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Jan Aasly

Showing results (51-60 of 77) with videos related to

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American Journal of Human Genetics|February 24, 2005
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populationsJennifer Kachergus, Ignacio F Mata, Mary Hulihan, et al.
Annals of Neurology|April 1, 2003
Homozygous mutations in caveolin-3 cause a severe form of rippling muscle diseaseChristian Kubisch, Benedikt G H Schoser, Monika von Düring, et al.
Annals of Neurology|March 15, 2011
Cerebrospinal fluid biomarkers for Parkinson disease diagnosis and progressionMin Shi, Joshua Bradner, Aneeka M Hancock, et al.
Annals of Neurology|June 10, 2022
Reply to: Cognitive Effects of Deep Brain Stimulation in GBA-Related Parkinson's DiseaseGian Pal, Graziella Mangone, Bichun Ouyang, et al.
The Lancet. Neurology|March 25, 2017
Serotonin and dopamine transporter PET changes in the premotor phase of LRRK2 parkinsonism: cross-sectional studiesDaryl J Wile, Pankaj A Agarwal, Michael Schulzer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 27, 2019
Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controlsIlir Agalliu, Roberto A Ortega, Marta San Luciano, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 20, 2016
Arm swing as a potential new prodromal marker of Parkinson's diseaseAnat Mirelman, Hagar Bernad-Elazari, Avner Thaler, et al.
Neurology|July 31, 2012
MRI characteristics and scoring in HDLS due to CSF1R gene mutationsChristina Sundal, Jay A Van Gerpen, Alexandra M Nicholson, et al.
The Lancet. Neurology|June 10, 2008
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control studyDaniel G Healy, Mario Falchi, Sean S O'Sullivan, et al.
Parkinsonism & Related Disorders|June 22, 2013
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutationsChristina Sundal, Shinsuke Fujioka, Jay A Van Gerpen, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|February 24, 2005
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populationsJennifer Kachergus, Ignacio F Mata, Mary Hulihan, et al.
Annals of Neurology|April 1, 2003
Homozygous mutations in caveolin-3 cause a severe form of rippling muscle diseaseChristian Kubisch, Benedikt G H Schoser, Monika von Düring, et al.
Annals of Neurology|March 15, 2011
Cerebrospinal fluid biomarkers for Parkinson disease diagnosis and progressionMin Shi, Joshua Bradner, Aneeka M Hancock, et al.
Annals of Neurology|June 10, 2022
Reply to: Cognitive Effects of Deep Brain Stimulation in GBA-Related Parkinson's DiseaseGian Pal, Graziella Mangone, Bichun Ouyang, et al.
The Lancet. Neurology|March 25, 2017
Serotonin and dopamine transporter PET changes in the premotor phase of LRRK2 parkinsonism: cross-sectional studiesDaryl J Wile, Pankaj A Agarwal, Michael Schulzer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 27, 2019
Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controlsIlir Agalliu, Roberto A Ortega, Marta San Luciano, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 20, 2016
Arm swing as a potential new prodromal marker of Parkinson's diseaseAnat Mirelman, Hagar Bernad-Elazari, Avner Thaler, et al.
Neurology|July 31, 2012
MRI characteristics and scoring in HDLS due to CSF1R gene mutationsChristina Sundal, Jay A Van Gerpen, Alexandra M Nicholson, et al.
The Lancet. Neurology|June 10, 2008
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control studyDaniel G Healy, Mario Falchi, Sean S O'Sullivan, et al.
Parkinsonism & Related Disorders|June 22, 2013
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutationsChristina Sundal, Shinsuke Fujioka, Jay A Van Gerpen, et al.
Pageof 8