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Year | Number of Results |
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2022 | 2 |
2023 | 5 |
2024 | 1 |
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Page 1
Megaconial congenital muscular dystrophy due to novel CHKB variants: a case report and literature review.
Skelet Muscle. 2022 Sep 29;12(1):23. doi: 10.1186/s13395-022-00306-8.
Skelet Muscle. 2022.
PMID: 36175989
Free PMC article.
Review.
Clinical and molecular features of patients with amyotrophic lateral sclerosis and SOD1 mutations: a monocentric study.
Gagliardi D, Ripellino P, Meneri M, Del Bo R, Antognozzi S, Comi GP, Gobbi C, Ratti A, Ticozzi N, Silani V, Ronchi D, Corti S.
Gagliardi D, et al. Among authors: antognozzi s.
Front Neurol. 2023 May 17;14:1169689. doi: 10.3389/fneur.2023.1169689. eCollection 2023.
Front Neurol. 2023.
PMID: 37265463
Free PMC article.
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Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis.
Manini A, Gagliardi D, Meneri M, Antognozzi S, Del Bo R, Scaglione C, Comi GP, Corti S, Ronchi D.
Manini A, et al. Among authors: antognozzi s.
Ann Clin Transl Neurol. 2022 Nov;9(11):1820-1825. doi: 10.1002/acn3.51673. Epub 2022 Oct 25.
Ann Clin Transl Neurol. 2022.
PMID: 36285345
Free PMC article.
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NOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patients.
Manini A, Gagliardi D, Meneri M, Antognozzi S, Del Bo R, Comi GP, Corti S, Ronchi D.
Manini A, et al. Among authors: antognozzi s.
Sci Rep. 2023 Feb 23;13(1):3187. doi: 10.1038/s41598-023-30393-6.
Sci Rep. 2023.
PMID: 36823368
Free PMC article.
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Case report: A novel patient presenting TRIM32-related limb-girdle muscular dystrophy.
Rimoldi M, Romagnoli G, Magri F, Antognozzi S, Cinnante C, Saccani E, Ciscato P, Zanotti S, Velardo D, Corti S, Comi GP, Ronchi D.
Rimoldi M, et al. Among authors: antognozzi s.
Front Neurol. 2024 Jan 18;14:1281953. doi: 10.3389/fneur.2023.1281953. eCollection 2023.
Front Neurol. 2024.
PMID: 38304327
Free PMC article.
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Case report: Clinical and molecular characterization of two siblings affected by Brody myopathy.
Velardo D, Antognozzi S, Rimoldi M, Pagliarani S, Cogiamanian F, Barbieri S, Corti S, Comi GP, Ronchi D.
Velardo D, et al. Among authors: antognozzi s.
Front Neurol. 2023 Jun 2;14:1170071. doi: 10.3389/fneur.2023.1170071. eCollection 2023.
Front Neurol. 2023.
PMID: 37332993
Free PMC article.
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Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant.
Rimoldi M, Magri F, Antognozzi S, Ripolone M, Salani S, Piga D, Bertolasi L, Zanotti S, Ciscato P, Fortunato F, Moggio M, Corti S, Comi GP, Ronchi D.
Rimoldi M, et al. Among authors: antognozzi s.
Front Genet. 2023 Nov 30;14:1278572. doi: 10.3389/fgene.2023.1278572. eCollection 2023.
Front Genet. 2023.
PMID: 38098475
Free PMC article.
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