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Page 1
Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin.
Hakonen AH, Heiskanen S, Juvonen V, Lappalainen I, Luoma PT, Rantamaki M, Goethem GV, Lofgren A, Hackman P, Paetau A, Kaakkola S, Majamaa K, Varilo T, Udd B, Kaariainen H, Bindoff LA, Suomalainen A. Hakonen AH, et al. Among authors: heiskanen s. Am J Hum Genet. 2005 Sep;77(3):430-41. doi: 10.1086/444548. Epub 2005 Jul 27. Am J Hum Genet. 2005. PMID: 16080118 Free PMC article.
Local energy depletion in the basal forebrain increases sleep.
Kalinchuk AV, Urrila AS, Alanko L, Heiskanen S, Wigren HK, Suomela M, Stenberg D, Porkka-Heiskanen T. Kalinchuk AV, et al. Among authors: heiskanen s. Eur J Neurosci. 2003 Feb;17(4):863-9. doi: 10.1046/j.1460-9568.2003.02532.x. Eur J Neurosci. 2003. PMID: 12603276
Maternal Risk Factors for Congenital Vertebral Anomalies: A Population-Based Study.
Raitio A, Heiskanen S, Syvänen J, Leinonen MK, Kemppainen T, Löyttyniemi E, Ahonen M, Gissler M, Helenius I. Raitio A, et al. Among authors: heiskanen s. J Bone Joint Surg Am. 2023 Jul 19;105(14):1087-1092. doi: 10.2106/JBJS.22.01370. Epub 2023 May 22. J Bone Joint Surg Am. 2023. PMID: 37216430
Surgical and Health-related Quality of life Outcomes in Children With Congenital Scoliosis During 5-year Follow-up. Comparison to Age and Sex-matched Healthy Controls.
Haapala H, Heiskanen S, Syvänen J, Raitio A, Helenius L, Ahonen M, Diarbakerli E, Gerdhem P, Helenius I. Haapala H, et al. Among authors: heiskanen s. J Pediatr Orthop. 2023 Jul 1;43(6):e451-e457. doi: 10.1097/BPO.0000000000002408. Epub 2023 Mar 30. J Pediatr Orthop. 2023. PMID: 36998176
14 results