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L G Goldfarb

Showing results (11-20 of 91) with videos related to

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Annals of the New York Academy of Sciences|June 6, 1994
Familial Creutzfeldt-Jakob diseaseD 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 diseaseP 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 phenotypeC Majtényi, P Brown, L Cervenáková, et al.
Brain : a Journal of Neurology|January 16, 2004
Desmin myopathyL 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 studiesM Haltia, J Kovanen, L G Goldfarb, et al.
Annals of Neurology|April 20, 2001
Gluten sensitivity in sporadic and hereditary cerebellar ataxiaK 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 originL 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 SlovakiaL G Goldfarb, E Mitrová, P Brown, et al.
JAMA|November 4, 1992
Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsyJ M Bertoni, P Brown, L G Goldfarb, et al.
Pageof 10

Showing results (11-20 of 91) with videos related to

Sort By:
Pageof 10
Annals of the New York Academy of Sciences|June 6, 1994
Familial Creutzfeldt-Jakob diseaseD 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 diseaseP 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 phenotypeC Majtényi, P Brown, L Cervenáková, et al.
Brain : a Journal of Neurology|January 16, 2004
Desmin myopathyL 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 studiesM Haltia, J Kovanen, L G Goldfarb, et al.
Annals of Neurology|April 20, 2001
Gluten sensitivity in sporadic and hereditary cerebellar ataxiaK 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 originL 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 SlovakiaL G Goldfarb, E Mitrová, P Brown, et al.
JAMA|November 4, 1992
Familial Creutzfeldt-Jakob disease (codon 200 mutation) with supranuclear palsyJ M Bertoni, P Brown, L G Goldfarb, et al.
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