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Christophe Verny

Showing results (11-20 of 92) with videos related to

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Brain and Cognition|January 5, 2005
Arithmetic word-problem-solving in Huntington's diseasePhilippe Allain, Christophe Verny, Ghislaine Aubin, et al.
Neuromuscular Disorders : NMD|August 29, 2006
Refsum's disease may mimic familial Guillain Barre syndromeChristophe Verny, Adriana Prundean, Guillaume Nicolas, et al.
Journal of the Peripheral Nervous System : JPNS|October 11, 2008
Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African originJulien Cassereau, Christian Lavigne, Franck Letournel, et al.
European Journal of Neurology|October 2, 2025
Camptocormia as a Phenotypic Variant of FSHD in the Elderly: Clinical, Genetic, and Imaging FeaturesEleonora Torchia, Patrick Vandeputte, Mauro Monforte, et al.
Brain Communications|December 11, 2024
Opa1 and MT-Nd6 mutations induce early mitochondrial changes in the retina and prelaminar optic nerve of hereditary optic neuropathy mouse modelsJacques Bureau, Florence Manero, Olivier Baris, et al.
Clinical Neurology and Neurosurgery|June 12, 2013
Adult-onset cerebral X-linked adrenoleukodystrophy with major contrast-enhancement mimicking acquired diseaseClarisse Carra-Dalliere, Clarisse Scherer, Xavier Ayrignac, et al.
Archives of Dermatology|March 19, 2008
Heterozygosity for a single mutation in the ABCC6 gene may closely mimic PXE: consequences of this phenotype overlap for the definition of PXELudovic Martin, Frédéric Maître, Pierre Bonicel, et al.
American Journal of Human Genetics|August 6, 2003
Estimation of the inbreeding coefficient through use of genomic dataAnne-Louise Leutenegger, Bernard Prum, Emmanuelle Génin, et al.
Neuropsychology|July 7, 2011
Evidence for deficits on different components of theory of mind in Huntington's diseasePhilippe Allain, Valérie Havet-Thomassin, Christophe Verny, et al.
Neuromuscular Disorders : NMD|August 15, 2025
McLeod syndrome mimicking mitochondrial myopathy due to a novel in-frame duplication in the XK geneMaelle Garnier, Juliette Nectoux, Thomas Smol, et al.
Pageof 10

Showing results (11-20 of 92) with videos related to

Sort By:
Pageof 10
Brain and Cognition|January 5, 2005
Arithmetic word-problem-solving in Huntington's diseasePhilippe Allain, Christophe Verny, Ghislaine Aubin, et al.
Neuromuscular Disorders : NMD|August 29, 2006
Refsum's disease may mimic familial Guillain Barre syndromeChristophe Verny, Adriana Prundean, Guillaume Nicolas, et al.
Journal of the Peripheral Nervous System : JPNS|October 11, 2008
Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African originJulien Cassereau, Christian Lavigne, Franck Letournel, et al.
European Journal of Neurology|October 2, 2025
Camptocormia as a Phenotypic Variant of FSHD in the Elderly: Clinical, Genetic, and Imaging FeaturesEleonora Torchia, Patrick Vandeputte, Mauro Monforte, et al.
Brain Communications|December 11, 2024
Opa1 and MT-Nd6 mutations induce early mitochondrial changes in the retina and prelaminar optic nerve of hereditary optic neuropathy mouse modelsJacques Bureau, Florence Manero, Olivier Baris, et al.
Clinical Neurology and Neurosurgery|June 12, 2013
Adult-onset cerebral X-linked adrenoleukodystrophy with major contrast-enhancement mimicking acquired diseaseClarisse Carra-Dalliere, Clarisse Scherer, Xavier Ayrignac, et al.
Archives of Dermatology|March 19, 2008
Heterozygosity for a single mutation in the ABCC6 gene may closely mimic PXE: consequences of this phenotype overlap for the definition of PXELudovic Martin, Frédéric Maître, Pierre Bonicel, et al.
American Journal of Human Genetics|August 6, 2003
Estimation of the inbreeding coefficient through use of genomic dataAnne-Louise Leutenegger, Bernard Prum, Emmanuelle Génin, et al.
Neuropsychology|July 7, 2011
Evidence for deficits on different components of theory of mind in Huntington's diseasePhilippe Allain, Valérie Havet-Thomassin, Christophe Verny, et al.
Neuromuscular Disorders : NMD|August 15, 2025
McLeod syndrome mimicking mitochondrial myopathy due to a novel in-frame duplication in the XK geneMaelle Garnier, Juliette Nectoux, Thomas Smol, et al.
Pageof 10