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

M Anheim

Showing results (31-40 of 49) with videos related to

Pageof 5
Sort By:
Neurology|January 28, 2012
Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriersM Anheim, A Elbaz, S Lesage, et al.
Revue Neurologique|December 13, 2005
[Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) in patients with solid organ transplantation: a clinical, neurophysiological and neuropathological study of 4 cases]A Echaniz-Laguna, M Anheim, P Wolf, et al.
Journal of Neurology|January 16, 2020
Brain MRI of multiple system atrophy of cerebellar type: a prospective study with implications for diagnosis criteriaG Carré, J L Dietemann, O Gebus, et al.
Neurology|January 19, 2011
Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North AfricaS Lesage, C Condroyer, N Hecham, et al.
Cerebellum (London, England)|April 10, 2026
RFC1-related disorders: A case series of 4-aminopyridine and acetyl-DL-leucine treatmentF Heindl, A Traschütz, M Synofzik, et al.
Revue Neurologique|September 24, 2022
Early hyperdopaminergic state following sub-thalamic nucleus deep brain stimulation in Parkinson diseaseF Lamy, O Lagha-Boukbiza, T Wirth, et al.
NPJ Parkinson'S Disease|April 24, 2025
Improvement of apathy in early Parkinson's diseaseA Castrioto, E Schmitt, M Anheim, et al.
Journal of Neurology|August 8, 2014
Anti-Hu-associated brainstem encephalitis with ganglioneuroblastoma in a young adultS Montaut, M Mallaret, A Echaniz Laguna, et al.
Brain : a Journal of Neurology|May 2, 2007
A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23M Gribaa, M Salih, M Anheim, et al.
Neurogenetics|May 15, 2009
Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical managementM Anheim, M Fleury, B Monga, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Neurology|January 28, 2012
Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriersM Anheim, A Elbaz, S Lesage, et al.
Revue Neurologique|December 13, 2005
[Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) in patients with solid organ transplantation: a clinical, neurophysiological and neuropathological study of 4 cases]A Echaniz-Laguna, M Anheim, P Wolf, et al.
Journal of Neurology|January 16, 2020
Brain MRI of multiple system atrophy of cerebellar type: a prospective study with implications for diagnosis criteriaG Carré, J L Dietemann, O Gebus, et al.
Neurology|January 19, 2011
Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North AfricaS Lesage, C Condroyer, N Hecham, et al.
Cerebellum (London, England)|April 10, 2026
RFC1-related disorders: A case series of 4-aminopyridine and acetyl-DL-leucine treatmentF Heindl, A Traschütz, M Synofzik, et al.
Revue Neurologique|September 24, 2022
Early hyperdopaminergic state following sub-thalamic nucleus deep brain stimulation in Parkinson diseaseF Lamy, O Lagha-Boukbiza, T Wirth, et al.
NPJ Parkinson'S Disease|April 24, 2025
Improvement of apathy in early Parkinson's diseaseA Castrioto, E Schmitt, M Anheim, et al.
Journal of Neurology|August 8, 2014
Anti-Hu-associated brainstem encephalitis with ganglioneuroblastoma in a young adultS Montaut, M Mallaret, A Echaniz Laguna, et al.
Brain : a Journal of Neurology|May 2, 2007
A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23M Gribaa, M Salih, M Anheim, et al.
Neurogenetics|May 15, 2009
Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical managementM Anheim, M Fleury, B Monga, et al.
Pageof 5