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Jan Aasly

Showing results (31-40 of 77) with videos related to

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Brain : a Journal of Neurology|February 2, 2008
POLG1 mutations cause a syndromic epilepsy with occipital lobe predilectionBernt A Engelsen, Charalampos Tzoulis, Bjørn Karlsen, et al.
Neuroscience Letters|April 18, 2002
The tau H1 haplotype is associated with Parkinson's disease in the Norwegian populationMatt Farrer, Lisa Skipper, Marianne Berg, et al.
Scientific Reports|June 25, 2026
Variable mitochondrial phenotypes and reduced complex IV assembly factor SCO2 in LRRK2-G2019S fibroblastsRuby Wallis, Ella Simmonite, Harry Cooper, et al.
Biological Trace Element Research|July 2, 2003
Manganese, copper, and zinc in cerebrospinal fluid from patients with multiple sclerosisTorun M Melø, Cecilie Larsen, Linda R White, et al.
International Journal of Geriatric Psychiatry|May 20, 2008
Risk-reducing effect of education in Alzheimer's diseaseSigrid Botne Sando, Stacey Melquist, Ashley Cannon, et al.
American Journal of Human Genetics|August 7, 2004
Linkage disequilibrium and association of MAPT H1 in Parkinson diseaseLisa Skipper, Kristen Wilkes, Mathias Toft, et al.
Brain : a Journal of Neurology|April 28, 2006
The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 casesCharalampos Tzoulis, Bernt A Engelsen, Wenche Telstad, et al.
Journal of Neurology|July 28, 2011
Leukoencephalopathy with brainstem and spinal cord involvement caused by a novel mutation in the DARS2 geneCharalampos Tzoulis, Gia Tuong Tran, Ivar Otto Gjerde, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Parkinsonism, FXTAS, and FMR1 premutationsMathias Toft, Jan Aasly, Gina Bisceglio, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 5, 2016
Cerebrospinal fluid biomarkers and clinical features in leucine-rich repeat kinase 2 (LRRK2) mutation carriersDolores Vilas, Leslie M Shaw, Peggy Taylor, et al.
Pageof 8

Showing results (31-40 of 77) with videos related to

Sort By:
Pageof 8
Brain : a Journal of Neurology|February 2, 2008
POLG1 mutations cause a syndromic epilepsy with occipital lobe predilectionBernt A Engelsen, Charalampos Tzoulis, Bjørn Karlsen, et al.
Neuroscience Letters|April 18, 2002
The tau H1 haplotype is associated with Parkinson's disease in the Norwegian populationMatt Farrer, Lisa Skipper, Marianne Berg, et al.
Scientific Reports|June 25, 2026
Variable mitochondrial phenotypes and reduced complex IV assembly factor SCO2 in LRRK2-G2019S fibroblastsRuby Wallis, Ella Simmonite, Harry Cooper, et al.
Biological Trace Element Research|July 2, 2003
Manganese, copper, and zinc in cerebrospinal fluid from patients with multiple sclerosisTorun M Melø, Cecilie Larsen, Linda R White, et al.
International Journal of Geriatric Psychiatry|May 20, 2008
Risk-reducing effect of education in Alzheimer's diseaseSigrid Botne Sando, Stacey Melquist, Ashley Cannon, et al.
American Journal of Human Genetics|August 7, 2004
Linkage disequilibrium and association of MAPT H1 in Parkinson diseaseLisa Skipper, Kristen Wilkes, Mathias Toft, et al.
Brain : a Journal of Neurology|April 28, 2006
The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 casesCharalampos Tzoulis, Bernt A Engelsen, Wenche Telstad, et al.
Journal of Neurology|July 28, 2011
Leukoencephalopathy with brainstem and spinal cord involvement caused by a novel mutation in the DARS2 geneCharalampos Tzoulis, Gia Tuong Tran, Ivar Otto Gjerde, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Parkinsonism, FXTAS, and FMR1 premutationsMathias Toft, Jan Aasly, Gina Bisceglio, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 5, 2016
Cerebrospinal fluid biomarkers and clinical features in leucine-rich repeat kinase 2 (LRRK2) mutation carriersDolores Vilas, Leslie M Shaw, Peggy Taylor, et al.
Pageof 8