1. 2018
  2. Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations

    Stouffs, K., Moortgat, S., Vanderhasselt, T., Vandervore, L., Dica, A., Mathot, M., Keymolen, K., Seneca, S., Gheldof, A., De Meirleir, L. & Jansen, A. C., 1 Dec 2018, In : European Journal of Medical Genetics. 61, 12, p. 733-737 5 p.

    Research output: Contribution to journalArticleResearchpeer-review

  3. Expanding the clinical spectrum of biallelic ZNF335 variants

    Stouffs, K., Stergachis, A. B., Vanderhasselt, T., Dica, A., Janssens, S., Vandervore, L., Gheldof, A., Bodamer, O., Keymolen, K., Seneca, S., Liebaers, I., Jayaraman, D., Hill, H. E., Partlow, J. N., Walsh, C. A. & Jansen, A. C., Aug 2018, In : Clinical Genetics. 94, 2, p. 246-251 6 p.

    Research output: Contribution to journalArticleResearchpeer-review

  4. Three Siblings with Progressive Encephalopathy and Destructive White Matter Lesions

    Franckx, H., Stouffs, K., Vanderhasselt, T., Seneca, S., Gheldof, A. & De Meirleir, L., 2018, In : Journal of the International Child Neurology Association. 18, p. 110-110 1 p.

    Research output: Contribution to journalArticleResearchpeer-review

  5. 2017
  6. Bi-allelic variants in COL3A1 encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cysts

    Vandervore, L., Stouffs, K., Tanyalçin, I., Vanderhasselt, T., Roelens, F., Holder-Espinasse, M., Jørgensen, A., Pepin, M. G., Petit, F., Khau Van Kien, P., Bahi-Buisson, N., Lissens, W., Gheldof, A., Byers, P. H. & Jansen, A. C., Jun 2017, In : Journal of Medical Genetics. 54, 6, p. 432-440 9 p.

    Research output: Contribution to journalArticleResearchpeer-review

  7. 2016
  8. Interhemispheric Connections between the Primary Visual Cortical Areas via the Anterior Commissure in Human Callosal Agenesis

    van Meer, N., Houtman, A. C., Van Schuerbeek, P., Vanderhasselt, T., Milleret, C. & Ten Tusscher, M. P., 2016, In : Frontiers in Systems Neuroscience. 10, p. 101

    Research output: Contribution to journalArticleResearchpeer-review

  9. 2014
  10. Thin genu of the corpus callosum points to mutation in FOXG1 in a child with acquired microcephaly, trigonocephaly, and intellectual developmental disorder: A case report and review of literature

    De Bruyn, C., Vanderhasselt, T., Tanyalcin, I., Keymolen, K., Van Rompaey, K., De Meirleir, L. & Jansen, A., May 2014, In : Eur J Paediatr Neurol. 18, 3, p. 420-426

    Research output: Contribution to journalArticleResearchpeer-review

  11. Multi-modality imaging in an exceptional case of aborted sudden cardiac death

    Sonck, J., Tanaka, K., Czapla, J., Vanderhasselt, T., Kayaert, P., Scott, B. & Van Camp, G., 1 Feb 2014, In : International Journal of Cardiology. 171, 2, p. 57-58 2 p.

    Research output: Contribution to journalArticleResearchpeer-review

  12. Polymicrogyria with dysmorphic basal ganglia? Think tubulin!

    Amrom, D., Tanyalcin, I., Verhelst, H., Deconinck, N., Brouhard, G., Decarie, J-C., Vanderhasselt, T., Das, S., Hamdan, F. F., Lissens, W., Michaud, J., Jansen, A. & Hayden, M. R. (ed.), Feb 2014, In : Clinical Genetics. 85, p. 178-183 6 p.

    Research output: Contribution to journalArticleResearchpeer-review

  13. Hemangioperiocytoma simulating meningioma in a 41-year-old man

    Rabaey, E., Desmet, K., De Maeseneer, M., Vanderhasselt, T. & Stadnik, T., 2014, In : JBR-BTR. 97, 5, p. 315 1 p.

    Research output: Contribution to journalComment/debateResearch

  14. Thin genu of the corpus callosum points to mutation in FOXG1 in a child with acquiredmicrocephaly, trigonocephaly, and intellectual developmental disorder: A case report and review of literature

    De Bruyn, C., Vanderhasselt, T., Tanyalcin, I., Keymolen, K., Van Rompaey, K., De Meirleir, L., Jansen, A. & Lagae, L. (ed.), 2014, In : European Journal of Paediatric Neurology. 18, p. 420-426 7 p.

    Research output: Contribution to journalArticleResearchpeer-review

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