Nigro G - Search Results

1

Improvement of survival in Duchenne Muscular Dystrophy: retrospective analysis of 835 patients.

Passamano L, Taglia A, Palladino A, Viggiano E, D'Ambrosio P, Scutifero M, Rosaria Cecio M, Torre V, DE Luca F, Picillo E, Paciello O, Piluso G, Nigro G, Politano L. Passamano L, et al. Among authors: nigro g. Acta Myol. 2012 Oct;31(2):121-5. Acta Myol. 2012. PMID: 23097603 Free PMC article.

2

The cardiomyopathy of Duchenne/Becker consultands.

Comi LI, Nigro G, Politano L, Petretta VR. Comi LI, et al. Among authors: nigro g. Int J Cardiol. 1992 Mar;34(3):297-305. doi: 10.1016/0167-5273(92)90028-2. Int J Cardiol. 1992. PMID: 1563855

3

Skeletal muscle cytochrome c in X-linked muscle dystrophies.

Nigro G, Comi LI, Politano L, Limongelli FM. Nigro G, et al. 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.

4

The incidence and evolution of cardiomyopathy in Duchenne muscular dystrophy.

Nigro G, Comi LI, Politano L, Bain RJ. Nigro G, et al. Int J Cardiol. 1990 Mar;26(3):271-7. doi: 10.1016/0167-5273(90)90082-g. Int J Cardiol. 1990. PMID: 2312196

5

Prospective study of X-linked progressive muscular dystrophy in Campania.

Nigro G, Comi LI, Limongelli FM, Giugliano MA, Politano L, Petretta V, Passamano L, Stefanelli S. Nigro G, et al. Muscle Nerve. 1983 May;6(4):253-62. doi: 10.1002/mus.880060403. Muscle Nerve. 1983. PMID: 6683357

6

Dilated cardiomyopathy of muscular dystrophy: a multifaceted approach to management.

Nigro G, Comi LI, Politano L, Nigro V. Nigro G, et al. Among authors: nigro v. Semin Neurol. 1995 Mar;15(1):90-2. doi: 10.1055/s-2008-1041012. Semin Neurol. 1995. PMID: 7638465 Clinical Trial. No abstract available.

7

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: nigro v. Muscle Nerve. 1995 Mar;18(3):283-91. doi: 10.1002/mus.880180304. Muscle Nerve. 1995. PMID: 7870105

8

Mutation of dystrophin gene and cardiomyopathy.

Nigro G, Politano L, Nigro V, Petretta VR, Comi LI. Nigro G, et al. Among authors: nigro v. Neuromuscul Disord. 1994 Jul;4(4):371-9. doi: 10.1016/0960-8966(94)90073-6. Neuromuscul Disord. 1994. PMID: 7981594

9

SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function.

Nigro V, Bruni P, Ciccodicola A, Politano L, Nigro G, Piluso G, Cappa V, Covone AE, Romeo G, D'Urso M. Nigro V, et al. Among authors: nigro g. Hum Mol Genet. 1995 Oct;4(10):2003-4. doi: 10.1093/hmg/4.10.2003. Hum Mol Genet. 1995. PMID: 8595433 No abstract available.

10

Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies.

Politano L, Nigro V, Nigro G, Petretta VR, Passamano L, Papparella S, Di Somma S, Comi LI. Politano L, et al. Among authors: nigro v, nigro g. JAMA. 1996 May 1;275(17):1335-8. JAMA. 1996. PMID: 8614119

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