Laing NG - Search Results

1

Muscle disease caused by mutations in the skeletal muscle alpha-actin gene (ACTA1).

Sparrow JC, Nowak KJ, Durling HJ, Beggs AH, Wallgren-Pettersson C, Romero N, Nonaka I, Laing NG. Sparrow JC, et al. Among authors: laing ng. Neuromuscul Disord. 2003 Sep;13(7-8):519-31. doi: 10.1016/s0960-8966(03)00101-9. Neuromuscul Disord. 2003. PMID: 12921789 Review.

2

A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1.

Beggs AH, Phillips HA, Kozman H, Mulley JC, Wilton SD, Kunkel LM, Laing NG. Beggs AH, et al. Among authors: laing ng. Genomics. 1992 Aug;13(4):1314-5. doi: 10.1016/0888-7543(92)90054-v. Genomics. 1992. PMID: 1505962

3

40th ENMC Sponsored International Workshop: Nemaline Myopathy. 2-4 February 1996, Naarden, The Netherlands.

Wallgren-Pettersson C, Laing N. Wallgren-Pettersson C, et al. Neuromuscul Disord. 1996 Oct;6(5):389-91. doi: 10.1016/0960-8966(96)00354-9. Neuromuscul Disord. 1996. PMID: 8938704 Review. No abstract available.

4

Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy.

North KN, Laing NG, Wallgren-Pettersson C. North KN, et al. Among authors: laing ng. J Med Genet. 1997 Sep;34(9):705-13. doi: 10.1136/jmg.34.9.705. J Med Genet. 1997. PMID: 9321754 Free PMC article. Review. No abstract available.

5

51st ENMC International Workshop: Nemaline Myopathy. 13-15 June 1997, Naarden, The Netherlands.

Wallgren-Pettersson C, Beggs AH, Laing NG. Wallgren-Pettersson C, et al. Among authors: laing ng. Neuromuscul Disord. 1998 Feb;8(1):53-6. Neuromuscul Disord. 1998. PMID: 9565992 No abstract available.

6

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy.

Pelin K, Hilpelä P, Donner K, Sewry C, Akkari PA, Wilton SD, Wattanasirichaigoon D, Bang ML, Centner T, Hanefeld F, Odent S, Fardeau M, Urtizberea JA, Muntoni F, Dubowitz V, Beggs AH, Laing NG, Labeit S, de la Chapelle A, Wallgren-Pettersson C. Pelin K, et al. Among authors: laing ng. Proc Natl Acad Sci U S A. 1999 Mar 2;96(5):2305-10. doi: 10.1073/pnas.96.5.2305. Proc Natl Acad Sci U S A. 1999. PMID: 10051637 Free PMC article.

7

Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy.

Mastaglia FL, Nowak KJ, Stell R, Phillips BA, Edmondston JE, Dorosz SM, Wilton SD, Hallmayer J, Kakulas BA, Laing NG. Mastaglia FL, et al. Among authors: laing ng. J Neurol Neurosurg Psychiatry. 1999 Aug;67(2):174-9. doi: 10.1136/jnnp.67.2.174. J Neurol Neurosurg Psychiatry. 1999. PMID: 10406984 Free PMC article.

8

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.

Nowak KJ, Wattanasirichaigoon D, Goebel HH, Wilce M, Pelin K, Donner K, Jacob RL, Hübner C, Oexle K, Anderson JR, Verity CM, North KN, Iannaccone ST, Müller CR, Nürnberg P, Muntoni F, Sewry C, Hughes I, Sutphen R, Lacson AG, Swoboda KJ, Vigneron J, Wallgren-Pettersson C, Beggs AH, Laing NG. Nowak KJ, et al. Among authors: laing ng. Nat Genet. 1999 Oct;23(2):208-12. doi: 10.1038/13837. Nat Genet. 1999. PMID: 10508519

9

Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy.

Wallgren-Pettersson C, Pelin K, Hilpelä P, Donner K, Porfirio B, Graziano C, Swoboda KJ, Fardeau M, Urtizberea JA, Muntoni F, Sewry C, Dubowitz V, Iannaccone S, Minetti C, Pedemonte M, Seri M, Cusano R, Lammens M, Castagna-Sloane A, Beggs AH, Laing NG, de la Chapelle A. Wallgren-Pettersson C, et al. Among authors: laing ng. Neuromuscul Disord. 1999 Dec;9(8):564-72. doi: 10.1016/s0960-8966(99)00061-9. Neuromuscul Disord. 1999. PMID: 10619714

10

Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy.

Tan P, Briner J, Boltshauser E, Davis MR, Wilton SD, North K, Wallgren-Pettersson C, Laing NG. Tan P, et al. Among authors: laing ng. Neuromuscul Disord. 1999 Dec;9(8):573-9. doi: 10.1016/s0960-8966(99)00053-x. Neuromuscul Disord. 1999. PMID: 10619715

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