Articles dans des revues avec comité de lecture (84)
  1. 8. Jacquemin, V., Versbraegen, N., Duerinckx, S., Massart, A., Soblet, J., Perazzolo, C., Deconinck, N., Brischoux-Boucher, E., De Leener, A., Revencu, N., Janssens, S., Moorgat, S., Blaumeiser, B., Avela, K., Touraine, R., Abou Jaoude, I., Keymolen, K., Saugier-Veber, P., Lenaerts, T., Abramowicz, M., & Pirson, I. (2023). Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance. Human genomics, 17(1), 16. doi:10.1186/s40246-023-00464-w
  2. 9. Van Dyck, D., Deconinck, N., Aeby, A., Baijot, S., Coquelet, N., De Tiege, X., & Urbain, C. (2022). Atypical procedural learning skills in children with Developmental Coordination Disorder. Neuropsychology, development, and cognition. Section C, Child neuropsychology, 1-23. doi:10.1080/09297049.2022.2152433
  3. 10. Van Dyck, D., Baijot, S., Aeby, A., De Tiege, X., & Deconinck, N. (2022). Cognitive, perceptual, and motor profiles of school-aged children with developmental coordination disorder. Frontiers in Psychology, 13, 860766. doi:10.3389/fpsyg.2022.860766
  4. 11. Van Dyck, D., Deconinck, N., Aeby, A., Baijot, S., Coquelet, N., Trotta, N., Rovai, A., Goldman, S., Urbain, C., Wens, V., & De Tiege, X. (2022). Atypical resting-state functional brain connectivity in children with developmental coordination disorder. NeuroImage: Clinical, 33, 102928. doi:10.1016/j.nicl.2021.102928
  5. 12. Boemer, F., Caberg, J.-H., Beckers, P., Dideberg, V., di Fiore, S., Bours, V., Marie, S., Dewulf, J. J., Marcelis, L., Deconinck, N., Daron, A., Blasco-Perez, L., Tizzano, E., Hiligsmann, M., Lombet, J., Pereira, T., Lopez-Granados, L., Shalchian-Tehran, S., van Assche, V., Willems, A., Huybrechts, S., Mast, B., van Olden, R., Dangouloff, T., & Servais, L. (2021). Three years pilot of spinal muscular atrophy newborn screening turned into official program in Southern Belgium. Scientific reports, 11(1), 19922. doi:10.1038/s41598-021-99496-2
  6. 13. Duerinckx, S., Désir, J., Perazzolo, C., Badoer, C., Jacquemin, V., Soblet, J., Maystadt, I., Tunca, Y., Blaumeiser, B., Ceulemans, B., Courtens, W., Debray, F.-G., Donckier De Donceel, A., Devriendt, K., Jansen, A. C. M. A., Keymolen, K., Lederer, D., Loeys, B., Meuwissen, M. E. C., Moortgat, S., Mortier, G., Nassogne, M.-C., Sekhara, T., Van Coster, R., Van Den Ende, J., Van Der Aa, N., Van Esch, H., Vanakker, O., Verhelst, H., Vilain, C., Weckhuysen, S., Passemard, S., Verloes, A., Aeby, A., Deconinck, N., Van Bogaert, P., Pirson, I., & Abramowicz, M. (2021). Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy. Molecular genetics & genomic medicine. doi:10.1002/mgg3.1768
  7. 14. Van Dyck, D., Deconinck, N., Aeby, A., Baijot, S., Coquelet, N., Trotta, N., Rovai, A., Goldman, S., Urbain, C., Wens, V., & De Tiege, X. (2021). Resting-state functional brain connectivity is related to subsequent procedural learning skills in school-aged children. NeuroImage, 240, 118368. doi:10.1016/j.neuroimage.2021.118368
  8. 15. Kissine, M., Bertels, J., Deconinck, N., Passeri, G., & Deliens, G. (2021). Audio-visual integration in nonverbal or minimally verbal young autistic children. Journal of experimental psychology. General. doi:10.1037/xge0001040
  9. 16. Albajara Saenz, A., Villemonteix, T., Van Schuerbeek, P., Baijot, S., Septier, M., Defresne, P., Delvenne, V., Passeri, G., Raeymaekers, H., Victoor, L., Willaye, E., Peigneux, P., Deconinck, N., & Massat, I. (2021). Motor Abnormalities in Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Are Associated With Regional Grey Matter Volumes. Frontiers in neurology, 12, 666980. doi:10.3389/fneur.2021.666980
  10. 17. Aeby, A., Santalucia, R., Van Hecke, A., Nebbioso, A., Vermeiren, J., Deconinck, N., De Tiege, X., & Van Bogaert, P. (2021). A qualitative awake EEG score for the diagnosis of continuous spike and waves during sleep (CSWS) syndrome in self-limited focal epilepsy (SFE): A case-control study. Seizure, 84, 34-39.
  11. 18. Albajara Saenz, A., Van Schuerbeek, P., Baijot, S., Septier, M., Deconinck, N., Defresne, P., Delvenne, V., Passeri, G., Raeymaekers, H., Slama, H., Victoor, L., Willaye, E., Peigneux, P., Villemonteix, T., & Massat, I. (2020). Disorder-specific brain volumetric abnormalities in Attention-Deficit/Hyperactivity Disorder relative to Autism Spectrum Disorder. PloS one, 15(11), e0241856. doi:10.1371/journal.pone.0241856
  12. 19. Paternoster, L., Soblet, J., Aeby, A., De Tiege, X., Goldman, S., Yue, W. W., Coppens, S., Smits, G., Vilain, C., & Deconinck, N. (2020). Novel homozygous variant of carbonic anhydrase 8 gene expanding the phenotype of cerebellar ataxia, mental retardation, and disequilibrium syndrome subtype 3. American journal of medical genetics. Part A, 182(11), 2685-2693. doi:10.1002/ajmg.a.61805
    13. << Précédent 1 2 3 4 5 6 7 8 9 10 Suivant >>