MD, Neurologist
Location: Italy
In February 2009, during the post-graduation he participated in the management of clinical trial "Quantitative muscle strength assessment in Duchenne muscular dystrophy: longitudinal study and correlation with functional measures". In 2011 he access to residency in Neurology at the University of Milan, and he practice clinical activities in Neurology Unit and Stroke Unit at the IRCCS Auxologico Institute, with particular interest in neurodegenerative diseases. He graduated the 1st multimedia course on headaches organized by the ASC. In May 2015 complete Neurology residency with honors (final vote 70/70), he drafted a thesis entitled "Manual Dexterity in amyotrophic lateral sclerosis: relationship with apraxia and cognitive disorders". Afterward he manage clinical trials and clinical research studies on Amyotrophic Lateral Sclerosis. Since 2016 he has been a consultant neurologist relating to rare diseases network of Neuromuscular and Rare Diseases at IRCCS Ca’ Granda foundation Ospedale Maggiore Policlinico, Milan, Italy; moreover he performs muscular biopsies report. He is the contact person for clinical management and research studies on glycogenesis type 2 (Pompe disease). He completed the workshop for medical writer, “Rising Medical Stars” by Springer Healthcare.
alberto Lerario, Santagostino Medical Center.
“MD”
Telemedicine for management of patients with amyotrophic lateral sclerosis through COVID-19 tail.
Bombaci A, Abbadessa G, Trojsi F, Leocani L, Bonavita S, Lavorgna L; Digital Technologies, Web and Social Media Study Group of the Italian Society of Neurology.Neurol Sci. 2021 Jan;42(1):9-13. doi: 10.1007/s10072-020-04783-x. Epub 2020 Oct 6.PMID: 33025327 Free PMC article. Review.
Immune-mediated necrotizing myopathy due to statins exposure.
Villa L, Lerario A, Calloni S, Peverelli L, Matinato C, DE Liso F, Ceriotti F, Tironi R, Sciacco M, Moggio M, Triulzi F, Cinnante C.Acta Myol. 2018 Dec 1;37(4):257-262. eCollection 2018 Dec.PMID: 30944904 Free PMC article.
A case report with the peculiar concomitance of 2 different genetic syndromes.
Lerario A, Colombo I, Milani D, Peverelli L, Villa L, Del Bo R, Sciacco M, Comi GP, Esposito S, Moggio M.Medicine (Baltimore). 2016 Dec;95(49):e5567. doi: 10.1097/MD.0000000000005567.PMID: 27930565 Free PMC article. Review.
Charles Bonnet syndrome: two case reports and review of the literature.
Lerario A, Ciammola A, Poletti B, Girotti F, Silani V.J Neurol. 2013 Apr;260(4):1180-6. doi: 10.1007/s00415-013-6857-7. Epub 2013 Feb 5.PMID: 23381616 Review.
The Use of Social Media and Digital Devices Among Italian Neurologists.
Lavorgna L, Brigo F, Abbadessa G, Bucello S, Clerico M, Cocco E, Iodice R, Lanzillo R, Leocani L, Lerario A, Moccia M, Padovani A, Prosperini L, Repice A, Stromillo M, Trojsi F, Mancardi G, Tedeschi G, Bonavita S.Front Neurol. 2020 Jun 16;11:583. doi: 10.3389/fneur.2020.00583. eCollection 2020.PMID: 32612572 Free PMC article.
New missense variants of NDUFA11 associated with late-onset myopathy.
Peverelli L, Legati A, Lamantea E, Nasca A, Lerario A, Galimberti V, Ghezzi D, Lamperti C.Muscle Nerve. 2019 Aug;60(2):E11-E14. doi: 10.1002/mus.26511. Epub 2019 May 30.PMID: 31074871 No abstract available.
Lerario A, Girotti F, Sassone J, Poletti B, Ciammola A, Silani V.Neurol Sci. 2021 Aug;42(8):3467-3469. doi: 10.1007/s10072-021-05290-3. Epub 2021 May 1.PMID: 33931820 No abstract available.
Filosto M, Cotti Piccinelli S, Ravaglia S, Servidei S, Moggio M, Musumeci O, Donati MA, Pegoraro E, Di Muzio A, Maggi L, Tonin P, Marrosu G, Sancricca C, Lerario A, Sacchini M, Semplicini C, Bozzoni V, Telese R, Bonanno S, Piras R, Maioli MA, Ricci G, Vercelli L, Galvagni A, Gallo Cassarino S, Caria F, Mongini T, Siciliano G, Padovani A, Toscano A.Adv Ther. 2019 May;36(5):1177-1189. doi: 10.1007/s12325-019-00926-5. Epub 2019 Mar 16.PMID: 30879255
MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form.
Telese R, Pagliarani S, Lerario A, Ciscato P, Fagiolari G, Cassandrini D, Grimoldi N, Conte G, Cinnante C, Santorelli FM, Comi GP, Sciacco M, Peverelli L.Mol Genet Genomic Med. 2020 Sep;8(9):e1320. doi: 10.1002/mgg3.1320. Epub 2020 Jun 24.PMID: 32578970 Free PMC article.
Miele G, Straccia G, Moccia M, Leocani L, Tedeschi G, Bonavita S, Lavorgna L; Digital Technologies, Web and Social Media Study Group of the Italian Society of Neurology.Telemed J E Health. 2020 Dec;26(12):1533-1536. doi: 10.1089/tmj.2020.0184. Epub 2020 Jul 13.PMID: 32667839
Lerario A, Girotti F, Sassone J, Poletti B, Ciammola A, Silani V.Neurol Sci. 2021 Aug;42(8):3515. doi: 10.1007/s10072-021-05446-1.PMID: 34216309 No abstract available.
Lerario A, Bonfiglio S, Sormani M, Tettamanti A, Marktel S, Napolitano S, Previtali S, Scarlato M, Natali-Sora M, Mercuri E, Bresolin N, Mongini T, Comi G, Gatti R, Ciceri F, Cossu G, Torrente Y.BMC Neurol. 2012 Sep 13;12:91. doi: 10.1186/1471-2377-12-91.PMID: 22974002 Free PMC article.
Effects of rituximab in two patients with dysferlin-deficient muscular dystrophy.
Lerario A, Cogiamanian F, Marchesi C, Belicchi M, Bresolin N, Porretti L, Torrente Y.BMC Musculoskelet Disord. 2010 Jul 11;11:157. doi: 10.1186/1471-2474-11-157.PMID: 20618995 Free PMC article. Clinical Trial.
No Grants Mentioned !!