Stefano Previtali

Stefano Previtali
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专科:
神经内科 罕见病
职业:
神经科医生
医疗机构:
神经内科与神经康复科 @ 圣拉斐尔科学研究医院
语言:
IT
EN
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个人简介

Stefano Previtali医生就职于IRCCS圣拉斐尔科学研究医院的神经内科，在Massimo Filippi教授的指导下开展工作。

1990年，Previtali从米兰大学医学院毕业后，于1994年专修神经病学，并于1998年在米兰大学获得神经病学博士学位。

Previtali医生负责肌肉活检科（形态学、组织酶学、免疫组织化学和Western印记），是神经肌肉疾病方面的专家，特别关注成人和儿童的肌病（遗传性和获得性）和遗传性神经病（CMT）。

在研究活动方面，Previtali医生负责神经肌肉再生研究部。Previtali医生的工作主要是确定新的治疗策略、发现某些疾病背后的分子机制，如杜兴氏肌营养不良（进行性肌营养不良）、面肩肱型肌营养不良症、Merosin缺陷性先天性营养不良症（LAMA2）、核纤层蛋白病、进行性神经性腓骨肌萎缩症（CMT）。Previtali医生以作者或共同作者的身份在行业学术期刊上发表了多篇论文，也参与了书籍章节的编写，共计100余篇文章，H指数为37。他经常参加意大利国内外的行业会议。

