ENFERMEDAD POLIQUISTICA RENAL AUTOSOMICA RECESIVA PDF

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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The spectrum of polycystic kidney disease in children. An Esp Pediatr, 28pp. Identification of patients with autosomal dominant polycystic kidney disease at highest risk for end-stage renal disease.

Discussion The clinical and pathological findings are poliquishica and the most important necropsy findings are described.

Unruptured intracranial aneurysms–risk of rupture and risks of surgical intervention. Get a more complete global picture by discovering new insights from research in Latin America, Spain, Portugal, the Caribbean and South Africa. Renxl Nucl Med, 18pp. Print Send to a friend Export reference Mendeley Statistics.

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Recomendaciones del Grupo de Trabajo de Obesidad de la Principios de Medicina Interna. Pediatr Nephrol, 12pp. Mayo Clin Proc, 73pp. Imaging classification of autosomal dominant polycystic kidney disease: Scopus is a bibliographic database publishing summaries and aktosomica concerning articles from scientific journals. Views View Edit History. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.

ENFERMEDAD RENAL POLIQUISTICA Y OTROS TRASTORNOS HEREDITARIO by on Prezi

Combined cystic disease of the rscesiva and kidney. Autosomal Dominant Polycystic Kidney Disease. Microscopically a diagnosis of autosomal recessive polycystic kidney disease with biliary dysgenesis was made. This is a cause of end-stage kidney disease and a common indication for dialysis and kidney transplantation.

Autosomal recessive polycystic kidney disease. Recommendations of the Spanish Paediatric Endocrinology Management of Intracranial Aneurysms.

Previous article Next article. Print Send to a friend Export reference Mendeley Statistics. Pregnancy outcome and its relationship to progression of renal failure in autosomal dominant polycystic kidney disease. It’s a one stop shop for users of OA Journals.

Revista de la Facultad de Medicina

Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate. Access nearly titles, over 4 million cited references, and open access with links to full text through a local language interface with an easy search experience. Adult renal cystic disease: Renal artery embolization for the symptomatic treatment of adult polycystic kidney disease.

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SRJ is a prestige metric based on the idea that not all citations are the same. Subscribe to our Newsletter. Renap for the use of tolvaptan in autosomal dominant polycystic kidney disease: I, the copyright holder of this work, release this work into the public domain.

Scopus Scopus is a bibliographic database publishing summaries and references concerning articles from scientific journals.

Acta Pediatr, 84pp. Effect of pravastatin on total kidney volume, left ventricular mass index, and microalbuminuria in pediatric autosomal dominant polycystic kidney disease.

Combined cystic disease of the liver and kidney. I grant anyone the right to use this enfeermedad for any purposewithout any conditions, unless such conditions are required by law. Ludwig symposium on biliary disorders – part I.

Autosomal recessive polycystic kidney disease ARPKD is a genetic disorder caused by a mutation in the PKD1 autosoomica, which codes for protein polycystin 1, mapped on chromosome 6p