Nigro G - Search Results

1

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein.

Nigro V, Piluso G, Belsito A, Politano L, Puca AA, Papparella S, Rossi E, Viglietto G, Esposito MG, Abbondanza C, Medici N, Molinari AM, Nigro G, Puca GA. Nigro V, et al. Among authors: nigro g. Hum Mol Genet. 1996 Aug;5(8):1179-86. doi: 10.1093/hmg/5.8.1179. Hum Mol Genet. 1996. PMID: 8842738

2

Detection of a nonsense mutation in the dystrophin gene by multiple SSCP.

Nigro V, Politano L, Nigro G, Romano SC, Molinari AM, Puca GA. Nigro V, et al. Among authors: nigro g. Hum Mol Genet. 1992 Oct;1(7):517-20. doi: 10.1093/hmg/1.7.517. Hum Mol Genet. 1992. PMID: 1307253

3

Novel small mutations along the DMD/BMD gene associated with different phenotypes.

Nigro V, Nigro G, Esposito MG, Comi LI, Molinari AM, Puca GA, Politano L. Nigro V, et al. Among authors: nigro g. Hum Mol Genet. 1994 Oct;3(10):1907-8. doi: 10.1093/hmg/3.10.1907. Hum Mol Genet. 1994. PMID: 7849724 No abstract available.

4

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.

5

Identification of the Syrian hamster cardiomyopathy gene.

Nigro V, Okazaki Y, Belsito A, Piluso G, Matsuda Y, Politano L, Nigro G, Ventura C, Abbondanza C, Molinari AM, Acampora D, Nishimura M, Hayashizaki Y, Puca GA. Nigro V, et al. Among authors: nigro g. Hum Mol Genet. 1997 Apr;6(4):601-7. doi: 10.1093/hmg/6.4.601. Hum Mol Genet. 1997. PMID: 9097966

6

Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complex.

Lancioni A, Rotundo IL, Kobayashi YM, D'Orsi L, Aurino S, Nigro G, Piluso G, Acampora D, Cacciottolo M, Campbell KP, Nigro V. Lancioni A, et al. Among authors: nigro v, nigro g. Hum Mol Genet. 2011 Dec 1;20(23):4644-54. doi: 10.1093/hmg/ddr398. Epub 2011 Sep 2. Hum Mol Genet. 2011. PMID: 21890494 Free PMC article.

7

Evaluation of cardiac and respiratory involvement in sarcoglycanopathies.

Politano L, Nigro V, Passamano L, Petretta V, Comi LI, Papparella S, Nigro G, Rambaldi PF, Raia P, Pini A, Mora M, Giugliano MA, Esposito MG, Nigro G. Politano L, et al. Among authors: nigro v, nigro g. Neuromuscul Disord. 2001 Mar;11(2):178-85. doi: 10.1016/s0960-8966(00)00174-7. Neuromuscul Disord. 2001. PMID: 11257475

8

Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes.

Piluso G, Politano L, Aurino S, Fanin M, Ricci E, Ventriglia VM, Belsito A, Totaro A, Saccone V, Topaloglu H, Nascimbeni AC, Fulizio L, Broccolini A, Canki-Klain N, Comi LI, Nigro G, Angelini C, Nigro V. Piluso G, et al. Among authors: nigro v, nigro g. J Med Genet. 2005 Sep;42(9):686-93. doi: 10.1136/jmg.2004.028738. J Med Genet. 2005. PMID: 16141003 Free PMC article.

9

Use of a lower dosage liver-detargeted AAV vector to prevent hamster muscular dystrophy.

Rotundo IL, Lancioni A, Savarese M, D'Orsi L, Iacomino M, Nigro G, Piluso G, Auricchio A, Nigro V. Rotundo IL, et al. Among authors: nigro v, nigro g. Hum Gene Ther. 2013 Apr;24(4):424-30. doi: 10.1089/hum.2012.121. Epub 2013 Apr 4. Hum Gene Ther. 2013. PMID: 23427808 Free PMC article.

10

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

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