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Biochemical and Biophysical Research Communications
|
July 30, 2015
Lack of enzyme activity in GBA2 mutants associated with hereditary spastic paraplegia/cerebellar ataxia (SPG46)
Saki Sultana, Jennifer Reichbauer, Rebecca Schüle, et al.
Plos One
|
June 30, 2017
Absence of EEG correlates of self-referential processing depth in ALS
Tatiana Fomina, Sebastian Weichwald, Matthis Synofzik, et al.
Dysphagia
|
January 10, 2018
Validation and Psychometric Properties of the German Version of the SWAL-QOL
Eva-Maria Kraus, Natalie Rommel, Lisa H Stoll, et al.
Journal of Neurology
|
May 9, 2018
Serum neurofilament light is increased in multiple system atrophy of cerebellar type and in repeat-expansion spinocerebellar ataxias: a pilot study
Carlo Wilke, Friedemann Bender, Stefanie N Hayer, et al.
Molecular Therapy. Nucleic Acids
|
July 29, 2025
Tailored antisense oligonucleotides for ultrarare CNS diseases: An experience-based best practice framework for individual patient evaluation
Rebecca Schüle, Holm Graessner, Annemieke Aartsma-Rus, et al.
Journal of Neurology
|
March 10, 2026
Development and validation of the dysarthria impact scale: a patient-reported outcome for motor speech disorders
Adam P Vogel, Lisa Graf, Merit Weiß, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
June 13, 2020
Multifocal, hypoechogenic nerve thickening in Cerebrotendinous Xanthomatosis
Benjamin Roeben, Jennifer Just, Holger Hengel, et al.
Parkinsonism & Related Disorders
|
June 19, 2018
Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism
Milan Zimmermann, Carlo Wilke, Claudia Schulte, et al.
Neurology. Clinical Practice
|
September 6, 2021
Fampridine and Acetazolamide in EA2 and Related Familial EA: A Prospective Randomized Placebo-Controlled Trial
Carolin Muth, Julian Teufel, Ludger Schöls, et al.
Cerebellum (London, England)
|
January 15, 2013
Friedreich ataxia: dysarthria profile and clinical data
Bettina Brendel, Hermann Ackermann, Daniela Berg, et al.
Page
of 52
Search research articles
Search
Showing results (91-100 of 511) with videos related to
Sort By:
Page
of 52
Biochemical and Biophysical Research Communications
|
July 30, 2015
Lack of enzyme activity in GBA2 mutants associated with hereditary spastic paraplegia/cerebellar ataxia (SPG46)
Saki Sultana, Jennifer Reichbauer, Rebecca Schüle, et al.
Plos One
|
June 30, 2017
Absence of EEG correlates of self-referential processing depth in ALS
Tatiana Fomina, Sebastian Weichwald, Matthis Synofzik, et al.
Dysphagia
|
January 10, 2018
Validation and Psychometric Properties of the German Version of the SWAL-QOL
Eva-Maria Kraus, Natalie Rommel, Lisa H Stoll, et al.
Journal of Neurology
|
May 9, 2018
Serum neurofilament light is increased in multiple system atrophy of cerebellar type and in repeat-expansion spinocerebellar ataxias: a pilot study
Carlo Wilke, Friedemann Bender, Stefanie N Hayer, et al.
Molecular Therapy. Nucleic Acids
|
July 29, 2025
Tailored antisense oligonucleotides for ultrarare CNS diseases: An experience-based best practice framework for individual patient evaluation
Rebecca Schüle, Holm Graessner, Annemieke Aartsma-Rus, et al.
Journal of Neurology
|
March 10, 2026
Development and validation of the dysarthria impact scale: a patient-reported outcome for motor speech disorders
Adam P Vogel, Lisa Graf, Merit Weiß, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
June 13, 2020
Multifocal, hypoechogenic nerve thickening in Cerebrotendinous Xanthomatosis
Benjamin Roeben, Jennifer Just, Holger Hengel, et al.
Parkinsonism & Related Disorders
|
June 19, 2018
Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism
Milan Zimmermann, Carlo Wilke, Claudia Schulte, et al.
Neurology. Clinical Practice
|
September 6, 2021
Fampridine and Acetazolamide in EA2 and Related Familial EA: A Prospective Randomized Placebo-Controlled Trial
Carolin Muth, Julian Teufel, Ludger Schöls, et al.
Cerebellum (London, England)
|
January 15, 2013
Friedreich ataxia: dysarthria profile and clinical data
Bettina Brendel, Hermann Ackermann, Daniela Berg, et al.
Page
of 52