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J S Kuipers

Showing results (11-20 of 21) with videos related to

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Archivum Chirurgicum Neerlandicum|January 1, 1972
How well do autoclaves function?J S Kuipers, K J Balmus, R F Cohen
Parkinsonism & Related Disorders|October 18, 2019
Primary familial brain calcification caused by MYORG mutations in an Italian familyIlaria Taglia, Demy J S Kuipers, Guido J Breedveld, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2022
Isolated Paroxysmal Non-kinesigenic Dystonia Associated with Homozygous PDHB Variant in an Indian FamilyPankaj A Agarwal, Demy J S Kuipers, Christina Fevga, et al.
Parkinsonism & Related Disorders|August 22, 2019
Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish familyDemy J S Kuipers, Zeynep Tufekcioglu, Başar Bilgiç, et al.
Journal of Alzheimer'S Disease : JAD|June 30, 2020
Clinical and Pathological Phenotypes of LRP10 Variant Carriers with DementiaLeonie J M Vergouw, Hanneke Geut, Guido Breedveld, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 7, 2018
PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disabilityDemy J S Kuipers, Jonathan Carr, Soraya Bardien, et al.
Neurobiology of Aging|June 13, 2020
LRP10 variants in progressive supranuclear palsyLeonie J M Vergouw, Shamiram Melhem, Laura Donker Kaat, et al.
Parkinsonism & Related Disorders|December 10, 2021
WARS2 mutations cause dopa-responsive early-onset parkinsonism and progressive myoclonus ataxiaMatej Skorvanek, Irena Rektorova, Wim Mandemakers, et al.
Brain : a Journal of Neurology|September 8, 2022
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disabilityChristina Fevga, Christelle Tesson, Ana Carreras Mascaro, et al.
Brain Communications|July 20, 2022
A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementiaAlessandra Fanciulli, Fabian Leys, Fabienne Lehner, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Archivum Chirurgicum Neerlandicum|January 1, 1972
How well do autoclaves function?J S Kuipers, K J Balmus, R F Cohen
Parkinsonism & Related Disorders|October 18, 2019
Primary familial brain calcification caused by MYORG mutations in an Italian familyIlaria Taglia, Demy J S Kuipers, Guido J Breedveld, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2022
Isolated Paroxysmal Non-kinesigenic Dystonia Associated with Homozygous PDHB Variant in an Indian FamilyPankaj A Agarwal, Demy J S Kuipers, Christina Fevga, et al.
Parkinsonism & Related Disorders|August 22, 2019
Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish familyDemy J S Kuipers, Zeynep Tufekcioglu, Başar Bilgiç, et al.
Journal of Alzheimer'S Disease : JAD|June 30, 2020
Clinical and Pathological Phenotypes of LRP10 Variant Carriers with DementiaLeonie J M Vergouw, Hanneke Geut, Guido Breedveld, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 7, 2018
PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disabilityDemy J S Kuipers, Jonathan Carr, Soraya Bardien, et al.
Neurobiology of Aging|June 13, 2020
LRP10 variants in progressive supranuclear palsyLeonie J M Vergouw, Shamiram Melhem, Laura Donker Kaat, et al.
Parkinsonism & Related Disorders|December 10, 2021
WARS2 mutations cause dopa-responsive early-onset parkinsonism and progressive myoclonus ataxiaMatej Skorvanek, Irena Rektorova, Wim Mandemakers, et al.
Brain : a Journal of Neurology|September 8, 2022
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disabilityChristina Fevga, Christelle Tesson, Ana Carreras Mascaro, et al.
Brain Communications|July 20, 2022
A multiplex pedigree with pathologically confirmed multiple system atrophy and Parkinson's disease with dementiaAlessandra Fanciulli, Fabian Leys, Fabienne Lehner, et al.
Pageof 3