Laing N - Search Results

1

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

Wallgren-Pettersson C, Laing N. Wallgren-Pettersson C, et al. Among authors: laing n. 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.

2

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.

3

Refined localisation of the genes for nebulin and titin on chromosome 2q allows the assignment of nebulin as a candidate gene for autosomal recessive nemaline myopathy.

Pelin K, Ridanpää M, Donner K, Wilton S, Krishnarajah J, Laing N, Kolmerer B, Millevoi S, Labeit S, de la Chapelle A, Wallgren-Petterson C. Pelin K, et al. Among authors: laing n. Eur J Hum Genet. 1997 Jul-Aug;5(4):229-34. Eur J Hum Genet. 1997. PMID: 9359044

4

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.

5

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.

6

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

7

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

8

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

9

Report of the 70th ENMC International Workshop: nemaline myopathy, 11-13 June 1999, Naarden, The Netherlands.

Wallgren-Pettersson C, Laing NG. Wallgren-Pettersson C, et al. Among authors: laing ng. Neuromuscul Disord. 2000 Jun;10(4-5):299-306. doi: 10.1016/s0960-8966(99)00129-7. Neuromuscul Disord. 2000. PMID: 10838258 No abstract available.

10

Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene.

Jungbluth H, Sewry CA, Brown SC, Nowak KJ, Laing NG, Wallgren-Pettersson C, Pelin K, Manzur AY, Mercuri E, Dubowitz V, Muntoni F. Jungbluth H, et al. Among authors: laing ng. Neuromuscul Disord. 2001 Jan;11(1):35-40. doi: 10.1016/s0960-8966(00)00167-x. Neuromuscul Disord. 2001. PMID: 11166164

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