Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Autosomal Dominant/complications"'
Autor:
Niek F. Casteleijn, Paul Geertsema, Iris W. Koorevaar, Friso D.J. Inkelaar, Marnix R. Jansen, Steven J. Lohuis, Esther Meijer, Robert A. Pol, Jan-Stephan Sanders, Peter E. van de Streek, Anna M. Leliveld, Ron T. Gansevoort
Publikováno v:
Urologia internationalis, 107(2). KARGER
Introduction: There is no consensus if nor when a native nephrectomy should be performed in the workup for kidney transplantation in ADPKD patients. In our PKD Expertise Center, a restrictive approach is pursued in which nephrectomy is performed only
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad2c9097c906e27854edef2a3d35971b
https://research.rug.nl/en/publications/7d72ba50-220e-4af1-a66d-048642c2549d
https://research.rug.nl/en/publications/7d72ba50-220e-4af1-a66d-048642c2549d
Publikováno v:
BMJ Case Rep
BMJ Case Reports
BMJ Case Reports, BMJ Publishing Group, 2020, 13 (1), pp.e231334. ⟨10.1136/bcr-2019-231334⟩
BMJ Case Reports
BMJ Case Reports, BMJ Publishing Group, 2020, 13 (1), pp.e231334. ⟨10.1136/bcr-2019-231334⟩
A 76-year-old renal transplant patient due to autosomal dominant polycystic kidney disease who resumed chronic haemodialysis was admitted to our hospital for confusion and lassitude. He was afebrile and physical examination revealed diffuse bilateral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2972168bbd1f00ad82a7475928be5a1
https://europepmc.org/articles/PMC7021179/
https://europepmc.org/articles/PMC7021179/
Autor:
Pieter Evenepoel, Jean De Schepper, Maria Van Dyck, Pieter Vermeersch, Elena Levtchenko, Djalila Mekahli, Stéphanie De Rechter, Patrick C. D'Haese, Justine Bacchetta, Julie Maquet, Laurence Dubourg, Nathalie Godefroid, Pierre Cochat, Ann Raes
Publikováno v:
The journal of clinical endocrinology and metabolism
Ghent University Academic Bibliography
Ghent University Academic Bibliography
Context: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease. Hypophosphatemia was demonstrated in adult patients with preserved renal function, together with high fibroblast growth factor 23 (FGF23) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3ec2d1db8fac6995275ae2bb13f450f
https://hdl.handle.net/20.500.14017/a490d388-72ae-4fce-9085-fc61244d0482
https://hdl.handle.net/20.500.14017/a490d388-72ae-4fce-9085-fc61244d0482
Autor:
Marina Grbić, Lada Zibar
Publikováno v:
Medicinski vjesnik
Volume 44
Issue (1-4)
Volume 44
Issue (1-4)
Cilj istraživanja bio je ispitati pojavljuje li se završni stupanj kronične bubrežne bolesti (KBB) u oboljelih od autosomne dominantne policistične bubrežne bolesti (ADPBB) ranije u bolesnika rođenih u drugoj polovici 20. stoljeća u odnosu na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______951::962a5f9f8dd899d054ec32fe49cfa837
https://hrcak.srce.hr/186331
https://hrcak.srce.hr/186331
Publikováno v:
Università degli studi di Modena e Reggio Emilia-IRIS
Cerebral aneurysm in autosomal dominant polycystic kidney disease (ADPKD) is an uncommon event (documented in 6-13% of cases) but frequently characterized by severe neurological sequelae and potentially fatal in case of rupture. The arterial vascular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e037dad11f77dabaa02b7399ab15f982
http://www.ncbi.nlm.nih.gov/pubmed/22167609
http://www.ncbi.nlm.nih.gov/pubmed/22167609
Publikováno v:
Pediatric Nephrology. 26:643-644
Pediatr Nephrol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95f01c07ea832834ad672b0c1cf99e23
https://doi.org/10.1007/s00467-010-1710-z
https://doi.org/10.1007/s00467-010-1710-z