Nigro V - Search Results

1

Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in Italian patients with hypertrophic cardiomyopathy.

Roncarati R, Latronico MV, Musumeci B, Aurino S, Torella A, Bang ML, Jotti GS, Puca AA, Volpe M, Nigro V, Autore C, Condorelli G. Roncarati R, et al. Among authors: nigro v. J Cell Physiol. 2011 Nov;226(11):2894-900. doi: 10.1002/jcp.22636. J Cell Physiol. 2011. PMID: 21302287 Free PMC article.

2

Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.

Nigro V, de Sá Moreira E, Piluso G, Vainzof M, Belsito A, Politano L, Puca AA, Passos-Bueno MR, Zatz M. Nigro V, et al. Nat Genet. 1996 Oct;14(2):195-8. doi: 10.1038/ng1096-195. Nat Genet. 1996. PMID: 8841194

3

Identification and characterization of a novel member of the dystrobrevin gene family.

Puca AA, Nigro V, Piluso G, Belsito A, Sampaolo S, Quaderi N, Rossi E, Di Iorio G, Ballabio A, Franco B. Puca AA, et al. Among authors: nigro v. FEBS Lett. 1998 Mar 20;425(1):7-13. doi: 10.1016/s0014-5793(98)00097-0. FEBS Lett. 1998. PMID: 9540997 Free article.

4

Lack of sodium channel mutation in an Italian family with paramyotonia congenita.

Sampaolo S, Puca AA, Nigro V, Cappa V, Sannino V, Sanges G, Bonavita V, Di Iorio G. Sampaolo S, et al. Among authors: nigro v. Neurology. 1999 Oct 22;53(7):1549-55. doi: 10.1212/wnl.53.7.1549. Neurology. 1999. PMID: 10534266

5

Scanning for mutations of the ryanodine receptor (RYR1) gene by denaturing HPLC: detection of three novel malignant hyperthermia alleles.

Tammaro A, Bracco A, Cozzolino S, Esposito M, Di Martino A, Savoia G, Zeuli L, Piluso G, Aurino S, Nigro V. Tammaro A, et al. Among authors: nigro v. Clin Chem. 2003 May;49(5):761-8. doi: 10.1373/49.5.761. Clin Chem. 2003. PMID: 12709367

6

On symptomatic heterozygous alpha-sarcoglycan gene mutation carriers.

Fischer D, Aurino S, Nigro V, Schröder R. Fischer D, et al. Among authors: nigro v. Ann Neurol. 2003 Nov;54(5):674-8. doi: 10.1002/ana.10738. Ann Neurol. 2003. PMID: 14595658

7

Readthrough strategies for stop codons in Duchenne muscular dystrophy.

Aurino S, Nigro V. Aurino S, et al. Among authors: nigro v. Acta Myol. 2006 Jun;25(1):5-12. Acta Myol. 2006. PMID: 17039975 Review.

8

Log-PCR: a new tool for immediate and cost-effective diagnosis of up to 85% of dystrophin gene mutations.

Trimarco A, Torella A, Piluso G, Maria Ventriglia V, Politano L, Nigro V. Trimarco A, et al. Among authors: nigro v. Clin Chem. 2008 Jun;54(6):973-81. doi: 10.1373/clinchem.2007.097881. Epub 2008 Apr 10. Clin Chem. 2008. PMID: 18403565

9

A missense mutation in CASK causes FG syndrome in an Italian family.

Piluso G, D'Amico F, Saccone V, Bismuto E, Rotundo IL, Di Domenico M, Aurino S, Schwartz CE, Neri G, Nigro V. Piluso G, et al. Among authors: nigro v. Am J Hum Genet. 2009 Feb;84(2):162-77. doi: 10.1016/j.ajhg.2008.12.018. Epub 2009 Feb 5. Am J Hum Genet. 2009. PMID: 19200522 Free PMC article.

10

Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes.

Fanin M, Nascimbeni AC, Aurino S, Tasca E, Pegoraro E, Nigro V, Angelini C. Fanin M, et al. Among authors: nigro v. Neurology. 2009 Apr 21;72(16):1432-5. doi: 10.1212/WNL.0b013e3181a1885e. Neurology. 2009. PMID: 19380703

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