Arnaud Vanlander

Arnaud Vanlander

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Arnaud Vanlander

Arnaud Vanlander

Publications by authors named "Arnaud Vanlander"

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26Publications

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TANGO2 deficiency as a cause of neurodevelopmental delay with indirect effects on mitochondrial energy metabolism.

J Inherit Metab Dis 2019 Sep 24;42(5):898-908. Epub 2019 Jul 24.

Department of Paediatrics, Institute of Clinical Sciences, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.

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http://dx.doi.org/10.1002/jimd.12149DOI Listing
September 2019

Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in .

Neurol Genet 2018 Dec 27;4(6):e298. Epub 2018 Nov 27.

Department of Neurology (D.M.H.), Ghent University Hospital; Department of Pediatrics (A.V.V., J.S., E.V., R.V.C.), Division of Pediatric Neurology and Metabolism, Ghent University Hospital; Department of Radiology (M.A.), Ghent University Hospital; Department of Nuclear Medicine (I.G.), Ghent University Hospital; Center for Medical Genetics Ghent (T.S., B.M.), Ghent University, Belgium; and Center for Medical Genetics (S.S.), UZ Brussel and Reproduction Genetics and Regenerative Medicine, Vrije Universiteit Brussel, Brussels, Belgium.

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http://dx.doi.org/10.1212/NXG.0000000000000298DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278240PMC
December 2018

A novel IKAROS haploinsufficiency kindred with unexpectedly late and variable B-cell maturation defects.

J Allergy Clin Immunol 2018 01 18;141(1):432-435.e7. Epub 2017 Sep 18.

Clinical Immunology Research Laboratory, Department of Pulmonary Medicine, Ghent University Hospital, Ghent, Belgium; Center for Primary Immunodeficiency, Jeffrey Modell Diagnosis and Research Centre, Ghent University Hospital, Ghent, Belgium; Laboratory of Immunoregulation, VIB Inflammation Research Center, Ghent, Belgium; Department of Internal Medicine, Ghent University, Ghent, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.jaci.2017.08.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588539PMC
January 2018

New insights into the phenotype of FARS2 deficiency.

Mol Genet Metab 2017 12 12;122(4):172-181. Epub 2017 Oct 12.

Department of Pediatric Neurology and Metabolism, Ghent University Hospital, Ghent, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2017.10.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5734183PMC
December 2017

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 bumpy ride on the diagnostic bench of massive parallel sequencing, the case of the mitochondrial genome.

PLoS One 2014 10;9(11):e112950. Epub 2014 Nov 10.

Research Group Reproduction and Genetics (REGE), Vrije Universiteit Brussel (VUB), Brussels, Belgium; Center for Medical Genetics, UZ Brussel, Vrije Universiteit Brussel (VUB), Brussels, Belgium.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0112950PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4226615PMC
December 2015

Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy.

J Inherit Metab Dis 2015 Nov 14;38(6):1147-53. Epub 2015 May 14.

Division of Pediatric Neurology and Metabolism, Department of Pediatrics, Gent University Hospital, Gent, Belgium.

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http://dx.doi.org/10.1007/s10545-015-9857-1DOI Listing
November 2015

Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder.

J Med Genet 2015 Aug 18;52(8):532-40. Epub 2015 Mar 18.

Department of Pediatrics, Section of Genetics, University of Colorado School of Medicine, Aurora, Colorado, USA Intellectual and Developmental Disabilities Research Center, University of Colorado School of Medicine, Aurora, Colorado, USA.

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http://dx.doi.org/10.1136/jmedgenet-2015-103049DOI Listing
August 2015

Forearm deoxyhemoglobin and deoxymyoglobin (deoxy[Hb + Mb]) measured by near-infrared spectroscopy (NIRS) using a handgrip test in mitochondrial myopathy.

Appl Spectrosc 2015 Mar 1;69(3):342-7. Epub 2015 Feb 1.

Department of Movement and Sports Sciences, Ghent University, Watersportlaan 2, 9000 Ghent, Belgium.

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http://dx.doi.org/10.1366/14-07604DOI Listing
March 2015

Extremely high mutation load of the mitochondrial 8993 T>G mutation in a newborn: implications for prognosis and family planning decisions.

Eur J Pediatr 2015 Feb 10;174(2):267-70. Epub 2014 Jul 10.

Department of Neonatology, Ghent University Hospital, De Pintelaan 185, 9000, Ghent, Belgium,

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http://link.springer.com/10.1007/s00431-014-2370-y
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http://dx.doi.org/10.1007/s00431-014-2370-yDOI Listing
February 2015

Possible pathogenic mechanism of propofol infusion syndrome involves coenzyme q.

Anesthesiology 2015 Feb;122(2):343-52

From the Department of Pediatrics, Division of Pediatric Neurology and Metabolism (A.V.V., J.S., E.D.L., B.D.P., R.V.C.), Department of Critical Care Medicine, Division of Pediatric Intensive Care Medicine (A.d.J.), Department of Clinical Chemistry (B.W.), Department of Emergency Medicine (P.D.P.), Ghent University Hospital, Ghent, Belgium; Department of General Pediatrics, Division of Inherited Metabolic Diseases, University Children's Hospital, Heidelberg, Germany (J.G.O.); Department of Pediatrics, University of Ghent, Ghent, Belgium (G.D.); Physiology Group, Department of Basic Medical Sciences, Ghent University, Ghent, Belgium (B.V.); Department of Critical Care Medicine, Antwerp University Hospital, Antwerp University, Edegem, Belgium (P.G.J., N.V.R.); and Department of Critical Care Medicine, ZNA Antwerp, Belgium (N.V.R.).

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http://dx.doi.org/10.1097/ALN.0000000000000484DOI Listing
February 2015

Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation.

Biochim Biophys Acta 2015 Feb 20;1853(2):285-98. Epub 2014 Nov 20.

KU Leuven - University of Leuven, Department of Pharmaceutical and Pharmacological Sciences, Laboratory of Cell Metabolism, B-3000 Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.bbamcr.2014.11.017DOI Listing
February 2015

Analysis of the whole mitochondrial genome: translation of the Ion Torrent Personal Genome Machine system to the diagnostic bench?

Eur J Hum Genet 2015 Jan 26;23(1):41-8. Epub 2014 Mar 26.

1] Research Group Reproduction and Genetics, Vrije Universiteit Brussel (VUB), Brussels, Belgium [2] Department of Pediatric Neurology, UZ Brussel, Vrije Universiteit Brussel (VUB), Brussels, Belgium.

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http://dx.doi.org/10.1038/ejhg.2014.49DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266735PMC
January 2015

Effect of resveratrol on cultured skin fibroblasts from patients with oxidative phosphorylation defects.

Phytother Res 2014 Feb 26;28(2):312-6. Epub 2013 Apr 26.

Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Ghent University Hospital, Ghent, Belgium.

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http://dx.doi.org/10.1002/ptr.4988DOI Listing
February 2014

Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for the detection of oxidative phosphorylation defects.

Pediatr Res 2012 Sep 22;72(3):232-40. Epub 2012 Jun 22.

Department of Pediatrics, Division of Pediatric Neurology and Metabolism, Ghent University Hospital, Ghent, Belgium.

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http://dx.doi.org/10.1038/pr.2012.84DOI Listing
September 2012

Propranolol as a novel treatment for congenital visceral haemangioma.

Neonatology 2010 13;98(3):229-31. Epub 2010 Apr 13.

Neonatal Intensive Care Unit, AZ-St-Jan Bruges-Ostend AV, Bruges, Belgium.

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http://dx.doi.org/10.1159/000291300DOI Listing
January 2011