Your browser doesn't support javascript.
loading
The different clinical facets of SYN1-related neurodevelopmental disorders.
Parenti, Ilaria; Leitão, Elsa; Kuechler, Alma; Villard, Laurent; Goizet, Cyril; Courdier, Cécile; Bayat, Allan; Rossi, Alessandra; Julia, Sophie; Bruel, Ange-Line; Tran Mau-Them, Frédéric; Nambot, Sophie; Lehalle, Daphné; Willems, Marjolaine; Lespinasse, James; Ghoumid, Jamal; Caumes, Roseline; Smol, Thomas; El Chehadeh, Salima; Schaefer, Elise; Abi-Warde, Marie-Thérèse; Keren, Boris; Afenjar, Alexandra; Tabet, Anne-Claude; Levy, Jonathan; Maruani, Anna; Aledo-Serrano, Ángel; Garming, Waltraud; Milleret-Pignot, Clara; Chassevent, Anna; Koopmans, Marije; Verbeek, Nienke E; Person, Richard; Belles, Rebecca; Bellus, Gary; Salbert, Bonnie A; Kaiser, Frank J; Mazzola, Laure; Convers, Philippe; Perrin, Laurine; Piton, Amélie; Wiegand, Gert; Accogli, Andrea; Brancati, Francesco; Benfenati, Fabio; Chatron, Nicolas; Lewis-Smith, David; Thomas, Rhys H; Zara, Federico; Striano, Pasquale.
Affiliation
  • Parenti I; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
  • Leitão E; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
  • Kuechler A; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
  • Villard L; INSERM, MMG, Faculté de Médecine, Aix-Marseille University, Marseille, France.
  • Goizet C; Département de Génétique Médicale, APHM, Hôpital d'Enfants de La Timone, Marseille, France.
  • Courdier C; Service de Génétique Médicale, Bordeaux, France.
  • Bayat A; Centre de Référence Maladies Rares Neurogénétique, Service de Génétique Médicale, Bordeaux, France.
  • Rossi A; NRGEN Team, INCIA, CNRS UMR 5287, University of Bordeaux, Bordeaux, France.
  • Julia S; Service de Génétique Médicale, Bordeaux, France.
  • Bruel AL; Centre de Référence Maladies Rares Neurogénétique, Service de Génétique Médicale, Bordeaux, France.
  • Tran Mau-Them F; NRGEN Team, INCIA, CNRS UMR 5287, University of Bordeaux, Bordeaux, France.
  • Nambot S; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.
  • Lehalle D; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.
  • Willems M; Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.
  • Lespinasse J; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.
  • Ghoumid J; Pediatric Clinic, IRCCS Policlinico San Matteo Foundation, University of Pavia, Pavia, Italy.
  • Caumes R; Service de Génétique Médicale, Pôle de Biologie, CHU de Toulouse - Hôpital Purpan, Toulouse, France.
  • Smol T; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.
  • El Chehadeh S; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.
  • Schaefer E; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.
  • Abi-Warde MT; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.
  • Keren B; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.
  • Afenjar A; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.
  • Tabet AC; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.
  • Levy J; Department of Medical Genetics, Rare diseases and Personalized Medicine, CHU Montpellier, University of Montpellier, Montpellier, France.
  • Maruani A; Inserm U1298, INM, CHU Montpellier, University of Montpellier, Montpellier, France.
  • Aledo-Serrano Á; Service de Cytogenetique, Centre Hospitalier de Chambéry, Chambéry, France.
  • Garming W; Univ. Lille, ULR7364 RADEME, Lille, France.
  • Milleret-Pignot C; CHU Lille, Clinique de Génétique, Guy Fontaine, Lille, France.
  • Chassevent A; Univ. Lille, ULR7364 RADEME, Lille, France.
  • Koopmans M; CHU Lille, Clinique de Génétique, Guy Fontaine, Lille, France.
  • Verbeek NE; Univ. Lille, ULR7364 RADEME, Lille, France.
  • Person R; CHU Lille, Institut de Génétique Médicale, Lille, France.
  • Belles R; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, Strasbourg, France.
  • Bellus G; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Hôpital de Hautepierre, Strasbourg, France.
  • Salbert BA; Département de NeuroPédiatrie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
  • Kaiser FJ; APHP, Département de Génétique, UF de Génomique du Développement, Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, Sorbonne Université, Paris, France.
  • Mazzola L; Département de Génétique, Centre de Référence déficiences Intellectuelles de Causes Rares, APHP, Hôpital Armand Trousseau, Sorbonne Université, Paris, France.
  • Convers P; APHP, Département de Génétique, Hôpital Robert-Debré, Paris, France.
  • Perrin L; APHP, Département de Génétique, Hôpital Robert-Debré, Paris, France.
  • Piton A; Department of Child and Adolescent Psychiatry, Robert Debré Hospital, APHP, Paris, France.
  • Wiegand G; Epilepsy and Neurogenetics Program, Neurology Department, Ruber Internacional Hospital, Madrid, Spain.
  • Accogli A; Sozialpädiatrisches Zentrum, Kinder-und Jugendklinik Gelsenkirchen, Gelsenkirchen, Germany.
  • Brancati F; Service de Pédiatrie, CH de Mâcon, Mâcon, France.
  • Benfenati F; Department of Neurogenetics, Kennedy Krieger Institute, Baltimore, MD, United States.
  • Chatron N; Department of Genetics, Utrecht University Medical Center, Utrecht, Netherlands.
  • Lewis-Smith D; Department of Genetics, Utrecht University Medical Center, Utrecht, Netherlands.
  • Thomas RH; GeneDx, Gaithersburg, MD, United States.
  • Zara F; Medical Genetics, Geisinger Medical Center, Danville, PA, United States.
  • Striano P; Medical Genetics, Geisinger Medical Center, Danville, PA, United States.
Front Cell Dev Biol ; 10: 1019715, 2022.
Article in En | MEDLINE | ID: mdl-36568968
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Front Cell Dev Biol Year: 2022 Document type: Article Affiliation country: Alemania Country of publication: Suiza
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Front Cell Dev Biol Year: 2022 Document type: Article Affiliation country: Alemania Country of publication: Suiza