Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a First National Institutes of Health/Office of Rare Diseases conference

Autor:	Patricia D. Wilson, Joseph T. Flynn, Julie R. Ingelfinger, Peter C. Harris, Theo Heller, Gregory G. Germino, Vicente E. Torres, Benjamin L. Shneider, Nicholas F. LaRusso, Colleen Zak, Jing Zhou, Robert Kleta, Peter L. Choyke, Robert Bacallao, Ellis D. Avner, Lisa M. Guay-Woodford, Parvathi Mohan, William A. Gahl, Frederick Kaskel, Gregory J. Pazour, Meral Gunay-Aygun
Rok vydání:	2006
Předmět:	Pathology medicine.medical_specialty Pediatrics biology business.industry education Fibrocystin Autosomal dominant polycystic kidney disease Phosphoric Diester Hydrolases urologic and male genital diseases medicine.disease Article female genital diseases and pregnancy complications humanities Autosomal Recessive Polycystic Kidney Disease Pediatrics Perinatology and Child Health Polycystic kidney disease medicine biology.protein Congenital hepatic fibrosis business health care economics and organizations Rare disease Kidney disease
Zdroj:	The Journal of Pediatrics. 149:159-164
ISSN:	0022-3476
DOI:	10.1016/j.jpeds.2006.03.014
Popis:	Researchers and clinicians with expertise in autosomal recessive polycystic kidney disease and congenital hepatic fibrosis (ARPKD/CHF) and related fields met on May 5-6, 2005, on the National Institutes of Health (NIH) campus for a 1.5-day symposium sponsored by the NIH Office of Rare Diseases, the National Human Genome Research Institute (NHGRI), and in part by the ARPKD/CHF Alliance. The meeting addressed the present status and the future of ARPKD/CHF research.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa76fbd2326c59042a8cf20b6806583f https://doi.org/10.1016/j.jpeds.2006.03.014 Zobrazit plný text záznamu Full Text from ScienceDirect