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Frontiers in Digital Health
|
September 19, 2025
Clinic vs. daily life gait characteristics in patients with spinocerebellar ataxia
Vrutangkumar V Shah, Daniel Muzyka, Adam Jagodinsky, et al.
Plos One
|
April 12, 2011
Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)
Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al.
Neuron
|
March 30, 2019
α1ACT Is Essential for Survival and Early Cerebellar Programming in a Critical Neonatal Window
Xiaofei Du, Cenfu Wei, Daniel Parviz Hejazi Pastor, et al.
Cerebellum (London, England)
|
April 25, 2026
MT-ATP6 9035T>C Variant Causes Ataxia With Azoospermia and Apparent Anticipation in a Four-generation Kindred
Changrui Xiao, David Zhu, Jon Pryor, et al.
Experimental Neurology
|
December 3, 2014
Fluoxetine is neuroprotective in slow-channel congenital myasthenic syndrome
Haipeng Zhu, Gary E Grajales-Reyes, Vivianette Alicea-Vázquez, et al.
Frontiers in Neurology
|
April 1, 2025
Gait characteristics in people with Friedreich ataxia: daily life versus clinic measures
Hannah L Casey, Vrutangkumar V Shah, Daniel Muzyka, et al.
Movement Disorders Clinical Practice
|
September 21, 2019
Sensitivity of Volumetric Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy to Progression of Spinocerebellar Ataxia Type 1
Dinesh K Deelchand, James M Joers, Adarsh Ravishankar, et al.
American Journal of Medical Genetics
|
July 13, 2002
Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7
Rong Mao, Arthur S Aylsworth, Nicholas Potter, et al.
Molecular and Cellular Neurosciences
|
April 21, 2006
Novel beta subunit mutation causes a slow-channel syndrome by enhancing activation and decreasing the rate of agonist dissociation
Manuel F Navedo, José A Lasalde-Dominicci, Carlos A Báez-Pagán, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 22, 2013
Stable respiratory activity requires both P/Q-type and N-type voltage-gated calcium channels
Henner Koch, Sebastien Zanella, Gina E Elsen, et al.
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of 13
Search research articles
Search
Showing results (71-80 of 128) with videos related to
Sort By:
Page
of 13
Frontiers in Digital Health
|
September 19, 2025
Clinic vs. daily life gait characteristics in patients with spinocerebellar ataxia
Vrutangkumar V Shah, Daniel Muzyka, Adam Jagodinsky, et al.
Plos One
|
April 12, 2011
Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)
Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al.
Neuron
|
March 30, 2019
α1ACT Is Essential for Survival and Early Cerebellar Programming in a Critical Neonatal Window
Xiaofei Du, Cenfu Wei, Daniel Parviz Hejazi Pastor, et al.
Cerebellum (London, England)
|
April 25, 2026
MT-ATP6 9035T>C Variant Causes Ataxia With Azoospermia and Apparent Anticipation in a Four-generation Kindred
Changrui Xiao, David Zhu, Jon Pryor, et al.
Experimental Neurology
|
December 3, 2014
Fluoxetine is neuroprotective in slow-channel congenital myasthenic syndrome
Haipeng Zhu, Gary E Grajales-Reyes, Vivianette Alicea-Vázquez, et al.
Frontiers in Neurology
|
April 1, 2025
Gait characteristics in people with Friedreich ataxia: daily life versus clinic measures
Hannah L Casey, Vrutangkumar V Shah, Daniel Muzyka, et al.
Movement Disorders Clinical Practice
|
September 21, 2019
Sensitivity of Volumetric Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy to Progression of Spinocerebellar Ataxia Type 1
Dinesh K Deelchand, James M Joers, Adarsh Ravishankar, et al.
American Journal of Medical Genetics
|
July 13, 2002
Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7
Rong Mao, Arthur S Aylsworth, Nicholas Potter, et al.
Molecular and Cellular Neurosciences
|
April 21, 2006
Novel beta subunit mutation causes a slow-channel syndrome by enhancing activation and decreasing the rate of agonist dissociation
Manuel F Navedo, José A Lasalde-Dominicci, Carlos A Báez-Pagán, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 22, 2013
Stable respiratory activity requires both P/Q-type and N-type voltage-gated calcium channels
Henner Koch, Sebastien Zanella, Gina E Elsen, et al.
Page
of 13