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Science Translational Medicine
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September 13, 2021
4-Aminopyridine is a promising treatment option for patients with gain-of-function <i>KCNA2</i>-encephalopathy
Ulrike B S Hedrich, Stephan Lauxmann, Markus Wolff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 29, 2021
Characterization of Lifestyle in Spinocerebellar Ataxia Type 3 and Association with Disease Severity
Holger Hengel, Peter Martus, Jennifer Faber, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 4, 2022
Autosomal Recessive Cerebellar Ataxias in South America: A Multicenter Study of 1338 Patients
Maria Thereza D Gama, Pedro Braga-Neto, Deborah M Rangel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 9, 2022
Differential Temporal Dynamics of Axial and Appendicular Ataxia in SCA3
Roderick P P W M Maas, Steven Teerenstra, Manuela Lima, et al.
Current Medical Research and Opinion
|
March 10, 2017
The hidden Niemann-Pick type C patient: clinical niches for a rare inherited metabolic disease
Christian J Hendriksz, Mathieu Anheim, Peter Bauer, et al.
Journal of Neurology
|
December 21, 2024
Subtypes of cognitive impairment in cerebellar disease identified by cross-diagnostic cluster-analysis: results from a German multicenter study
Qi Liu, Kerstin Rubarth, Jennifer Faber, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 26, 2024
Neuroradiological findings in GAA-<i>FGF14</i> ataxia (SCA27B): more than cerebellar atrophy
Shihan Chen, Catherine Ashton, Rawan Sakalla, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 14, 2022
Adult-Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERD<sub>ND</sub> ): Time to Move Beyond the Skin
Isabell Cordts, Demet Önder, Andreas Traschütz, et al.
Journal of Neurology
|
November 3, 2022
The frequency of non-motor symptoms in SCA3 and their association with disease severity and lifestyle factors
Holger Hengel, Peter Martus, Jennifer Faber, et al.
Alzheimer'S Research & Therapy
|
May 3, 2022
Comparative analysis of machine learning algorithms for multi-syndrome classification of neurodegenerative syndromes
Leonie Lampe, Sebastian Niehaus, Hans-Jürgen Huppertz, et al.
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of 52
Search research articles
Search
Showing results (311-320 of 511) with videos related to
Sort By:
Page
of 52
Science Translational Medicine
|
September 13, 2021
4-Aminopyridine is a promising treatment option for patients with gain-of-function <i>KCNA2</i>-encephalopathy
Ulrike B S Hedrich, Stephan Lauxmann, Markus Wolff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 29, 2021
Characterization of Lifestyle in Spinocerebellar Ataxia Type 3 and Association with Disease Severity
Holger Hengel, Peter Martus, Jennifer Faber, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 4, 2022
Autosomal Recessive Cerebellar Ataxias in South America: A Multicenter Study of 1338 Patients
Maria Thereza D Gama, Pedro Braga-Neto, Deborah M Rangel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 9, 2022
Differential Temporal Dynamics of Axial and Appendicular Ataxia in SCA3
Roderick P P W M Maas, Steven Teerenstra, Manuela Lima, et al.
Current Medical Research and Opinion
|
March 10, 2017
The hidden Niemann-Pick type C patient: clinical niches for a rare inherited metabolic disease
Christian J Hendriksz, Mathieu Anheim, Peter Bauer, et al.
Journal of Neurology
|
December 21, 2024
Subtypes of cognitive impairment in cerebellar disease identified by cross-diagnostic cluster-analysis: results from a German multicenter study
Qi Liu, Kerstin Rubarth, Jennifer Faber, et al.
Medrxiv : the Preprint Server for Health Sciences
|
February 26, 2024
Neuroradiological findings in GAA-<i>FGF14</i> ataxia (SCA27B): more than cerebellar atrophy
Shihan Chen, Catherine Ashton, Rawan Sakalla, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 14, 2022
Adult-Onset Neurodegeneration in Nucleotide Excision Repair Disorders (NERD<sub>ND</sub> ): Time to Move Beyond the Skin
Isabell Cordts, Demet Önder, Andreas Traschütz, et al.
Journal of Neurology
|
November 3, 2022
The frequency of non-motor symptoms in SCA3 and their association with disease severity and lifestyle factors
Holger Hengel, Peter Martus, Jennifer Faber, et al.
Alzheimer'S Research & Therapy
|
May 3, 2022
Comparative analysis of machine learning algorithms for multi-syndrome classification of neurodegenerative syndromes
Leonie Lampe, Sebastian Niehaus, Hans-Jürgen Huppertz, et al.
Page
of 52