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Neurologia I Neurochirurgia Polska
|
July 21, 2020
Spinocerebellar ataxia type 6 family with phenotypic overlap with Multiple System Atrophy
Rana Hanna Al-Shaikh, Anna I Wernick, Audrey J Strongosky, et al.
Brain Pathology (Zurich, Switzerland)
|
April 2, 2020
Clinicopathologic and genetic features of multiple system atrophy with Lewy body disease
Shunsuke Koga, Fuyao Li, Na Zhao, et al.
Parkinsonism & Related Disorders
|
July 6, 2020
GBA variation and susceptibility to multiple system atrophy
Anna I Wernick, Ronald L Walton, Shunsuke Koga, et al.
Neuroscience Letters
|
February 18, 2021
Investigating ELOVL7 coding variants in multiple system atrophy
Anna I Wernick, Ronald L Walton, Alexandra I Soto-Beasley, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society
|
January 27, 2021
Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy
Anna I Wernick, Ronald L Walton, Alexandra I Soto-Beasley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 15, 2018
Multiple system atrophy and apolipoprotein E
Kotaro Ogaki, Yuka A Martens, Michael G Heckman, et al.
NPJ Parkinson'S Disease
|
November 24, 2022
Protein aggregation and calcium dysregulation are hallmarks of familial Parkinson's disease in midbrain dopaminergic neurons
Gurvir S Virdi, Minee L Choi, James R Evans, et al.
Nature Neuroscience
|
August 30, 2022
Pathological structural conversion of α-synuclein at the mitochondria induces neuronal toxicity
Minee L Choi, Alexandre Chappard, Bhanu P Singh, et al.
Nature Neuroscience
|
October 19, 2022
Author Correction: Pathological structural conversion of α-synuclein at the mitochondria induces neuronal toxicity
Minee L Choi, Alexandre Chappard, Bhanu P Singh, et al.
Science Advances
|
June 26, 2024
The annotation of <i>GBA1</i> has been concealed by its protein-coding pseudogene <i>GBAP1</i>
Emil K Gustavsson, Siddharth Sethi, Yujing Gao, et al.
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of 1
Search research articles
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Neurologia I Neurochirurgia Polska
|
July 21, 2020
Spinocerebellar ataxia type 6 family with phenotypic overlap with Multiple System Atrophy
Rana Hanna Al-Shaikh, Anna I Wernick, Audrey J Strongosky, et al.
Brain Pathology (Zurich, Switzerland)
|
April 2, 2020
Clinicopathologic and genetic features of multiple system atrophy with Lewy body disease
Shunsuke Koga, Fuyao Li, Na Zhao, et al.
Parkinsonism & Related Disorders
|
July 6, 2020
GBA variation and susceptibility to multiple system atrophy
Anna I Wernick, Ronald L Walton, Shunsuke Koga, et al.
Neuroscience Letters
|
February 18, 2021
Investigating ELOVL7 coding variants in multiple system atrophy
Anna I Wernick, Ronald L Walton, Alexandra I Soto-Beasley, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society
|
January 27, 2021
Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy
Anna I Wernick, Ronald L Walton, Alexandra I Soto-Beasley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 15, 2018
Multiple system atrophy and apolipoprotein E
Kotaro Ogaki, Yuka A Martens, Michael G Heckman, et al.
NPJ Parkinson'S Disease
|
November 24, 2022
Protein aggregation and calcium dysregulation are hallmarks of familial Parkinson's disease in midbrain dopaminergic neurons
Gurvir S Virdi, Minee L Choi, James R Evans, et al.
Nature Neuroscience
|
August 30, 2022
Pathological structural conversion of α-synuclein at the mitochondria induces neuronal toxicity
Minee L Choi, Alexandre Chappard, Bhanu P Singh, et al.
Nature Neuroscience
|
October 19, 2022
Author Correction: Pathological structural conversion of α-synuclein at the mitochondria induces neuronal toxicity
Minee L Choi, Alexandre Chappard, Bhanu P Singh, et al.
Science Advances
|
June 26, 2024
The annotation of <i>GBA1</i> has been concealed by its protein-coding pseudogene <i>GBAP1</i>
Emil K Gustavsson, Siddharth Sethi, Yujing Gao, et al.
Page
of 1