Beggs AH - Search Results

1

Rod distribution and muscle fiber type modification in the progression of nemaline myopathy.

Gurgel-Giannetti J, Reed UC, Marie SK, Zanoteli E, Fireman MA, Oliveira AS, Werneck LC, Beggs AH, Zatz M, Vainzof M. Gurgel-Giannetti J, et al. Among authors: beggs ah. J Child Neurol. 2003 Mar;18(3):235-40. doi: 10.1177/08830738030180031501. J Child Neurol. 2003. PMID: 12731651

2

Deficiency of muscle alpha-actinin-3 is compatible with high muscle performance.

Zanoteli E, Lotuffo RM, Oliveira AS, Beggs AH, Canovas M, Zatz M, Vainzof M. Zanoteli E, et al. Among authors: beggs ah. J Mol Neurosci. 2003 Feb;20(1):39-42. doi: 10.1385/JMN:20:1:39. J Mol Neurosci. 2003. PMID: 12663933

3

Telethonin protein expression in neuromuscular disorders.

Vainzof M, Moreira ES, Suzuki OT, Faulkner G, Valle G, Beggs AH, Carpen O, Ribeiro AF, Zanoteli E, Gurgel-Gianneti J, Tsanaclis AM, Silva HC, Passos-Bueno MR, Zatz M. Vainzof M, et al. Among authors: beggs ah. Biochim Biophys Acta. 2002 Oct 9;1588(1):33-40. doi: 10.1016/s0925-4439(02)00113-8. Biochim Biophys Acta. 2002. PMID: 12379311 Free article.

4

Deficiency of alpha-actinin-3 (ACTN3) occurs in different forms of muscular dystrophy.

Vainzof M, Costa CS, Marie SK, Moreira ES, Reed U, Passos-Bueno MR, Beggs AH, Zatz M. Vainzof M, et al. Among authors: beggs ah. Neuropediatrics. 1997 Aug;28(4):223-8. doi: 10.1055/s-2007-973704. Neuropediatrics. 1997. PMID: 9309713

5

Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?

Passos-Bueno MR, Byth BC, Rosenberg S, Takata RI, Bakker E, Beggs AH, Pavanello RC, Vainzof M, Davies KE, Zatz M. Passos-Bueno MR, et al. Among authors: beggs ah. Am J Med Genet. 1993 Apr 15;46(2):172-5. doi: 10.1002/ajmg.1320460214. Am J Med Genet. 1993. PMID: 8484404

6

Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations.

Agrawal PB, Strickland CD, Midgett C, Morales A, Newburger DE, Poulos MA, Tomczak KK, Ryan MM, Iannaccone ST, Crawford TO, Laing NG, Beggs AH. Agrawal PB, et al. Among authors: beggs ah. Ann Neurol. 2004 Jul;56(1):86-96. doi: 10.1002/ana.20157. Ann Neurol. 2004. PMID: 15236405

7

Adult-onset nemaline myopathy and monoclonal gammopathy.

Keller CE, Hays AP, Rowland LP, Moghadaszadeh B, Beggs AH, Bhagat G. Keller CE, et al. Among authors: beggs ah. Arch Neurol. 2006 Jan;63(1):132-4. doi: 10.1001/archneur.63.1.132. Arch Neurol. 2006. PMID: 16401746

8

Thin filament length dysregulation contributes to muscle weakness in nemaline myopathy patients with nebulin deficiency.

Ottenheijm CA, Witt CC, Stienen GJ, Labeit S, Beggs AH, Granzier H. Ottenheijm CA, et al. Among authors: beggs ah. Hum Mol Genet. 2009 Jul 1;18(13):2359-69. doi: 10.1093/hmg/ddp168. Epub 2009 Apr 4. Hum Mol Genet. 2009. PMID: 19346529 Free PMC article.

9

Skeletal muscle repair in a mouse model of nemaline myopathy.

Sanoudou D, Corbett MA, Han M, Ghoddusi M, Nguyen MA, Vlahovich N, Hardeman EC, Beggs AH. Sanoudou D, et al. Among authors: beggs ah. Hum Mol Genet. 2006 Sep 1;15(17):2603-12. doi: 10.1093/hmg/ddl186. Epub 2006 Jul 28. Hum Mol Genet. 2006. PMID: 16877500 Free PMC article.

10

Genotype-phenotype correlations in nemaline myopathy caused by mutations in the genes for nebulin and skeletal muscle alpha-actin.

Wallgren-Pettersson C, Pelin K, Nowak KJ, Muntoni F, Romero NB, Goebel HH, North KN, Beggs AH, Laing NG; ENMC International Consortium On Nemaline Myopathy. Wallgren-Pettersson C, et al. Among authors: beggs ah. Neuromuscul Disord. 2004 Sep;14(8-9):461-70. doi: 10.1016/j.nmd.2004.03.006. Neuromuscul Disord. 2004. PMID: 15336686

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