Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Richard S G Knight"'
Autor:
Pascual Sanchez-Juan, Matthew T Bishop, Gabor G Kovacs, Miguel Calero, Yurii S Aulchenko, Anna Ladogana, Alison Boyd, Victoria Lewis, Claudia Ponto, Olga Calero, Anna Poleggi, Ángel Carracedo, Sven J van der Lee, Thomas Ströbel, Fernando Rivadeneira, Albert Hofman, Stéphane Haïk, Onofre Combarros, José Berciano, Andre G Uitterlinden, Steven J Collins, Herbert Budka, Jean-Philippe Brandel, Jean Louis Laplanche, Maurizio Pocchiari, Inga Zerr, Richard S G Knight, Robert G Will, Cornelia M van Duijn
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0123654 (2014)
We performed a genome-wide association (GWA) study in 434 sporadic Creutzfeldt-Jakob disease (sCJD) patients and 1939 controls from the United Kingdom, Germany and The Netherlands. The findings were replicated in an independent sample of 1109 sCJD an
Externí odkaz:
https://doaj.org/article/cce2b1a8c1a44c87b1539cdd95ccb3a7
Publikováno v:
Transfusion. 51(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fe1386b65efc1235f9e7a54d010c4af8
https://pubmed.ncbi.nlm.nih.gov/21214582
https://pubmed.ncbi.nlm.nih.gov/21214582
Autor:
Gábor G, Kovács, Gianriccardo, Trabattoni, Johannes A, Hainfellner, James W, Ironside, Richard S G, Knight, Herbert, Budka
Publikováno v:
Journal of neurology. 249(11)
Prion diseases are inherited in 5-15 % of cases. They are classified according to changes in the prion protein gene ( PRNP) or conventionally according to phenotype as Gerstmann-Sträussler-Scheinker disease (GSS), fatal familial insomnia (FFI), or f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f37eaead98cb9efcbd4e2688324f28d4
https://pubmed.ncbi.nlm.nih.gov/12420099
https://pubmed.ncbi.nlm.nih.gov/12420099
Publikováno v:
Electrophoresis. 23(14)
The ability to perform an ante mortem differential diagnosis of Creutzfeld-Jakob disease (CJD) is aided by several clinical and molecular tests. There is a need for molecular tests which can reliably distinguish ante mortem variant CJD (vCJD) from an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ef66beac683d69e2110051119f24c3ca
https://pubmed.ncbi.nlm.nih.gov/12210228
https://pubmed.ncbi.nlm.nih.gov/12210228
Autor:
Craig A. Heath, Sarah A. Cooper, Katy Murray, Andrea Lowman, Colm Henry, Margaret A. MacLeod, Gillian E. Stewart, Martin Zeidler, Jan M. MacKenzie, James W. Ironside, David M. Summers, Richard S. G. Knight, Robert G. Will
Publikováno v:
Annals of Neurology. 69:212-213
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0da9aa37f64c6b89356f772677a3a7d2
https://doi.org/10.1002/ana.22287
https://doi.org/10.1002/ana.22287
Autor:
Hester J. T. Ward, Dawn Everington, Simon N. Cousens, Blaire Smith‐Bathgate, Margaret Leitch, Sarah Cooper, Craig Heath, Richard S. G. Knight, Peter G. Smith, Robert G. Will
Publikováno v:
Annals of Neurology; Jan2006, Vol. 59 Issue 1, p111-120, 0p