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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Hypertension in autosomal dominant polycystic kidney disease. Relationship between renal volume growth and renal function in autosomal dominant polycystic kidney disease: Pulmonary cysts in smoking-related interstitial fibrosis: From Wikimedia Commons, the free media repository.
Autosomal Recessive Polycystic Kidney Disease. 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. Everolimus in patients pooiquistica autosomal dominant polycystic kidney disease. This item has received. Case report We report the autopsy findings in a 2 h old, term female infant with severe oligohydramnios. Imaging approaches to patients with polycystic kidney disease.
SJR uses a similar algorithm as the Google page rank; it provides a quantitative enfermedav qualitative measure of the poliquistjca impact.
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Enfermedad Poliquistica Renal by Sergio Noga on Prezi
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Autosomal Dominant Polycystic Kidney Disease. To improve our services and revesiva, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. Pei Y, Watnick T. Acta Pediatr, 84pp. Full text is only aviable in PDF.
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This page was last edited on 14 Mayat Systematic literature review conducted in recessiva PubMed, Lilacs, UptoDate and Medline databases with the following terms: CiteScore measures average citations received per document published. The molecular biology of polycystic kidney disease. January – March Pages Microscopically a diagnosis of autosomal recessive polycystic kidney disease with biliary dysgenesis was made.
Effect of pravastatin on total kidney volume, left ventricular mass index, and microalbuminuria in pediatric autosomal dominant polycystic enfermedaad disease. The clinical and pathological findings are correlated and the most important necropsy findings are described. Caroli’s diseaseversus polycystic hepatic disease. Scopus is a bibliographic database publishing summaries and references concerning articles from scientific journals.
Renal transplantation in autosomal dominant polycystic kidney disease. Mayo Clin Proc, 73pp. Si continua navegando, consideramos que acepta su uso. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.
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SRJ is a prestige metric based on the idea that not all citations are the same. Pediatr Nephrol, 12pp. Human Genet, 68pp.
Gross pathology of polycystic kidney disease. ARPKD is characterised by the formation of cysts from coalescing dilated renal collecting ducts coexisting with congenital hepatic fibrosis secondary to biliar dysgenesis. You can change the settings or obtain more information by clicking here.
Pregnancy outcome and its relationship to progression of renal failure in autosomal dominant polycystic kidney disease. Diverticulitis and polycystic kidney disease. The relevant literature is reviewed and recent advances in the pathology, genetics, diagnosis, ultrasonography, prevention and treatment of ARPKD are discussed. Polycystic disease of kidney presenting in childhood.