Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Tale N. Wien"'
Autor:
Dorota Rowczenio, Maria Stensland, Gustavo A. de Souza, Erik H. Strøm, Janet A. Gilbertson, Graham Taylor, Nigel Rendell, Shane Minogue, Yvonne A. Efebera, Helen J. Lachmann, Ashutosh D. Wechalekar, Philip N. Hawkins, Ketil R. Heimdal, Kristian Selvig, Inger K. Lægreid, Nathalie Demoulin, Selda Aydin, Julian D. Gillmore, Tale N. Wien
Publikováno v:
Kidney International Reports, Vol 2, Iss 3, Pp 461-469 (2017)
Fibrinogen A alpha chain amyloidosis is an autosomal dominant disease associated with mutations in the fibrinogen A alpha chain (FGA) gene, and it is the most common cause of hereditary renal amyloidosis in the UK. Patients typically present with kid
Externí odkaz:
https://doaj.org/article/eafc8316f25e41acb96af87f66ab9d68
Autor:
Wien, Tale N.1 t.n.wien@klinmed.uio.no, Sørby, Randi2, Espenes, Arild2, Gunnes, Gjermund2, Nordstoga, Knut2, Landsverk, Thor2, Husby, Gunnar1
Publikováno v:
Amyloid. Dec2003, Vol. 10 Issue 4, p240-249. 10p.
Publikováno v:
Clinical Physiology & Functional Imaging; May2016, Vol. 36 Issue 3, p237-241, 5p, 2 Black and White Photographs, 4 Charts
This authoritative volume contains 179 chapters by international experts on recent developments in our understanding of amyloid proteins, protein folding disorders, and new and proposed clinical trials in amyloidosis. Topics include detection and cha
