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Page 1
An Overview of Molecular Mechanisms in Fabry Disease.
Amodio F, Caiazza M, Monda E, Rubino M, Capodicasa L, Chiosi F, Simonelli V, Dongiglio F, Fimiani F, Pepe N, Chimenti C, Calabrò P, Limongelli G. Amodio F, et al. Among authors: simonelli v. Biomolecules. 2022 Oct 12;12(10):1460. doi: 10.3390/biom12101460. Biomolecules. 2022. PMID: 36291669 Free PMC article. Review.
Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes.
Monda E, Lioncino M, Caiazza M, Simonelli V, Nesti C, Rubino M, Perna A, Mauriello A, Budillon A, Pota V, Bruno G, Varone A, Nigro V, Santorelli FM, Pacileo G, Russo MG, Frisso G, Sampaolo S, Limongelli G. Monda E, et al. Among authors: simonelli v. Int J Mol Sci. 2023 May 22;24(10):9108. doi: 10.3390/ijms24109108. Int J Mol Sci. 2023. PMID: 37240454 Free PMC article.
Pathophysiology, Functional Assessment and Prognostic Implications of Nutritional Disorders in Systemic Amyloidosis.
Dongiglio F, Monda E, Palmiero G, Verrillo F, Rubino M, Diana G, Cirillo A, Fusco A, Vetrano E, Lioncino M, Caiazza M, Cerciello G, Capodicasa L, Chiosi F, Simonelli V, De Rimini ML, Natale F, Di Santo A, Moscarella E, Calabrò P, Limongelli G. Dongiglio F, et al. Among authors: simonelli v. J Clin Med. 2023 Jan 9;12(2):528. doi: 10.3390/jcm12020528. J Clin Med. 2023. PMID: 36675458 Free PMC article. Review.
Combined Clinical, Molecular, and Muscle Biopsy Approach to Unveil Prevalence and Clinical Features of Rare Neuromuscular and Mitochondrial Diseases in Patients With Cardiomyopathies.
Lioncino M, Monda E, Caiazza M, Simonelli V, Nesti C, Mauriello A, Budillon A, Di Santo A, Bruno G, Varone A, Nigro V, Santorelli FM, Pacileo G, Russo MG, Frisso G, Sampaolo S, Limongelli G. Lioncino M, et al. Among authors: simonelli v. Circ Genom Precis Med. 2023 Aug;16(4):412-414. doi: 10.1161/CIRCGEN.123.004122. Epub 2023 May 17. Circ Genom Precis Med. 2023. PMID: 37194584 No abstract available.