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G Goldfarb

Showing results (101-110 of 244) with videos related to

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Lancet (London, England)|January 16, 1993
Real and imagined clinicopathological limits of "prion dementia"P Brown, P Kaur, M P Sulima, et al.
Neuromuscular Disorders : NMD|January 22, 2014
A new disease allele for the p.C30071R mutation in titin causing hereditary myopathy with early respiratory failureGerald Pfeffer, Nyamkhishig Sambuughin, Montse Olivé, et al.
Journal of Neuropathology and Experimental Neurology|January 18, 2012
Kuru: genes, cannibals and neuropathologyPawel P Liberski, Beata Sikorska, Shirley Lindenbaum, 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.
The Journal of Antimicrobial Chemotherapy|August 2, 2001
Genetic and phenotypic characterization of macrolide resistance in group A streptococci isolated from adults with pharyngo-tonsillitis in FranceP Weber, J Filipecki, E Bingen, 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.
Folia Neuropathologica|July 21, 2009
Viliuisk encephalomyelitis in Eastern Siberia - analysis of 390 casesLev G Goldfarb, Vsevolod A Vladimirtsev, Fyodor A Platanov, et al.
Neurology|December 8, 2010
Dominant-negative effects of a novel mutation in the filamin myopathyPeter F M van der Ven, Zagaa Odgerel, Dieter O Fürst, et al.
Pageof 25

Showing results (101-110 of 244) with videos related to

Sort By:
Pageof 25
Lancet (London, England)|January 16, 1993
Real and imagined clinicopathological limits of "prion dementia"P Brown, P Kaur, M P Sulima, et al.
Neuromuscular Disorders : NMD|January 22, 2014
A new disease allele for the p.C30071R mutation in titin causing hereditary myopathy with early respiratory failureGerald Pfeffer, Nyamkhishig Sambuughin, Montse Olivé, et al.
Journal of Neuropathology and Experimental Neurology|January 18, 2012
Kuru: genes, cannibals and neuropathologyPawel P Liberski, Beata Sikorska, Shirley Lindenbaum, 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.
The Journal of Antimicrobial Chemotherapy|August 2, 2001
Genetic and phenotypic characterization of macrolide resistance in group A streptococci isolated from adults with pharyngo-tonsillitis in FranceP Weber, J Filipecki, E Bingen, 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.
Folia Neuropathologica|July 21, 2009
Viliuisk encephalomyelitis in Eastern Siberia - analysis of 390 casesLev G Goldfarb, Vsevolod A Vladimirtsev, Fyodor A Platanov, et al.
Neurology|December 8, 2010
Dominant-negative effects of a novel mutation in the filamin myopathyPeter F M van der Ven, Zagaa Odgerel, Dieter O Fürst, et al.
Pageof 25