Wallgren-Pettersson C - Search Results

1

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. 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.

2

Genetics of congenital nemaline myopathy: a study of 10 families.

Wallgren-Pettersson C, Kääriäinen H, Rapola J, Salmi T, Jääskeläinen J, Donner M. Wallgren-Pettersson C, et al. J Med Genet. 1990 Aug;27(8):480-7. doi: 10.1136/jmg.27.8.480. J Med Genet. 1990. PMID: 2213842 Free PMC article.

3

Electromyography in congenital nemaline myopathy.

Wallgren-Pettersson C, Sainio K, Salmi T. Wallgren-Pettersson C, et al. Muscle Nerve. 1989 Jul;12(7):587-93. doi: 10.1002/mus.880120710. Muscle Nerve. 1989. PMID: 2674705 Review.

4

Pathology of congenital nemaline myopathy. A follow-up study.

Wallgren-Pettersson C, Rapola J, Donner M. Wallgren-Pettersson C, et al. J Neurol Sci. 1988 Feb;83(2-3):243-57. doi: 10.1016/0022-510x(88)90072-x. J Neurol Sci. 1988. PMID: 3356991

5

Pregnancy and delivery in congenital nemaline myopathy.

Wallgren-Pettersson C, Hiilesmaa VK, Paatero H. Wallgren-Pettersson C, et al. Acta Obstet Gynecol Scand. 1995 Sep;74(8):659-61. doi: 10.3109/00016349509013486. Acta Obstet Gynecol Scand. 1995. PMID: 7660780 No abstract available.

6

Alpha-actinin in nemaline bodies in congenital nemaline myopathy: immunological confirmation by light and electron microscopy.

Wallgren-Pettersson C, Jasani B, Newman GR, Morris GE, Jones S, Singhrao S, Clarke A, Virtanen I, Holmberg C, Rapola J. Wallgren-Pettersson C, et al. Neuromuscul Disord. 1995 Mar;5(2):93-104. doi: 10.1016/0960-8966(94)00035-8. Neuromuscul Disord. 1995. PMID: 7767098

7

Exclusion of two candidate loci for autosomal recessive nemaline myopathy.

Tahvanainen E, Beggs AH, Wallgren-Pettersson C. Tahvanainen E, et al. J Med Genet. 1994 Jan;31(1):79-80. doi: 10.1136/jmg.31.1.79. J Med Genet. 1994. PMID: 8151647 Free PMC article.

8

The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies.

Wallgren-Pettersson C, Clarke A, Samson F, Fardeau M, Dubowitz V, Moser H, Grimm T, Barohn RJ, Barth PG. Wallgren-Pettersson C, et al. J Med Genet. 1995 Sep;32(9):673-9. doi: 10.1136/jmg.32.9.673. J Med Genet. 1995. PMID: 8544184 Free PMC article. Review.

9

A gene for autosomal recessive nemaline myopathy assigned to chromosome 2q by linkage analysis.

Wallgren-Pettersson C, Avela K, Marchand S, Kolehmainen J, Tahvanainen E, Hansen FJ, Muntoni F, Dubowitz V, De Visser M, Van Langen IM, et al. Wallgren-Pettersson C, et al. Neuromuscul Disord. 1995 Nov;5(6):441-3. doi: 10.1016/0960-8966(95)00022-f. Neuromuscul Disord. 1995. PMID: 8580725

10

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.

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