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Annals of the New York Academy of Sciences
|
June 6, 1994
Familial Creutzfeldt-Jakob disease
D L Camenga, L G Goldfarb, D Bierke-Nelson, et al.
European Journal of Epidemiology
|
September 11, 1991
The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease
P Brown, L G Goldfarb, C J Gibbs, et al.
Neurology
|
June 14, 2000
A three-sister sibship of Gerstmann-Sträussler-Scheinker disease with a CJD phenotype
C Majtényi, P Brown, L Cervenáková, et al.
Brain : a Journal of Neurology
|
January 16, 2004
Desmin myopathy
L G Goldfarb, P Vicart, H H Goebel, et al.
Annals of Neurology
|
July 1, 1996
Is hereditary inclusion body myopathy a "familial prion disease" ?
L Cervernáková, K Sivakumar, J Nagle, et al.
European Journal of Epidemiology
|
September 1, 1991
Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies
M Haltia, J Kovanen, L G Goldfarb, et al.
Annals of Neurology
|
April 20, 2001
Gluten sensitivity in sporadic and hereditary cerebellar ataxia
K O Bushara, S U Goebel, H Shill, et al.
Lancet (London, England)
|
September 8, 1990
Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin
L G Goldfarb, A D Korczyn, P Brown, et al.
Lancet (London, England)
|
August 25, 1990
Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia
L G Goldfarb, E Mitrová, P Brown, et al.
JAMA
|
November 4, 1992
Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy
J M Bertoni, P Brown, L G Goldfarb, et al.
Page
of 10
Search research articles
Search
Showing results (11-20 of 91) with videos related to
Sort By:
Page
of 10
Annals of the New York Academy of Sciences
|
June 6, 1994
Familial Creutzfeldt-Jakob disease
D L Camenga, L G Goldfarb, D Bierke-Nelson, et al.
European Journal of Epidemiology
|
September 11, 1991
The phenotypic expression of different mutations in transmissible familial Creutzfeldt-Jakob disease
P Brown, L G Goldfarb, C J Gibbs, et al.
Neurology
|
June 14, 2000
A three-sister sibship of Gerstmann-Sträussler-Scheinker disease with a CJD phenotype
C Majtényi, P Brown, L Cervenáková, et al.
Brain : a Journal of Neurology
|
January 16, 2004
Desmin myopathy
L G Goldfarb, P Vicart, H H Goebel, et al.
Annals of Neurology
|
July 1, 1996
Is hereditary inclusion body myopathy a "familial prion disease" ?
L Cervernáková, K Sivakumar, J Nagle, et al.
European Journal of Epidemiology
|
September 1, 1991
Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studies
M Haltia, J Kovanen, L G Goldfarb, et al.
Annals of Neurology
|
April 20, 2001
Gluten sensitivity in sporadic and hereditary cerebellar ataxia
K O Bushara, S U Goebel, H Shill, et al.
Lancet (London, England)
|
September 8, 1990
Mutation in codon 200 of scrapie amyloid precursor gene linked to Creutzfeldt-Jakob disease in Sephardic Jews of Libyan and non-Libyan origin
L G Goldfarb, A D Korczyn, P Brown, et al.
Lancet (London, England)
|
August 25, 1990
Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia
L G Goldfarb, E Mitrová, P Brown, et al.
JAMA
|
November 4, 1992
Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsy
J M Bertoni, P Brown, L G Goldfarb, et al.
Page
of 10