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Page 1
Genetics architecture of spontaneous coronary artery dissection in an Italian cohort.
Casula M, Marchetti D, Trevisan L, Pezzoli L, Bellini M, Patrone S, Zingarelli A, Gotta F, Iascone M, Mandich P. Casula M, et al. Among authors: trevisan l. Front Cardiovasc Med. 2024 Nov 25;11:1486273. doi: 10.3389/fcvm.2024.1486273. eCollection 2024. Front Cardiovasc Med. 2024. PMID: 39654947 Free PMC article.
Case report: Episodic ataxia without ataxia?
Gaudio A, Gotta F, Ponti C, Sanguineri F, Trevisan L, Geroldi A, Patrone S, Gemelli C, Cabona C, Astrea G, Fiorillo C, Gustincich S, Grandis M, Mandich P. Gaudio A, et al. Among authors: trevisan l. Front Neurol. 2023 Oct 26;14:1224241. doi: 10.3389/fneur.2023.1224241. eCollection 2023. Front Neurol. 2023. PMID: 37965175 Free PMC article.
Early Onset Inherited Peripheral Neuropathies: The Experience of a Specialized Referral Center for Genetic Diagnosis Achievement.
Geroldi A, Ponti C, Mammi A, Patrone S, Gotta F, Trevisan L, Sanguineri F, Origone P, Gaudio A, La Barbera A, Cataldi M, Gemelli C, Massucco S, Schenone A, Lanteri P, Fiorillo C, Grandis M, Mandich P, Bellone E. Geroldi A, et al. Among authors: trevisan l. Pediatr Neurol. 2024 May;154:4-8. doi: 10.1016/j.pediatrneurol.2024.02.002. Epub 2024 Feb 10. Pediatr Neurol. 2024. PMID: 38428336
Spinocerebellar ataxia 17: full phenotype in a 41 CAG/CAA repeats carrier.
Origone P, Gotta F, Lamp M, Trevisan L, Geroldi A, Massucco D, Grazzini M, Massa F, Ticconi F, Bauckneht M, Marchese R, Abbruzzese G, Bellone E, Mandich P. Origone P, et al. Among authors: trevisan l. Cerebellum Ataxias. 2018 Mar 14;5:7. doi: 10.1186/s40673-018-0086-x. eCollection 2018. Cerebellum Ataxias. 2018. PMID: 29564144 Free PMC article.
A novel mutation of Twinkle in Perrault syndrome: A not rare diagnosis?
Gotta F, Lamp M, Geroldi A, Trevisan L, Origone P, Fugazza G, Fabbri S, Nesti C, Rubegni A, Morani F, Santorelli FM, Bellone E, Mandich P. Gotta F, et al. Among authors: trevisan l. Ann Hum Genet. 2020 Sep;84(5):417-422. doi: 10.1111/ahg.12384. Epub 2020 Apr 12. Ann Hum Genet. 2020. PMID: 32281099
Genetic Workup for Charcot-Marie-Tooth Neuropathy: A Retrospective Single-Site Experience Covering 15 Years.
Gemelli C, Geroldi A, Massucco S, Trevisan L, Callegari I, Marinelli L, Ursino G, Hamedani M, Mennella G, Stara S, Maggi G, Mori L, Schenone C, Gotta F, Patrone S, Mammi A, Origone P, Prada V, Nobbio L, Mandich P, Schenone A, Bellone E, Grandis M. Gemelli C, et al. Among authors: trevisan l. Life (Basel). 2022 Mar 10;12(3):402. doi: 10.3390/life12030402. Life (Basel). 2022. PMID: 35330153 Free PMC article.
A misleading presentation of Mohr-Tranebjaerg syndrome: What is hidden behind an axonal neuropathy?
Geroldi A, Trevisan L, Gaudio A, Gotta F, Patrone S, Origone P, Grandis M, Gemelli C, Schenone A, Accogli A, Zara F, Mandich P, Bellone E. Geroldi A, et al. Among authors: trevisan l. Parkinsonism Relat Disord. 2022 Sep;102:54-56. doi: 10.1016/j.parkreldis.2022.07.021. Epub 2022 Aug 5. Parkinsonism Relat Disord. 2022. PMID: 35947939 No abstract available.
100 results