Publications by authors named "Cesar Loris"

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Claudin-19 mutations and clinical phenotype in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Félix Claverie-Martín, Víctor García-Nieto, Cesar Loris, Gema Ariceta, Inmaculada Nadal

PLoS One· August 2013

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Gitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of life.
José David Herrero-Morín, Julián Rodríguez, Eliecer Coto, Helena Gil-Peña, Victoria Alvarez, César Loris

Nephrol Dial Transplant· January 2011

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Quality of life of adolescents with end-stage renal disease and kidney transplant.
Isolina Riaño-Galán, Serafín Málaga, Luis Rajmil, Gema Ariceta, Mercedes Navarro, Cesar Loris

Pediatr Nephrol· August 2009

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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, Mustapha Amyere, Janine Wagenstaller, César Loris

Nat Genet· November 2006

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A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies.
Eliecer Coto, Julian Rodriguez, Nikola Jeck, Victoria Alvarez, Rosario Stone, Cesar Loris

Kidney Int· January 2004

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Novel truncating mutations in the ClC-5 chloride channel gene in patients with Dent's disease.
Irma Carballo-Trujillo, Victor Garcia-Nieto, Francisco J Moya-Angeler, Montserrat Antón-Gamero, Cesar Loris

Nephrol Dial Transplant· April 2003

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Renin-angiotensin system polymorphisms and renal scarring.
Rafael Pardo, Serafín Málaga, Eliecer Coto, Mercedes Navarro, Victoria Alvarez, Cesar Loris

Pediatr Nephrol· February 2003

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