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出版物

最新出版物

Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation.
Hum Mol Genet 2020 2020;29(2):177–188. doi: 10.1093/hmg/ddz211. PMID 31868880
Longo F, Benedetti S, Zambon AA, Natali Sora MG, Di Resta C, Quattrini A, Maltecca F, Ferrari M, Previtali SC.
Expanding the spectrum of genes responsible for hereditary motor neuropathies.
J Neurol Neurosurg Psychiatry. 2019;90(10):1171–1179.. doi: 10.1136/jnnp-2019-320717. PMID 31167812
Previtali SC, Zhao E, Lazarevic D, Pipitone GB, Fabrizi GM, Manganelli F, Mazzeo A, Pareyson D, Schenone A, Taroni F, Vita G, Bellone E, Ferrarini M, Garibaldi M, Magri S, Padua L, Pennisi E, Pisciotta C, Riva N, Scaioli V, Scarlato M, Tozza S, Geroldi A, Jordanova A, Ferrari M, Molineris I, Reilly MM, Comi G, Carrera P, Devoto M, Bolino A.
A multicentre retrospective study of Charcot-Marie-Tooth disease type 4B (CMT4B) due to mutations in Myotubularin-related proteins (MTMRs).
Ann Neurol. 2019;86(1):55–67. doi: 10.1002/ana.25500. PMID
Pareyson D, Stojkovic T, Reilly MM, Leonard-Louis S, Laurà M, Blake J, Parman Y, Battaloglu E, Tazir M, Bellatache M, Bonello-Palot N, Lévy N, Sacconi S, Guimarães-Costa R, Attarian S, Latour P, Solé G, Megarbane A, Horvath R, Ricci G, Choi BO, Schenone A, Gemelli C, Geroldi A, Sabatelli M, Luigetti M, Santoro L, Manganelli F, Quattrone A, Valentino P, Murakami T, Scherer SS, Dankwa L, Shy ME, Bac
Expanding The Central Nervous System Disease Spectrum Associated WITH Flnc Mutation. Muscle Nerve.
2019;59(5):E33–E37. doi: 10.1002/mus.26443. PMID 30734317
Previtali SC, Scarlato M, Vezzulli P, Ruggieri A, Velardo D, Benedetti S, Torini G, Colombo B, Maggi L, Bella DD, Gellera C, D'Angelo G, Mora M.
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: critical issues and areas for improvements.
Neuromuscul Disord. 2017 May;27(5):447-451. doi: 10.1016/j.nmd.2017.02.006. PMID:28262469
D'Amico A, Catteruccia M, Baranello G, Politano L, Govoni A, Previtali SC, Pane M, D'Angelo MG, Bruno C, Messina S, Ricci F, Pegoraro E, Pini A, Berardinelli A, Gorni K, Battini R, Vita G, Trucco F, Scutifero M, Petillo R, D'Ambrosio P, Ardissone A, Pasanisi B, Vita G, Mongini T, Moggio M, Comi GP, Mercuri E, Bertini E.
Niacin-mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination.
EMBO Mol Med 2016 Dec 1;8(12):1438-1454. doi: 10.15252/emmm.201606349. PMID 27799291
Bolino A, Piguet F, Alberizzi V, Pellegatta M, Rivellini C, Guerrero-Valero M, Noseda R, Brombin C, Nonis A, D'Adamo P, Taveggia C, Previtali SC.
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne Muscular Dystrophy.
EMBO MolMed 2015 Nov 5. pii: e201505636. doi: 10.15252/emmm.201505636. PMID:26543057
Cossu G*, Previtali SC*, Napolitano S, Cicalese MP, Tedesco FS, Nicastro F, Noviello M, Roostalu U, Natali Sora MG, Scarlato M, De Pellegrin M, Godi C, Giuliani S, Ciotti F, Tonlorenzi R, Lorenzetti I, Rivellini C, Benedetti S, Gatti R, Marktel S, Mazzi B, Tettamanti A, Ragazzi M, Imro MA, Marano G, Ambrosi A, Fiori R, Sormani MP, Bonini C, Venturini M, Politi LS, Torrente Y*, Ciceri F*.
Mesoangioblast delivery of miniagrin ameliorates murine model of Merosin Deficient Congenital Muscular Dystrophy type 1A.
Skelet Muscle. 2015 Sep 3;5:30. doi: 10.1186/s13395-015-0055-5. eCollection 2015.. PMID:26347253
Domi T, Porrello E, Velardo D, Capotondo A, Biffi A, Tonlorenzi R, Amadio S, Ambrosi A, MiyagoeSuzuki Y, Takeda S, Ruegg MA, Previtali SC.
Muscle MRI findings in Facioscapulohumeral muscular dystrophy.
Eur Radiol. 2016 Mar;26(3):693-705. doi: 10.1007/s00330-015-3890-1. Epub 2015 Jun 27. PMID:26115655
Gerevini S, Scarlato M, Maggi L, Cava M, Caliendo G, Pasanisi B, Falini A, Previtali SC*, Morandi L.
A new double trouble phenotype: facioscapulohumeral muscular dystrophy ameliorates spastic paraparesis due to spastin mutation.
J Neurol. 2015 Feb;262(2):476-8. doi: 10.1007/s00415-014-7606-2. Epub 2014 Dec 16.PMID:25511172
Scarlato M, Nuara A, Gerevini S, Benedetti S, Rossi P, Ferrari M, Previtali SC.
Loss of function mutations in HINT1 are a major cause of peripheral neuropathy with neuromyotonia
Nat Genet. 2012 Oct;44(10):1080-3. doi: 10.1038/ng.2406. PMID 22961002
Zimoń M, Baets J, Almeida-Souza L, De Vriendt E, Nikodinovic J, Parman Y, Battalo Gcaron Lu E, Matur Z, Guergueltcheva V, Tournev I, Auer-Grumbach M, De Rijk P, Petersen BS, Müller T, Fransen E, Van Damme P, Löscher WN, Barišić N, Mitrovic Z, Previtali SC, Topalo Gcaron Lu H, Bernert G, BelezaMeireles A, Todorovic S, Savic-Pavicevic D, Ishpekova B, Lechner S, Peeters K, Ooms T, Hahn AF, Züchner S,
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy.
Neurology 2012 Jul 10;79(2):159-62. PMID 22744661
Bello L, Piva L, Barp A, Taglia A, Picillo E, Vasco G, Pane M, Previtali SC, Torrente Y, Gazzerro E, Motta MC, Grieco GS, Napolitano S, Magri F, D'Amico A, Astrea G, Messina S, Sframeli M, Vita GL, Boffi P, Mongini T, Ferlini A, Gualandi F, Soraru' G, Ermani M, Vita G, Battini R, Bertini E, Comi GP, Berardinelli A, Minetti C, Bruno C, Mercuri E, Politano L, Angelini C, Hoffman EP, Pegoraro E.
Vimentin regulates peripheral nerve myelination.
Development 2012 Apr;139(7):1359-67. PMID 22357929
Triolo D, Dina G, Taveggia C, Vaccari I, Porrello E, Rivellini C, Domi T, La Marca R, Cerri F, Bolino A, Quattrini A, Previtali SC.
Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study
Neurology 2011 Jul 19;77(3):250-6. PMID 21734183
Mazzone E, Vasco G, Sormani MP, Torrente Y, Berardinelli A, Messina S, Adele D’Amico, Doglio L, Politano L, Martinelli D, Cavallaro F, Frosini S, Bello L, Bonfiglio S, Zucchini E, De Sanctis R, Scutifero M, Bianco F, Rossi F, Motta MC, Sacco A, Donati MA, Mongini T, Pini A, Battini R, Pegoraro E, Pane M, Gasperini S, Previtali S, Napolitano S, Bruno C, Vita G, Comi GP, Bertini E, Mercuri E.

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