Annick Vogels

Annick Vogels

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Annick Vogels

Annick Vogels

Publications by authors named "Annick Vogels"

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Low-Dose Aripiprazole and Risperidone for Treating Problem Behavior in Children With Pitt-Hopkins Syndrome.

J Clin Psychopharmacol 2018 06;38(3):260-261

University Psychiatric Centre KU Leuven Catholic University of Leuven Leuven, Belgium Centre for Human Genetics Catholic University Leuven Leuven, Belgium.

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http://Insights.ovid.com/crossref?an=00004714-201806000-0001
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http://dx.doi.org/10.1097/JCP.0000000000000871DOI Listing
June 2018

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.

Neurology 2018 06 11;90(23):e2059-e2067. Epub 2018 May 11.

From The Dalglish Family 22q Clinic for Adults and Department of Psychiatry (E.B., A.M.F., A.S.B.), Toronto General Research Institute (A.S.B.), and Division of Cardiology, Department of Medicine (A.S.B.), University Health Network, Toronto, Canada; De Hartekamp Groep (E.B.), Centre for People with Intellectual Disability, Haarlem; Department of Nuclear Medicine (E.B., J.B.), Academic Medical Center, Amsterdam, the Netherlands; Clinical Genetics Research Program and Campbell Family Mental Health Research Institute (N.J.B., A.M.F., A.S.B.), Centre for Addiction and Mental Health, Toronto; Institute of Medical Science (N.J.B., M.M., A.E.L., A.S.B.), Division of Neurology, Department of Medicine (C.M., M.M., A.E.L.), and Department of Psychiatry (A.S.B.), University of Toronto; Deer Lodge Movement Disorders Centre (S.U.); Section of Neurology (S.U.), Division of Internal Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg; Morton and Gloria Shulman Movement Disorders Centre and the Edmond J. Safra Program in Parkinson's Disease Research (C.M., A.E.L.), Toronto Western Hospital and University of Toronto, Canada; Department of Molecular Neuroscience (K.Y.M., N.W.W.), UCL Institute of Neurology, London, UK; Department of Neurology (S.K.), Kansai Medical University, Osaka, Japan; Department of Neurology (M.J.B.), University of Virginia School of Medicine, Charlottesville; Medical Genetics Unit (P.P.), Perugia University Hospital, Italy; Department of Neurology (B.D.B.), University of Colorado Anschutz Medical Campus, Aurora; Neurology Section (B.D.B.), VA Eastern Colorado Health Care System, Denver; Cognitive & Movement Disorders Clinic and Hurvitz Brain Sciences Research Program (M.M.), Sunnybrook Health Sciences Centre, Toronto, Canada; Departments of Clinical Neurosciences (Movement Disorders) (B.D.) and Genetics (Neurogenetics) (K.N.), Timone University Hospital (AP-HM), Provence-Alpes-Côte d'Azur; Aix-Marseille University (B.D., K.N.), Marseille; Department of Genetics (Neurogenetics) (P.C., A.J.), Pitié-Salpêtrière University Hospital; Sorbonne University (P.C., A.J.), Paris; Department of Neurosciences (Movement Disorders) (E.M.), Lille University Hospital; Lille University (E.M.); Department of Neurology (Movement Disorders) (T.D.), Pierre Wertheimer University Hospital, Lyon; Marc Jeannerod Center for Cognitive Neurosciences (T.D.), Lyon-1 University; Department of Neurology (Movement Disorders) and Clinical Investigation Center (Clinical and Experimental Neurosciences) (O.C.), Poitiers University Hospital; Department of Neurology (Movement Disorders) (S.D.), Rennes University Hospital; Rennes-1 University (S.D.); Department of Clinical Neurosciences (Movement Disorders) (M.B.), Nice University Hospital, France; Department of Psychiatry (A.M.F.), Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, the Netherlands; Center for Human Genetics (E.V., A.S., A.V.), University Hospital Leuven; Department of Human Genetics (A.S.), KU Leuven, Belgium; Department of Neurology (A.P.), University of Munich, Germany; Scientific and Technological Coordination Unit of the ANLIS Directorate (C.P.), National Administration of Laboratories and Institutes of Health, Argentina; Department of Neurodegenerative Diseases (T.G.), Center of Neurology and Hertie-Institute for Clinical Brain Research, University of Tübingen; German Center for Neurodegenerative Diseases (DZNE) (T.G.); Department of Neurology (K.C.), AZ Turnhout, Antwerp, Belgium; Neurology Unit and Stroke Center (F.B.), Hôpital Foch, Suresnes, France; Movement Disorder Division (K.M.), Johns Hopkins University, Baltimore, MD; and Psychological Medicine and Clinical Neurosciences (N.M.W.), MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University School of Medicine, Cardiff University, UK.

