Fibrosis hepática congénita y enfermedad poliquística renal autosómica recesiva . Author links open overlay érrez Junquera Fibrosis hepática congénita y enfermedad poliquística renal autosómica recesiva . Article in Anales de Pediatría 52(5) · December with 3 Reads. La enfermedad renal poliquística (PKD, por su sigla en inglés) es una enfermedad genética . Durán-Álvarez S. Enfermedad poliquística autosómica recesiva.
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Autosomal Dominant Polycystic Kidney Disease. You can change the settings or obtain more information by clicking here. Subscribe to our Newsletter. International Society of Nefrology. The Spanish Association of Pediatrics has as one of its main objectives the dissemination of rigorous and updated scientific information on the different areas of pediatrics.
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This item has received. Public domain Public domain false false. Recommendations of the Spanish Paediatric Endocrinology Mc Graw Hill; The Impact Factor measures the average number of citations received in a particular year by poliqiistica published in the journal during the two receding years. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.
Chapman AB, Wei W. Introduction Autosomal recessive polycystic kidney disease ARPKD is a genetic disorder caused by a mutation in the PKD1 gene, which codes for protein polycystin 1, mapped on chromosome 6p Renal artery embolization for the symptomatic treatment of adult polycystic kidney disease.
Pathogenesis of ductal plate abnormalities. From Wikimedia Commons, the free media repository. Tolvaptan in patients with autosomal dominant polycystic kidney disease. It’s a one stop shop for users of OA Journals.
Actualización en enfermedad renal poliquística | Montaña | Revista de la Facultad de Medicina
Mayo Clin Proc, 73pp. Combined cystic disease of the liver and kidney.
IBN Publindex Publindex is a Colombian bibliographic index for classifying, updating, rating and certifying scientific and technological publications. Gross pathology of polycystic kidney disease. Full text is only aviable in PDF. Continuing navigation will be considered as acceptance of this use. Molecular pathways and therapies in autosomal-dominant polycystic kidney disease.
Revista de la Facultad de Medicina
Views View Edit History. SRJ is a prestige metric based on the idea that not all citations are the same. CiteScore measures average citations received per document published. Search and view critically important regional content with international impact to get a comprehensive picture of the influencers and drivers of regional research. J Med Genet, 8pp. Existen dos presentaciones de esta enfermedad que se distinguen por sus patrones de herencia: I grant anyone the right to use this work for any purposewithout any conditions, unless such conditions are required by law.
Mayo Clin Proc, 73pp.
Discussion The clinical and pathological findings are correlated and the most important necropsy findings are described. Pediatr Nephrol, 12pp.