Bart Dermaut

Bart Dermaut

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Bart Dermaut

Bart Dermaut

Publications by authors named "Bart Dermaut"

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42Publications

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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

Future perspectives of genome-scale sequencing.

Acta Clin Belg 2018 Feb;73(1):7-10

a Center for Medical Genetics , Ghent University Hospital , Ghent , Belgium.

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http://dx.doi.org/10.1080/17843286.2017.1413809DOI Listing
February 2018

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.

Hum Mutat 2017 03 19;38(3):297-309. Epub 2017 Jan 19.

Center for Molecular Neurology, VIB, Antwerp, Belgium.

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http://dx.doi.org/10.1002/humu.23161DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324646PMC
March 2017

RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder.

Neurology 2015 Apr 3;84(17):1760-6. Epub 2015 Apr 3.

From the Department of Neurology (P.S., B.D.) and the Center for Medical Genetics (T.V.D., W.S., A.W., A.D.P., P.J.C., B.D.), Ghent University Hospital, Belgium; and Inserm U1172, Centre de Recherches J-P Aubert (B.S.), and Inserm U1167, Institut Pasteur de Lille (B.D.), Université de Lille, France.

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http://www.neurology.org/content/84/17/1760.full.pdf
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http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000152
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http://dx.doi.org/10.1212/WNL.0000000000001521DOI Listing
April 2015

Functional complementation in Drosophila to predict the pathogenicity of TARDBP variants: evidence for a loss-of-function mechanism.

Neurobiol Aging 2015 Feb 28;36(2):1121-9. Epub 2014 Sep 28.

Inserm U744, Institut Pasteur de Lille, Université de Lille Nord de France, Lille, France; Center for Medical Genetics, Ghent University Hospital, Gent, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2014.09.001DOI Listing
February 2015

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.

Acta Neuropathol 2014 Sep 5;128(3):397-410. Epub 2014 Jun 5.

Department of Molecular Genetics, VIB, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s00401-014-1298-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131163PMC
September 2014

HDAC6 is a Bruchpilot deacetylase that facilitates neurotransmitter release.

Cell Rep 2014 Jul 26;8(1):94-102. Epub 2014 Jun 26.

VIB Center for the Biology of Disease, Herestraat 49 bus 602, 3000 Leuven, Belgium; KU Leuven, Center for Human Genetics and Leuven Research Institute for Neuroscience and Disease (LIND), Herestraat 49 bus 602, 3000 Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2014.05.051DOI Listing
July 2014

TDP-43-mediated neurodegeneration: towards a loss-of-function hypothesis?

Trends Mol Med 2014 Feb 16;20(2):66-71. Epub 2013 Dec 16.

Inserm U744, Institut Pasteur de Lille, Université de Lille Nord de France, 59019 Lille, France. Electronic address:

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http://www.cell.com/trends/molecular-medicine/pdf/S1471-4914
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http://linkinghub.elsevier.com/retrieve/pii/S147149141300196
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http://dx.doi.org/10.1016/j.molmed.2013.11.003DOI Listing
February 2014

Drosophila models of tauopathies: what have we learned?

Int J Alzheimers Dis 2012 4;2012:970980. Epub 2012 Jun 4.

Laboratory of Behavioral and Developmental Genetics, Center for Human Genetics, University of Leuven, 3000 Leuven, Belgium.

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http://dx.doi.org/10.1155/2012/970980DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3373119PMC
August 2012

Vagus nerve stimulation for refractory status epilepticus.

Eur J Paediatr Neurol 2009 May 27;13(3):286-9. Epub 2008 Jun 27.

Department of Neurology, Reference Center for Refractory Epilepsy, Ghent University Hospital, Belgium.

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http://linkinghub.elsevier.com/retrieve/pii/S109037980800106
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http://dx.doi.org/10.1016/j.ejpn.2008.05.004DOI Listing
May 2009

Mean age-of-onset of familial alzheimer disease caused by presenilin mutations correlates with both increased Abeta42 and decreased Abeta40.

Hum Mutat 2006 Jul;27(7):686-95

Neurodegenerative Brain Diseases Group, Department of Molecular Genetics, Flanders Interuniversity Institute of Biotechnology, University of Antwerp, Antwerpen, Belgium.

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http://dx.doi.org/10.1002/humu.20336DOI Listing
July 2006

A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.

Brain 2006 Apr 22;129(Pt 4):841-52. Epub 2006 Feb 22.

Neurodegenerative Brain Diseases Group, Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Antwerpen, Belgium.

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http://dx.doi.org/10.1093/brain/awl029DOI Listing
April 2006

Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family.

J Neuropathol Exp Neurol 2006 Mar;65(3):289-301

Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology (VIB8), Institute Born-Bunge, University of Antwerp, Belgium.

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http://dx.doi.org/10.1097/01.jnen.0000205147.39210.c7DOI Listing
March 2006

The UBQLN1 polymorphism, UBQ-8i, at 9q22 is not associated with Alzheimer's disease with onset before 70 years.

Neurosci Lett 2006 Jan 6;392(1-2):72-4. Epub 2005 Oct 6.

Department of Molecular Genetics, Flanders Interuniversity Institute of Biotechnology and Institute Born-Bunge, University of Antwerp, Universiteitsplein 1, Belgium.

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http://dx.doi.org/10.1016/j.neulet.2005.08.064DOI Listing
January 2006

Tau is central in the genetic Alzheimer-frontotemporal dementia spectrum.

Trends Genet 2005 Dec 10;21(12):664-72. Epub 2005 Oct 10.

Department of Molecular Genetics (VIB 8), Flanders Interuniversity Institute for Biotechnology, Neurodegenerative Brain Diseases Group, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, B-2610 Antwerpen, Belgium.

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http://dx.doi.org/10.1016/j.tig.2005.09.005DOI Listing
December 2005

Genetic testing has no place as a routine diagnostic test in sporadic and familial cases of Alzheimer's disease.

J Am Geriatr Soc 2004 Dec;52(12):2110-3

Memory Clinic, Section of Geriatric Medicine, Department of Internal Medicine, Erasmus MC, Rotterdam, the Netherlands.

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http://dx.doi.org/10.1111/j.1532-5415.2004.52573.xDOI Listing
December 2004

Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy.

Eur J Hum Genet 2003 Jul;11(7):547-9

Neuromuscular Reference Center and Department of Neurology, University Hospital of Antwerp (UZA), Antwerpen, Belgium.

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http://dx.doi.org/10.1038/sj.ejhg.5201002DOI Listing
July 2003

PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease.

Ann Neurol 2003 Mar;53(3):409-12

Department of Molecular Genetics, Flanders Interuniversity Institute of Biotechnology (VIB8), University of Antwerp, Antwerpen, Belgium.

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http://dx.doi.org/10.1002/ana.10507DOI Listing
March 2003