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Page 1
Epilepsy in neuropathologically verified Alzheimer's disease.
Rauramaa T, Saxlin A, Lohvansuu K, Alafuzoff I, Pitkänen A, Soininen H. Rauramaa T, et al. Among authors: lohvansuu k. Seizure. 2018 May;58:9-12. doi: 10.1016/j.seizure.2018.03.014. Epub 2018 Mar 16. Seizure. 2018. PMID: 29602145 Free article.
Predictors of developmental dyslexia in European orthographies with varying complexity.
Landerl K, Ramus F, Moll K, Lyytinen H, Leppänen PH, Lohvansuu K, O'Donovan M, Williams J, Bartling J, Bruder J, Kunze S, Neuhoff N, Tóth D, Honbolygó F, Csépe V, Bogliotti C, Iannuzzi S, Chaix Y, Démonet JF, Longeras E, Valdois S, Chabernaud C, Delteil-Pinton F, Billard C, George F, Ziegler JC, Comte-Gervais I, Soares-Boucaud I, Gérard CL, Blomert L, Vaessen A, Gerretsen P, Ekkebus M, Brandeis D, Maurer U, Schulz E, van der Mark S, Müller-Myhsok B, Schulte-Körne G. Landerl K, et al. Among authors: lohvansuu k. J Child Psychol Psychiatry. 2013 Jun;54(6):686-94. doi: 10.1111/jcpp.12029. Epub 2012 Dec 10. J Child Psychol Psychiatry. 2013. PMID: 23227813
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
Becker J, Czamara D, Scerri TS, Ramus F, Csépe V, Talcott JB, Stein J, Morris A, Ludwig KU, Hoffmann P, Honbolygó F, Tóth D, Fauchereau F, Bogliotti C, Iannuzzi S, Chaix Y, Valdois S, Billard C, George F, Soares-Boucaud I, Gérard CL, van der Mark S, Schulz E, Vaessen A, Maurer U, Lohvansuu K, Lyytinen H, Zucchelli M, Brandeis D, Blomert L, Leppänen PH, Bruder J, Monaco AP, Müller-Myhsok B, Kere J, Landerl K, Nöthen MM, Schulte-Körne G, Paracchini S, Peyrard-Janvid M, Schumacher J. Becker J, et al. Among authors: lohvansuu k. Eur J Hum Genet. 2014 May;22(5):675-80. doi: 10.1038/ejhg.2013.199. Epub 2013 Sep 11. Eur J Hum Genet. 2014. PMID: 24022301 Free PMC article.
15 results