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Mathieu Anheim

Showing results (1-10 of 189) with videos related to

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Presse Medicale (Paris, France : 1983)|May 16, 2009
[Autosomal recessive cerebellar ataxias]Christine Tranchant, Mathieu Anheim
La Revue Du Praticien|November 21, 2007
[Motor and sensory deficit in the limbs]Mathieu Anheim, Christine Tranchant
La Revue Du Praticien|December 6, 2011
[Sudden onset sensorimotor deficit: first consider stroke]Christine Tranchant, Mathieu Anheim
The New England Journal of Medicine|February 17, 2012
The autosomal recessive cerebellar ataxiasMathieu Anheim, Christine Tranchant, Michel Koenig
JAMA Neurology|February 10, 2015
Autosomal recessive cerebellar ataxia 3 due to homozygote c.132dupA mutation within the ANO10 gene--replyMichel Koenig, Christine Tranchant, Mathieu Anheim
Parkinsonism & Related Disorders|March 4, 2017
Parkinsonian-Pyramidal syndromes: A systematic reviewChristine Tranchant, Meriam Koob, Mathieu Anheim
Frontiers in Psychology|August 28, 2020
Joint Consultation by a Neurogeneticist of Movement Disorders and a Psychodynamic Psychotherapist: An Occasion for SubjectivizationOlivier Putois, Marie-Frédérique Bacqué, Mathieu Anheim
Movement Disorders : Official Journal of the Movement Disorder Society|October 12, 2020
Autosomal Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common BiomarkerMathilde Renaud, Christine Tranchant, Michel Koenig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 22, 2021
Reply to: "Autosomal-Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common Biomarker"Mathilde Renaud, Christine Tranchant, Michel Koenig, et al.
Cerebellum (London, England)|January 15, 2020
Recessive Ataxia Differential Diagnosis Algorithm (RADIAL) Versus Specific Niemann-Pick Type C Suspicion Indices: A Retrospective Algorithm ComparisonMathieu Anheim, Juan V Torres Martin, Stefan A Kolb
Pageof 19

Showing results (1-10 of 189) with videos related to

Sort By:
Pageof 19
Presse Medicale (Paris, France : 1983)|May 16, 2009
[Autosomal recessive cerebellar ataxias]Christine Tranchant, Mathieu Anheim
La Revue Du Praticien|November 21, 2007
[Motor and sensory deficit in the limbs]Mathieu Anheim, Christine Tranchant
La Revue Du Praticien|December 6, 2011
[Sudden onset sensorimotor deficit: first consider stroke]Christine Tranchant, Mathieu Anheim
The New England Journal of Medicine|February 17, 2012
The autosomal recessive cerebellar ataxiasMathieu Anheim, Christine Tranchant, Michel Koenig
JAMA Neurology|February 10, 2015
Autosomal recessive cerebellar ataxia 3 due to homozygote c.132dupA mutation within the ANO10 gene--replyMichel Koenig, Christine Tranchant, Mathieu Anheim
Parkinsonism & Related Disorders|March 4, 2017
Parkinsonian-Pyramidal syndromes: A systematic reviewChristine Tranchant, Meriam Koob, Mathieu Anheim
Frontiers in Psychology|August 28, 2020
Joint Consultation by a Neurogeneticist of Movement Disorders and a Psychodynamic Psychotherapist: An Occasion for SubjectivizationOlivier Putois, Marie-Frédérique Bacqué, Mathieu Anheim
Movement Disorders : Official Journal of the Movement Disorder Society|October 12, 2020
Autosomal Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common BiomarkerMathilde Renaud, Christine Tranchant, Michel Koenig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 22, 2021
Reply to: "Autosomal-Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common Biomarker"Mathilde Renaud, Christine Tranchant, Michel Koenig, et al.
Cerebellum (London, England)|January 15, 2020
Recessive Ataxia Differential Diagnosis Algorithm (RADIAL) Versus Specific Niemann-Pick Type C Suspicion Indices: A Retrospective Algorithm ComparisonMathieu Anheim, Juan V Torres Martin, Stefan A Kolb
Pageof 19