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K Gwinn

Showing results (31-40 of 49) with videos related to

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Neurology|September 20, 2000
Spinocerebellar ataxia type 2 with parkinsonism in ethnic ChineseK Gwinn-Hardy, J Y Chen, H C Liu, et al.
Neuroscience Letters|February 23, 1999
No pathogenic mutations in the persyn gene in Parkinson's diseaseS Lincoln, K Gwinn-Hardy, J Goudreau, et al.
Acta Neuropathologica|March 21, 2002
Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonismZ K Wszolek, K Gwinn-Hardy, E K Wszolek, et al.
Annals of Neurology|September 18, 2001
Lewy bodies and parkinsonism in families with parkin mutationsM Farrer, P Chan, R Chen, et al.
Brain : a Journal of Neurology|October 24, 2001
A clinical and pathological study of motor neurone disease on GuamH R Morris, S Al-Sarraj, C Schwab, et al.
Human Molecular Genetics|January 15, 1999
A chromosome 4p haplotype segregating with Parkinson's disease and postural tremorM Farrer, K Gwinn-Hardy, M Muenter, et al.
European Journal of Medicinal Chemistry|February 24, 2026
Structure-activity relationship profiling of N-substituted 8-trifluoromethyl-9H-purin-6-amines as mitochondrial protonophoresEmily L Krinos, Rei J Fields, Isabella M DeLuca, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 15, 2004
Analysis of polyglutamine-coding repeats in the TATA-binding protein in different neurodegenerative diseasesY R Wu, H C Fung, G J Lee-Chen, et al.
Nature Medicine|April 18, 1998
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1R Crook, A Verkkoniemi, J Perez-Tur, et al.
Neurology|December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteriaM K Bruno, M Hallett, K Gwinn-Hardy, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Neurology|September 20, 2000
Spinocerebellar ataxia type 2 with parkinsonism in ethnic ChineseK Gwinn-Hardy, J Y Chen, H C Liu, et al.
Neuroscience Letters|February 23, 1999
No pathogenic mutations in the persyn gene in Parkinson's diseaseS Lincoln, K Gwinn-Hardy, J Goudreau, et al.
Acta Neuropathologica|March 21, 2002
Neuropathology of two members of a German-American kindred (Family C) with late onset parkinsonismZ K Wszolek, K Gwinn-Hardy, E K Wszolek, et al.
Annals of Neurology|September 18, 2001
Lewy bodies and parkinsonism in families with parkin mutationsM Farrer, P Chan, R Chen, et al.
Brain : a Journal of Neurology|October 24, 2001
A clinical and pathological study of motor neurone disease on GuamH R Morris, S Al-Sarraj, C Schwab, et al.
Human Molecular Genetics|January 15, 1999
A chromosome 4p haplotype segregating with Parkinson's disease and postural tremorM Farrer, K Gwinn-Hardy, M Muenter, et al.
European Journal of Medicinal Chemistry|February 24, 2026
Structure-activity relationship profiling of N-substituted 8-trifluoromethyl-9H-purin-6-amines as mitochondrial protonophoresEmily L Krinos, Rei J Fields, Isabella M DeLuca, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 15, 2004
Analysis of polyglutamine-coding repeats in the TATA-binding protein in different neurodegenerative diseasesY R Wu, H C Fung, G J Lee-Chen, et al.
Nature Medicine|April 18, 1998
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1R Crook, A Verkkoniemi, J Perez-Tur, et al.
Neurology|December 30, 2004
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteriaM K Bruno, M Hallett, K Gwinn-Hardy, et al.
Pageof 5