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G Goldfarb

Showing results (111-120 of 244) with videos related to

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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.
Neurology|January 1, 1996
Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph diseaseJ J Higgins, L E Nee, O Vasconcelos, et al.
Journal of the Neurological Sciences|October 11, 1991
The molecular genetics of familial Creutzfeldt-Jakob disease in FranceP Brown, L G Goldfarb, F Cathala, et al.
Annals of Neurology|March 11, 1992
Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutationP Brown, L G Goldfarb, J Kovanen, et al.
Lung|June 9, 2026
Worsened longitudinal visit-to-visit-FEV<sub>1</sub>-variation and mortality in WTC exposed FDNY workers: a 23-year landmark analysisMarie-Hélène Walraedt, Amber Vanhauwaert, David G Goldfarb, et al.
Occupational and Environmental Medicine|January 17, 2024
Association of firefighting exposures with lung function using a novel job exposure matrix (JEM)David G Goldfarb, David J Prezant, Rachel Zeig-Owens, et al.
Journal of the Neurological Sciences|January 8, 1999
Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15N Sambuughin, K Sivakumar, B Selenge, et al.
Pageof 25

Showing results (111-120 of 244) with videos related to

Sort By:
Pageof 25
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.
Neurology|January 1, 1996
Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph diseaseJ J Higgins, L E Nee, O Vasconcelos, et al.
Journal of the Neurological Sciences|October 11, 1991
The molecular genetics of familial Creutzfeldt-Jakob disease in FranceP Brown, L G Goldfarb, F Cathala, et al.
Annals of Neurology|March 11, 1992
Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutationP Brown, L G Goldfarb, J Kovanen, et al.
Lung|June 9, 2026
Worsened longitudinal visit-to-visit-FEV<sub>1</sub>-variation and mortality in WTC exposed FDNY workers: a 23-year landmark analysisMarie-Hélène Walraedt, Amber Vanhauwaert, David G Goldfarb, et al.
Occupational and Environmental Medicine|January 17, 2024
Association of firefighting exposures with lung function using a novel job exposure matrix (JEM)David G Goldfarb, David J Prezant, Rachel Zeig-Owens, et al.
Journal of the Neurological Sciences|January 8, 1999
Autosomal dominant distal spinal muscular atrophy type V (dSMA-V) and Charcot-Marie-Tooth disease type 2D (CMT2D) segregate within a single large kindred and map to a refined region on chromosome 7p15N Sambuughin, K Sivakumar, B Selenge, et al.
Pageof 25