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TYMP Variants Result in Late-Onset Mitochondrial Myopathy With Altered Muscle Mitochondrial DNA Homeostasis.
Front Genet. 2020 Aug 5;11:860. doi: 10.3389/fgene.2020.00860. eCollection 2020.
Front Genet. 2020.
PMID: 32849836
Free PMC article.
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG.
Villa D, Cinnante C, Valcamonica G, Manenti G, Lanfranconi S, Colombi A, Ghione I, Saetti MC, D'Amico M, Bonato S, Bresolin N, Comi GP, Ronchi D.
Villa D, et al.
BMC Neurol. 2020 Aug 26;20(1):316. doi: 10.1186/s12883-020-01890-2.
BMC Neurol. 2020.
PMID: 32847536
Free PMC article.
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Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutations.
Abati E, Magri S, Meneri M, Manenti G, Velardo D, Balistreri F, Pisciotta C, Saveri P, Bresolin N, Comi GP, Ronchi D, Pareyson D, Taroni F, Corti S.
Abati E, et al.
Ann Clin Transl Neurol. 2021 May;8(5):1158-1164. doi: 10.1002/acn3.51364. Epub 2021 May 4.
Ann Clin Transl Neurol. 2021.
PMID: 33943041
Free PMC article.
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Clinical, neuroradiological and genetic findings in a cohort of patients with multiple Cerebral Cavernous Malformations.
Lanfranconi S, Piergallini L, Ronchi D, Valcamonica G, Conte G, Marazzi E, Manenti G, Bertani GA, Locatelli M, Triulzi F, Bresolin N, Scola E, Comi GP.
Lanfranconi S, et al.
Metab Brain Dis. 2021 Oct;36(7):1871-1878. doi: 10.1007/s11011-021-00809-1. Epub 2021 Aug 6.
Metab Brain Dis. 2021.
PMID: 34357553
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Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study.
Piccinini A, Bailo P, Barbara G, Miozzo M, Tabano S, Colapietro P, Farè C, Sirchia SM, Battaglioli E, Bertuccio P, Manenti G, Micci L, La Vecchia C, Kustermann A, Gaudi S.
Piccinini A, et al.
Healthcare (Basel). 2023 Jan 6;11(2):173. doi: 10.3390/healthcare11020173.
Healthcare (Basel). 2023.
PMID: 36673541
Free PMC article.
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