Christine Verellen-Dumoulin

Christine Verellen-Dumoulin

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Christine Verellen-Dumoulin

Christine Verellen-Dumoulin

Publications by authors named "Christine Verellen-Dumoulin"

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Attentional impairments in Huntington's disease: A specific deficit for the executive conflict.

Neuropsychology 2017 May 27;31(4):424-436. Epub 2017 Feb 27.

Department of Psychiatry, Saint-Luc University Hospital.

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http://dx.doi.org/10.1037/neu0000321DOI Listing
May 2017

Dissociating emotional and cognitive empathy in pre-clinical and clinical Huntington's disease.

Psychiatry Res 2016 Mar 28;237:103-8. Epub 2016 Jan 28.

Department of Adult Psychiatry, Saint-Luc University Hospital, 10 Avenue Hippocrate, B-1200 Brussels, Belgium.

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http://dx.doi.org/10.1016/j.psychres.2016.01.070DOI Listing
March 2016

The Association of H1N1 Pandemic Influenza with Congenital Anomaly Prevalence in Europe: An Ecological Time Series Study.

Epidemiology 2015 Nov;26(6):853-61

From the aInstitute of Nursing Research/School of Nursing, University of Ulster, Newtownabbey, United Kingdom; bDivision of Medical Genetics, Lausanne, Switzerland; cPublic Health Division of Gipuzkoa, Instituto BIO-Donostia, Basque Government, CIBER Epidemiología y Salud Pública-CIBERESP, Madrid, Spain; dUnit of Epidemiology, Institute of Clinical Physiology, Pisa, Italy; eDepartment of Paediatrics, Hospital Lillebaelt, Kolding, Denmark; fINSERM U953, Paris, France; gProvinciaal Instituut voor Hygiene, Antwerp, Belgium; hIMER Registry-Azienda Ospedaliero-Universitaria di Ferrara, Ferrara, Italy; iUniversity Medical Center of the Johannes Gutenberg University, Mainz, Germany; jInstitute of Health & Society, Newcastle University, Newcastle-upon-Tyne, United Kingdom; kNational Perinatal Epidemiology Unit, University of Oxford, Oxford, United Kingdom; lInstitut de Pathologie et de Génétique, Charleroi, Belgium; mDepartment of Genetics, University Medical Center Groningen, University of Groningen, Eurocat, Groningen, The Netherlands; nWessex Clinical Genetics Service, Princess Anne Hospital, Southampton, United Kingdom; oSchool of Clinical Sciences, University of Bristol, Bristol, United Kingdom; pOMNI-Net for Children, Rivne Medical Diagnostic Center, Rivne, Ukraine; qDivision of Pharmacy, Department of Pharmacoepidemiology and Pharmacoeconomics, University of Groningen, Groningen, The Netherlands; and rCentre for Environmental and Preventive Medicine, Queen Mary University of London, London, United Kingdom.

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http://dx.doi.org/10.1097/EDE.0000000000000372DOI Listing
November 2015

A three generation X-linked family with Kabuki syndrome phenotype and a frameshift mutation in KDM6A.

Am J Med Genet A 2014 May 24;164A(5):1289-92. Epub 2014 Mar 24.

Center for Human Genetics, IPG, Charleroi, (Gosselies), Belgium.

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http://dx.doi.org/10.1002/ajmg.a.36442DOI Listing
May 2014

Intron 22 homologous regions are implicated in exons 1-22 duplications of the F8 gene.

Eur J Hum Genet 2013 Sep 9;21(9):970-6. Epub 2013 Jan 9.

Center of Human Genetics UCLouvain, Cliniques Universitaires Saint-Luc, Bruxelles, Belgium.

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http://dx.doi.org/10.1038/ejhg.2012.275DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3746252PMC
September 2013

Atypical findings in three patients with Pai syndrome and literature review.

Am J Med Genet A 2012 Nov 17;158A(11):2899-904. Epub 2012 Sep 17.

Center for Human Genetics, IPG, Charleroi (Gosselies), Belgium.

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http://dx.doi.org/10.1002/ajmg.a.35592DOI Listing
November 2012

Discordant monozygotic twins for macrocephaly-capillary malformation.

Am J Med Genet A 2012 Jun 14;158A(6):1509-11. Epub 2012 May 14.

Center For Human Genetics, IPG, Charleroi (Gosselies), Belgium.

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http://dx.doi.org/10.1002/ajmg.a.35382DOI Listing
June 2012

NF1 microduplication first clinical report: association with mild mental retardation, early onset of baldness and dental enamel hypoplasia?

Eur J Hum Genet 2008 Mar 9;16(3):305-11. Epub 2008 Jan 9.

Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium.

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http://dx.doi.org/10.1038/sj.ejhg.5201978DOI Listing
March 2008

Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population.

Eur J Hum Genet 2005 Nov;13(11):1239-42

Laboratory of Human Molecular Genetics, Christian de Duve Institute of Cellular Pathology and University of Louvain Medical School, Brussels, Belgium.

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http://dx.doi.org/10.1038/sj.ejhg.5201486DOI Listing
November 2005

Congenital diaphragmatic eventration and bilateral uretero-hydronephrosis in a patient with neonatal Marfan syndrome caused by a mutation in exon 25 of the FBN1 gene and review of the literature.

Eur J Pediatr 2004 Jan 30;163(1):33-7. Epub 2003 Oct 30.

Center for Human Genetics and Medical Genetics Unit, Cliniques universitaires Saint-Luc and Université catholique de Louvain, Av. Mounier 5220, 1200 Brussels, Belgium.

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http://dx.doi.org/10.1007/s00431-003-1330-8DOI Listing
January 2004

Free fetal DNA concentration in maternal plasma during normal labour at term.

Prenat Diagn 2003 Dec;23(13):1077-82

Department of Obstetrics, Université Catholique de Louvain, Cliniques Universitaires Saint Luc, Bruxelles, Belgium.

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http://dx.doi.org/10.1002/pd.757DOI Listing
December 2003

Polymicrogyria in chromosome 22q11 deletion syndrome.

Eur J Paediatr Neurol 2002 ;6(1):73-7

Department of Pediatric Neurology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

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http://dx.doi.org/10.1053/ejpn.2001.0544DOI Listing
August 2002