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Parkinsonism & Related Disorders|June 3, 2014
Three families with Perry syndrome from distinct parts of the worldPawel Tacik, Fabienne C Fiesel, Shinsuke Fujioka, et al.
Genes|July 29, 2023
Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar DisordersSaadia Maryam Saadi, Elisa Cali, Lubaba Bintee Khalid, et al.
Nature Communications|October 1, 2024
The genetic landscape of basal ganglia and implications for common brain disordersShahram Bahrami, Kaja Nordengen, Jaroslav Rokicki, et al.
Molecular Genetics and Genomics : MGG|May 21, 2024
Exome sequencing in four families with neurodevelopmental disorders: genotype-phenotype correlation and identification of novel disease-causing variants in VPS13B and RELNTehseen Ullah Khan Afridi, Ambrin Fatima, Humayoon Shafique Satti, et al.
Parkinsonism & Related Disorders|December 3, 2014
Three sib-pairs of autopsy-confirmed progressive supranuclear palsyShinsuke Fujioka, Monica Y Sanchez Contreras, Audrey J Strongosky, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 26, 2011
Genetic variants of α-synuclein are not associated with essential tremorOwen A Ross, Karen N Conneely, Tao Wang, et al.
Neurobiology of Aging|October 22, 2013
SLC1A2 rs3794087 does not associate with essential tremorJay P Ross, Sruti Rayaprolu, Cecily Q Bernales, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 4, 2016
Cerebellar ataxia in progressive supranuclear palsy: An autopsy study of PSP-CShunsuke Koga, Keith A Josephs, Kotaro Ogaki, et al.
AIDS Research and Therapy|September 30, 2025
The association of antiretroviral therapy type and duration of use with stroke in people living with HIV in ZambiaStanley Zimba, Owen Ngalamika, Emmanuel Mukambo, et al.
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