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Showing results (561-570 of 586) with videos related to

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Multiple Sclerosis (Houndmills, Basingstoke, England)|January 14, 2015
Analysis of genes, pathways and networks involved in disease severity and age at onset in primary-progressive multiple sclerosisG Giacalone, F Clarelli, A M Osiceanu, et al.
Neurology|November 15, 2011
Acute myeloid leukemia in Italian patients with multiple sclerosis treated with mitoxantroneV Martinelli, E Cocco, R Capra, et al.
Nature Genetics|June 30, 2001
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondriaJ N Spelbrink, F Y Li, V Tiranti, et al.
Neurology|July 8, 2011
Breastfeeding is not related to postpartum relapses in multiple sclerosisE Portaccio, A Ghezzi, B Hakiki, et al.
Journal of Neurology|July 11, 2025
Analysis of the Italian cohort of late-onset Pompe disease (LOPD) patients after 10 and 15 years of therapy with alglucosidase alfaT Mongini, G Gadaleta, P Alonge, et al.
Journal of Neuroimmunology|December 18, 2021
Burden of rare coding variants in an Italian cohort of familial multiple sclerosisE Mascia, F Clarelli, A Zauli, et al.
Neuromuscular Disorders : NMD|June 26, 2012
Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiencyM Pane, S Messina, G Vasco, et al.
American Journal of Human Genetics|April 29, 1998
Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlationB M Manning, K A Quane, H Ording, et al.
Neurology|April 6, 2011
Interferon β-1b and glatiramer acetate effects on permanent black hole evolutionM Filippi, M A Rocca, F Camesasca, et al.
Neurology|November 17, 2010
Pregnancy and fetal outcomes after interferon-β exposure in multiple sclerosisM P Amato, E Portaccio, A Ghezzi, et al.
Pageof 59

Showing results (561-570 of 586) with videos related to

Sort By:
Pageof 59
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 14, 2015
Analysis of genes, pathways and networks involved in disease severity and age at onset in primary-progressive multiple sclerosisG Giacalone, F Clarelli, A M Osiceanu, et al.
Neurology|November 15, 2011
Acute myeloid leukemia in Italian patients with multiple sclerosis treated with mitoxantroneV Martinelli, E Cocco, R Capra, et al.
Nature Genetics|June 30, 2001
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondriaJ N Spelbrink, F Y Li, V Tiranti, et al.
Neurology|July 8, 2011
Breastfeeding is not related to postpartum relapses in multiple sclerosisE Portaccio, A Ghezzi, B Hakiki, et al.
Journal of Neurology|July 11, 2025
Analysis of the Italian cohort of late-onset Pompe disease (LOPD) patients after 10 and 15 years of therapy with alglucosidase alfaT Mongini, G Gadaleta, P Alonge, et al.
Journal of Neuroimmunology|December 18, 2021
Burden of rare coding variants in an Italian cohort of familial multiple sclerosisE Mascia, F Clarelli, A Zauli, et al.
Neuromuscular Disorders : NMD|June 26, 2012
Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiencyM Pane, S Messina, G Vasco, et al.
American Journal of Human Genetics|April 29, 1998
Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlationB M Manning, K A Quane, H Ording, et al.
Neurology|April 6, 2011
Interferon β-1b and glatiramer acetate effects on permanent black hole evolutionM Filippi, M A Rocca, F Camesasca, et al.
Neurology|November 17, 2010
Pregnancy and fetal outcomes after interferon-β exposure in multiple sclerosisM P Amato, E Portaccio, A Ghezzi, et al.
Pageof 59