Autoren-Indexdatei meiner TSE-Literatur-Datenbank

File of the authors index for my TSE-Literature-Collection

Mead,S.

AOQF - Beck,J.A.; Poulter,M.; Campbell,T.A.; Uphill,J.B.; Adamson,G.; Mead,S.; Collinge,J. - PRNP haplotype analysis in PNG populations - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - DG-64

ABDR - Beck,J.A.; Mead,S.; Campbell,T.A.; Dickinson,A.; Wientjens,D.P.W.M.; Croes,E.A.; van Duijn,C.M.; Collinge,J. - Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia - Neurology 2001 Jul 24; 57(2): 354-6

AUTQ - Collinge,J.; Whitfield,J.; McKintosh,E.; Beck,J.; Mead,S.; Thomas,D.J.; Alpers,M.P. - Kuru in the 21st century - an acquired human prion disease with very long incubation periods - Lancet 2006 Jun 24; 367(9528): 2068-74

ANRF - King,A.; Doey,L.; Rossor,M.; Mead,S.; Collinge,J.; Lantos,P. - Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene - Neuropathology and Applied Neurobiology 2003 Apr; 29(2): 98-105

AXSP - Mead,S.; Webb,T.E.F.; Collinge,J. - Age of Onset and Death in Inherited Prion Diseases are Highly Heritable - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Pathology and Pathogenesis P03.27

AXSQ - Mead,S.; Beck,J.; Adamson,G.; Campbell,T.; Uphill,J.; Bostantjopoulou,S.; Bazak,N.; Collinge,J. - A PRNP Missense Allele Series in Patients and Healthy Populations - International Conference - Prion 2007 (26.-28.9.2007) Edinburgh International Conference Centre, Edinburgh, Scotland, UK - Book of Abstracts: Pathology and Pathogenesis P03.30

AYCL - Mead,S.; Webb,T.E.F.; Campbell,T.A.; Beck,J.; Linehan,J.M.; Rutherfoord,S.; Joiner,S.; Wadsworth,J.D.F.; Heckmann,J.; Wroe,S.; Doey,L.; King,A.; Collinge,J. - Inherited prion disease with 5-OPRI: phenotype modification by repeat length and codon 129. - Neurology 2007 Aug 21; 69(8): 730-8

AVGE - Mead,S.; Poulter,M.; Beck,J.; Webb,T.E.F.; Campbell,T.A.; Linehan,J.M.; Desbruslais,M.; Joiner,S.; Wadsworth,J.D.F.; King,A.; Lantos,P.; Collinge,J. - Inherited prion disease with six octapeptide repeat insertional mutation - molecular analysis of phenotypic heterogeneity - Brain: A Journal of Neurology 2006 Sep; 129(9): 2297-317

AUIR - Mead,S. - Prion disease genetics - European Journal of Human Genetics 2006 Mar; 14(3): 273-81

AUCX - Mead,S.; Prout,K.; Collinge,J. - Questionnaire to reduce the risk of iatrogenic prion disease transmission - The Journal of Hospital Infection 2005 Aug; 60(4): 378-9

ANUX - Mead,S.; Stumpf,M.P.; Whitfield,J.; Beck,J.A.; Poulter,M.; Campbell,T.A.; Uphill,J.B.; Goldstein,D.; Alpers,M.P.; Fisher,E.M.C.; Collinge,J. - Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics - Science 2003 Apr 25; 300(5619): 640-3

AIFY - Mead,S.; Mahal,S.P.; Beck,J.A.; Campbell,T.A.; Farrall,M.; Fisher,E.; Collinge,J. - Sporadic - but not variant - Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1 - American Journal of Human Genetics 2001 Dec; 69(6): 1225-35

AIFZ - Mead,S.; Beck,J.A.; Dickinson,A.; Fisher,E.M.C.; Collinge,J. - Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease - Neuroscience Letters 2000 Aug 25; 290(2): 117-20

AOXZ - Poulter,M.; Beck,J.A.; Campbell,T.A.; Uphill,J.B.; Adamson,G.; Mead,S.; Collinge,J. - Small Pool PCR to test for somatic octapeptide repeat variation in sporadic CJD patients - International Conference - Prion diseases: from basic research to intervention concepts - TSE-Forum, 08.10.-10.10.2003, Gasteig, München - Poster session - DG-65

AVRL - Rohrer,J.D.; Mead,S.; Omar,R.; Poulter,M.; Warren,J.D.; Collinge,J.; Rossor,M.N. - Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes - Annals of Neurology 2006 Nov; 60(5): 616; author reply 617

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