Haapasalo H - 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: haapasalo h. Duodecim. 2006;122(17):2130-6. Duodecim. 2006. PMID: 17115630 Finnish. No abstract available.

2

Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibers.

Raheem O, Huovinen S, Suominen T, Haapasalo H, Udd B. Raheem O, et al. Among authors: haapasalo h. Acta Neuropathol. 2010 Apr;119(4):495-500. doi: 10.1007/s00401-010-0643-8. Epub 2010 Jan 28. Acta Neuropathol. 2010. PMID: 20107819

3

[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: haapasalo h. Duodecim. 2003;119(7):625-8. Duodecim. 2003. PMID: 12762202 Finnish. No abstract available.

4

Mutant (CCTG)n expansion causes abnormal expression of zinc finger protein 9 (ZNF9) in myotonic dystrophy type 2.

Raheem O, Olufemi SE, Bachinski LL, Vihola A, Sirito M, Holmlund-Hampf J, Haapasalo H, Li YP, Udd B, Krahe R. Raheem O, et al. Among authors: haapasalo h. Am J Pathol. 2010 Dec;177(6):3025-36. doi: 10.2353/ajpath.2010.100179. Epub 2010 Oct 22. Am J Pathol. 2010. PMID: 20971734 Free PMC article.

5

Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish family.

Palmio J, Sandell S, Suominen T, Penttilä S, Raheem O, Hackman P, Huovinen S, Haapasalo H, Udd B. Palmio J, et al. Among authors: haapasalo h. Neuromuscul Disord. 2011 Aug;21(8):551-5. doi: 10.1016/j.nmd.2011.05.008. Neuromuscul Disord. 2011. PMID: 21684747

6

New immunohistochemical method for improved myotonia and chloride channel mutation diagnostics.

Raheem O, Penttilä S, Suominen T, Kaakinen M, Burge J, Haworth A, Sud R, Schorge S, Haapasalo H, Sandell S, Metsikkö K, Hanna M, Udd B. Raheem O, et al. Among authors: haapasalo h. Neurology. 2012 Nov 27;79(22):2194-200. doi: 10.1212/WNL.0b013e31827595e2. Epub 2012 Nov 14. Neurology. 2012. PMID: 23152584 Free PMC article. Clinical Trial.

7

[Hypothyroidism-associated alveolar hypoventilation and myopathy].

Saarelainen S, Jäntti V, Kalimo H, Haapasalo H. Saarelainen S, et al. Among authors: haapasalo h. Duodecim. 1993;109(9):759-63. Duodecim. 1993. PMID: 8062755 Finnish. No abstract available.

8

[Inflammatory muscle diseases].

Kalimo H, Alanen A, Falck B, Haapasalo H, Halonen P, Kalimo K, Salonen R, Aärimaa T. Kalimo H, et al. Among authors: haapasalo h. Duodecim. 1993;109(16):1373-84. Duodecim. 1993. PMID: 7720596 Review. Finnish. No abstract available.

9

The enigma of 7q36 linked autosomal dominant limb girdle muscular dystrophy.

Sandell S, Huovinen S, Sarparanta J, Luque H, Raheem O, Haapasalo H, Hackman P, Udd B. Sandell S, et al. Among authors: haapasalo h. J Neurol Neurosurg Psychiatry. 2010 Aug;81(8):834-9. doi: 10.1136/jnnp.2009.192351. J Neurol Neurosurg Psychiatry. 2010. PMID: 20682716

10

Aivojen osmoottinen myelinolyysi.

Jolma P, Leinonen J, Kähärä V, Haapasalo H, Keränen T, Honkaniemi J. Jolma P, et al. Among authors: haapasalo h. Duodecim. 2007;123(9):1096-102. Duodecim. 2007. PMID: 17612271 Finnish. No abstract available.

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