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Andrew Singleton

Showing results (61-70 of 286) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|February 11, 2009
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutationsSarah Teixeira Camargos, Leonardo Oliveira Dornas, Parastoo Momeni, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2007
Novel GCH1 mutation in a Brazilian family with dopa-responsive dystoniaSarah Teixeira Camargos, Francisco Cardoso, Parastoo Momeni, et al.
Trauma Surgery & Acute Care Open|August 31, 2019
Family satisfaction in the trauma and surgical intensive care unit: another important quality measureTom Maxim, Agustin Alvarez, Yvonne Hojberg, et al.
Studies in Health Technology and Informatics|October 4, 2007
Assessing the impact of recording quality target data on the GP consultation using multi-channel videoMaigaelle V Moulene, Simon de Lusignan, George Freeman, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 7, 2005
Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's diseaseJordi Clarimon, Janel Johnson, Okan Dogu, et al.
Research Square|April 24, 2023
Analysis of rare Parkinson's disease variants in millions of peopleVanessa Pitz, Mary Makarious, Sara Bandrés-Ciga, et al.
European Heart Journal|May 14, 2009
Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older peopleAnna Murray, Christie Cluett, Stefania Bandinelli, et al.
JMIR Research Protocols|April 7, 2025
Racial Disparities in Parkinson Disease Clinical Phenotype, Management, and Genetics: Protocol for a Prospective Observational StudyDeborah A Hall, Josh M Shulman, Andrew Singleton, et al.
Neurobiology of Aging|December 28, 2007
Complete screening for glucocerebrosidase mutations in Parkinson disease patients from PortugalJose Bras, Coro Paisan-Ruiz, Rita Guerreiro, et al.
Neurobiology of Aging|March 4, 2017
Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association studyAri Siitonen, Michael A Nalls, Dena Hernández, et al.
Pageof 29

Showing results (61-70 of 286) with videos related to

Sort By:
Pageof 29
Movement Disorders : Official Journal of the Movement Disorder Society|February 11, 2009
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutationsSarah Teixeira Camargos, Leonardo Oliveira Dornas, Parastoo Momeni, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2007
Novel GCH1 mutation in a Brazilian family with dopa-responsive dystoniaSarah Teixeira Camargos, Francisco Cardoso, Parastoo Momeni, et al.
Trauma Surgery & Acute Care Open|August 31, 2019
Family satisfaction in the trauma and surgical intensive care unit: another important quality measureTom Maxim, Agustin Alvarez, Yvonne Hojberg, et al.
Studies in Health Technology and Informatics|October 4, 2007
Assessing the impact of recording quality target data on the GP consultation using multi-channel videoMaigaelle V Moulene, Simon de Lusignan, George Freeman, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 7, 2005
Defining the ends of Parkin exon 4 deletions in two different families with Parkinson's diseaseJordi Clarimon, Janel Johnson, Okan Dogu, et al.
Research Square|April 24, 2023
Analysis of rare Parkinson's disease variants in millions of peopleVanessa Pitz, Mary Makarious, Sara Bandrés-Ciga, et al.
European Heart Journal|May 14, 2009
Common lipid-altering gene variants are associated with therapeutic intervention thresholds of lipid levels in older peopleAnna Murray, Christie Cluett, Stefania Bandinelli, et al.
JMIR Research Protocols|April 7, 2025
Racial Disparities in Parkinson Disease Clinical Phenotype, Management, and Genetics: Protocol for a Prospective Observational StudyDeborah A Hall, Josh M Shulman, Andrew Singleton, et al.
Neurobiology of Aging|December 28, 2007
Complete screening for glucocerebrosidase mutations in Parkinson disease patients from PortugalJose Bras, Coro Paisan-Ruiz, Rita Guerreiro, et al.
Neurobiology of Aging|March 4, 2017
Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association studyAri Siitonen, Michael A Nalls, Dena Hernández, et al.
Pageof 29