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L G Goldfarb

Showing results (61-70 of 91) with videos related to

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Clinical Genetics|July 25, 2000
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutationK Y Park, M C Dalakas, C Semino-Mora, et al.
Neurology|April 1, 1998
Creutzfeldt-Jakob disease in a husband and wifeP Brown, L Cervenáková, L McShane, et al.
Annals of Neurology|March 1, 1992
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European originL G Goldfarb, P Brown, M Haltia, et al.
Neurology|September 1, 1996
Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutationE J Cochran, D A Bennett, L Cervenáková, et al.
Neurology|March 1, 1996
Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutationJ Chapman, A Arlazoroff, L G Goldfarb, et al.
Science (New York, N.Y.)|October 30, 1992
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphismL G Goldfarb, R B Petersen, M Tabaton, et al.
Journal of Medical Virology|April 1, 1990
Detection of measles virus genomic sequences in SSPE brain tissue by the polymerase chain reactionM S Godec, D M Asher, P T Swoveland, et al.
Molecular Neurobiology|April 1, 1994
A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene)R B Petersen, L G Goldfarb, M Tabaton, et al.
Lancet (London, England)|January 15, 1994
Molecular genetic testing of a fetus at risk of Gerstmann-Sträussler-Scheinker syndromeP Brown, L Cervenáková, L G Goldfarb, et al.
Annals of Neurology|April 1, 1996
Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1L G Goldfarb, O Vasconcelos, F A Platonov, et al.
Pageof 10

Showing results (61-70 of 91) with videos related to

Sort By:
Pageof 10
Clinical Genetics|July 25, 2000
Sporadic cardiac and skeletal myopathy caused by a de novo desmin mutationK Y Park, M C Dalakas, C Semino-Mora, et al.
Neurology|April 1, 1998
Creutzfeldt-Jakob disease in a husband and wifeP Brown, L Cervenáková, L McShane, et al.
Annals of Neurology|March 1, 1992
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European originL G Goldfarb, P Brown, M Haltia, et al.
Neurology|September 1, 1996
Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutationE J Cochran, D A Bennett, L Cervenáková, et al.
Neurology|March 1, 1996
Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutationJ Chapman, A Arlazoroff, L G Goldfarb, et al.
Science (New York, N.Y.)|October 30, 1992
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphismL G Goldfarb, R B Petersen, M Tabaton, et al.
Journal of Medical Virology|April 1, 1990
Detection of measles virus genomic sequences in SSPE brain tissue by the polymerase chain reactionM S Godec, D M Asher, P T Swoveland, et al.
Molecular Neurobiology|April 1, 1994
A novel mechanism of phenotypic heterogeneity demonstrated by the effect of a polymorphism on a pathogenic mutation in the PRNP (prion protein gene)R B Petersen, L G Goldfarb, M Tabaton, et al.
Lancet (London, England)|January 15, 1994
Molecular genetic testing of a fetus at risk of Gerstmann-Sträussler-Scheinker syndromeP Brown, L Cervenáková, L G Goldfarb, et al.
Annals of Neurology|April 1, 1996
Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1L G Goldfarb, O Vasconcelos, F A Platonov, et al.
Pageof 10