Chantal Ceuterick-de Groote

Chantal Ceuterick-de Groote

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Chantal Ceuterick-de Groote

Chantal Ceuterick-de Groote

Publications by authors named "Chantal Ceuterick-de Groote"

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Teenage-onset progressive myoclonic epilepsy due to a familial repeat expansion.

Neurology 2018 02 19;90(8):e658-e663. Epub 2018 Jan 19.

From the Department of Neurology (J.v.d.A., A.S., A.M., P.S., B.D.) and Center for Medical Genetics (B.D.), Ghent University Hospital, Belgium; Institute for Inherited Metabolic Disorders (I.J., A.P., H.H., S.K.), Prague, First Faculty of Medicine, Charles University in Prague, Czech Republic; Neurodegenerative Brain Diseases Group (A.S., S.V.M., C.V.B.), Center for Molecular Neurology, VIB; Neuropathology and Laboratory of Neurochemistry and Behavior (A.S.), Laboratory of Neurogenetics (S.V.M., C.V.B.), and Laboratory of Neuromuscular Pathology and Translational Neurosciences (C.C.-d.G.), Institute Born-Bunge, University of Antwerp, Belgium; Institute of Pathology, First Faculty of Medicine (H.H., R.M.), Charles University and General University Hospital; Department of Pathology and Molecular Medicine (R.M.), National Reference Laboratory for Diagnostics of Human Prion Diseases, Thomayer Hospital, Prague, Czech Republic; Epilepsy Research Centre, Department of Medicine (S.F.B.), University of Melbourne, Austin Health, Heidelberg, Australia; and Inserm U1167 (B.D.), Laboratoire d'Excellence Distalz, Institut Pasteur de Lille, Longevity Research Center, Université de Lille, France. J.v.d.A. is currently affiliated with the Department of Clinical Neurosciences and WT/CRUK Gurdon Institute, University of Cambridge, UK.

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http://dx.doi.org/10.1212/WNL.0000000000004999DOI Listing
February 2018

A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8.

Acta Neuropathol 2018 01 5;135(1):131-148. Epub 2017 Aug 5.

Peripheral Neuropathy Research Group, Department of Biomedical Sciences and Institute Born Bunge, University of Antwerp, Universiteitsplein 1, 2610, Antwerpen, Belgium.

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http://dx.doi.org/10.1007/s00401-017-1756-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5756276PMC
January 2018

Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD.

Neurol Genet 2016 Oct 16;2(5):e102. Epub 2016 Sep 16.

Neurodegenerative Brain Diseases Group (J.v.d.Z., S.V.M., L.D., F.P., A.S., C.V.B.), Department of Molecular Genetics, VIB, Antwerp; Institute Born-Bunge (J.v.d.Z., S.V.M., L.D., F.P., S.E., C.C.-D.G., A.S., P.C., J.-J.M., C.V.B.), CLIPS, Computational Linguistics and Psycholinguistics (J. Verhoeven), University of Antwerp; Department of Neurology and Memory Clinic (P.M., R.C., S.V.M., S.E.), ZNA Middelheim and Hoge Beuken, Antwerp; Clinical and Experimental Neurolinguistics (P.M., T.D.), Vrije Universiteit Brussel, Belgium; Department of Language and Communication Science (J. Verhoeven), City University, London, UK; Department of Neurology (A.S.), University Hospital Ghent and University of Ghent; Department of Neurology (S.V.M., P.C.), Antwerp University Hospital; and Department of Neurology (J. Versijpt), University Hospital Brussels, Belgium.

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http://dx.doi.org/10.1212/NXG.0000000000000102DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5027801PMC
October 2016

Cathepsin A-related arteriopathy with strokes and leukoencephalopathy (CARASAL).

Neurology 2016 Oct 24;87(17):1777-1786. Epub 2016 Sep 24.

From the Departments of Child Neurology (M.B., S.H.K., H.S.B., T.E.M.A., M.S.v.d.K.) and Pathology (M.B., H.W.M.N.), Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam; Department of Clinical Genetics (Q.W.), VU University Medical Center, Amsterdam, the Netherlands; Laboratory for Ultrastructural Neuropathology (C.C.-d.G.), Institute Born-Bunge and University of Antwerp, Belgium; Department of Clinical genetics (S.A.M.J.L.O.), Leiden University Medical Center, Leiden; and Department of Functional Genomics (M.S.v.d.K.), Center for Neurogenomics and Cognitive Research, VU University, Amsterdam, the Netherlands.

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http://dx.doi.org/10.1212/WNL.0000000000003251DOI Listing
October 2016

Motor neuron degeneration in spastic paraplegia 11 mimics amyotrophic lateral sclerosis lesions.

Brain 2016 06 25;139(Pt 6):1723-34. Epub 2016 Mar 25.

