Zobrazeno 1 - 10
of 52
pro vyhledávání: '"David, Auguste"'
Autor:
David, Auguste.
Th. licence--Droit--Lyon, 1879-08-01.
Externí odkaz:
http://catalogue.bnf.fr/ark:/12148/cb36842995w
Autor:
David, Auguste-Henri.
Th. licence--Droit--Paris, 1857.
Mention parallèle de titre ou de responsabilité : [Droit français : des donations entre vifs et des testaments].
Mention parallèle de titre ou de responsabilité : [Droit français : des donations entre vifs et des testaments].
Externí odkaz:
http://catalogue.bnf.fr/ark:/12148/cb36836340q
Autor:
Sonia Jean, Fabrice Mac-Way, Lynne Moore, David Auguste, Louis-Charles Desbiens, Aboubacar Sidibé, C. Fortier, Yue Pei Wang
Publikováno v:
JBMR Plus. 3:45-55
Chronic kidney disease is associated with an increased risk of fracture and cardiovascular mortality. The risk of fracture in hemodialysis (HD), peritoneal dialysis (PD) and kidney transplant (KT) patients is higher when compared with the general pop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab8f4576fce6041bd9a1738991f76aaa
https://doi.org/10.1002/jbm4.10067
https://doi.org/10.1002/jbm4.10067
Autor:
Aboubacar, Sidibé, David, Auguste, Louis-Charles, Desbiens, Catherine, Fortier, Yue Pei, Wang, Sonia, Jean, Lynne, Moore, Fabrice, Mac-Way
Publikováno v:
JBMR Plus
Chronic kidney disease is associated with an increased risk of fracture and cardiovascular mortality. The risk of fracture in hemodialysis (HD), peritoneal dialysis (PD) and kidney transplant (KT) patients is higher when compared with the general pop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::719155682da9f24c34c95bec99964bbb
https://pubmed.ncbi.nlm.nih.gov/30680363
https://pubmed.ncbi.nlm.nih.gov/30680363
Autor:
Tomoko Takano, Mirela Maier, Indra R. Gupta, David Auguste, Cindy Baldwin, Richard Robins, Lamine Aoudjit
Publikováno v:
Small GTPases. 7(2)
Nephrotic syndrome (NS) describes a group of kidney disorders in which there is injury to podocyte cells, specialized cells within the kidney's glomerular filtration barrier, allowing proteins to leak into the urine. Three mutations in ARHGDIA, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71e93ab107bc4e5cb7704d642a37f6f0
https://pubmed.ncbi.nlm.nih.gov/26726844
https://pubmed.ncbi.nlm.nih.gov/26726844
Autor:
Martin Bitzan, Somayyeh Fahiminiya, Jasmine El Andalousi, Chantal Bernard, Cindy Baldwin, Tomoko Takano, Steven A. Narod, David Auguste, David S. Rosenblatt, Indra R. Gupta, Jacek Majewski, Kevin C.H. Ha, Mohammad R. Akbari
Publikováno v:
Journal of Medical Genetics
Background Congenital nephrotic syndrome arises from a defect in the glomerular filtration barrier that permits the unrestricted passage of protein across the barrier, resulting in proteinuria, hypoalbuminaemia, and severe oedema. While most cases ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::357fb462c16f2f85a6e4c5260abe2559
https://pubmed.ncbi.nlm.nih.gov/23434736
https://pubmed.ncbi.nlm.nih.gov/23434736