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L G Goldfarb

Showing results (31-40 of 91) with videos related to

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The American Journal of Tropical Medicine and Hygiene|March 1, 1980
An epidemiological model of Crimean hemorrhagic feverL G Goldfarb, M P Chumakov, A A Myskin, et al.
Lancet (London, England)|January 16, 1993
Real and imagined clinicopathological limits of "prion dementia"P Brown, P Kaur, M P Sulima, et al.
The New England Journal of Medicine|March 16, 2000
Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin geneM C Dalakas, K Y Park, C Semino-Mora, et al.
Clinical Genetics|November 4, 2004
Small de novo duplication in the repeat region of the TATA-box-binding protein gene manifest with a phenotype similar to variant Creutzfeldt-Jakob diseaseA Shatunov, E A Fridman, F I Pagan, et al.
Journal of the Neurological Sciences|October 11, 1992
Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20P Brown, S Gálvez, L G Goldfarb, et al.
Annals of Neurology|May 13, 1999
Novel exon 3B proteolipid protein gene mutation causing late-onset spastic paraplegia type 2 with variable penetrance in female family membersK Sivakumar, N Sambuughin, B Selenge, et al.
Lancet (London, England)|July 21, 1990
Identical mutation in unrelated patients with Creutzfeldt-Jakob diseaseL G Goldfarb, P Brown, D Goldgaber, et al.
Neurology|November 1, 1993
A new (two-repeat) octapeptide coding insert mutation in Creutzfeldt-Jakob diseaseL G Goldfarb, P Brown, B W Little, et al.
Lancet (London, England)|March 9, 1991
Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease familiesA Nieto, L G Goldfarb, P Brown, et al.
The Journal of Infectious Diseases|December 20, 2000
Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotypeH S Lee, P Brown, L Cervenáková, et al.
Pageof 10

Showing results (31-40 of 91) with videos related to

Sort By:
Pageof 10
The American Journal of Tropical Medicine and Hygiene|March 1, 1980
An epidemiological model of Crimean hemorrhagic feverL G Goldfarb, M P Chumakov, A A Myskin, et al.
Lancet (London, England)|January 16, 1993
Real and imagined clinicopathological limits of "prion dementia"P Brown, P Kaur, M P Sulima, et al.
The New England Journal of Medicine|March 16, 2000
Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin geneM C Dalakas, K Y Park, C Semino-Mora, et al.
Clinical Genetics|November 4, 2004
Small de novo duplication in the repeat region of the TATA-box-binding protein gene manifest with a phenotype similar to variant Creutzfeldt-Jakob diseaseA Shatunov, E A Fridman, F I Pagan, et al.
Journal of the Neurological Sciences|October 11, 1992
Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20P Brown, S Gálvez, L G Goldfarb, et al.
Annals of Neurology|May 13, 1999
Novel exon 3B proteolipid protein gene mutation causing late-onset spastic paraplegia type 2 with variable penetrance in female family membersK Sivakumar, N Sambuughin, B Selenge, et al.
Lancet (London, England)|July 21, 1990
Identical mutation in unrelated patients with Creutzfeldt-Jakob diseaseL G Goldfarb, P Brown, D Goldgaber, et al.
Neurology|November 1, 1993
A new (two-repeat) octapeptide coding insert mutation in Creutzfeldt-Jakob diseaseL G Goldfarb, P Brown, B W Little, et al.
Lancet (London, England)|March 9, 1991
Codon 178 mutation in ethnically diverse Creutzfeldt-Jakob disease familiesA Nieto, L G Goldfarb, P Brown, et al.
The Journal of Infectious Diseases|December 20, 2000
Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotypeH S Lee, P Brown, L Cervenáková, et al.
Pageof 10