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F Cathala

Showing results (81-90 of 85) with videos related to

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Journal of the Neurological Sciences|October 11, 1991
The molecular genetics of familial Creutzfeldt-Jakob disease in FranceP Brown, L G Goldfarb, F Cathala, et al.
Annals of Neurology|March 11, 1992
Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutationP Brown, L G Goldfarb, J Kovanen, et al.
Journal of the Neurological Sciences|September 11, 1992
An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker familyL G Goldfarb, P Brown, A Vrbovská, et al.
Annals of Neurology|March 1, 1992
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European originL G Goldfarb, P Brown, M Haltia, et al.
Revue Neurologique|January 1, 1981
[Creutzfeldt-Jakob disease in the squirrel monkeys]F Cathala, L Court, P Breton, et al.
Pageof 9

Showing results (81-90 of 85) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 85 results.
Journal of the Neurological Sciences|October 11, 1991
The molecular genetics of familial Creutzfeldt-Jakob disease in FranceP Brown, L G Goldfarb, F Cathala, et al.
Annals of Neurology|March 11, 1992
Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutationP Brown, L G Goldfarb, J Kovanen, et al.
Journal of the Neurological Sciences|September 11, 1992
An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker familyL G Goldfarb, P Brown, A Vrbovská, et al.
Annals of Neurology|March 1, 1992
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European originL G Goldfarb, P Brown, M Haltia, et al.
Revue Neurologique|January 1, 1981
[Creutzfeldt-Jakob disease in the squirrel monkeys]F Cathala, L Court, P Breton, et al.
Pageof 9