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Epidemiology of lissencephaly type I.
de Rijk-van Andel JF, Arts WF, Hofman A, Staal A, Niermeijer MF. de Rijk-van Andel JF, et al. Neuroepidemiology. 1991;10(4):200-4. doi: 10.1159/000110270. Neuroepidemiology. 1991. PMID: 1745330
Neuroimaging in lissencephaly type I.
de Rijk-van Andel JF, van der Knaap MS, Valk J, Arts WF. de Rijk-van Andel JF, et al. Neuroradiology. 1991;33(3):230-3. doi: 10.1007/BF00588223. Neuroradiology. 1991. PMID: 1881540
EEG in type I lissencephaly.
de Rijk-van Andel JF, Arts WF, de Weerd AW. de Rijk-van Andel JF, et al. Dev Med Child Neurol. 1988 Feb;30(1):126-7. doi: 10.1111/j.1469-8749.1988.tb04736.x. Dev Med Child Neurol. 1988. PMID: 3371564 No abstract available.
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.
Namavar Y, Barth PG, Kasher PR, van Ruissen F, Brockmann K, Bernert G, Writzl K, Ventura K, Cheng EY, Ferriero DM, Basel-Vanagaite L, Eggens VR, Krägeloh-Mann I, De Meirleir L, King M, Graham JM Jr, von Moers A, Knoers N, Sztriha L, Korinthenberg R; PCH Consortium; Dobyns WB, Baas F, Poll-The BT. Namavar Y, et al. Brain. 2011 Jan;134(Pt 1):143-56. doi: 10.1093/brain/awq287. Epub 2010 Oct 15. Brain. 2011. PMID: 20952379 Free PMC article.
Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders.
van Harssel JJ, Weckhuysen S, van Kempen MJ, Hardies K, Verbeek NE, de Kovel CG, Gunning WB, van Daalen E, de Jonge MV, Jansen AC, Vermeulen RJ, Arts WF, Verhelst H, Fogarasi A, de Rijk-van Andel JF, Kelemen A, Lindhout D, De Jonghe P, Koeleman BP, Suls A, Brilstra EH. van Harssel JJ, et al. Among authors: de rijk van andel jf. Neurogenetics. 2013 Feb;14(1):23-34. doi: 10.1007/s10048-013-0353-1. Epub 2013 Jan 20. Neurogenetics. 2013. PMID: 23334464
29 results