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L G Goldfarb

Showing results (21-30 of 91) with videos related to

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Annals of the New York Academy of Sciences|January 1, 1991
A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian originA D Korczyn, J Chapman, L G Goldfarb, et al.
Neurology|October 24, 2007
T cell receptor profiling in muscle and blood lymphocytes in sporadic inclusion body myositisM Salajegheh, G Rakocevic, R Raju, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1993
Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrilsL G Goldfarb, P Brown, M Haltia, et al.
Lancet (London, England)|October 14, 1995
Familial Alzheimer's disease associated with S182 codon 286 mutationJ Chapman, A Asherov, N Wang, et al.
Lancet (London, England)|July 9, 1994
Identification of a PRNP gene mutation in Jakob's original Creutzfeldt-Jakob disease familyP Brown, L Cervenáková, J W Boellaard, et al.
Neurology|November 1, 1989
Olivopontocerebellar atrophy in a large Iakut kinship in eastern SiberiaL G Goldfarb, M P Chumakov, P A Petrov, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob diseaseL Cervenáková, L G Goldfarb, R Garruto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1993
Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutationJ Chapman, P Brown, L G Goldfarb, et al.
Neurology|August 23, 2000
Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical studyC M Bütefisch, P Gambetti, L Cervenakova, et al.
Genomics|February 1, 1991
Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pterM C Speer, D Goldgaber, L G Goldfarb, et al.
Pageof 10

Showing results (21-30 of 91) with videos related to

Sort By:
Pageof 10
Annals of the New York Academy of Sciences|January 1, 1991
A mutation in the prion protein gene in Creutzfeldt-Jakob disease in Jewish patients of Libyan, Greek, and Tunisian originA D Korczyn, J Chapman, L G Goldfarb, et al.
Neurology|October 24, 2007
T cell receptor profiling in muscle and blood lymphocytes in sporadic inclusion body myositisM Salajegheh, G Rakocevic, R Raju, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1993
Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrilsL G Goldfarb, P Brown, M Haltia, et al.
Lancet (London, England)|October 14, 1995
Familial Alzheimer's disease associated with S182 codon 286 mutationJ Chapman, A Asherov, N Wang, et al.
Lancet (London, England)|July 9, 1994
Identification of a PRNP gene mutation in Jakob's original Creutzfeldt-Jakob disease familyP Brown, L Cervenáková, J W Boellaard, et al.
Neurology|November 1, 1989
Olivopontocerebellar atrophy in a large Iakut kinship in eastern SiberiaL G Goldfarb, M P Chumakov, P A Petrov, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob diseaseL Cervenáková, L G Goldfarb, R Garruto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1993
Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutationJ Chapman, P Brown, L G Goldfarb, et al.
Neurology|August 23, 2000
Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical studyC M Bütefisch, P Gambetti, L Cervenakova, et al.
Genomics|February 1, 1991
Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pterM C Speer, D Goldgaber, L G Goldfarb, et al.
Pageof 10