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Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease.
Vilariño-Güell C, Zimprich A, Martinelli-Boneschi F, Herculano B, Wang Z, Matesanz F, Urcelay E, Vandenbroeck K, Leyva L, Gris D, Massaad C, Quandt JA, Traboulsee AL, Encarnacion M, Bernales CQ, Follett J, Yee IM, Criscuoli MG, Deutschländer A, Reinthaler EM, Zrzavy T, Mascia E, Zauli A, Esposito F, Alcina A, Izquierdo G, Espino-Paisán L, Mena J, Antigüedad A, Urbaneja-Romero P, Ortega-Pinazo J, Song W, Sadovnick AD. Vilariño-Güell C, et al. Among authors: mascia e. PLoS Genet. 2019 Jun 6;15(6):e1008180. doi: 10.1371/journal.pgen.1008180. eCollection 2019 Jun. PLoS Genet. 2019. PMID: 31170158 Free PMC article.
Inverse correlation of genetic risk score with age at onset in bout-onset and progressive-onset multiple sclerosis.
Sorosina M, Esposito F, Guaschino C, Clarelli F, Barizzone N, Osiceanu AM, Brambilla P, Mascia E, Cavalla P, Gallo P; PROGRESSO; PROGEMUS; Martinelli V, Leone M, Comi G, D'Alfonso S, Martinelli Boneschi F. Sorosina M, et al. Among authors: mascia e. Mult Scler. 2015 Oct;21(11):1463-7. doi: 10.1177/1352458514561910. Epub 2014 Dec 22. Mult Scler. 2015. PMID: 25533292
Impact of MS genetic loci on familial aggregation, clinical phenotype, and disease prediction.
Esposito F, Guaschino C, Sorosina M, Clarelli F, Ferre' L, Mascia E, Santoro S, Pagnesi M, Radaelli M, Colombo B, Moiola L, Rodegher M, Stupka E, Martinelli V, Comi G, Martinelli Boneschi F. Esposito F, et al. Among authors: mascia e. Neurol Neuroimmunol Neuroinflamm. 2015 Jul 9;2(4):e129. doi: 10.1212/NXI.0000000000000129. eCollection 2015 Aug. Neurol Neuroimmunol Neuroinflamm. 2015. PMID: 26185776 Free PMC article.
Impact of multiple sclerosis risk loci in postinfectious neurological syndromes.
Martinelli-Boneschi F, Currò R, Santoro S, Berzero G, Sorosina M, Ferrè L, Mascia E, Peroni S, Comi G, Gugliemi A, Vegezzi E, Callegari I, Filippi M, Cortese A, Esposito F, Clarelli F, Marchioni E. Martinelli-Boneschi F, et al. Among authors: mascia e. Mult Scler Relat Disord. 2020 Sep;44:102326. doi: 10.1016/j.msard.2020.102326. Epub 2020 Jun 24. Mult Scler Relat Disord. 2020. PMID: 32615529
Identification of differential DNA methylation associated with multiple sclerosis: A family-based study.
Garcia-Manteiga JM, Clarelli F, Bonfiglio S, Mascia E, Giannese F, Barbiera G, Guaschino C, Sorosina M, Santoro S, Protti A, Martinelli V, Cittaro D, Lazarevic D, Stupka E, Filippi M, Esposito F, Martinelli-Boneschi F. Garcia-Manteiga JM, et al. Among authors: mascia e. J Neuroimmunol. 2021 Jul 15;356:577600. doi: 10.1016/j.jneuroim.2021.577600. Epub 2021 Apr 30. J Neuroimmunol. 2021. PMID: 33991750
Transcriptomic Analysis of Peripheral Monocytes upon Fingolimod Treatment in Relapsing Remitting Multiple Sclerosis Patients.
Sferruzza G, Clarelli F, Mascia E, Ferrè L, Ottoboni L, Sorosina M, Santoro S, Moiola L, Martinelli V, Comi G, Martinelli Boneschi F, Filippi M, Provero P, Esposito F. Sferruzza G, et al. Among authors: mascia e. Mol Neurobiol. 2021 Oct;58(10):4816-4827. doi: 10.1007/s12035-021-02465-z. Epub 2021 Jun 28. Mol Neurobiol. 2021. PMID: 34181235
An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients.
Barizzone N, Cagliani R, Basagni C, Clarelli F, Mendozzi L, Agliardi C, Forni D, Tosi M, Mascia E, Favero F, Corà D, Corrado L, Sorosina M, Esposito F, Zuccalà M, Vecchio D, Liguori M, Comi C, Comi G, Martinelli V, Filippi M, Leone M, Martinelli-Boneschi F, Caputo D, Sironi M, Guerini FR, D'Alfonso S. Barizzone N, et al. Among authors: mascia e. Genes (Basel). 2021 Oct 13;12(10):1607. doi: 10.3390/genes12101607. Genes (Basel). 2021. PMID: 34681001 Free PMC article.
40 results