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G Goetz

Showing results (741-750 of 755) with videos related to

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Neurology|March 14, 2007
DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkersC F Lippa, J E Duda, M Grossman, et al.
Human Molecular Genetics|October 23, 2003
Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson diseaseYi-Ju Li, Sofia A Oliveira, Puting Xu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 9, 2012
Validation of the Italian version of the Movement Disorder Society--Unified Parkinson's Disease Rating ScaleAngelo Antonini, Giovanni Abbruzzese, Luigi Ferini-Strambi, et al.
JAMA|November 17, 2001
Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson diseaseE R Martin, W K Scott, M A Nance, et al.
American Journal of Human Genetics|March 5, 2002
Age at onset in two common neurodegenerative diseases is genetically controlledYi-Ju Li, William K Scott, Dale J Hedges, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 10, 2017
Past, present, and future of Parkinson's disease: A special essay on the 200th Anniversary of the Shaking PalsyJ A Obeso, M Stamelou, C G Goetz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 26, 2022
Validation of the Arabic Version of the Movement Disorder Society-Unified Parkinson's Disease Rating ScaleHanan Khalil, Zakiyah F Aldaajani, Mayis Aldughmi, et al.
Parkinsonism & Related Disorders|April 8, 2018
Relationship between the MDS-UPDRS and Quality of Life: A large multicenter study of 3206 patientsMatej Skorvanek, Pablo Martinez-Martin, Norbert Kovacs, et al.
Neurology|October 21, 2005
Diagnosis and management of dementia with Lewy bodies: third report of the DLB ConsortiumI G McKeith, D W Dickson, J Lowe, et al.
The Journal of Clinical Investigation|October 4, 2017
Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like featuresRaphael Carapito, Martina Konantz, Catherine Paillard, et al.
Pageof 76

Showing results (741-750 of 755) with videos related to

Sort By:
Pageof 76
Neurology|March 14, 2007
DLB and PDD boundary issues: diagnosis, treatment, molecular pathology, and biomarkersC F Lippa, J E Duda, M Grossman, et al.
Human Molecular Genetics|October 23, 2003
Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson diseaseYi-Ju Li, Sofia A Oliveira, Puting Xu, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 9, 2012
Validation of the Italian version of the Movement Disorder Society--Unified Parkinson's Disease Rating ScaleAngelo Antonini, Giovanni Abbruzzese, Luigi Ferini-Strambi, et al.
JAMA|November 17, 2001
Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson diseaseE R Martin, W K Scott, M A Nance, et al.
American Journal of Human Genetics|March 5, 2002
Age at onset in two common neurodegenerative diseases is genetically controlledYi-Ju Li, William K Scott, Dale J Hedges, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 10, 2017
Past, present, and future of Parkinson's disease: A special essay on the 200th Anniversary of the Shaking PalsyJ A Obeso, M Stamelou, C G Goetz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 26, 2022
Validation of the Arabic Version of the Movement Disorder Society-Unified Parkinson's Disease Rating ScaleHanan Khalil, Zakiyah F Aldaajani, Mayis Aldughmi, et al.
Parkinsonism & Related Disorders|April 8, 2018
Relationship between the MDS-UPDRS and Quality of Life: A large multicenter study of 3206 patientsMatej Skorvanek, Pablo Martinez-Martin, Norbert Kovacs, et al.
Neurology|October 21, 2005
Diagnosis and management of dementia with Lewy bodies: third report of the DLB ConsortiumI G McKeith, D W Dickson, J Lowe, et al.
The Journal of Clinical Investigation|October 4, 2017
Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like featuresRaphael Carapito, Martina Konantz, Catherine Paillard, et al.
Pageof 76