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Movement Disorders Clinical Practice
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September 29, 2023
Comparison of Live and Remote Video Ratings of the Scale for Assessment and Rating of Ataxia
Arian Taheri Amin, Jennifer Faber, Demet Önder, et al.
Mitochondrion
|
June 22, 2017
Speech and swallowing abnormalities in adults with POLG associated ataxia (POLG-A)
Adam P Vogel, Natalie Rommel, Andreas Oettinger, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 23, 2011
Retinal nerve fiber layer loss in multiple system atrophy
M Dominik Fischer, Matthis Synofzik, Robert Heidlauf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 15, 2018
The genetic nomenclature of recessive cerebellar ataxias
Malco Rossi, Mathieu Anheim, Alexandra Durr, et al.
Annals of Clinical and Translational Neurology
|
July 17, 2018
Serum neurofilament light chain is increased in hereditary spastic paraplegias
Carlo Wilke, Tim W Rattay, Holger Hengel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 24, 2022
Real-Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia
Annika Thierfelder, Jens Seemann, Natalie John, et al.
Brain : a Journal of Neurology
|
November 24, 2020
PCYT2 mutations disrupting etherlipid biosynthesis: phenotypes converging on the CDP-ethanolamine pathway
Jonathan De Winter, Danique Beijer, Willem De Ridder, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 19, 2016
Neurofilament light chain in FTD is elevated not only in cerebrospinal fluid, but also in serum
Carlo Wilke, Oliver Preische, Christian Deuschle, et al.
Molecular Neurobiology
|
April 10, 2025
Most L1CAM Is not Associated with Extracellular Vesicles in Human Biofluids and iPSC-Derived Neurons
Vaibhavi Kadam, Madeleine Wacker, Patrick Oeckl, et al.
Molecular Genetics & Genomic Medicine
|
October 22, 2014
AP5Z1/SPG48 frequency in autosomal recessive and sporadic spastic paraplegia
Nina A Schlipf, Rebecca Schüle, Sven Klimpe, et al.
Page
of 52
Search research articles
Search
Showing results (121-130 of 511) with videos related to
Sort By:
Page
of 52
Movement Disorders Clinical Practice
|
September 29, 2023
Comparison of Live and Remote Video Ratings of the Scale for Assessment and Rating of Ataxia
Arian Taheri Amin, Jennifer Faber, Demet Önder, et al.
Mitochondrion
|
June 22, 2017
Speech and swallowing abnormalities in adults with POLG associated ataxia (POLG-A)
Adam P Vogel, Natalie Rommel, Andreas Oettinger, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 23, 2011
Retinal nerve fiber layer loss in multiple system atrophy
M Dominik Fischer, Matthis Synofzik, Robert Heidlauf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 15, 2018
The genetic nomenclature of recessive cerebellar ataxias
Malco Rossi, Mathieu Anheim, Alexandra Durr, et al.
Annals of Clinical and Translational Neurology
|
July 17, 2018
Serum neurofilament light chain is increased in hereditary spastic paraplegias
Carlo Wilke, Tim W Rattay, Holger Hengel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 24, 2022
Real-Life Turning Movements Capture Subtle Longitudinal and Preataxic Changes in Cerebellar Ataxia
Annika Thierfelder, Jens Seemann, Natalie John, et al.
Brain : a Journal of Neurology
|
November 24, 2020
PCYT2 mutations disrupting etherlipid biosynthesis: phenotypes converging on the CDP-ethanolamine pathway
Jonathan De Winter, Danique Beijer, Willem De Ridder, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 19, 2016
Neurofilament light chain in FTD is elevated not only in cerebrospinal fluid, but also in serum
Carlo Wilke, Oliver Preische, Christian Deuschle, et al.
Molecular Neurobiology
|
April 10, 2025
Most L1CAM Is not Associated with Extracellular Vesicles in Human Biofluids and iPSC-Derived Neurons
Vaibhavi Kadam, Madeleine Wacker, Patrick Oeckl, et al.
Molecular Genetics & Genomic Medicine
|
October 22, 2014
AP5Z1/SPG48 frequency in autosomal recessive and sporadic spastic paraplegia
Nina A Schlipf, Rebecca Schüle, Sven Klimpe, et al.
Page
of 52