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http://dx.doi.org/10.1212/WNL.0000000000005660DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5993183PMC
June 2018

Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia.

Am J Hum Genet 2018 05 12;102(5):744-759. Epub 2018 Apr 12.

Service de Génétique Médicale, CHU Nantes, 9 quai Moncousu, 44093 Nantes Cedex 1, France; l'institut du thorax, INSERM, CNRS, UNIV Nantes, 44007 Nantes, France. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2018.02.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5986661PMC
May 2018

Autism spectrum disorder profile in neurofibromatosis type I.

J Autism Dev Disord 2015 Jun;45(6):1649-57

Institute of Brain Behaviour and Mental Health, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.

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http://link.springer.com/10.1007/s10803-014-2321-5
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http://dx.doi.org/10.1007/s10803-014-2321-5DOI Listing
June 2015

Presenting symptoms in adults with the 22q11 deletion syndrome.

Eur J Med Genet 2014 Mar 24;57(4):157-62. Epub 2014 Feb 24.

Center for Human Genetics, KU Leuven, Belgium.

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http://dx.doi.org/10.1016/j.ejmg.2014.02.008DOI Listing
March 2014

Simvastatin for cognitive deficits and behavioural problems in patients with neurofibromatosis type 1 (NF1-SIMCODA): a randomised, placebo-controlled trial.

Lancet Neurol 2013 Nov 1;12(11):1076-83. Epub 2013 Oct 1.

Department of Neuroscience, Erasmus University Medical Centre, Rotterdam, Netherlands; Department of Paediatrics, Erasmus University Medical Centre, Rotterdam, Netherlands; ENCORE Expertise Centre For Neurodevelopmental Disorders, Erasmus University Medical Centre, Rotterdam, Netherlands.

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http://www.thelancet.com/pdfs/journals/laneur/PIIS1474-4422(
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http://linkinghub.elsevier.com/retrieve/pii/S147444221370227
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http://dx.doi.org/10.1016/S1474-4422(13)70227-8DOI Listing
November 2013

Testicular histology in boys with Prader-Willi syndrome: fertile or infertile?

J Urol 2008 Oct 21;180(4 Suppl):1800-4. Epub 2008 Aug 21.

Department of Human Genetics, University Hospitals Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1016/j.juro.2008.03.113DOI Listing
October 2008

The oro-dental phenotype in Prader-Willi syndrome: a survey of 15 patients.

Int J Paediatr Dent 2008 Jan;18(1):40-7

Paediatric Dentistry, Garancière Hotel-Dieu Hospital, AP-HP France.

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http://dx.doi.org/10.1111/j.1365-263X.2007.00857.xDOI Listing
January 2008

Pfeiffer syndrome.

Orphanet J Rare Dis 2006 Jun 1;1:19. Epub 2006 Jun 1.

Center for Human Genetics, University Hospital Leuven, Herestraat 49, B-3000 Leuven, Belgium.

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http://dx.doi.org/10.1186/1750-1172-1-19DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1482682PMC
June 2006

Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders.

Eur J Hum Genet 2004 Mar;12(3):238-40

Centre for Human Genetics, University of Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/sj.ejhg.5201135DOI Listing
March 2004

Atypical presentation of the Prader-Willi syndrome. Mosaic trisomy 15?

Ann Genet 2002 Jan-Mar;45(1):1-3

Centre for Human Genetics, University Hospital Leuven, Leuven, Belgium

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October 2002