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Pirjo Isohanni

  • Finland

1990 …2019
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Publications 1990 2019

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Review Article
2019

Veltto imeväinen

Seppä-Moilanen, M., Isohanni, P. & Lönnqvist, T., 2019, In : Duodecim. 135, 4, p. 359-366 8 p.

Research output: Contribution to journalReview ArticleScientificpeer-review

2018

PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature

Reijnders, M. R. F., Janowski, R., Alvi, M., Self, J. E., van Essen, T. J., Vreeburg, M., Rouhl, R. P. W., Stevens, S. J. C., Stegmann, A. P. A., Schieving, J., Pfundt, R., van Dijk, K., Smeets, E., Stumpel, C. T. R. M., Bok, L. A., Cobben, J. M., Engelen, M., Mansour, S., Whiteford, M., Chandler, K. E. & 31 others, Douzgou, S., Cooper, N. S., Tan, E-C., Foo, R., Lai, A. H. M., Rankin, J., Green, A., Lönnqvist, T., Isohanni, P., Williams, S., Ruhoy, I., Carvalho, K. S., Dowling, J. J., Lev, D. L., Sterbova, K., Lassuthova, P., Neupauerova, J., Waugh, J. L., Keros, S., Clayton-Smith, J., Smithson, S. F., Brunner, H. G., van Hoeckel, C., Anderson, M., Clowes, V. E., Siu, V. M., Selber, P., Leventer, R. J., Nellaker, C., Niessing, D. & DDD Study, Feb 2018, In : Journal of Medical Genetics. 55, 2, p. 104-113 10 p.

Research output: Contribution to journalReview ArticleScientificpeer-review

Open Access
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2015

Leigh Syndrome: Neuropathology and Pathogenesis

Lake, N. J., Bird, M. J., Isohanni, P. & Paetau, A., Jun 2015, In : Journal of Neuropathology and Experimental Neurology. 74, 6, p. 482-492 11 p.

Research output: Contribution to journalReview ArticleScientificpeer-review

2010

Mitochondrial DNA depletion syndromes - Many genes, common mechanisms

Wartiovaara, A. & Isohanni, P., 2010, In : Neuromuscular Disorders. 20, 7, p. 429-437 9 p.

Research output: Contribution to journalReview ArticleScientificpeer-review