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Developmental Medicine and Child Neurology
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June 7, 2022
Early identification of children with myoclonus-dystonia: Is it time for a revision of diagnostic criteria?
Emmanuel Roze
Movement Disorders Clinical Practice
|
May 8, 2019
GLUT1 Deficiency in a Patient Diagnosed as Cerebral Palsy: Is NGS a Valuable Tool to Be Considered in All Cases of CP to Detect Underlying Genetic Disorders?
Aurélie Méneret, Emmanuel Roze
The Lancet. Neurology
|
October 25, 2020
Dystonia: genetics, phenomenology, and pathophysiology
Marie Vidailhet, Aurelie Méneret, Emmanuel Roze
Pediatric Neurology
|
August 1, 2015
Spasmus Nutans: More Than Meets the Eye
Cécile Delorme, Domitille Gras, Emmanuel Roze
Current Opinion in Neurology
|
June 11, 2009
Pathophysiology of dystonia
Marie Vidailhet, David Grabli, Emmanuel Roze
Pediatric Neurology
|
February 19, 2017
Alternating Upper Limb Monoplegia due to ATP1A3 Mutation
Cécile Delorme, Elodie Hainque, Emmanuel Roze
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 25, 2025
Corticospinal Tract Development, Evolution, and Skilled Movements
Emmanuel Roze, Caroline Dubacq, Quentin Welniarz
Current Opinion in Neurology
|
July 9, 2008
Pathophysiology of Huntington's disease: from huntingtin functions to potential treatments
Emmanuel Roze, Frédéric Saudou, Jocelyne Caboche
Developmental Neurobiology
|
October 6, 2016
The corticospinal tract: Evolution, development, and human disorders
Quentin Welniarz, Isabelle Dusart, Emmanuel Roze
Current Opinion in Neurology
|
June 29, 2018
Myoclonus-dystonia: classification, phenomenology, pathogenesis, and treatment
Emmanuel Roze, Anthony E Lang, Marie Vidailhet
Page
of 34
Search research articles
Search
Showing results (1-10 of 331) with videos related to
Sort By:
Page
of 34
Developmental Medicine and Child Neurology
|
June 7, 2022
Early identification of children with myoclonus-dystonia: Is it time for a revision of diagnostic criteria?
Emmanuel Roze
Movement Disorders Clinical Practice
|
May 8, 2019
GLUT1 Deficiency in a Patient Diagnosed as Cerebral Palsy: Is NGS a Valuable Tool to Be Considered in All Cases of CP to Detect Underlying Genetic Disorders?
Aurélie Méneret, Emmanuel Roze
The Lancet. Neurology
|
October 25, 2020
Dystonia: genetics, phenomenology, and pathophysiology
Marie Vidailhet, Aurelie Méneret, Emmanuel Roze
Pediatric Neurology
|
August 1, 2015
Spasmus Nutans: More Than Meets the Eye
Cécile Delorme, Domitille Gras, Emmanuel Roze
Current Opinion in Neurology
|
June 11, 2009
Pathophysiology of dystonia
Marie Vidailhet, David Grabli, Emmanuel Roze
Pediatric Neurology
|
February 19, 2017
Alternating Upper Limb Monoplegia due to ATP1A3 Mutation
Cécile Delorme, Elodie Hainque, Emmanuel Roze
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 25, 2025
Corticospinal Tract Development, Evolution, and Skilled Movements
Emmanuel Roze, Caroline Dubacq, Quentin Welniarz
Current Opinion in Neurology
|
July 9, 2008
Pathophysiology of Huntington's disease: from huntingtin functions to potential treatments
Emmanuel Roze, Frédéric Saudou, Jocelyne Caboche
Developmental Neurobiology
|
October 6, 2016
The corticospinal tract: Evolution, development, and human disorders
Quentin Welniarz, Isabelle Dusart, Emmanuel Roze
Current Opinion in Neurology
|
June 29, 2018
Myoclonus-dystonia: classification, phenomenology, pathogenesis, and treatment
Emmanuel Roze, Anthony E Lang, Marie Vidailhet
Page
of 34