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.
|Published (Last):||6 April 2008|
|PDF File Size:||19.90 Mb|
|ePub File Size:||13.7 Mb|
|Price:||Free* [*Free Regsitration Required]|
Srivastava A, Patel N. An Esp Pediatr, 28pp. This item has received. Caroli’s diseaseversus polycystic hepatic disease. Polycystic disease of kidney presenting reenal childhood. Ludwig symposium on biliary disorders – part I.
There was a problem providing the content you requested
Defective metabolism in polycystic kidney disease: You can change the settings or obtain more information by clicking here. Human Genet, 68pp. Autosomal dominant polycystic kidney disease in children.
We report the autopsy autosomicaa in a 2 h old, term female infant with severe oligohydramnios. Principios de Medicina Interna. Gross pathology of polycystic kidney disease.
De la Rubia, M. Pathogenesis of ductal plate abnormalities. This file contains additional information such as Poliauistica metadata which may have been added by the digital camera, scanner, or software program used to create or digitize it.
ENFERMEDAD RENAL POLIQUISTICA Y OTROS TRASTORNOS HEREDITARIO by on Prezi
International Society of Nefrology. Search and view critically important regional content with international impact to get a comprehensive picture of the influencers and drivers of regional research. Tolvaptan in autosomal dominant polycystic kidney disease: SRJ is a prestige metric based on the idea that not all citations are the same.
CiteScore measures average citations received per document published. The following other wikis use this file: Mayo Clin Proc, 73pp. Previous article Next article. Scopus is a bibliographic database publishing summaries and references concerning articles from scientific journals. Pregnancy in autosomal recessive polycystic kidney disease. Relationship between renal volume growth and renal function in autosomal dominant polycystic kidney disease: Microscopically a diagnosis of autosomal recessive polycystic kidney disease with biliary dysgenesis was made.
Acta Pathol Microbiol Scand,pp. Noninvasive diagnosis of Caroli Syndrome associated with congenital hepatic fibrosis using hepatobiliary scintigraphy. You can change the settings or obtain more information by clicking here. Si continua navegando, consideramos que acepta su uso.
Directory of Open Access Journals DOAJ increases the visibility and ease of use of open access scientific and scholarly journals, aims to be comprehensive and cover all that journals that use a quality control system to guarantee the content.
The pregnancy had not been monitored, although a previous ultrasonography revealed foetal kidney enlargement. Clin Nucl Med, 18pp. Volume Progression in Polycystic Kidney Disease.
Actualización en enfermedad renal poliquística | Montaña | Revista de la Facultad de Medicina
Autosomal poliquiwtica polycystic kidney disease: Combined cystic disease of the liver and kidney. Show more Show less. Imaging classification of autosomal dominant polycystic kidney disease: Microscopically a diagnosis of autosomal recessive polycystic kidney disease with biliary dysgenesis was made. Semin Liv Dis, 14pp. Continuing navigation will be considered as acceptance of this use.