Publications by authors named "Nicolas Deconinck"

36Publications

MEG and high-density EEG resting-state networks mapping in children.

Clin Neurophysiol 2020 Nov 23;131(11):2713-2715. Epub 2020 Sep 23.

Laboratoire de Cartographie fonctionnelle du Cerveau, UNI - ULB, Neurosciences Institute, Université libre de Bruxelles (ULB), Brussels, Belgium; Department of Functional Neuroimaging, Service of Nuclear Medicine, CUB Hôpital Erasme, Université libre de Bruxelles, Brussels, Belgium.

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http://dx.doi.org/10.1016/j.clinph.2020.09.003DOI Listing
November 2020

Novel homozygous variant of carbonic anhydrase 8 gene expanding the phenotype of cerebellar ataxia, mental retardation, and disequilibrium syndrome subtype 3.

Am J Med Genet A 2020 Aug 18. Epub 2020 Aug 18.

Department of Pediatric Neurology, Hôpital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles (ULB), Brussels, Belgium.

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http://dx.doi.org/10.1002/ajmg.a.61805DOI Listing
August 2020

ADHD and ASD: distinct brain patterns of inhibition-related activation?

Transl Psychiatry 2020 01 22;10(1):24. Epub 2020 Jan 22.

Neuropsychology and Functional Neuroimaging Research Group (UR2NF) at the Centre for Research in Cognition and Neurosciences (CRCN), Université Libre de Bruxelles (ULB), Brussels, Belgium.

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http://dx.doi.org/10.1038/s41398-020-0707-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026183PMC
January 2020

Sitting in patients with spinal muscular atrophy type 1 treated with nusinersen.

Dev Med Child Neurol 2020 03 4;62(3):310-314. Epub 2019 Dec 4.

Institute I-motion, Armand Trousseau Hospital, Paris, France.

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http://dx.doi.org/10.1111/dmcn.14412DOI Listing
March 2020

Duplication 2p16 is associated with perisylvian polymicrogyria.

Am J Med Genet A 2019 12 29;179(12):2343-2356. Epub 2019 Oct 29.

Department of Pediatrics (Genetics) and Neurology, University of Washington, and Seattle Children's Research Institute, Seattle, Washington.

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http://dx.doi.org/10.1002/ajmg.a.61342DOI Listing
December 2019

Congenital Titinopathy: Comprehensive characterization and pathogenic insights.

Ann Neurol 2018 06;83(6):1105-1124

Harry Perkins Institute, University of Western Australia, Nedlands, Western Australia, Australia.

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http://dx.doi.org/10.1002/ana.25241DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105519PMC
June 2018

EEG Dynamics of a Go/Nogo Task in Children with ADHD.

Brain Sci 2017 Dec 20;7(12). Epub 2017 Dec 20.

Laboratory of Neurophysiology and Movement Biomechanics, Université Libre de Bruxelles, CP640, 808 route de Lennik, 1070 Brussels, Belgium.

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http://dx.doi.org/10.3390/brainsci7120167DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742770PMC
December 2017

BCL11A frameshift mutation associated with dyspraxia and hypotonia affecting the fine, gross, oral, and speech motor systems.

Am J Med Genet A 2018 01 27;176(1):201-208. Epub 2017 Sep 27.

Department of Pediatric Neurology, Hôpital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles, Brussels, Belgium.

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http://dx.doi.org/10.1002/ajmg.a.38479DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765401PMC
January 2018

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders.

Brain 2017 May;140(5):1316-1336

The Danish Epilepsy Centre, Dianalund, Denmark.

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http://dx.doi.org/10.1093/brain/awx054DOI Listing
May 2017

Multiple sclerosis in Belgian children: A multicentre retrospective study.

Eur J Paediatr Neurol 2017 Mar 25;21(2):358-366. Epub 2016 Oct 25.

Department of Paediatrics, Division of Paediatric Neurology, Ghent University Hospital, Ghent, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.ejpn.2016.10.005DOI Listing
March 2017

Neuropsychological and neurophysiological benefits from white noise in children with and without ADHD.

Behav Brain Funct 2016 Mar 15;12(1):11. Epub 2016 Mar 15.

Department of Neurology, Queen Fabiola Children's University Hospital (HUDERF), Université Libre de Bruxelles (ULB), Avenue Jean-Joseph Crocq, 15, 1020, Brussels, Belgium.

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http://behavioralandbrainfunctions.biomedcentral.com/article
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http://dx.doi.org/10.1186/s12993-016-0095-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4791764PMC
March 2016

Anti-GQ1b antibody syndrome presenting as acute isolated bilateral ophthalmoplegia: Report on two patients and review of the literature.

Eur J Paediatr Neurol 2016 May 18;20(3):439-43. Epub 2016 Feb 18.

Department of Paediatric Neurology, Centre Hospitalier Universitaire Saint-Pierre (U.L.B.), Rue Haute 322, 1000 Brussels, Belgium; Department of Paediatric Neurology, Hôpital Universitaire des Enfants Reine Fabiola (U.L.B.), Avenue Crocq 15, 1020 Brussels, Belgium.

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http://dx.doi.org/10.1016/j.ejpn.2016.02.002DOI Listing
May 2016

Recurrent episodes of myoglobinuria, mental retardation and seizures but no hemolysis in two brothers with phosphoglycerate kinase deficiency.

Neuromuscul Disord 2016 Mar 30;26(3):207-10. Epub 2015 Nov 30.

Neuromuscular Reference Centre, Department of Pediatric Neurology, Hôpital Erasme, Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

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http://dx.doi.org/10.1016/j.nmd.2015.11.008DOI Listing
March 2016

Toward better recognition of early predictors for autism spectrum disorders.

Pediatr Neurol 2013 Oct 6;49(4):225-31. Epub 2013 Aug 6.

Department of Neurology, Hôpital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles (ULB), Brussels, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.pediatrneurol.2013.05.012DOI Listing
October 2013

Rett syndrome associated with continuous spikes and waves during sleep.

Acta Neurol Belg 2011 Dec;111(4):328-32

Department of Neurology - Hôpital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles (ULB), Brussels, Belgium.

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December 2011

Novel LMNA mutation presenting as severe congenital muscular dystrophy.

Pediatr Neurol 2010 Oct;43(4):283-6

Department of Neurology, Queen Fabiola Children's University Hospital, Free University of Brussels, Brussels, Belgium.

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http://dx.doi.org/10.1016/j.pediatrneurol.2010.05.016DOI Listing
October 2010

Metachromatic leukodystrophy without arylsulfatase A deficiency: a new case of saposin-B deficiency.

Eur J Paediatr Neurol 2008 Jan 5;12(1):46-50. Epub 2007 Jul 5.

Department of Neurology, Hôpital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles, Av. J.J. Crocq 15, 1020 Brussels, Belgium.

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http://dx.doi.org/10.1016/j.ejpn.2007.05.004DOI Listing
January 2008

Pathophysiology of duchenne muscular dystrophy: current hypotheses.

Pediatr Neurol 2007 Jan;36(1):1-7

Department of Neurology, Hôpital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles, Brussels, Belgium.

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http://dx.doi.org/10.1016/j.pediatrneurol.2006.09.016DOI Listing
January 2007

Opsoclonus-myoclonus associated with celiac disease.

Pediatr Neurol 2006 Apr;34(4):312-4

Department of Neurology, Hôpital Universitaire des Enfants Reine Fabiola, Université Libre de Bruxelles (ULB), Brussels, Belgium.

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http://dx.doi.org/10.1016/j.pediatrneurol.2005.08.034DOI Listing
April 2006