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Page 1
Acute and chronic synaptic pathology in multiple sclerosis gray matter.
Vercellino M, Marasciulo S, Grifoni S, Vallino-Costassa E, Bosa C, Pasanisi MB, Crociara P, Casalone C, Chiò A, Giordana MT, Corona C, Cavalla P. Vercellino M, et al. Among authors: pasanisi mb. Mult Scler. 2022 Mar;28(3):369-382. doi: 10.1177/13524585211022174. Epub 2021 Jun 14. Mult Scler. 2022. PMID: 34124960
Kappa free light chains index in the differential diagnosis of Multiple Sclerosis from Neuromyelitis optica spectrum disorders and other immune-mediated central nervous system disorders.
Cavalla P, Caropreso P, Limoncelli S, Bosa C, Pasanisi MB, Schillaci V, Alteno A, Costantini G, Giordana MT, Mengozzi G, Vercellino M. Cavalla P, et al. Among authors: pasanisi mb. J Neuroimmunol. 2020 Feb 15;339:577122. doi: 10.1016/j.jneuroim.2019.577122. Epub 2019 Dec 3. J Neuroimmunol. 2020. PMID: 31837636
Dietary habits, nutritional status and risk of a first demyelinating event: an incident case-control study in a southern European cohort.
Cavalla P, Golzio P, Maietta D, Bosa C, Pasanisi MB, Alteno A, Schillaci V, Costantini G, Durelli P, Cuffini E, Panizzolo S, De Francesco A, Chiò A, Vercellino M. Cavalla P, et al. Among authors: pasanisi mb. Neurol Sci. 2022 Jul;43(7):4373-4380. doi: 10.1007/s10072-022-05908-0. Epub 2022 Feb 15. Neurol Sci. 2022. PMID: 35166977
Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: results of a phase IIb double-blind study of salbutamol.
Tiziano FD, Lomastro R, Abiusi E, Pasanisi MB, Di Pietro L, Fiori S, Baranello G, Angelini C, Sorarù G, Gaiani A, Mongini T, Vercelli L, Mercuri E, Vasco G, Pane M, Vita G, Vita G, Messina S, Petillo R, Passamano L, Politano L, Campanella A, Mantegazza R, Morandi L. Tiziano FD, et al. Among authors: pasanisi mb. J Med Genet. 2019 May;56(5):293-300. doi: 10.1136/jmedgenet-2018-105482. Epub 2018 Dec 28. J Med Genet. 2019. PMID: 30593463 Clinical Trial.
SMA-miRs (miR-181a-5p, -324-5p, and -451a) are overexpressed in spinal muscular atrophy skeletal muscle and serum samples.
Abiusi E, Infante P, Cagnoli C, Lospinoso Severini L, Pane M, Coratti G, Pera MC, D'Amico A, Diano F, Novelli A, Spartano S, Fiori S, Baranello G, Moroni I, Mora M, Pasanisi MB, Pocino K, Le Pera L, D'Amico D, Travaglini L, Ria F, Bruno C, Locatelli D, Bertini ES, Morandi LO, Mercuri E, Di Marcotullio L, Tiziano FD. Abiusi E, et al. Among authors: pasanisi mb. Elife. 2021 Sep 20;10:e68054. doi: 10.7554/eLife.68054. Elife. 2021. PMID: 34542403 Free PMC article.
Amifampridine phosphate in the treatment of muscle-specific kinase myasthenia gravis: a phase IIb, randomized, double-blind, placebo-controlled, double crossover study.
Bonanno S, Pasanisi MB, Frangiamore R, Maggi L, Antozzi C, Andreetta F, Campanella A, Brenna G, Cottini L, Mantegazza R. Bonanno S, et al. Among authors: pasanisi mb. SAGE Open Med. 2018 Dec 17;6:2050312118819013. doi: 10.1177/2050312118819013. eCollection 2018. SAGE Open Med. 2018. PMID: 30574306 Free PMC article.
Interpreting Genetic Variants in Titin in Patients With Muscle Disorders.
Savarese M, Maggi L, Vihola A, Jonson PH, Tasca G, Ruggiero L, Bello L, Magri F, Giugliano T, Torella A, Evilä A, Di Fruscio G, Vanakker O, Gibertini S, Vercelli L, Ruggieri A, Antozzi C, Luque H, Janssens S, Pasanisi MB, Fiorillo C, Raimondi M, Ergoli M, Politano L, Bruno C, Rubegni A, Pane M, Santorelli FM, Minetti C, Angelini C, De Bleecker J, Moggio M, Mongini T, Comi GP, Santoro L, Mercuri E, Pegoraro E, Mora M, Hackman P, Udd B, Nigro V. Savarese M, et al. Among authors: pasanisi mb. JAMA Neurol. 2018 May 1;75(5):557-565. doi: 10.1001/jamaneurol.2017.4899. JAMA Neurol. 2018. PMID: 29435569 Free PMC article.
Quantitative Muscle MRI Protocol as Possible Biomarker in Becker Muscular Dystrophy.
Maggi L, Moscatelli M, Frangiamore R, Mazzi F, Verri M, De Luca A, Pasanisi MB, Baranello G, Tramacere I, Chiapparini L, Bruzzone MG, Mantegazza R, Aquino D. Maggi L, et al. Among authors: pasanisi mb. Clin Neuroradiol. 2021 Mar;31(1):257-266. doi: 10.1007/s00062-019-00875-0. Epub 2020 Jan 23. Clin Neuroradiol. 2021. PMID: 31974637
Sleep breathing disorders in 40 Italian patients with Myotonic dystrophy type 1.
Pincherle A, Patruno V, Raimondi P, Moretti S, Dominese A, Martinelli-Boneschi F, Pasanisi MB, Canioni E, Salerno F, Deleo F, Spreafico R, Mantegazza R, Villani F, Morandi L. Pincherle A, et al. Among authors: pasanisi mb. Neuromuscul Disord. 2012 Mar;22(3):219-24. doi: 10.1016/j.nmd.2011.08.010. Epub 2011 Dec 3. Neuromuscul Disord. 2012. PMID: 22137426
26 results