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Page 1
[A technological platform for cerebral palsy - the ICT4Rehab project].
Van Sint Jan S, Wermenbol V, Van Bogaert P, Desloovere K, Degelaen M, Dan B, Salvia P, Ortibus E, Bonnechère B, Le Borgne YA, Bontempi G, Vansummeren S, Sholukha V, Moiseev F, Rooze M. Van Sint Jan S, et al. Among authors: wermenbol v. Med Sci (Paris). 2013 May;29(5):529-36. doi: 10.1051/medsci/2013295017. Epub 2013 May 28. Med Sci (Paris). 2013. PMID: 23732103 Free article. French.
A familial heterozygous null mutation of MET in autism spectrum disorder.
Lambert N, Wermenbol V, Pichon B, Acosta S, van den Ameele J, Perazzolo C, Messina D, Musumeci MF, Dessars B, De Leener A, Abramowicz M, Vilain C. Lambert N, et al. Among authors: wermenbol v. Autism Res. 2014 Oct;7(5):617-22. doi: 10.1002/aur.1396. Epub 2014 Jun 6. Autism Res. 2014. PMID: 24909855
[Systematic follow-up of infants born preterm].
Aeby A, Wermenbol V, Ciardelli R, Mûller MF, Wetzburger C, Van Bogaert P. Aeby A, et al. Among authors: wermenbol v. Rev Med Brux. 2015 Sep;36(4):219-22. Rev Med Brux. 2015. PMID: 26591304 Review. French.
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus.
Anderson BH, Kasher PR, Mayer J, Szynkiewicz M, Jenkinson EM, Bhaskar SS, Urquhart JE, Daly SB, Dickerson JE, O'Sullivan J, Leibundgut EO, Muter J, Abdel-Salem GM, Babul-Hirji R, Baxter P, Berger A, Bonafé L, Brunstom-Hernandez JE, Buckard JA, Chitayat D, Chong WK, Cordelli DM, Ferreira P, Fluss J, Forrest EH, Franzoni E, Garone C, Hammans SR, Houge G, Hughes I, Jacquemont S, Jeannet PY, Jefferson RJ, Kumar R, Kutschke G, Lundberg S, Lourenço CM, Mehta R, Naidu S, Nischal KK, Nunes L, Ounap K, Philippart M, Prabhakar P, Risen SR, Schiffmann R, Soh C, Stephenson JB, Stewart H, Stone J, Tolmie JL, van der Knaap MS, Vieira JP, Vilain CN, Wakeling EL, Wermenbol V, Whitney A, Lovell SC, Meyer S, Livingston JH, Baerlocher GM, Black GC, Rice GI, Crow YJ. Anderson BH, et al. Among authors: wermenbol v. Nat Genet. 2012 Jan 22;44(3):338-42. doi: 10.1038/ng.1084. Nat Genet. 2012. PMID: 22267198 Free article.
Prevalence of cerebral palsy and factors associated with cerebral palsy subtype: A population-based study in Belgium.
Dhondt E, Dan B, Plasschaert F, Degelaen M, Dielman C, Dispa D, Ebetiuc I, Hasaerts D, Kenis S, Lombardo C, Pelc K, Wermenbol V, Ortibus E; Belgian Cerebral Palsy Register. Dhondt E, et al. Among authors: wermenbol v. Eur J Paediatr Neurol. 2023 Sep;46:8-23. doi: 10.1016/j.ejpn.2023.06.003. Epub 2023 Jun 14. Eur J Paediatr Neurol. 2023. PMID: 37364404
15 results