Neurology. Genetics, 2376-7839

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Related Publications
  1. Clinical and pathologic phenotype of a large family with heterozygous STUB1 mutation

    Mol, M. O., van Rooij, J. G. J., Brusse, E., Verkerk, A. J. M. H., Melhem, S., den Dunnen, W. F. A., Rizzu, P., Cupidi, C., van Swieten, J. C. & Donker Kaat, L., Jun-2020, In : Neurology. Genetics. 6, 3, p. e417

    Research output: Contribution to journalArticleAcademicpeer-review

  2. Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes

    Atrial Fibrillation Genetics Conso, Int Stroke Genetics Consortium, Rienstra, M., Geelhoed, B., Hagemeijer, Y. P., Verweij, N., Siland, J. E. & van der Harst, P., Dec-2018, In : Neurology. Genetics. 4, 6, 8 p., 293.

    Research output: Contribution to journalArticleAcademicpeer-review

  3. ACO2 homozygous missense mutation associated with complicated Hereditary spastic paraplegia

    Bouwkamp, C. G., Afawi, Z., Fattal-Valevski, A., Krabbendam, I. E., Rivetti, S., Masalha, R., Quadri, M., Breedveld, G. J., Mandel, H., Tailakh, M. A., Beverloo, H. B., Stevanin, G., Brice, A., van IJcken, W. F. J., Vernooij, M. W., Dolga, A. M., de Vrij, F. M. S., Bonifati, V. & Kushner, S. A., Apr-2018, In : Neurology. Genetics. 4, 2, p. e223

    Research output: Contribution to journalArticleAcademicpeer-review

  4. Expanding thephenotype toward spastic paraparesis: A mutation in the M2 domain

    Waalkens, A. J. E., Vansenne, F., van der Hout, A. H., Zutt, R., Mourmans, J., Tolosa, E., de Koning, T. J. & Tijssen, M. A. J., Feb-2018, In : Neurology. Genetics. 4, 1, 2 p., e214.

    Research output: Contribution to journalArticleAcademicpeer-review

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