Showing 1 - 5 results of 5 for search 'H. Martikainen', query time: 0.03s Refine Results
  1. 1
    Incidence and prevalence of mtDNA-related adult mitochondrial disease in Southwest Finland, 2009–2022: an observational, population-based study

    Incidence and prevalence of mtDNA-related adult mitochondrial disease in Southwest Finland, 2009–2022: an observational, population-based study by Kari Majamaa, Mika H Martikainen

    Published 2024-02-01
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    Article
  2. 2
    Magnetic resonance imaging negative myelopathy in Leber’s hereditary optic neuropathy: a case report

    Magnetic resonance imaging negative myelopathy in Leber’s hereditary optic neuropathy: a case report by Mika H. Martikainen, Miika Suomela, Kari Majamaa

    Published 2022-12-01
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  3. 3
    Consensus-based statements for the management of mitochondrial stroke-like episodes [version 1; peer review: 2 approved]

    Consensus-based statements for the management of mitochondrial stroke-like episodes [version 1; peer review: 2 approved] by Yi Shiau Ng, Laurence A. Bindoff, Gráinne S. Gorman, Rita Horvath, Thomas Klopstock, Michelangelo Mancuso, Mika H. Martikainen, Robert Mcfarland, Victoria Nesbitt, Robert D. S. Pitceathly, Andrew M. Schaefer, Doug M. Turnbull

    Published 2019-12-01
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  4. 4
    Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

    Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis by C. S. Gallagher, N. Mäkinen, H. R. Harris, N. Rahmioglu, O. Uimari, J. P. Cook, N. Shigesi, T. Ferreira, D. R. Velez-Edwards, T. L. Edwards, S. Mortlock, Z. Ruhioglu, F. Day, C. M. Becker, V. Karhunen, H. Martikainen, M.-R. Järvelin, R. M. Cantor, P. M. Ridker, K. L. Terry, J. E. Buring, S. D. Gordon, S. E. Medland, G. W. Montgomery, D. R. Nyholt, D. A. Hinds, J. Y. Tung, the 23andMe Research Team, J. R. B. Perry, P. A. Lind, J. N. Painter, N. G. Martin, A. P. Morris, D. I. Chasman, S. A. Missmer, K. T. Zondervan, C. C. Morton

    Published 2022-09-01
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  5. 5
    Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

    Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis by C. S. Gallagher, N. Mäkinen, H. R. Harris, N. Rahmioglu, O. Uimari, J. P. Cook, N. Shigesi, T. Ferreira, D. R. Velez-Edwards, T. L. Edwards, S. Mortlock, Z. Ruhioglu, F. Day, C. M. Becker, V. Karhunen, H. Martikainen, M.-R. Järvelin, R. M. Cantor, P. M. Ridker, K. L. Terry, J. E. Buring, S. D. Gordon, S. E. Medland, G. W. Montgomery, D. R. Nyholt, D. A. Hinds, J. Y. Tung, the 23andMe Research Team, J. R. B. Perry, P. A. Lind, J. N. Painter, N. G. Martin, A. P. Morris, D. I. Chasman, S. A. Missmer, K. T. Zondervan, C. C. Morton

    Published 2019-10-01
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    Article

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