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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Pathophysiology of childhood polycystic kidney diseases: Are you a health professional able to prescribe or dispense drugs? Renal artery embolization for the symptomatic treatment of adult polycystic kidney disease. Combined cystic disease of the liver and kidney. Principios de Medicina Interna. International Society of Loliquistica. If the file has been modified from its original state, some details such as the timestamp may not fully reflect those of the original file.
Enfermedad Poliquistica Renal by Sergio Noga on Prezi
Defective glucose metabolism in polycystic kidney disease identifies a new therapeutic strategy. Acta Pediatr, 84pp. You can change the settings or obtain more information by clicking here. Mayo Clin Proc, 73pp. Verghese P, Miyashita Y. Mc Graw Hill; Noninvasive diagnosis of Caroli Syndrome associated with congenital hepatic fibrosis using hepatobiliary scintigraphy. Pei Y, Watnick T.
An Esp Pediatr, 28pp. Molecular pathways and therapies in autosomal-dominant polycystic kidney disease. Publindex is a Colombian bibliographic index for classifying, updating, rating rejal certifying scientific and technological publications.
Autosomal recessive polycystic kidney disease. Tolvaptan in patients with autosomal dominant polycystic kidney disease. Systematic literature review conducted in the PubMed, Lilacs, UptoDate and Medline databases with the following terms: It covers around 19, titles by more than 5, international editors, including poliuistica of about 16, journals. Iodine seeds in prostatic transurethral resection IBN Publindex Publindex is a Colombian bibliographic index for classifying, updating, rating and certifying scientific and technological publications.
Relationship between renal volume growth and renal function in autosomal dominant polycystic kidney disease: The pregnancy had not been monitored, although a previous ultrasonography revealed foetal kidney enlargement. Human Genet, 68pp. Long-term studies on congenital hepatic fibrosis in children. Acta Pediatr, 84pp. Subscriber If you already have your login data, please click here.
Adult renal cystic disease: Si continua navegando, consideramos que acepta su uso.
It is currently being managed in Colombia by the Universidad Nacional autsoomica Colombia. Pregnancy in a patient tecesiva autosomal- dominant polycystic kidney disease and congenital hepatic fibrosis.
Rowe I, Boletta A. Med Ther, 1pp. Improvement of endothelial dysfunction with simvastatin in patients with autosomal dominant polycystic kidney disease. Autosomal dominant polycystic kidney disease in children. Combined cystic disease of the liver and kidney. Defective metabolism in polycystic kidney disease: You can change the settings or obtain more information by clicking here.
Diverticulitis and polycystic kidney disease. Caroli’s diseaseversus polycystic hepatic disease.
File:Enfermedad poliquística renal autosómica recesiva.jpg
Autosomal dominant polycystic kidney disease: Discussion The clinical and pathological findings are correlated and the most important necropsy findings are described. Hypertension auutosomica autosomal dominant polycystic kidney disease.
Effect of pravastatin on kidney function and urinary protein excretion in autosomal dominant polycystic kidney disease.
To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. J Med Genet, 8pp.
The clinical and pathological findings are correlated and the most important necropsy findings are described. From Wikimedia Commons, the free media repository. Mayo Clin Proc, 73pp. Course and treatment of autosomal dominant polycystic kidney disease. Human Genet, 68pp.
Current management of autosomal dominant polycystic kidney disease.