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	1.	Quality of life of adolescents with end-stage renal disease and kidney transplant. [electronic resource] by Riaño-Galán, Isolina Málaga, Serafín Rajmil, Luis Ariceta, Gema Navarro, Mercedes Loris, Cesar Vallo, Alfredo Producer: 20090824 In: Pediatric nephrology (Berlin, Germany) vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Renin-angiotensin system polymorphisms and renal scarring. [electronic resource] by Pardo, Rafael Málaga, Serafín Coto, Eliecer Navarro, Mercedes Alvarez, Victoria Espinosa, Laura Alvarez, Ruth Vallo, Alfredo Loris, Cesar Braga, Socorro Producer: 20030916 In: Pediatric nephrology (Berlin, Germany) vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Novel truncating mutations in the ClC-5 chloride channel gene in patients with Dent's disease. [electronic resource] by Carballo-Trujillo, Irma Garcia-Nieto, Victor Moya-Angeler, Francisco J Antón-Gamero, Montserrat Loris, Cesar Méndez-Alvarez, Sebastián Claverie-Martin, Felix Producer: 20031125 In: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies. [electronic resource] by Coto, Eliecer Rodriguez, Julian Jeck, Nikola Alvarez, Victoria Stone, Rosario Loris, Cesar Rodriguez, Luis M Fischbach, Michel Seyberth, Hannsjörg W Santos, Fernando Producer: 20040928 In: Kidney international vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Gitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of life. [electronic resource] by Herrero-Morín, José David Rodríguez, Julián Coto, Eliecer Gil-Peña, Helena Alvarez, Victoria Espinosa, Laura Loris, César Gil-Calvo, Marta Santos, Fernando Producer: 20110512 In: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis. [electronic resource] by Lorenz-Depiereux, Bettina Bastepe, Murat Benet-Pagès, Anna Amyere, Mustapha Wagenstaller, Janine Müller-Barth, Ursula Badenhoop, Klaus Kaiser, Stephanie M Rittmaster, Roger S Shlossberg, Alan H Olivares, José L Loris, César Ramos, Feliciano J Glorieux, Francis Vikkula, Miikka Jüppner, Harald Strom, Tim M Producer: 20070118 In: Nature genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Claudin-19 mutations and clinical phenotype in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis. [electronic resource] by Claverie-Martín, Félix García-Nieto, Víctor Loris, Cesar Ariceta, Gema Nadal, Inmaculada Espinosa, Laura Fernández-Maseda, Ángeles Antón-Gamero, Montserrat Avila, Africa Madrid, Álvaro González-Acosta, Hilaria Córdoba-Lanus, Elizabeth Santos, Fernando Gil-Calvo, Marta Espino, Mar García-Martinez, Elena Sanchez, Ana Muley, Rafael Producer: 20130820 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)