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Page 1
A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H.
Bisceglia L, Zoccolella S, Torraco A, Piemontese MR, Dell'Aglio R, Amati A, De Bonis P, Artuso L, Copetti M, Santorelli FM, Serlenga L, Zelante L, Bertini E, Petruzzella V. Bisceglia L, et al. Among authors: serlenga l. Eur J Hum Genet. 2010 Jun;18(6):636-41. doi: 10.1038/ejhg.2009.235. Epub 2010 Jan 13. Eur J Hum Genet. 2010. PMID: 20068593 Free PMC article.
Mitochondrial genome aberrations in skeletal muscle of patients with motor neuron disease.
Artuso L, Zoccolella S, Favia P, Amati A, Capozzo R, Logroscino G, Serlenga L, Simone I, Gasparre G, Petruzzella V. Artuso L, et al. Among authors: serlenga l. Amyotroph Lateral Scler Frontotemporal Degener. 2013 May;14(4):261-6. doi: 10.3109/21678421.2012.735239. Epub 2012 Oct 24. Amyotroph Lateral Scler Frontotemporal Degener. 2013. PMID: 23134511
Autophagy markers LC3 and p62 accumulate in immune-mediated necrotizing myopathy.
Girolamo F, Lia A, Annese T, Giannini M, Amati A, D'Abbicco D, Tampoia M, Virgintino D, Ribatti D, Serlenga L, Iannone F, Trojano M. Girolamo F, et al. Among authors: serlenga l. Muscle Nerve. 2019 Sep;60(3):315-327. doi: 10.1002/mus.26608. Epub 2019 Jun 21. Muscle Nerve. 2019. PMID: 31172530
Mitochondrial disease mimicking polymyositis: a case report.
Corrado A, Cantatore FP, Serlenga L, Amati A, Petruzzella V, Lapadula G. Corrado A, et al. Among authors: serlenga l. Clin Rheumatol. 2002 Sep;21(5):411-4. doi: 10.1007/s100670200110. Clin Rheumatol. 2002. PMID: 12223994
Cerebellar ataxia as atypical manifestation of the 3243A>G MELAS mutation.
Petruzzella V, Zoccolella S, Amati A, Torraco A, Lamberti P, Carnicella F, Serlenga L, Papa S. Petruzzella V, et al. Among authors: serlenga l. Clin Genet. 2004 Jan;65(1):64-5. doi: 10.1111/j..2004.00185.x. Clin Genet. 2004. PMID: 15032978 No abstract available.
55 results