manejo del reflujo vesicoureteral primario

C. Loris, G. Fraga, J. Escribano, 2009 .

Gitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of life.

V. Álvarez, E. Coto, H. Gil-Peña, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.