Haapasalo H - Search Results

1

Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2.

Vihola A, Bassez G, Meola G, Zhang S, Haapasalo H, Paetau A, Mancinelli E, Rouche A, Hogrel JY, Laforêt P, Maisonobe T, Pellissier JF, Krahe R, Eymard B, Udd B. Vihola A, et al. Among authors: haapasalo h. Neurology. 2003 Jun 10;60(11):1854-7. doi: 10.1212/01.wnl.0000065898.61358.09. Neurology. 2003. PMID: 12796551 Free article.

2

Proliferative activity and DNA index do not significantly predict survival in primary central nervous system lymphoma.

Aho R, Haapasalo H, Alanen K, Haltia M, Paetau A, Kalimo H. Aho R, et al. Among authors: haapasalo h. J Neuropathol Exp Neurol. 1995 Nov;54(6):826-32. doi: 10.1097/00005072-199511000-00009. J Neuropathol Exp Neurol. 1995. PMID: 7595655

3

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: haapasalo h. Neuromuscul Disord. 2004 Apr;14(4):274-83. doi: 10.1016/j.nmd.2004.01.002. Neuromuscul Disord. 2004. PMID: 15019706

4

A quantitative method for the assessment of intraepidermal nerve fibers in small-fiber neuropathy.

Koskinen M, Hietaharju A, Kyläniemi M, Peltola J, Rantala I, Udd B, Haapasalo H. Koskinen M, et al. Among authors: haapasalo h. J Neurol. 2005 Jul;252(7):789-94. doi: 10.1007/s00415-005-0743-x. Epub 2005 Mar 29. J Neurol. 2005. PMID: 15789134

5

Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2.

Vihola A, Bachinski LL, Sirito M, Olufemi SE, Hajibashi S, Baggerly KA, Raheem O, Haapasalo H, Suominen T, Holmlund-Hampf J, Paetau A, Cardani R, Meola G, Kalimo H, Edström L, Krahe R, Udd B. Vihola A, et al. Among authors: haapasalo h. Acta Neuropathol. 2010 Apr;119(4):465-79. doi: 10.1007/s00401-010-0637-6. Epub 2010 Jan 12. Acta Neuropathol. 2010. PMID: 20066428 Free PMC article.

6

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

7

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

8

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.

9

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.

10

An unusual phenotype of late-onset desminopathy.

Palmio J, Penttilä S, Huovinen S, Haapasalo H, Udd B. Palmio J, et al. Among authors: haapasalo h. Neuromuscul Disord. 2013 Nov;23(11):922-3. doi: 10.1016/j.nmd.2013.06.374. Epub 2013 Jul 30. Neuromuscul Disord. 2013. PMID: 23911073 No abstract available.

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