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Showing results (531-540 of 561) with videos related to

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Neurology|December 24, 2013
Characterizing mild cognitive impairment in incident Parkinson disease: the ICICLE-PD studyAlison J Yarnall, David P Breen, Gordon W Duncan, et al.
Brain : a Journal of Neurology|July 21, 2019
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease studyManuela M X Tan, Naveed Malek, Michael A Lawton, et al.
Neurology|October 27, 2004
Clinical and neuropathologic variation in neuronal intermediate filament inclusion diseaseN J Cairns, M Grossman, S E Arnold, et al.
Human Genetics|September 12, 2000
Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13M Takahashi, E Rapley, P J Biggs, et al.
Neurology|August 12, 2004
SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodiesJ Johnson, S M Hague, M Hanson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 14, 2006
A multicentre longitudinal observational study of changes in self reported health status in people with Parkinson's disease left untreated at diagnosisD Grosset, L Taurah, D J Burn, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2012
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's diseaseLaura L Kilarski, Justin P Pearson, Victoria Newsway, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 23, 2006
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease familiesLianna Ishihara, Rachel A Gibson, Liling Warren, et al.
Annals of Neurology|December 26, 2009
Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease geneMatthias Elstner, Christopher M Morris, Katharina Heim, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 14, 2023
A Statement of the MDS on Biological Definition, Staging, and Classification of Parkinson's DiseaseFrancisco Cardoso, Christopher G Goetz, Tiago A Mestre, et al.
Pageof 57

Showing results (531-540 of 561) with videos related to

Sort By:
Pageof 57
Neurology|December 24, 2013
Characterizing mild cognitive impairment in incident Parkinson disease: the ICICLE-PD studyAlison J Yarnall, David P Breen, Gordon W Duncan, et al.
Brain : a Journal of Neurology|July 21, 2019
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease studyManuela M X Tan, Naveed Malek, Michael A Lawton, et al.
Neurology|October 27, 2004
Clinical and neuropathologic variation in neuronal intermediate filament inclusion diseaseN J Cairns, M Grossman, S E Arnold, et al.
Human Genetics|September 12, 2000
Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13M Takahashi, E Rapley, P J Biggs, et al.
Neurology|August 12, 2004
SNCA multiplication is not a common cause of Parkinson disease or dementia with Lewy bodiesJ Johnson, S M Hague, M Hanson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 14, 2006
A multicentre longitudinal observational study of changes in self reported health status in people with Parkinson's disease left untreated at diagnosisD Grosset, L Taurah, D J Burn, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2012
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's diseaseLaura L Kilarski, Justin P Pearson, Victoria Newsway, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 23, 2006
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease familiesLianna Ishihara, Rachel A Gibson, Liling Warren, et al.
Annals of Neurology|December 26, 2009
Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease geneMatthias Elstner, Christopher M Morris, Katharina Heim, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 14, 2023
A Statement of the MDS on Biological Definition, Staging, and Classification of Parkinson's DiseaseFrancisco Cardoso, Christopher G Goetz, Tiago A Mestre, et al.
Pageof 57