Isabelle Bailleul-Forestier

Isabelle Bailleul-Forestier

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Isabelle Bailleul-Forestier

Isabelle Bailleul-Forestier

Publications by authors named "Isabelle Bailleul-Forestier"

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22Publications

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Necrotizing Periodontal Diseases in Children: A Literature Review and Adjustment of Treatment.

J Trop Pediatr 2016 08 10;62(4):331-7. Epub 2016 Mar 10.

Department of Paediatric Dentistry, CHU Rangueil, Paul Sabatier University, Toulouse 31069, France.

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http://dx.doi.org/10.1093/tropej/fmw005DOI Listing
August 2016

Recurrent Aphthous Stomatitis As a Marker of Celiac Disease in Children.

Pediatr Dermatol 2016 Mar-Apr;33(2):241

Dental Service, Toulouse University Hospital, University of Toulouse III, Toulouse, France.

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http://dx.doi.org/10.1111/pde.12783DOI Listing
July 2016

A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.

J Med Genet 2016 Feb 26;53(2):98-110. Epub 2015 Oct 26.

Centre de Référence des Manifestations Odontologiques des Maladies Rares, Pôle de Médecine et Chirurgie Bucco-dentaires, Hôpitaux Universitaires de Strasbourg (HUS), Strasbourg, France Faculté de Chirurgie Dentaire, Université de Strasbourg, Strasbourg, France Institut de Génétique et de Biologie Moléculaire and Cellulaire-Centre Européen de Recherche en Biologie et en Médecine, CNRS UMR7104, INSERM U964 Université de Strasbourg, Illkirch, France.

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http://dx.doi.org/10.1136/jmedgenet-2015-103302DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752661PMC
February 2016

Direct Microscopy: A Useful Tool to Diagnose Oral Candidiasis in Children and Adolescents.

Mycopathologia 2015 Dec 2;180(5-6):373-7. Epub 2015 Sep 2.

Department of Pediatric Dentistry, Toulouse Dental School, University of Toulouse III, Toulouse, France.

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http://dx.doi.org/10.1007/s11046-015-9933-yDOI Listing
December 2015

Genotypic and phenotypic variation in six patients with solitary median maxillary central incisor syndrome.

Am J Med Genet A 2015 Oct 16;167A(10):2451-8. Epub 2015 Jun 16.

Department of Oral Health Sciences-Orthodontics, KU Leuven and Dentistry, University Hospitals Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1002/ajmg.a.37207DOI Listing
October 2015

Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta.

Hum Mol Genet 2015 Jun 10;24(11):3038-49. Epub 2015 Feb 10.

Université de Strasbourg, Laboratoire de Génétique Médicale, INSERM UMR 1112, Faculté de Médecine, FMTS, 11 rue Humann 67000 Strasbourg, France Université de Strasbourg, Laboratoire de Génétique Médicale, INSERM UMR 1112, Faculté de Médecine, FMTS, 11 rue Humann 67000 Strasbourg, France Université de Strasbourg, Laboratoire de Génétique Médicale, INSERM UMR 1112, Faculté de Médecine, FMTS, 11 rue Humann 67000 Strasbourg, France

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http://dx.doi.org/10.1093/hmg/ddv053DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4424950PMC
June 2015

Proteus syndrome: Report of a case with AKT1 mutation in a dental cyst.

Eur J Med Genet 2015 May 14;58(5):300-4. Epub 2015 Mar 14.

University Paul Sabatier, Toulouse III, France; Department of Paediatric Dentistry, CHU of Toulouse, Toulouse, France; LU 51, Faculty of Dentistry, Toulouse, France.

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http://dx.doi.org/10.1016/j.ejmg.2015.02.008DOI Listing
May 2015

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.

Nucleic Acids Res 2014 Jan 11;42(Database issue):D966-74. Epub 2013 Nov 11.

Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany, Berlin-Brandenburg Center for Regenerative Therapies, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany, Lawrence Berkeley National Laboratory, Mail Stop 84R0171, Berkeley, CA 94720, USA, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK, Department of Medical Genetics, Cambridge University Addenbrooke's Hospital, Cambridge CB2 2QQ, UK, Université Paul Sabatier, Faculté de Chirurgie Dentaire, CHU Toulouse, France, Centre for Genomic Medicine, Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Sciences Centre (MAHSC), Manchester, UK, Centre for Genomic Medicine, Institute of Human Development, Faculty of Medical and Human Sciences, University of Manchester, MAHSC, Manchester M13 9WL, UK, Institute of Genetic Medicine. Newcastle University, Central Parkway, Newcastle upon Tyne, NE1 3BZ, UK, Department of Computer Science, University of Toronto, Ontario, Canada, Centre for Computational Medicine, Hospital for Sick Children, Toronto, Ontario, Canada, Department of Clinical Genetics, Leeds Teaching Hospitals NHS Trust, Leeds LS2 9NS, UK, MRC Human Genetics Unit, MRC Institute of Genetic and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, UK, The Jackson Laboratory, Bar Harbor, ME 04609, USA, Center for Molecular and Vascular Biology, University of Leuven, Belgium, Department of Neuropediatrics, University Medical Center Schleswig-Holstein, Kiel Campus, 24105 Kiel, Germany, NE Thames Genetics Service, Great Ormond Street Hospital, London WC1N 3JH, UK, Drexel University College of Medicine, Philadelphia, PA 19102, USA, Department of Haematology, University of Cambridge and NHS Blood and Transplant Cambridge, CB2 0PT Cambridge, UK, Autism and Developmental Medicine Institute, Geisinger Health System

