Nigro V - Search Results

1

A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F.

Dinçer P, Bönnemann CG, Erdir Aker O, Akçoren Z, Nigro V, Kunkel LM, Topalolu H. Dinçer P, et al. Among authors: nigro v. Neuromuscul Disord. 2000 Jun;10(4-5):247-50. doi: 10.1016/s0960-8966(00)00100-0. Neuromuscul Disord. 2000. PMID: 10838250

2

Beta-sarcoglycan gene mutations in Turkey.

Balci B, Wilichowski E, Haliloğlu G, Talim B, Aurino S, Kremer E, Ebinger F, Senbil N, Anlar B, Kale G, Nigro V, Topaloğlu H, Bonnemann C, Dinçer P. Balci B, et al. Among authors: nigro v. Acta Myol. 2004 Dec;23(3):154-8. Acta Myol. 2004. PMID: 15938573

3

Calpain-3 mutations in Turkey.

Balci B, Aurino S, Haliloglu G, Talim B, Erdem S, Akcören Z, Tan E, Caglar M, Richard I, Nigro V, Topaloglu H, Dincer P. Balci B, et al. Among authors: nigro v. Eur J Pediatr. 2006 May;165(5):293-8. doi: 10.1007/s00431-005-0046-3. Epub 2006 Jan 13. Eur J Pediatr. 2006. PMID: 16411092

4

The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.

Vainzof M, Passos-Bueno MR, Canovas M, Moreira ES, Pavanello RC, Marie SK, Anderson LV, Bonnemann CG, McNally EM, Nigro V, Kunkel LM, Zatz M. Vainzof M, et al. Among authors: nigro v. Hum Mol Genet. 1996 Dec;5(12):1963-9. doi: 10.1093/hmg/5.12.1963. Hum Mol Genet. 1996. PMID: 8968750

5

Delta-sarcoglycan is required for early zebrafish muscle organization.

Guyon JR, Mosley AN, Jun SJ, Montanaro F, Steffen LS, Zhou Y, Nigro V, Zon LI, Kunkel LM. Guyon JR, et al. Among authors: nigro v. Exp Cell Res. 2005 Mar 10;304(1):105-15. doi: 10.1016/j.yexcr.2004.10.032. Epub 2004 Dec 8. Exp Cell Res. 2005. PMID: 15707578

6

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

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

A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.

Moreira ES, Vainzof M, Marie SK, Nigro V, Zatz M, Passos-Bueno MR. Moreira ES, et al. Among authors: nigro v. J Med Genet. 1998 Nov;35(11):951-3. doi: 10.1136/jmg.35.11.951. J Med Genet. 1998. PMID: 9832045 Free PMC article.

9

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

10

A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G).

Vieira NM, Naslavsky MS, Licinio L, Kok F, Schlesinger D, Vainzof M, Sanchez N, Kitajima JP, Gal L, Cavaçana N, Serafini PR, Chuartzman S, Vasquez C, Mimbacas A, Nigro V, Pavanello RC, Schuldiner M, Kunkel LM, Zatz M. Vieira NM, et al. Among authors: nigro v. Hum Mol Genet. 2014 Aug 1;23(15):4103-10. doi: 10.1093/hmg/ddu127. Epub 2014 Mar 18. Hum Mol Genet. 2014. PMID: 24647604

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