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L G Goldfarb

Showing results (71-80 of 91) with videos related to

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Neurology|February 1, 1994
Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicineP Brown, L Cervenáková, L G Goldfarb, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 11, 1991
Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP geneL G Goldfarb, P Brown, W R McCombie, et al.
Neurology|June 1, 1995
Clinical and genetic studies of fatal familial insomniaA T Reder, A S Mednick, P Brown, et al.
Annals of Neurology|January 1, 1988
Seroprevalence of antibodies to HTLV-I in patients with chronic neurological disorders other than tropical spastic paraparesisC A Mora, R M Garruto, P Brown, et al.
Brain Research. Brain Research Reviews|January 11, 1991
Regulation and genetic control of brain amyloid. FESN Study GroupD C Gajdusek, K Beyreuther, P Brown, et al.
Neurology|February 11, 1992
Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor geneP Brown, L G Goldfarb, W R McCombie, et al.
Experimental Neurology|June 1, 1990
Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndromeL G Goldfarb, P Brown, D Goldgaber, et al.
Neurology|March 1, 1991
Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndromeP Brown, L G Goldfarb, W T Brown, et al.
Experimental Neurology|November 1, 1989
Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndromeD Goldgaber, L G Goldfarb, P Brown, et al.
Nature Genetics|August 11, 1998
Missense mutations in desmin associated with familial cardiac and skeletal myopathyL G Goldfarb, K Y Park, L Cervenáková, et al.
Pageof 10

Showing results (71-80 of 91) with videos related to

Sort By:
Pageof 10
Neurology|February 1, 1994
Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicineP Brown, L Cervenáková, L G Goldfarb, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 11, 1991
Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP geneL G Goldfarb, P Brown, W R McCombie, et al.
Neurology|June 1, 1995
Clinical and genetic studies of fatal familial insomniaA T Reder, A S Mednick, P Brown, et al.
Annals of Neurology|January 1, 1988
Seroprevalence of antibodies to HTLV-I in patients with chronic neurological disorders other than tropical spastic paraparesisC A Mora, R M Garruto, P Brown, et al.
Brain Research. Brain Research Reviews|January 11, 1991
Regulation and genetic control of brain amyloid. FESN Study GroupD C Gajdusek, K Beyreuther, P Brown, et al.
Neurology|February 11, 1992
Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor geneP Brown, L G Goldfarb, W R McCombie, et al.
Experimental Neurology|June 1, 1990
Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndromeL G Goldfarb, P Brown, D Goldgaber, et al.
Neurology|March 1, 1991
Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndromeP Brown, L G Goldfarb, W T Brown, et al.
Experimental Neurology|November 1, 1989
Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndromeD Goldgaber, L G Goldfarb, P Brown, et al.
Nature Genetics|August 11, 1998
Missense mutations in desmin associated with familial cardiac and skeletal myopathyL G Goldfarb, K Y Park, L Cervenáková, et al.
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