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Mathias Toft

Showing results (51-60 of 129) with videos related to

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Neuroscience Letters|August 24, 2017
The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signalVictoria Berge-Seidl, Lasse Pihlstrøm, Jodi Maple-Grødem, 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.
Frontiers in Pediatrics|June 1, 2026
A homozygous splice-site variant in SAMHD1 shows variable expressivity of Aicardi-Goutières syndrome type 5: a case report and literature reviewHammad Yousaf, Zehra Zonash, Javeria Manzoor, et al.
Acta Neuropathologica|June 22, 2023
Transcriptomic profiling of Parkinson's disease brains reveals disease stage specific gene expression changesChiara Cappelletti, Sandra Pilar Henriksen, Hanneke Geut, et al.
The Journal of Headache and Pain|November 27, 2025
Prevalence of headache disorders in Norway: results from the population based PopHEAD studyMaria Bengtson Argren, Helene Engstrand, Andreas Kattem Husøy, et al.
Frontiers in Neurology|February 22, 2021
<i>APOE</i> and <i>MAPT</i> Are Associated With Dementia in Neuropathologically Confirmed Parkinson's DiseaseJon-Anders Tunold, Hanneke Geut, J M Annemieke Rozemuller, et al.
Neurology. Genetics|July 20, 2019
Missense mutations in DYT-TOR1A dystoniaZafar Iqbal, Jeanette Koht, Lasse Pihlstrøm, et al.
Archives of Neurology|June 16, 2005
FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophyValérie Biancalana, Mathias Toft, Isabelle Le Ber, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 10, 2011
Long-term efficacy and mortality in Parkinson's disease patients treated with subthalamic stimulationMathias Toft, Bård Lilleeng, Jon Ramm-Pettersen, 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.
Pageof 13

Showing results (51-60 of 129) with videos related to

Sort By:
Pageof 13
Neuroscience Letters|August 24, 2017
The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signalVictoria Berge-Seidl, Lasse Pihlstrøm, Jodi Maple-Grødem, 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.
Frontiers in Pediatrics|June 1, 2026
A homozygous splice-site variant in SAMHD1 shows variable expressivity of Aicardi-Goutières syndrome type 5: a case report and literature reviewHammad Yousaf, Zehra Zonash, Javeria Manzoor, et al.
Acta Neuropathologica|June 22, 2023
Transcriptomic profiling of Parkinson's disease brains reveals disease stage specific gene expression changesChiara Cappelletti, Sandra Pilar Henriksen, Hanneke Geut, et al.
The Journal of Headache and Pain|November 27, 2025
Prevalence of headache disorders in Norway: results from the population based PopHEAD studyMaria Bengtson Argren, Helene Engstrand, Andreas Kattem Husøy, et al.
Frontiers in Neurology|February 22, 2021
<i>APOE</i> and <i>MAPT</i> Are Associated With Dementia in Neuropathologically Confirmed Parkinson's DiseaseJon-Anders Tunold, Hanneke Geut, J M Annemieke Rozemuller, et al.
Neurology. Genetics|July 20, 2019
Missense mutations in DYT-TOR1A dystoniaZafar Iqbal, Jeanette Koht, Lasse Pihlstrøm, et al.
Archives of Neurology|June 16, 2005
FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophyValérie Biancalana, Mathias Toft, Isabelle Le Ber, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 10, 2011
Long-term efficacy and mortality in Parkinson's disease patients treated with subthalamic stimulationMathias Toft, Bård Lilleeng, Jon Ramm-Pettersen, 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.
Pageof 13