Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Philippe Petiot

Showing results (21-30 of 36) with videos related to

Pageof 4
Sort By:
Rheumatology (Oxford, England)|July 18, 2023
Inaugural dropped head syndrome and camptocormia in inflammatory myopathies: a retrospective studyMarie Robert, Lola E R Lessard, Françoise Bouhour, et al.
Journal of Neurology|August 4, 2023
Peripheral nervous system involvement accompanies central nervous system involvement in anti-glial fibrillary acidic protein (GFAP) antibody-related diseaseJulian Theuriet, Florent Cluse, Alice Gravier-Dumonceau, et al.
Neurology|October 25, 2013
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutationsKarine Auré, Odile Dubourg, Claude Jardel, et al.
European Journal of Neurology|April 16, 2026
Clinical Features and Prognosis of SEPTIN9-Related Hereditary Neuralgic AmyotrophyJulian Theuriet, Isabelle Quadrio, Frédéric Fer, et al.
Human Mutation|February 2, 2017
Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel MutationsAndoni Echaniz-Laguna, Thomas Geuens, Philippe Petiot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 27, 2017
Anti-MAG antibodies in 202 patients: clinicopathological and therapeutic featuresJuliette Svahn, Philippe Petiot, Jean-Christophe Antoine, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 14, 2021
Charcot-Marie-Tooth disease type 2CC due to <i>NEFH</i> variants causes a progressive, non-length-dependent, motor-predominant phenotypeMenelaos Pipis, Andrea Cortese, James M Polke, et al.
Neurology. Genetics|December 22, 2017
Clinical heterogeneity and phenotype/genotype findings in 5 families with <i>GYG1</i> deficiencyRabah Ben Yaou, Aurélie Hubert, Isabelle Nelson, et al.
Neurology|April 14, 2019
FSHD1 and FSHD2 form a disease continuumSabrina Sacconi, Audrey Briand-Suleau, Marilyn Gros, et al.
European Journal of Neurology|March 20, 2026
Multiple Mononeuropathy Secondary to Parvovirus B19 Infection: A Case SeriesJulian Theuriet, Maud Michaud, Guillaume Fargeot, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Rheumatology (Oxford, England)|July 18, 2023
Inaugural dropped head syndrome and camptocormia in inflammatory myopathies: a retrospective studyMarie Robert, Lola E R Lessard, Françoise Bouhour, et al.
Journal of Neurology|August 4, 2023
Peripheral nervous system involvement accompanies central nervous system involvement in anti-glial fibrillary acidic protein (GFAP) antibody-related diseaseJulian Theuriet, Florent Cluse, Alice Gravier-Dumonceau, et al.
Neurology|October 25, 2013
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutationsKarine Auré, Odile Dubourg, Claude Jardel, et al.
European Journal of Neurology|April 16, 2026
Clinical Features and Prognosis of SEPTIN9-Related Hereditary Neuralgic AmyotrophyJulian Theuriet, Isabelle Quadrio, Frédéric Fer, et al.
Human Mutation|February 2, 2017
Axonal Neuropathies due to Mutations in Small Heat Shock Proteins: Clinical, Genetic, and Functional Insights into Novel MutationsAndoni Echaniz-Laguna, Thomas Geuens, Philippe Petiot, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 27, 2017
Anti-MAG antibodies in 202 patients: clinicopathological and therapeutic featuresJuliette Svahn, Philippe Petiot, Jean-Christophe Antoine, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 14, 2021
Charcot-Marie-Tooth disease type 2CC due to <i>NEFH</i> variants causes a progressive, non-length-dependent, motor-predominant phenotypeMenelaos Pipis, Andrea Cortese, James M Polke, et al.
Neurology. Genetics|December 22, 2017
Clinical heterogeneity and phenotype/genotype findings in 5 families with <i>GYG1</i> deficiencyRabah Ben Yaou, Aurélie Hubert, Isabelle Nelson, et al.
Neurology|April 14, 2019
FSHD1 and FSHD2 form a disease continuumSabrina Sacconi, Audrey Briand-Suleau, Marilyn Gros, et al.
European Journal of Neurology|March 20, 2026
Multiple Mononeuropathy Secondary to Parvovirus B19 Infection: A Case SeriesJulian Theuriet, Maud Michaud, Guillaume Fargeot, et al.
Pageof 4