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Journal of Neurology
|
September 12, 2024
Pharmacogenomics of clinical response to Natalizumab in multiple sclerosis: a genome-wide multi-centric association study
Ferdinando Clarelli, Andrea Corona, Kimmo Pääkkönen, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
March 3, 2026
Pharmacogenomics of response to interferon-beta and glatiramer acetate in Multiple Sclerosis: A multi-centric study
Andrea Corona, Ferdinando Clarelli, Kimmo Pääkkönen, et al.
Genes
|
October 23, 2021
An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients
Nadia Barizzone, Rachele Cagliani, Chiara Basagni, et al.
Genes
|
December 23, 2022
A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility
Federica Esposito, Ana Maria Osiceanu, Melissa Sorosina, et al.
Journal of Neurology
|
May 11, 2022
A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility
Melissa Sorosina, Nadia Barizzone, Ferdinando Clarelli, et al.
Acta Neuropathologica
|
February 4, 2026
A HIF1A variant impacts long-term disability and smoldering inflammation in multiple sclerosis
Antonino Giordano, Pernilla Stridh, Paolo Preziosa, et al.
Plos Genetics
|
June 7, 2019
Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease
Carles Vilariño-Güell, Alexander Zimprich, Filippo Martinelli-Boneschi, et al.
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Search research articles
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Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 27 results.
Journal of Neurology
|
September 12, 2024
Pharmacogenomics of clinical response to Natalizumab in multiple sclerosis: a genome-wide multi-centric association study
Ferdinando Clarelli, Andrea Corona, Kimmo Pääkkönen, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
March 3, 2026
Pharmacogenomics of response to interferon-beta and glatiramer acetate in Multiple Sclerosis: A multi-centric study
Andrea Corona, Ferdinando Clarelli, Kimmo Pääkkönen, et al.
Genes
|
October 23, 2021
An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients
Nadia Barizzone, Rachele Cagliani, Chiara Basagni, et al.
Genes
|
December 23, 2022
A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility
Federica Esposito, Ana Maria Osiceanu, Melissa Sorosina, et al.
Journal of Neurology
|
May 11, 2022
A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility
Melissa Sorosina, Nadia Barizzone, Ferdinando Clarelli, et al.
Acta Neuropathologica
|
February 4, 2026
A HIF1A variant impacts long-term disability and smoldering inflammation in multiple sclerosis
Antonino Giordano, Pernilla Stridh, Paolo Preziosa, et al.
Plos Genetics
|
June 7, 2019
Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease
Carles Vilariño-Güell, Alexander Zimprich, Filippo Martinelli-Boneschi, et al.
Page
of 3