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http://dx.doi.org/10.1093/nar/gkt1026DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965098PMC
January 2014

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.

Nephron Physiol 2012 23;122(1-2):1-6. Epub 2013 Feb 23.

Centre for Nephrology, University College London, London, UK.

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http://dx.doi.org/10.1159/000349989DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782194PMC
October 2013

Oral manifestations of patients with Kenny-Caffey Syndrome.

Eur J Med Genet 2012 Aug-Sep;55(8-9):441-5. Epub 2012 Mar 30.

Paediatric Dentistry, Garancière Paris Diderot University, France.

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http://dx.doi.org/10.1016/j.ejmg.2012.03.005DOI Listing
November 2012

Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations.

Int J Paediatr Dent 2010 Jul;20(4):305-12

Paediatric Dentistry, Garancière Hotel-Dieu Hospital, Assistance Publique-Hôpitaux de Paris, Paris Diderot University, France.

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http://dx.doi.org/10.1111/j.1365-263X.2010.01056.xDOI Listing
July 2010

[Orthodontic treatment of children suffering from attention deficit disorder with hyperactivity (ADHD)].

Orthod Fr 2009 Sep 4;80(3):331-8. Epub 2009 Sep 4.

Département d'Orthodontie, Hôpital Garancière, Université Paris VII Denis-Diderot, 5 rue Garancière, 75006 Paris, France.

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http://www.orthodfr.org/10.1051/orthodfr/2009024
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http://dx.doi.org/10.1051/orthodfr/2009024DOI Listing
September 2009

The genetic basis of inherited anomalies of the teeth. Part 2: syndromes with significant dental involvement.

Eur J Med Genet 2008 Sep-Oct;51(5):383-408. Epub 2008 May 23.

Paediatric Dentistry Department, Paris 7 University; AP-HP, Hôtel-Dieu, Garancière, Paris, France.

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http://dx.doi.org/10.1016/j.ejmg.2008.05.003DOI Listing
November 2008

The genetic basis of inherited anomalies of the teeth. Part 1: clinical and molecular aspects of non-syndromic dental disorders.

Eur J Med Genet 2008 Jul-Aug;51(4):273-91. Epub 2008 Mar 26.

Paediatric Dentistry Department, Paris 7 University, AP-HP, Hôtel-Dieu - Garancière, Paris, France.

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http://linkinghub.elsevier.com/retrieve/pii/S176972120800042
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http://dx.doi.org/10.1016/j.ejmg.2008.02.009DOI Listing
October 2008

Generalized periodontitis associated with Chédiak-Higashi syndrome.

J Periodontol 2008 Jul;79(7):1263-70

Department of Pediatric Dentistry, Garancière, Public Assistance Hospitals of Paris, Hôtel-Dieu Hospital, University Paris 7, Paris, France.

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http://dx.doi.org/10.1902/jop.2008.070440DOI Listing
July 2008

Mesiodens.

Eur J Med Genet 2008 Mar-Apr;51(2):178-81. Epub 2008 Jan 4.

Centre for Human Genetics, University Hospital Leuven, Herestraat 49, 3000 Leuven, Belgium.

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http://dx.doi.org/10.1016/j.ejmg.2007.12.006DOI Listing
June 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

Caries experience in a severely obese adolescent population.

Int J Paediatr Dent 2007 Sep;17(5):358-63

Paediatric Dentistry, Garancière Hotel-Dieu Hospital, AP-HP, University Paris 7, Diderot, France.

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http://dx.doi.org/10.1111/j.1365-263X.2007.00848.xDOI Listing
September 2007

High proportion of pituitary abnormalities and other congenital defects in children with congenital nasal pyriform aperture stenosis.

Pediatr Res 2006 Oct 28;60(4):478-84. Epub 2006 Aug 28.

Pediatric Endocrinology and Diabetes Unit, Centre de Référence Maladies Endocriniennes Rares de la Croissance, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Paris VII University, 75019 Paris, France.

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http://dx.doi.org/10.1203/01.pdr.0000238380.03683.cbDOI Listing
October 2006