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Elizabeth Slow

Showing results (1-10 of 13) with videos related to

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Movement Disorders Clinical Practice|October 27, 2018
Dystonic Pseudo Foot DropCamila C Aquino, Elizabeth Slow, Anthony E Lang
Movement Disorders Clinical Practice|January 15, 2019
ADCK3-related Coenzyme Q10 Deficiency: A Potentially Treatable Genetic DiseaseAnna Chang, Marta Ruiz-Lopez, Elizabeth Slow, et al.
Neurobiology of Disease|May 27, 2008
Full length mutant huntingtin is required for altered Ca2+ signaling and apoptosis of striatal neurons in the YAC mouse model of Huntington's diseaseHua Zhang, Qin Li, Rona K Graham, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2017
C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonismMing Zhang, Zhengrui Xi, Karen Misquitta, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 8, 2005
Disturbed Ca2+ signaling and apoptosis of medium spiny neurons in Huntington's diseaseTie-Shan Tang, Elizabeth Slow, Vitalie Lupu, et al.
Neurobiology of Disease|February 6, 2007
Phenotypic abnormalities in the YAC128 mouse model of Huntington disease are penetrant on multiple genetic backgrounds and modulated by strainJeremy M Van Raamsdonk, Martina Metzler, Elizabeth Slow, et al.
Movement Disorders Clinical Practice|March 23, 2023
Demographics and Clinical Characteristics of Autosomal Dominant Spinocerebellar Ataxia in CanadaSohaila Alshimemeri, Danah Abo Alsamh, Lily Zhou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2020
A Distinct EEG Marker of Celiac Disease-Related Cortical MyoclonusEmily Swinkin, Karlo J Lizárraga, Musleh Algarni, et al.
Parkinsonism & Related Disorders|June 16, 2019
The clinical significance of lower limb tremorsRajasumi Rajalingam, David P Breen, Robert Chen, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 2, 2024
Rare Spinocerebellar Ataxia Types in Canada: A Case Series and Review of the LiteratureSohaila Alshimemeri, Lamya Alsaghan, Danah Abo Alsamh, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Movement Disorders Clinical Practice|October 27, 2018
Dystonic Pseudo Foot DropCamila C Aquino, Elizabeth Slow, Anthony E Lang
Movement Disorders Clinical Practice|January 15, 2019
ADCK3-related Coenzyme Q10 Deficiency: A Potentially Treatable Genetic DiseaseAnna Chang, Marta Ruiz-Lopez, Elizabeth Slow, et al.
Neurobiology of Disease|May 27, 2008
Full length mutant huntingtin is required for altered Ca2+ signaling and apoptosis of striatal neurons in the YAC mouse model of Huntington's diseaseHua Zhang, Qin Li, Rona K Graham, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2017
C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonismMing Zhang, Zhengrui Xi, Karen Misquitta, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 8, 2005
Disturbed Ca2+ signaling and apoptosis of medium spiny neurons in Huntington's diseaseTie-Shan Tang, Elizabeth Slow, Vitalie Lupu, et al.
Neurobiology of Disease|February 6, 2007
Phenotypic abnormalities in the YAC128 mouse model of Huntington disease are penetrant on multiple genetic backgrounds and modulated by strainJeremy M Van Raamsdonk, Martina Metzler, Elizabeth Slow, et al.
Movement Disorders Clinical Practice|March 23, 2023
Demographics and Clinical Characteristics of Autosomal Dominant Spinocerebellar Ataxia in CanadaSohaila Alshimemeri, Danah Abo Alsamh, Lily Zhou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2020
A Distinct EEG Marker of Celiac Disease-Related Cortical MyoclonusEmily Swinkin, Karlo J Lizárraga, Musleh Algarni, et al.
Parkinsonism & Related Disorders|June 16, 2019
The clinical significance of lower limb tremorsRajasumi Rajalingam, David P Breen, Robert Chen, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 2, 2024
Rare Spinocerebellar Ataxia Types in Canada: A Case Series and Review of the LiteratureSohaila Alshimemeri, Lamya Alsaghan, Danah Abo Alsamh, et al.
Pageof 2