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Items: 7

1.

GraphoGame - a catalyst for multi-level promotion of literacy in diverse contexts.

Ojanen E, Ronimus M, Ahonen T, Chansa-Kabali T, February P, Jere-Folotiya J, Kauppinen KP, Ketonen R, Ngorosho D, Pitkänen M, Puhakka S, Sampa F, Walubita G, Yalukanda C, Pugh K, Richardson U, Serpell R, Lyytinen H.

Front Psychol. 2015 Jun 10;6:671. doi: 10.3389/fpsyg.2015.00671. eCollection 2015.

2.

The associations of objectively measured physical activity and sedentary time with cognitive functions in school-aged children.

Syväoja HJ, Tammelin TH, Ahonen T, Kankaanpää A, Kantomaa MT.

PLoS One. 2014 Jul 25;9(7):e103559. doi: 10.1371/journal.pone.0103559. eCollection 2014.

3.

Physical activity and obesity mediate the association between childhood motor function and adolescents' academic achievement.

Kantomaa MT, Stamatakis E, Kankaanpää A, Kaakinen M, Rodriguez A, Taanila A, Ahonen T, Järvelin MR, Tammelin T.

Proc Natl Acad Sci U S A. 2013 Jan 29;110(5):1917-22. doi: 10.1073/pnas.1214574110. Epub 2012 Dec 31.

4.

Identification of tumor epithelium and stroma in tissue microarrays using texture analysis.

Linder N, Konsti J, Turkki R, Rahtu E, Lundin M, Nordling S, Haglund C, Ahonen T, Pietikäinen M, Lundin J.

Diagn Pathol. 2012 Mar 2;7:22. doi: 10.1186/1746-1596-7-22.

5.

Suspected motor problems and low preference for active play in childhood are associated with physical inactivity and low fitness in adolescence.

Kantomaa MT, Purtsi J, Taanila AM, Remes J, Viholainen H, Rintala P, Ahonen T, Tammelin TH.

PLoS One. 2011 Jan 18;6(1):e14554. doi: 10.1371/journal.pone.0014554.

6.

Gender differences relating to metabolic syndrome and proinflammation in Finnish subjects with elevated blood pressure.

Ahonen T, Saltevo J, Laakso M, Kautiainen H, Kumpusalo E, Vanhala M.

Mediators Inflamm. 2009;2009:959281. doi: 10.1155/2009/959281. Epub 2009 Aug 20.

7.

A dominant gene for developmental dyslexia on chromosome 3.

Nopola-Hemmi J, Myllyluoma B, Haltia T, Taipale M, Ollikainen V, Ahonen T, Voutilainen A, Kere J, Widén E.

J Med Genet. 2001 Oct;38(10):658-64.

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