Udd B - Search Results

1

Hartia-lantiodystrofioiden molekyyligenetiikka Suomessa.

Raheem O, Suominen T, Hackman P, Vihola A, Auranen M, Kalimo H, Mahjneh I, Kärppä M, Haapasalo H, Udd B. Raheem O, et al. Among authors: udd b. Duodecim. 2006;122(17):2130-6. Duodecim. 2006. PMID: 17115630 Finnish. No abstract available.

2

[Peripheral myopathies in Finland--a new kind of muscular dystrophy in the leg].

Udd B, Partanen J, Halonen P, Somer H, Falck B, Hakamies L, Heikkilä H, Ingo S, Kalimo H, Laulumaa V, et al. Udd B, et al. Duodecim. 1992;108(15):1331-8. Duodecim. 1992. PMID: 1366093 Review. Finnish. No abstract available.

3

[Respiratory arrests caused by congenital myasthenia gravis syndrome].

Byring RF, Ohno K, Pihko H, Gustafsson B, Hackman P, Engel A, Udd B. Byring RF, et al. Among authors: udd b. Duodecim. 2002;118(22):2323-6. Duodecim. 2002. PMID: 12523110 Finnish. No abstract available.

4

[Cases of oculopharyngeal muscular dystrophy even in Finland].

Hietaharju A, Juvonen V, Färkkilä M, Haapasalo H, Rantala I, Himanen SL, Kuusisto H, Sorri A, Udd B. Hietaharju A, et al. Among authors: udd b. Duodecim. 2003;119(7):625-8. Duodecim. 2003. PMID: 12762202 Finnish. No abstract available.

5

[A new type of myotonic dystrophy].

Auvinen S, Vihola A, Krahe R, Kupila J, Hackman P, Hietaharju A, Udd B. Auvinen S, et al. Among authors: udd b. Duodecim. 2003;119(8):707-13. Duodecim. 2003. PMID: 12806729 Review. Finnish. No abstract available.

6

New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).

Sallinen R, Vihola A, Bachinski LL, Huoponen K, Haapasalo H, Hackman P, Zhang S, Sirito M, Kalimo H, Meola G, Horelli-Kuitunen N, Wessman M, Krahe R, Udd B. Sallinen R, et al. Among authors: udd b. Neuromuscul Disord. 2004 Apr;14(4):274-83. doi: 10.1016/j.nmd.2004.01.002. Neuromuscul Disord. 2004. PMID: 15019706

7

Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3).

Haravuori H, Siitonen HA, Mahjneh I, Hackman P, Lahti L, Somer H, Peltonen L, Kestilä M, Udd B. Haravuori H, et al. Among authors: udd b. Neuromuscul Disord. 2004 Mar;14(3):183-7. doi: 10.1016/j.nmd.2003.12.003. Neuromuscul Disord. 2004. PMID: 15036327

8

Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophy.

Mahjneh I, Lamminen AE, Udd B, Paetau AE, Hackman P, Korhola OA, Somer HV. Mahjneh I, et al. Among authors: udd b. Acta Neurol Scand. 2004 Aug;110(2):87-93. doi: 10.1111/j.1600-0404.2004.00283.x. Acta Neurol Scand. 2004. PMID: 15242415

9

Titinopathies and extension of the M-line mutation phenotype beyond distal myopathy and LGMD2J.

Udd B, Vihola A, Sarparanta J, Richard I, Hackman P. Udd B, et al. Neurology. 2005 Feb 22;64(4):636-42. doi: 10.1212/01.WNL.0000151853.50144.82. Neurology. 2005. PMID: 15728284

10

Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patients.

Hackman P, Juvonen V, Sarparanta J, Penttinen M, Aärimaa T, Uusitalo M, Auranen M, Pihko H, Alén R, Junes M, Lönnqvist T, Kalimo H, Udd B. Hackman P, et al. Among authors: udd b. Muscle Nerve. 2005 Feb;31(2):199-204. doi: 10.1002/mus.20267. Muscle Nerve. 2005. PMID: 15736300

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