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Page 1
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. Among authors: politano l. 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
The cardiomyopathy of Duchenne/Becker consultands.
Comi LI, Nigro G, Politano L, Petretta VR. Comi LI, et al. Among authors: politano l. Int J Cardiol. 1992 Mar;34(3):297-305. doi: 10.1016/0167-5273(92)90028-2. Int J Cardiol. 1992. PMID: 1563855
Skeletal muscle cytochrome c in X-linked muscle dystrophies.
Nigro G, Comi LI, Politano L, Limongelli FM. Nigro G, et al. Among authors: politano l. Clin Chim Acta. 1991 Oct 14;202(1-2):89-93. doi: 10.1016/0009-8981(91)90259-f. Clin Chim Acta. 1991. PMID: 1666985 No abstract available.
Evaluation of the cardiomyopathy in Becker muscular dystrophy.
Nigro G, Comi LI, Politano L, Limongelli FM, Nigro V, De Rimini ML, Giugliano MA, Petretta VR, Passamano L, Restucci B, et al. Nigro G, et al. Among authors: politano l. Muscle Nerve. 1995 Mar;18(3):283-91. doi: 10.1002/mus.880180304. Muscle Nerve. 1995. PMID: 7870105
Mutation of dystrophin gene and cardiomyopathy.
Nigro G, Politano L, Nigro V, Petretta VR, Comi LI. Nigro G, et al. Among authors: politano l. Neuromuscul Disord. 1994 Jul;4(4):371-9. doi: 10.1016/0960-8966(94)90073-6. Neuromuscul Disord. 1994. PMID: 7981594
236 results