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G Goldfarb

Showing results (121-130 of 244) with videos related to

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Experimental Neurology|April 1, 1994
Autosomal dominant spinocerebellar ataxia (SCA) in a Siberian founder population: assignment to the SCA1 locusA Lunkes, L G Goldfarb, F A Platonov, et al.
Acta Neuropathologica|October 31, 2012
Filamin C-related myopathies: pathology and mechanismsDieter O Fürst, Lev G Goldfarb, Rudolf A Kley, et al.
Lancet (London, England)|February 16, 1991
New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindredL G Goldfarb, M Haltia, P Brown, et al.
Journal of Wildlife Diseases|October 1, 1992
White phosphorus poisoning of waterfowl in an Alaskan salt marshC H Racine, M E Walsh, B D Roebuck, et al.
Sleep & Breathing = Schlaf & Atmung|September 23, 2025
Response to letter to the editor: "association between obstructive sleep apnea and hearing loss among a cohort of emergency responders"David W Appel, David G Goldfarb, Rachel Zeig-Owens, et al.
Journal of the Neurological Sciences|September 11, 1992
An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker familyL G Goldfarb, P Brown, A Vrbovská, et al.
Sleep & Breathing = Schlaf & Atmung|May 6, 2025
Association between obstructive sleep apnea and hearing loss among a cohort of emergency respondersDavid W Appel, David G Goldfarb, Rachel Zeig-Owens, et al.
Clinical Genetics|September 5, 2001
Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry diseaseG M Altarescu, L G Goldfarb, K Y Park, et al.
Annals of Neurology|September 3, 2002
Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathyAyush Dagvadorj, Robert B Petersen, Hee Suk Lee, et al.
Neurology|June 11, 1992
Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutationJ Chapman, P Brown, J M Rabey, et al.
Pageof 25

Showing results (121-130 of 244) with videos related to

Sort By:
Pageof 25
Experimental Neurology|April 1, 1994
Autosomal dominant spinocerebellar ataxia (SCA) in a Siberian founder population: assignment to the SCA1 locusA Lunkes, L G Goldfarb, F A Platonov, et al.
Acta Neuropathologica|October 31, 2012
Filamin C-related myopathies: pathology and mechanismsDieter O Fürst, Lev G Goldfarb, Rudolf A Kley, et al.
Lancet (London, England)|February 16, 1991
New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindredL G Goldfarb, M Haltia, P Brown, et al.
Journal of Wildlife Diseases|October 1, 1992
White phosphorus poisoning of waterfowl in an Alaskan salt marshC H Racine, M E Walsh, B D Roebuck, et al.
Sleep & Breathing = Schlaf & Atmung|September 23, 2025
Response to letter to the editor: "association between obstructive sleep apnea and hearing loss among a cohort of emergency responders"David W Appel, David G Goldfarb, Rachel Zeig-Owens, et al.
Journal of the Neurological Sciences|September 11, 1992
An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker familyL G Goldfarb, P Brown, A Vrbovská, et al.
Sleep & Breathing = Schlaf & Atmung|May 6, 2025
Association between obstructive sleep apnea and hearing loss among a cohort of emergency respondersDavid W Appel, David G Goldfarb, Rachel Zeig-Owens, et al.
Clinical Genetics|September 5, 2001
Identification of fifteen novel mutations and genotype-phenotype relationship in Fabry diseaseG M Altarescu, L G Goldfarb, K Y Park, et al.
Annals of Neurology|September 3, 2002
Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathyAyush Dagvadorj, Robert B Petersen, Hee Suk Lee, et al.
Neurology|June 11, 1992
Transmission of spongiform encephalopathy from a familial Creutzfeldt-Jakob disease patient of Jewish Libyan origin carrying the PRNP codon 200 mutationJ Chapman, P Brown, J M Rabey, et al.
Pageof 25