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Distal myopathies in Finnish patients.
Palmio J, Jokela M, Sandell S, Suominen T, Penttilä S, Udd B. Palmio J, et al. Among authors: suominen t. Duodecim. 2016;132(18):1635-44. Duodecim. 2016. PMID: 29188941 Review.
Atypical phenotypes in titinopathies explained by second titin mutations.
Evilä A, Vihola A, Sarparanta J, Raheem O, Palmio J, Sandell S, Eymard B, Illa I, Rojas-Garcia R, Hankiewicz K, Negrão L, Löppönen T, Nokelainen P, Kärppä M, Penttilä S, Screen M, Suominen T, Richard I, Hackman P, Udd B. Evilä A, et al. Among authors: suominen t. Ann Neurol. 2014 Feb;75(2):230-40. doi: 10.1002/ana.24102. Epub 2014 Feb 24. Ann Neurol. 2014. PMID: 24395473
Differential isoform expression and selective muscle involvement in muscular dystrophies.
Huovinen S, Penttilä S, Somervuo P, Keto J, Auvinen P, Vihola A, Huovinen S, Pelin K, Raheem O, Salenius J, Suominen T, Hackman P, Udd B. Huovinen S, et al. Among authors: suominen t. Am J Pathol. 2015 Oct;185(10):2833-42. doi: 10.1016/j.ajpath.2015.06.018. Epub 2015 Aug 9. Am J Pathol. 2015. PMID: 26269091 Free article.
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: suominen t. Duodecim. 2006;122(17):2130-6. Duodecim. 2006. PMID: 17115630 Finnish. No abstract available.
213 results