Wallgren-Pettersson C - Search Results

1

Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin gene.

Kiiski KJ, Lehtokari VL, Vihola AK, Laitila JM, Huovinen S, Sagath LJ, Evilä AE, Paetau AE, Sewry CA, Hackman PB, Pelin KB, Wallgren-Pettersson C, Udd B. Kiiski KJ, et al. Neuromuscul Disord. 2019 Feb;29(2):97-107. doi: 10.1016/j.nmd.2018.12.007. Epub 2018 Dec 20. Neuromuscul Disord. 2019. PMID: 30679003

2

Ultrasonography, CT, and MRI of muscles in congenital nemaline myopathy.

Wallgren-Pettersson C, Kivisaari L, Jääskeläinen J, Lamminen A, Holmberg C. Wallgren-Pettersson C, et al. Pediatr Neurol. 1990 Jan-Feb;6(1):20-8. doi: 10.1016/0887-8994(90)90074-b. Pediatr Neurol. 1990. PMID: 2178616 Review.

3

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.

4

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.

5

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

6

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.

7

Report on the 20th ENMC sponsored international workshop: myotubular/centronuclear myopathy.

Wallgren-Pettersson C, Thomas NS. Wallgren-Pettersson C, et al. Neuromuscul Disord. 1994 Jan;4(1):71-4. doi: 10.1016/0960-8966(94)90050-7. Neuromuscul Disord. 1994. PMID: 8173354 No abstract available.

8

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

9

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.

10

Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?

Udd B, Krahe R, Wallgren-Pettersson C, Falck B, Kalimo H. Udd B, et al. Neuromuscul Disord. 1997 Jun;7(4):217-28. doi: 10.1016/s0960-8966(97)00041-2. Neuromuscul Disord. 1997. PMID: 9196902

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