1 Ecole Pratique des Hautes Etudes, EPHE, PSL université, laboratoire de neurogénétique, F-75013, Paris, France 2 Inserm, U1127, F-75013, Paris, France 3 CNRS, UMR7225, F-75013, Paris, France 4 Sorbonne Universités, UPMC Univ Paris 06, UMR_S1127, Institut du Cerveau et de la Moelle épinière - ICM, Pitié-Salpêtrière Hospital, F-75013, Paris, France.

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http://dx.doi.org/10.1093/brain/aww061DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5839621PMC
June 2016

Megaconial muscular dystrophy caused by mitochondrial membrane homeostasis defect, new insights from skeletal and heart muscle analyses.

Mitochondrion 2016 Mar 23;27:32-8. Epub 2016 Feb 23.

Laboratories of Neurogenetics and Ultrastructural Neuropathology and Biobank, Institute Born-Bunge, University of Antwerp, Universiteitsplein 1, B-2610 Antwerpen, Belgium; Neurogenetics Group, Department of Molecular Genetics, VIB, Universiteitsplein 1, B-2610 Antwerpen, Belgium; Department of Neurology, University Hospital Antwerp, Wilrijkstraat 10, B-2650 Edegem, Belgium.

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http://dx.doi.org/10.1016/j.mito.2016.02.001DOI Listing
March 2016

A novel hereditary extensive vascular leukoencephalopathy mapping to chromosome 20q13.

Neurology 2012 Dec 21;79(23):2283-7. Epub 2012 Nov 21.

Service de Neurologie, Centre de Référence des Maladies Vasculaires Rares du Cerveau et de l'Oeil (CERVCO), AP-HP, Groupe Hospitalier Lariboisière-Saint-Louis, Paris, France.

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http://dx.doi.org/10.1212/WNL.0b013e3182768954DOI Listing
December 2012

Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients.

Neuromuscul Disord 2012 Aug 15;22(8):699-711. Epub 2012 May 15.

Peripheral Neuropathy Group, Department of Molecular Genetics, VIB and University of Antwerp, Antwerpen 2610, Belgium.

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http://dx.doi.org/10.1016/j.nmd.2012.04.005DOI Listing
August 2012

Neuropathology in classical and variant ataxia-telangiectasia.

Neuropathology 2012 Jun 24;32(3):234-44. Epub 2011 Oct 24.

Department of Pediatric Neurology, Donders Institute for Brain, Cognition and Behaviour Pathology, Radboud University, Nijmegen Medical Centre, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1111/j.1440-1789.2011.01263.xDOI Listing
June 2012

Peripheral neuropathy and 46XY gonadal dysgenesis: a heterogeneous entity.

Neuromuscul Disord 2009 Feb 22;19(2):172-5. Epub 2009 Jan 22.

Neurogenetics group, VIB Department of Molecular Genetics, University of Antwerp, Universiteitsplein 1, B-2610 Antwerpen, Belgium.

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http://dx.doi.org/10.1016/j.nmd.2008.11.006DOI Listing
February 2009

Cap disease caused by heterozygous deletion of the beta-tropomyosin gene TPM2.

Neuromuscul Disord 2007 Jun 16;17(6):433-42. Epub 2007 Apr 16.

The Folkhälsan Institute of Genetics and the Department of Medical Genetics, University of Helsinki, Helsinki, Finland, and Division of Neurology, University Hospital of Antwerp, Antwerpen, Belgium.

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http://dx.doi.org/10.1016/j.nmd.2007.02.015DOI Listing
June 2007

Effect of an R69C mutation in the myelin protein zero gene on myelination and ion channel subtypes.

Arch Neurol 2006 Dec;63(12):1787-94

Department of Neurology, Wayne State University School of Medicine, Detroit, MI 48201, USA.

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http://dx.doi.org/10.1001/archneur.63.12.1787DOI Listing
December 2006

Linezolid-induced inhibition of mitochondrial protein synthesis.

Clin Infect Dis 2006 Apr 13;42(8):1111-7. Epub 2006 Mar 13.

Department of Internal Medicine, AZ Sint-Jan AV, Bruges, Belgium.

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http://dx.doi.org/10.1086/501356DOI Listing
April 2006

Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV.

Neuromuscul Disord 2006 Jan 20;16(1):19-25. Epub 2005 Dec 20.

Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, Institute Born-Bunge, University of Antwerp, Universiteitsplein 1, B-2610 Antwerpen, Belgium.

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http://dx.doi.org/10.1016/j.nmd.2005.10.007DOI Listing
January 2006

Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene.

Ann Neurol 2004 May;55(5):676-86

Institut National de la Santé et de la Recherche Médicale U582, Institut de Myologie, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.

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http://doi.wiley.com/10.1002/ana.20077
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http://dx.doi.org/10.1002/ana.20077DOI Listing
May 2004