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Neurology
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January 21, 2022
Cerebellum Dysfunction in Patients With <i>PRRT2</i>-Related Paroxysmal Dyskinesia
Asya Ekmen, Aurelie Meneret, Romain Valabregue, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 31, 2026
Psychiatric Disorders and Apathy in Mixed Movement Disorders Linked to ADCY5 (MxMD-ADCY5)
Aurélie Méneret, Clément Tarrano, Asya Ekmen, et al.
Journal of Alzheimer'S Disease : JAD
|
November 19, 2016
APP Mutations in Cerebral Amyloid Angiopathy with or without Cortical Calcifications: Report of Three Families and a Literature Review
François Sellal, David Wallon, Laurent Martinez-Almoyna, et al.
European Journal of Human Genetics : EJHG
|
April 2, 2015
Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy
Gaël Nicolas, David Wallon, Claudia Goupil, et al.
Brain Communications
|
November 11, 2025
Clinical and molecular landscape of paediatric cerebral and spinal cavernous malformations
Sandro Benichi, Estelle Balducci, Joseph Benzakoun, et al.
Brain : a Journal of Neurology
|
April 27, 2017
A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies
Marie Coutelier, Giulia Coarelli, Marie-Lorraine Monin, et al.
The Journal of Clinical Investigation
|
September 26, 2017
Mutations in the netrin-1 gene cause congenital mirror movements
Aurélie Méneret, Elizabeth A Franz, Oriane Trouillard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 8, 2021
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients
Marie Le Roux, Magalie Barth, Sophie Gueden, et al.
Neurology
|
October 15, 2021
Hemiplegic Migraine Associated With <i>PRRT2</i> Variations: A Clinical and Genetic Study
Florence Riant, Caroline Roos, Agathe Roubertie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 13, 2018
Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies
Stéphanie Valence, Emmanuelle Cochet, Christelle Rougeot, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 68) with videos related to
Sort By:
Page
of 7
Neurology
|
January 21, 2022
Cerebellum Dysfunction in Patients With <i>PRRT2</i>-Related Paroxysmal Dyskinesia
Asya Ekmen, Aurelie Meneret, Romain Valabregue, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 31, 2026
Psychiatric Disorders and Apathy in Mixed Movement Disorders Linked to ADCY5 (MxMD-ADCY5)
Aurélie Méneret, Clément Tarrano, Asya Ekmen, et al.
Journal of Alzheimer'S Disease : JAD
|
November 19, 2016
APP Mutations in Cerebral Amyloid Angiopathy with or without Cortical Calcifications: Report of Three Families and a Literature Review
François Sellal, David Wallon, Laurent Martinez-Almoyna, et al.
European Journal of Human Genetics : EJHG
|
April 2, 2015
Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy
Gaël Nicolas, David Wallon, Claudia Goupil, et al.
Brain Communications
|
November 11, 2025
Clinical and molecular landscape of paediatric cerebral and spinal cavernous malformations
Sandro Benichi, Estelle Balducci, Joseph Benzakoun, et al.
Brain : a Journal of Neurology
|
April 27, 2017
A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies
Marie Coutelier, Giulia Coarelli, Marie-Lorraine Monin, et al.
The Journal of Clinical Investigation
|
September 26, 2017
Mutations in the netrin-1 gene cause congenital mirror movements
Aurélie Méneret, Elizabeth A Franz, Oriane Trouillard, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 8, 2021
CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients
Marie Le Roux, Magalie Barth, Sophie Gueden, et al.
Neurology
|
October 15, 2021
Hemiplegic Migraine Associated With <i>PRRT2</i> Variations: A Clinical and Genetic Study
Florence Riant, Caroline Roos, Agathe Roubertie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 13, 2018
Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies
Stéphanie Valence, Emmanuelle Cochet, Christelle Rougeot, et al.
Page
of 7