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From phenomenology to neurophysiological understanding of hallucinations in children and adolescents.
Jardri R, Bartels-Velthuis AA, Debbané M, Jenner JA, Kelleher I, Dauvilliers Y, Plazzi G, Demeulemeester M, David CN, Rapoport J, Dobbelaere D, Escher S, Fernyhough C. Jardri R, et al. Among authors: dobbelaere d. Schizophr Bull. 2014 Jul;40 Suppl 4(Suppl 4):S221-32. doi: 10.1093/schbul/sbu029. Schizophr Bull. 2014. PMID: 24936083 Free PMC article. Review.
Hypoglycaemia related to inherited metabolic diseases in adults.
Douillard C, Mention K, Dobbelaere D, Wemeau JL, Saudubray JM, Vantyghem MC. Douillard C, et al. Among authors: dobbelaere d. Orphanet J Rare Dis. 2012 May 15;7:26. doi: 10.1186/1750-1172-7-26. Orphanet J Rare Dis. 2012. PMID: 22587661 Free PMC article. Review.
A novel HADHA variant associated with an atypical moderate and late-onset LCHAD deficiency.
Dessein AF, Hebbar E, Vamecq J, Lebredonchel E, Devos A, Ghoumid J, Mention K, Dobbelaere D, Chevalier-Curt MJ, Fontaine M, Defoort S, Smirnov V, Douillard C, Dhaenens CM. Dessein AF, et al. Among authors: dobbelaere d. Mol Genet Metab Rep. 2022 Mar 15;31:100860. doi: 10.1016/j.ymgmr.2022.100860. eCollection 2022 Jun. Mol Genet Metab Rep. 2022. PMID: 35782617 Free PMC article.
Mitochondrial acetoacetyl-CoA thiolase deficiency: basal ganglia impairment may occur independently of ketoacidosis.
Paquay S, Bourillon A, Pichard S, Benoist JF, de Lonlay P, Dobbelaere D, Fouilhoux A, Guffon N, Rouvet I, Labarthe F, Mention K, Touati G, Valayannopoulos V, Ogier de Baulny H, Elmaleh-Bergès M, Acquaviva-Bourdain C, Vianey-Saban C, Schiff M. Paquay S, et al. Among authors: dobbelaere d. J Inherit Metab Dis. 2017 May;40(3):415-422. doi: 10.1007/s10545-017-0021-y. Epub 2017 Mar 2. J Inherit Metab Dis. 2017. PMID: 28255778
195 results