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Risk of arrhythmia in type I myotonic dystrophy: the role of clinical and genetic variables.
Cudia P, Bernasconi P, Chiodelli R, Mangiola F, Bellocci F, Dello Russo A, Angelini C, Romeo V, Melacini P, Politano L, Palladino A, Nigro G, Siciliano G, Falorni M, Bongiorni MG, Falcone C, Mantegazza R, Morandi L. Cudia P, et al. J Neurol Neurosurg Psychiatry. 2009 Jul;80(7):790-3. doi: 10.1136/jnnp.2008.162594. Epub 2009 Feb 22. J Neurol Neurosurg Psychiatry. 2009. PMID: 19237383
Identification of novel mutations in five patients with mitochondrial encephalomyopathy.
Valente L, Piga D, Lamantea E, Carrara F, Uziel G, Cudia P, Zani A, Farina L, Morandi L, Mora M, Spinazzola A, Zeviani M, Tiranti V. Valente L, et al. Among authors: cudia p. Biochim Biophys Acta. 2009 May;1787(5):491-501. doi: 10.1016/j.bbabio.2008.10.001. Epub 2008 Oct 15. Biochim Biophys Acta. 2009. PMID: 18977334 Free article.
Autonomic regulation in muscular dystrophy.
Angelini C, Di Leo R, Cudia P. Angelini C, et al. Among authors: cudia p. Front Physiol. 2013 Sep 20;4:257. doi: 10.3389/fphys.2013.00257. eCollection 2013. Front Physiol. 2013. PMID: 24065927 Free PMC article. No abstract available.
A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score.
Lamperti C, Fabbri G, Vercelli L, D'Amico R, Frusciante R, Bonifazi E, Fiorillo C, Borsato C, Cao M, Servida M, Greco F, Di Leo R, Volpi L, Manzoli C, Cudia P, Pastorello E, Ricciardi L, Siciliano G, Galluzzi G, Rodolico C, Santoro L, Tomelleri G, Angelini C, Ricci E, Palmucci L, Moggio M, Tupler R. Lamperti C, et al. Among authors: cudia p. Muscle Nerve. 2010 Aug;42(2):213-7. doi: 10.1002/mus.21671. Muscle Nerve. 2010. PMID: 20544930
17 results