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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 phenotype
Ilaria 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 years
L 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 effect
E 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 patients
G Pasqualim, M G Ribeiro, G G G da Fonseca, et al.
Brain Research
|
January 20, 1992
GFAP expression of human Schwann cells in tissue culture
D Bianchini, I De Martini, A Cadoni, et al.
European Journal of Neurology
|
April 15, 2014
Contribution of copy number variations in CMT1X: a retrospective study
S 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 cases
A Schenone, M Abbruzzese, A Uccelli, et al.
Annals of Neurology
|
May 13, 1999
Congenital hypomyelination due to myelin protein zero Q215X mutation
P 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 analysis
S 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 Syndrome
Caterina Lapucci, Massimiliano Gambella, Emilio Cipriano, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 99) with videos related to
Sort By:
Page
of 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 phenotype
Ilaria 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 years
L 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 effect
E 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 patients
G Pasqualim, M G Ribeiro, G G G da Fonseca, et al.
Brain Research
|
January 20, 1992
GFAP expression of human Schwann cells in tissue culture
D Bianchini, I De Martini, A Cadoni, et al.
European Journal of Neurology
|
April 15, 2014
Contribution of copy number variations in CMT1X: a retrospective study
S 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 cases
A Schenone, M Abbruzzese, A Uccelli, et al.
Annals of Neurology
|
May 13, 1999
Congenital hypomyelination due to myelin protein zero Q215X mutation
P 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 analysis
S 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 Syndrome
Caterina Lapucci, Massimiliano Gambella, Emilio Cipriano, et al.
Page
of 10