Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Cristina Delco"'
Autor:
Sarah Belin, Cristina Delco, Paloma Parvex, Sylviane Hanquinet, Siv Fokstuen, Begoña Martinez de Tejada, Isabelle Eperon
Publikováno v:
Journal of Medical Case Reports, Vol 13, Iss 1, Pp 1-5 (2019)
Abstract Background Autosomal recessive renal polycystic kidney disease occurs in 1 in 20,000 live births. It is caused by mutations in both alleles of the PKHD1 gene. Management of delivery in cases of suspected autosomal recessive renal polycystic
Externí odkaz:
https://doaj.org/article/d7a6a01b0eca4814b7f3f85510f4ed97
Autor:
Belin, Sarah1 (AUTHOR), Delco, Cristina1 (AUTHOR), Parvex, Paloma1 (AUTHOR), Hanquinet, Sylviane2 (AUTHOR), Fokstuen, Siv3 (AUTHOR), Martinez de Tejada, Begoña1,4 (AUTHOR) begona.martinezdetejada@hcuge.ch, Eperon, Isabelle1 (AUTHOR)
Publikováno v:
Journal of Medical Case Reports. 12/12/2019, Vol. 13 Issue 1, p1-5. 5p.
Autor:
Keitel, Kristina1, Wagner, Noémie1, Lacroix, Laurence1, Manzano, Sergio1, Gervaix, Alain1,2 alain.gervaix@hcuge.ch, Wagner, Noémie (AUTHOR)
Publikováno v:
European Journal of Pediatrics. Apr2011, Vol. 170 Issue 4, p511-517. 7p. 4 Charts, 1 Graph.
Publikováno v:
Pharmacogenomics; Oct2011, Vol. 12 Issue 10, p1493-1501, 9p