Van Bogaert P - Search Results

1

A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome.

Vilain C, Rens C, Aeby A, Balériaux D, Van Bogaert P, Remiche G, Smet J, Van Coster R, Abramowicz M, Pirson I. Vilain C, et al. Among authors: van coster r, van bogaert p. Clin Genet. 2012 Sep;82(3):264-70. doi: 10.1111/j.1399-0004.2011.01743.x. Epub 2011 Jul 18. Clin Genet. 2012. PMID: 21696386

2

Mutation of a potassium channel-related gene in progressive myoclonic epilepsy.

Van Bogaert P, Azizieh R, Désir J, Aeby A, De Meirleir L, Laes JF, Christiaens F, Abramowicz MJ. Van Bogaert P, et al. Ann Neurol. 2007 Jun;61(6):579-86. doi: 10.1002/ana.21121. Ann Neurol. 2007. PMID: 17455289

3

Phenotypes and genotypes in non-consanguineous and consanguineous primary microcephaly: High incidence of epilepsy.

Duerinckx S, Désir J, Perazzolo C, Badoer C, Jacquemin V, Soblet J, Maystadt I, Tunca Y, Blaumeiser B, Ceulemans B, Courtens W, Debray FG, Destree A, Devriendt K, Jansen A, Keymolen K, Lederer D, Loeys B, Meuwissen M, Moortgat S, Mortier G, Nassogne MC, 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. Duerinckx S, et al. Among authors: van der aa n, van esch h, van coster r, van bogaert p, van den ende j. Mol Genet Genomic Med. 2021 Sep;9(9):e1768. doi: 10.1002/mgg3.1768. Epub 2021 Aug 17. Mol Genet Genomic Med. 2021. PMID: 34402213 Free PMC article.

4

Primary microcephaly with ASPM mutation shows simplified cortical gyration with antero-posterior gradient pre- and post-natally.

Desir J, Cassart M, David P, Van Bogaert P, Abramowicz M. Desir J, et al. Among authors: van bogaert p. Am J Med Genet A. 2008 Jun 1;146A(11):1439-43. doi: 10.1002/ajmg.a.32312. Am J Med Genet A. 2008. PMID: 18452193

5

Nonlinear microstructural changes in the right superior temporal sulcus and lateral occipitotemporal gyrus between 35 and 43 weeks in the preterm brain.

Aeby A, Van Bogaert P, David P, Balériaux D, Vermeylen D, Metens T, De Tiège X. Aeby A, et al. Among authors: van bogaert p. Neuroimage. 2012 Oct 15;63(1):104-10. doi: 10.1016/j.neuroimage.2012.06.013. Epub 2012 Jun 17. Neuroimage. 2012. PMID: 22713672

6

Neuroimaging fails to identify asymptomatic carriers of familial porencephaly.

Vilain C, Van Regemorter N, Verloes A, David P, Van Bogaert P. Vilain C, et al. Among authors: van regemorter n, van bogaert p. Am J Med Genet. 2002 Oct 1;112(2):198-202. doi: 10.1002/ajmg.10452. Am J Med Genet. 2002. PMID: 12244556

7

Posterior reversible encephalopathy syndrome revealing acute post-streptococcal glomerulonephritis.

Aeby A, David P, Fricx C, Jissendi P, Blecic S, Van Bogaert P. Aeby A, et al. Among authors: van bogaert p. J Child Neurol. 2006 Mar;21(3):250-1. doi: 10.2310/7010.2006.00057. J Child Neurol. 2006. PMID: 16901429

8

Biallelic gephyrin variants lead to impaired GABAergic inhibition in a patient with developmental and epileptic encephalopathy.

Macha A, Liebsch F, Fricke S, Hetsch F, Neuser F, Johannes L, Kress V, Djémié T, Santamaria-Araujo JA, Vilain C, Aeby A, Van Bogaert P, Dejanovic B, Weckhuysen S, Meier JC, Schwarz G. Macha A, et al. Among authors: van bogaert p. Hum Mol Genet. 2022 Mar 21;31(6):901-913. doi: 10.1093/hmg/ddab298. Hum Mol Genet. 2022. PMID: 34617111

9

MRI of patients with cerebral palsy and normal CT scan.

van Bogaert P, Baleriaux D, Christophe C, Szliwowski HB. van Bogaert P, et al. Neuroradiology. 1992;34(1):52-6. doi: 10.1007/BF00588433. Neuroradiology. 1992. PMID: 1553038

10

Addendum: contribution of magnetoencephalography to presurgical work-up of pharmacoresistant epilepsy.

De Tiège X, Balériaux D, Van Bogaert P. De Tiège X, et al. Among authors: van bogaert p. JBR-BTR. 2007 Jul-Aug;90(4):247. JBR-BTR. 2007. PMID: 17966237 No abstract available.

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