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Publications 1988 2019

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Conference article
2015

An economic model to assess the cost-benefit of BNCT

Kulvik, M., Hermans, R., Linnosmaa, I. & Shalowitz, J., Dec 2015, In : Applied Radiation and Isotopes. 106, p. 3-9 7 p.

Research output: Contribution to journalConference articleScientificpeer-review

2010

PERFECT Stroke - Aivohalvauksen hoidon aiheuttamat suorat terveydenhuollon kustannukset Suomessa 1999 - 2008

PERFECT Stroke, 2010, In : Avauksia. 2, p. 65-68 4 p.

Research output: Contribution to journalConference articleScientificpeer-review

2009

Capsid Modified Adenoviruses Display Robust, Long Term Gene Expression in Adult Skeletal Muscle Tissue\

Guse, K., Tyynismaa, H., Ahola-Erkkilä, S. T., Suomalainen, A., Pesonen, S., Cerullo, V. & Hemminki, A., 2009, In : Molecular therapy. 17, p. 363-364 2 p.

Research output: Contribution to journalConference articleScientificpeer-review

2008

Overexpression of Mitochondria DNA Helicase, Twinkle, Ameliorates Cardiac Remodeling and Failure in Mice

Inoue, T., Ide, T., Tyynismaa, H., Yoshida, M., Ando, M., Tanaka, A., Todaka, K., Kang, D., Suomalainen, A. & Sunagawa, K., 2008, In : Circulation Research. 118, p. S314-S315 2 p.

Research output: Contribution to journalConference articleScientificpeer-review

2005

ApoE e3 haplotype modulating the risk of Alzheimer's disease does not affect the risk of age-related macular degeneration

Immonen, I. J., Eerola, J., Tienari, P. J., Tervo, T., Moilanen, J., Ranta, P., Tommila, P. & Holopainen, J., 2005, In : Investigative Ophthalmology & Visual Science. 46, p. - 1 p.

Research output: Contribution to journalConference articleScientificpeer-review

2004

Cultured cell phenotypes of patients with Twinkle and POLG mutations

Lampinen, M., Tyynismaa, H., Ahlqvist, K. & Suomalainen, A., 2004, In : Biochimica et Biophysica Acta. Bioenergetics. 1657, p. 90-91 2 p.

Research output: Contribution to journalConference articleScientificpeer-review

Late-onset disease model for adPEO-Twinkle

Tyynismaa, H., Paetau, A., Rustin, P., Spelbrink, H. & Suomalainen, A., 2004, In : Biochimica et Biophysica Acta. Bioenergetics. 1657, p. 65-65 1 p.

Research output: Contribution to journalConference articleScientificpeer-review

2000

Exclusion of CACNA1A and KCNN1 as candidate genes for migraine in three 19p13-linked Finnish families.

Kaunisto, M., Hamalainen, E., Kallela, M., Harno, H., Marttila, P., Hovatta, I., Orpana, A., Peltonen, L., Farkkila, M., Palotie, A. & Wessman, M., 2000, In : American Journal of Human Genetics. 67, p. 329-329 1 p.

Research output: Contribution to journalConference articleScientificpeer-review

1999

Genetic studies on Finnish families with familial hemiplegic migraine.

Kaunisto, M., Kallela, M., Marttila, P., Farkkila, M., Havanka, H., Hamalainen, E., Hovatta, I., Orpana, A., Peltonen, L., Palotie, A. & Wessman, M., 1999, In : American Journal of Human Genetics. 65, p. A257-A257 1 p.

Research output: Contribution to journalConference articleScientificpeer-review