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Page 1
Laser capture microdissection for transcriptomic profiles in human skin biopsies.
Santoro S, Lopez ID, Lombardi R, Zauli A, Osiceanu AM, Sorosina M, Clarelli F, Peroni S, Cazzato D, Marchi M, Quattrini A, Comi G, Calogero RA, Lauria G, Martinelli Boneschi F. Santoro S, et al. BMC Mol Biol. 2018 Jun 19;19(1):7. doi: 10.1186/s12867-018-0108-5. BMC Mol Biol. 2018. PMID: 29921228 Free PMC article.
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: santoro s. Mol Neurobiol. 2021 Oct;58(10):4816-4827. doi: 10.1007/s12035-021-02465-z. Epub 2021 Jun 28. Mol Neurobiol. 2021. PMID: 34181235
COL6A5 variants in familial neuropathic chronic itch.
Martinelli-Boneschi F, Colombi M, Castori M, Devigili G, Eleopra R, Malik RA, Ritelli M, Zoppi N, Dordoni C, Sorosina M, Grammatico P, Fadavi H, Gerrits MM, Almomani R, Faber CG, Merkies IS, Toniolo D; INGI Network; Cocca M, Doglioni C, Waxman SG, Dib-Hajj SD, Taiana MM, Sassone J, Lombardi R, Cazzato D, Zauli A, Santoro S, Marchi M, Lauria G. Martinelli-Boneschi F, et al. Among authors: santoro s. Brain. 2017 Mar 1;140(3):555-567. doi: 10.1093/brain/aww343. Brain. 2017. PMID: 28073787
Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing.
Almomani R, Marchi M, Sopacua M, Lindsey P, Salvi E, Koning B, Santoro S, Magri S, Smeets HJM, Martinelli Boneschi F, Malik RR, Ziegler D, Hoeijmakers JGJ, Bönhof G, Dib-Hajj S, Waxman SG, Merkies ISJ, Lauria G, Faber CG, Gerrits MM; on behalf on the PROPANE Study Group. Almomani R, et al. Among authors: santoro s. PLoS One. 2020 Sep 2;15(9):e0238467. doi: 10.1371/journal.pone.0238467. eCollection 2020. PLoS One. 2020. PMID: 32877464 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: santoro s. 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
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis.
Mascia E, Clarelli F, Zauli A, Guaschino C, Sorosina M, Barizzone N, Basagni C, Santoro S, Ferrè L, Bonfiglio S, Biancolini D, Pozzato M, Guerini FR, Protti A, Liguori M, Moiola L, Vecchio D, Bresolin N, Comi G, Filippi M, Esposito F, D'Alfonso S, Martinelli-Boneschi F. Mascia E, et al. Among authors: santoro s. J Neuroimmunol. 2022 Jan 15;362:577760. doi: 10.1016/j.jneuroim.2021.577760. Epub 2021 Nov 5. J Neuroimmunol. 2022. PMID: 34922125
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: santoro s. 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.
467 results