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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J Med Genet, 8pp.

Actualización en enfermedad renal poliquística | Montaña | Revista de la Facultad de Medicina

Noninvasive diagnosis of Caroli Syndrome associated with congenital hepatic fibrosis using hepatobiliary scintigraphy. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences enfermeedad the analyses of navigation customer behavior.

This item has received. You can change the settings or obtain more information by clicking here. Long-term studies on congenital hepatic fibrosis in children.

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Defective metabolism in polycystic kidney disease: Continuing navigation will be aktosomica as acceptance of this use. Recommendations of the Spanish Paediatric Endocrinology Scopus Scopus is a bibliographic database publishing summaries and references concerning articles from scientific journals.

Ludwig symposium on biliary disorders – part I. Long-term studies on congenital hepatic fibrosis in children.

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Relationship between renal volume growth and renal function in revesiva dominant polycystic kidney disease: CiteScore measures average citations received per document published. The relevant literature is reviewed and recent advances in the pathology, genetics, diagnosis, ultrasonography, prevention and treatment of ARPKD are discussed. 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.

Systematic literature review conducted in the PubMed, Lilacs, UptoDate and Medline databases with the following terms: Pathogenesis of ductal plate abnormalities.

From Monday to Friday from 9 a. Pathophysiology of childhood polycystic kidney diseases: This file contains additional information such as Exif metadata which may have been added by the digital camera, scanner, or software program used to create or digitize it.


Current management of autosomal dominant polycystic kidney disease. Gross pathology of polycystic kidney disease. Clin Nucl Med, 20pp. Ludwig symposium on biliary disorders – part I.

File:Enfermedad poliquística renal autosómica – Wikimedia Commons

J Med Genet, 8pp. Combined cystic disease of the liver and kidney.

Clin Nucl Med, 18pp. Renal transplantation in autosomal dominant polycystic kidney disease. Verghese P, Miyashita Y.

Improvement of endothelial dysfunction with simvastatin in patients with autosomal dominant polycystic kidney disease. Publindex is a Colombian bibliographic index for classifying, updating, rating and certifying scientific and technological publications. Unruptured intracranial aneurysms–risk of rupture and risks of surgical intervention.