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L G Goldfarb

Showing results (81-90 of 91) with videos related to

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Journal of Medical Virology|April 11, 1991
Detection of flaviviruses by reverse-transcriptase polymerase chain reactionZ A Eldadah, D M Asher, M S Godec, et al.
Neuropathology and Applied Neurobiology|June 1, 1997
Viliuisk encephalomyelitis--review of the spectrum of pathological changesC A McLean, C L Masters, V A Vladimirtsev, et al.
Brain : a Journal of Neurology|April 6, 2006
Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteinsF Muntoni, G Bonne, L G Goldfarb, et al.
Neurology|August 26, 1998
APOE in non-Alzheimer amyloidoses: transmissible spongiform encephalopathiesJ Chapman, L Cervenáková, R B Petersen, et al.
Journal of the Neurological Sciences|September 12, 2000
Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS)L Cervenakova, I I Protas, A Hirano, et al.
Neurology|August 26, 1998
Spinocerebellar ataxia type 2 in China: molecular analysis and genotype-phenotype correlation in nine familiesY X Zhou, G X Wang, B S Tang, et al.
Archives of Neurology|May 18, 2001
Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 familiesY X Zhou, W H Qiao, W H Gu, et al.
American Journal of Human Genetics|March 26, 1999
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob diseaseH S Lee, N Sambuughin, L Cervenakova, et al.
Acta Neuropathologica Communications|February 5, 2016
New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analysesA Maerkens, M Olivé, A Schreiner, et al.
Journal of Proteomics|May 4, 2013
Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathyA Maerkens, R A Kley, M Olivé, et al.
Pageof 10

Showing results (81-90 of 91) with videos related to

Sort By:
Pageof 10
Journal of Medical Virology|April 11, 1991
Detection of flaviviruses by reverse-transcriptase polymerase chain reactionZ A Eldadah, D M Asher, M S Godec, et al.
Neuropathology and Applied Neurobiology|June 1, 1997
Viliuisk encephalomyelitis--review of the spectrum of pathological changesC A McLean, C L Masters, V A Vladimirtsev, et al.
Brain : a Journal of Neurology|April 6, 2006
Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteinsF Muntoni, G Bonne, L G Goldfarb, et al.
Neurology|August 26, 1998
APOE in non-Alzheimer amyloidoses: transmissible spongiform encephalopathiesJ Chapman, L Cervenáková, R B Petersen, et al.
Journal of the Neurological Sciences|September 12, 2000
Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS)L Cervenakova, I I Protas, A Hirano, et al.
Neurology|August 26, 1998
Spinocerebellar ataxia type 2 in China: molecular analysis and genotype-phenotype correlation in nine familiesY X Zhou, G X Wang, B S Tang, et al.
Archives of Neurology|May 18, 2001
Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 familiesY X Zhou, W H Qiao, W H Gu, et al.
American Journal of Human Genetics|March 26, 1999
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob diseaseH S Lee, N Sambuughin, L Cervenakova, et al.
Acta Neuropathologica Communications|February 5, 2016
New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analysesA Maerkens, M Olivé, A Schreiner, et al.
Journal of Proteomics|May 4, 2013
Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathyA Maerkens, R A Kley, M Olivé, et al.
Pageof 10