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A Schenone

Showing results (71-80 of 99) with videos related to

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Journal of Neurology|July 7, 2019
Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotypeIlaria Callegari, C Gemelli, A Geroldi, et al.
Journal of Neuroimmunology|November 3, 2019
Outcomes after single-cycle rituximab monotherapy in patients with anti-MAG polyneuropathy: A bi-center experience with an average follow-up of 11 yearsL Benedetti, M Garnero, C Demichelis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2004
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effectE Di Maria, R Gulli, P Balestra, et al.
Clinical Genetics|September 27, 2014
p.L18P: a novel IDUA mutation that causes a distinct attenuated phenotype in mucopolysaccharidosis type I patientsG Pasqualim, M G Ribeiro, G G G da Fonseca, et al.
Brain Research|January 20, 1992
GFAP expression of human Schwann cells in tissue cultureD Bianchini, I De Martini, A Cadoni, et al.
European Journal of Neurology|April 15, 2014
Contribution of copy number variations in CMT1X: a retrospective studyS Capponi, A Geroldi, I Pezzini, et al.
Journal of the Neurological Sciences|March 1, 1994
Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three casesA Schenone, M Abbruzzese, A Uccelli, et al.
Annals of Neurology|May 13, 1999
Congenital hypomyelination due to myelin protein zero Q215X mutationP Mandich, G L Mancardi, A Varese, et al.
Studies in Health Technology and Informatics|July 11, 2006
Early diagnosis of Alzheimer's disease using a grid implementation of statistical parametric mapping analysisS Bagnasco, F Beltrame, B Canesi, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|January 17, 2026
Brain Microstructural Damage as Potential Biomarker of Immune Cell-Associated Neurotoxicity SyndromeCaterina Lapucci, Massimiliano Gambella, Emilio Cipriano, et al.
Pageof 10

Showing results (71-80 of 99) with videos related to

Sort By:
Pageof 10
Journal of Neurology|July 7, 2019
Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotypeIlaria Callegari, C Gemelli, A Geroldi, et al.
Journal of Neuroimmunology|November 3, 2019
Outcomes after single-cycle rituximab monotherapy in patients with anti-MAG polyneuropathy: A bi-center experience with an average follow-up of 11 yearsL Benedetti, M Garnero, C Demichelis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 21, 2004
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effectE Di Maria, R Gulli, P Balestra, et al.
Clinical Genetics|September 27, 2014
p.L18P: a novel IDUA mutation that causes a distinct attenuated phenotype in mucopolysaccharidosis type I patientsG Pasqualim, M G Ribeiro, G G G da Fonseca, et al.
Brain Research|January 20, 1992
GFAP expression of human Schwann cells in tissue cultureD Bianchini, I De Martini, A Cadoni, et al.
European Journal of Neurology|April 15, 2014
Contribution of copy number variations in CMT1X: a retrospective studyS Capponi, A Geroldi, I Pezzini, et al.
Journal of the Neurological Sciences|March 1, 1994
Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three casesA Schenone, M Abbruzzese, A Uccelli, et al.
Annals of Neurology|May 13, 1999
Congenital hypomyelination due to myelin protein zero Q215X mutationP Mandich, G L Mancardi, A Varese, et al.
Studies in Health Technology and Informatics|July 11, 2006
Early diagnosis of Alzheimer's disease using a grid implementation of statistical parametric mapping analysisS Bagnasco, F Beltrame, B Canesi, et al.
Journal of Neuroimaging : Official Journal of the American Society of Neuroimaging|January 17, 2026
Brain Microstructural Damage as Potential Biomarker of Immune Cell-Associated Neurotoxicity SyndromeCaterina Lapucci, Massimiliano Gambella, Emilio Cipriano, et al.
Pageof 10