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M Anheim

Showing results (21-30 of 49) with videos related to

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Revue Neurologique|January 18, 2021
Paroxysmal dyskinesia: When a PRRT2 variant hides a curable causeV Schneider, M Ferrari-Henquinet, A O Diallo, et al.
Revue Neurologique|June 17, 2008
[Severe generalized dystonia due to postradiotherapy cerebral calcifications]J-B Chanson, M Anheim, O Lagha-Boukbiza, et al.
European Journal of Neurology|October 12, 2018
Mitochondrial disease and amyloidosis in a patient with familial polyneuropathyO Gebus, M Fleury, J-B Chanson, et al.
Revue Neurologique|December 17, 2004
[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy]B Degos, A Echaniz-Laguna, P Latour, et al.
Parkinsonism & Related Disorders|May 28, 2017
Severe early-onset impulsive compulsive behavior and psychosis in PLA2G6-related juvenile Parkinson's diseaseT Wirth, S Weibel, S Montaut, et al.
Clinical Genetics|August 11, 2010
Unexpected combination of inherited chorea-acanthocytosis with MDR3 (ABCB4) defect mimicking Wilson's diseaseM Anheim, P Chamouard, G Rudolf, et al.
Revue Neurologique|April 25, 2018
Progressive encephalomyelitis with rigidity and myoclonus, a diagnostic challengeT Wirth, C Kaeuffer, J B Chanson, et al.
Journal of the Neurological Sciences|April 23, 2017
Xeroderma pigmentosum complementation group F: A rare cause of cerebellar ataxia with choreaG Carré, C Marelli, M Anheim, et al.
Revue Neurologique|April 29, 2008
[Autosomal recessive spastic ataxia of Charlevoix-Saguenay: study of a family and review of the literature]M Anheim, D Chaigne, M Fleury, et al.
Journal of Neurology|June 30, 2018
Prospective study of relevance of <sup>123</sup>I-MIBG myocardial scintigraphy and clonidine GH test to distinguish Parkinson's disease and multiple system atrophyC Alves Do Rego, I J Namer, C Marcel, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Revue Neurologique|January 18, 2021
Paroxysmal dyskinesia: When a PRRT2 variant hides a curable causeV Schneider, M Ferrari-Henquinet, A O Diallo, et al.
Revue Neurologique|June 17, 2008
[Severe generalized dystonia due to postradiotherapy cerebral calcifications]J-B Chanson, M Anheim, O Lagha-Boukbiza, et al.
European Journal of Neurology|October 12, 2018
Mitochondrial disease and amyloidosis in a patient with familial polyneuropathyO Gebus, M Fleury, J-B Chanson, et al.
Revue Neurologique|December 17, 2004
[Hereditary neuropathy with liability to pressure palsy presenting with an acute inflammatory demyelinating polyneuropathy]B Degos, A Echaniz-Laguna, P Latour, et al.
Parkinsonism & Related Disorders|May 28, 2017
Severe early-onset impulsive compulsive behavior and psychosis in PLA2G6-related juvenile Parkinson's diseaseT Wirth, S Weibel, S Montaut, et al.
Clinical Genetics|August 11, 2010
Unexpected combination of inherited chorea-acanthocytosis with MDR3 (ABCB4) defect mimicking Wilson's diseaseM Anheim, P Chamouard, G Rudolf, et al.
Revue Neurologique|April 25, 2018
Progressive encephalomyelitis with rigidity and myoclonus, a diagnostic challengeT Wirth, C Kaeuffer, J B Chanson, et al.
Journal of the Neurological Sciences|April 23, 2017
Xeroderma pigmentosum complementation group F: A rare cause of cerebellar ataxia with choreaG Carré, C Marelli, M Anheim, et al.
Revue Neurologique|April 29, 2008
[Autosomal recessive spastic ataxia of Charlevoix-Saguenay: study of a family and review of the literature]M Anheim, D Chaigne, M Fleury, et al.
Journal of Neurology|June 30, 2018
Prospective study of relevance of <sup>123</sup>I-MIBG myocardial scintigraphy and clonidine GH test to distinguish Parkinson's disease and multiple system atrophyC Alves Do Rego, I J Namer, C Marcel, et al.
Pageof 5