Search Results - "LUQUE DE PABLOS, Augusto"
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Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis
Published in Kidney international (01-12-2009)“…Mutations in the NPHS1 gene cause congenital nephrotic syndrome of the Finnish type presenting before the first 3 months of life. Recently, NPHS1 mutations…”
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Severe manifestation of Bartter syndrome Type IV caused by a novel insertion mutation in the BSND gene
Published in Clinical nephrology (01-05-2014)“…Bartter syndrome Type IV is a rare subtype of the Bartter syndromes that leads to both severe renal salt wasting and sensorineural deafness. This autosomal…”
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New mutation in 2 paediatric patients with Alport syndrome. Prognostic significance of genotype
Published in Nefrología (01-05-2017)Get full text
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Mycobacterium fortuitum as a cause of peritoneal dialysis catheter port infection. A clinical case and a review of the literature
Published in Nefrología (01-11-2015)Get full text
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The influence of clinical situation on health-related quality of life in paediatric chronic kidney disease patients
Published in Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia (18-01-2013)“…Studies examining health-related quality of life (HRQOL) in adults with chronic kidney disease (CKD) have demonstrated that certain clinical situations such as…”
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Ibuprofen-induced acute interstitial nephritis in the paediatric population
Published in Nefrología (01-01-2016)Get full text
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Alteración genética no descrita previamente en 2 pacientes pediátricas con síndrome de Alport. Influencia pronóstica del genotipo
Published in Nefrología (01-05-2017)Get full text
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Mycobacterium fortuitum como causa de infección del orificio del catéter de diálisis peritoneal. Caso clínico y revisión de la literatura
Published in Nefrología (01-11-2015)Get full text
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Nefritis intersticial aguda por ibuprofeno en población pediátrica
Published in Nefrología (01-01-2016)Get full text
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TRPC6 mutational analysis in a large cohort of patients with focal segmental glomerulosclerosis
Published in Nephrology, dialysis, transplantation (01-10-2009)“…Background. Mutations in the TRPC6 gene have been reported in six families with adult-onset (17–57 years) autosomal dominant focal segmental glomerulosclerosis…”
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Cadaver donor kidney retransplantation in the pediatric patient: complications and long-term outcome
Published in The Journal of urology (01-06-2011)“…We compared the outcome of second and third kidney allografts with that of the first kidney allograft in pediatric recipients. We classified 173 cadaveric…”
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Results of the use of donors under 3 years of age for pediatric renal transplantation
Published in Archivos españoles de urología (01-07-2004)“…To evaluate the functional results and incidence of complications in a series of pediatric renal transplants using grafts from pediatric donors under 3 years…”
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Nephrin mutations cause childhood- and adult-onset focal segmental glomeruloscierosis
Published in Kidney international (2009)Get full text
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Re: En bloc transplantation of kidneys from pediatric donors
Published in The Journal of urology (01-01-1997)Get more information
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