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Page 1
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability.
Ronchi D, Di Fonzo A, Lin W, Bordoni A, Liu C, Fassone E, Pagliarani S, Rizzuti M, Zheng L, Filosto M, Ferrò MT, Ranieri M, Magri F, Peverelli L, Li H, Yuan YC, Corti S, Sciacco M, Moggio M, Bresolin N, Shen B, Comi GP. Ronchi D, et al. Among authors: peverelli l. Am J Hum Genet. 2013 Feb 7;92(2):293-300. doi: 10.1016/j.ajhg.2012.12.014. Epub 2013 Jan 24. Am J Hum Genet. 2013. PMID: 23352259 Free PMC article.
Mitochondrial disease heterogeneity: a prognostic challenge.
Moggio M, Colombo I, Peverelli L, Villa L, Xhani R, Testolin S, Di Mauro S, Sciacco M. Moggio M, et al. Among authors: peverelli l. Acta Myol. 2014 Oct;33(2):86-93. Acta Myol. 2014. PMID: 25709378 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. Lerario A, et al. Among authors: peverelli l. Medicine (Baltimore). 2016 Dec;95(49):e5567. doi: 10.1097/MD.0000000000005567. Medicine (Baltimore). 2016. PMID: 27930565 Free PMC article. Review.
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature.
Gagliardi D, Mauri E, Magri F, Velardo D, Meneri M, Abati E, Brusa R, Faravelli I, Piga D, Ronchi D, Triulzi F, Peverelli L, Sciacco M, Bresolin N, Comi GP, Corti S, Govoni A. Gagliardi D, et al. Among authors: peverelli l. Front Neurol. 2019 Jan 31;10:38. doi: 10.3389/fneur.2019.00038. eCollection 2019. Front Neurol. 2019. PMID: 30766507 Free PMC article.
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. Villa L, et al. Among authors: peverelli l. Acta Myol. 2018 Dec 1;37(4):257-262. eCollection 2018 Dec. Acta Myol. 2018. PMID: 30944904 Free PMC article.
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. Telese R, et al. Among authors: peverelli l. Mol Genet Genomic Med. 2020 Sep;8(9):e1320. doi: 10.1002/mgg3.1320. Epub 2020 Jun 24. Mol Genet Genomic Med. 2020. PMID: 32578970 Free PMC article.
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis.
Magri F, Brusa R, Bello L, Peverelli L, Del Bo R, Govoni A, Cinnante C, Colombo I, Fortunato F, Tironi R, Corti S, Grimoldi N, Sciacco M, Bresolin N, Pegoraro E, Moggio M, Comi GP. Magri F, et al. Among authors: peverelli l. Acta Myol. 2020 Jun 1;39(2):67-82. doi: 10.36185/2532-1900-009. eCollection 2020 Jun. Acta Myol. 2020. PMID: 32904964 Free PMC article.
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