부산대학교 도서관

Parra-Díaz, P; Monteil, A; Del Pino, I; Beltrán-Corbellini, A; Spinelli, E; Calame, D; Vera-Medialdea, R; Dieterich, K; Tevissen, H; Soliani, L; Cordelli, DM; Waltz, S; Riley, K; Kritzer, A; Caron, E; Román, ISM; Gil-Nagel, A

EPILEPSIA
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)

Parra-Díaz P; Department of Neurology, Hospital Ruber Internacional, Madrid, Spain.; Department of Neurology, Hospital Universitario Ramón y Cajal, Madrid, Spain.; Fundación Iniciativa para las Neurociencias (Fundación INCE), Madrid, Spain.; Monteil A; Institut de Génomique Fonctionnelle, Université de Montpellier, CNRS, INSERM, Montpellier, France.; LabEx 'Ion Channel Science and Therapeutics', Montpellier, France.; Department of Physiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.; Calame D; Section of Pediatric Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine, Houston, TX.; Texas Children's Hospital, Houston, TX.; Hadouiri N; Department of Physical Medicine and Rehabilitation, Dijon-Bourgogne University Hospital, Dijon, France.; UMR-Inserm 1231, Génétique des Anomalies du Développement (GAD), Bourgogne Franche-Comté University, Dijon, France.; INSERM, CIC 1432, Clinical Investigation Center, Plurithematic Module, Technological Investigation Platform, Dijon-Bourgogne University Hospital, Dijon, France.; Soliani L; UOC Neuropsichiatria dell'età Pediatrica, IRCCS Istituto delle Scienze Neurologiche di Bologna, Italy.; Spinelli E; Department of Pediatrics, Division of Pediatric Neurology, University of Western Ontario/London Health Sciences Centre, London, Ontario, Canada.; Caron EJ; The University of Tennessee Health Sciences Center, Le Bonheur Children's Hospital, Memphis.; Dieterich K; INSERM U1209, CHU Grenoble Alpes, Medical Genetics, Institute for Advanced Biosciences, Université Grenoble Alpes, Grenoble, France.; Kritzer A; Department of Genetics and Genomics, Boston Children's Hospital, MA.; Riley K; Department of Pediatric Medical Genetics, Duke University Hospital, Durham, NC.; Serratosa Fernández JM; Department of Neurology, Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.; Tanner JA; Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health San Antonio, TX.; Tevissen H; Department of Pediatrics, Centre Hospitalier de Valence, France.; Thauvin C; Centre de Génétique et Centre de Référence Neurogène, Hôpital d'Enfants, CHU Dijon, France.; Laboratoire de Génomique médicale - Centre NEOMICS, CHU Dijon Bourgogne, Dijon, France.; INSERM - Université de Bourgogne - UMR1231 GAD, Dijon, France.; Vera-Medialdea R; Department of Pediatrics, Hospital Regional Universitario de Málaga, Spain.; Waltz SM; Center for Neuropediatrics, Koeln, Germany; and.; Beltrán-Corbellini Á; Department of Neurology, Hospital Ruber Internacional, Madrid, Spain.; García Morales I; Department of Neurology, Hospital Ruber Internacional, Madrid, Spain.; Department of Neurology, Hospital Clínico San Carlos, Madrid, Spain.; Sánchez-Miranda Román I; Department of Neurology, Hospital Ruber Internacional, Madrid, Spain.; Toledano R; Department of Neurology, Hospital Ruber Internacional, Madrid, Spain.; Department of Neurology, Hospital Universitario Ramón y Cajal, Madrid, Spain.; Valls-Carbó A; Department of Neurology, Hospital Ruber Internacional, Madrid, Spain.; Fundación Iniciativa para las Neurociencias (Fundación INCE), Madrid, Spain.; Gil-Nagel A; Department of Neurology, Hospital Ruber Internacional, Madrid, Spain.; Fundación Iniciativa para las Neurociencias (Fundación INCE), Madrid, Spain.

Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1526-632X (Electronic) Linking ISSN: 00283878 NLM ISO Abbreviation: Neurology Subsets: MEDLINE

A.-F. Dumas; A. Grange; S. Munier; H. Tevissen; I. Dufrene; H. Hida

Le Pharmacien Clinicien. 57:e92

I de Montgolfier-Aubron; L Burglen; M.S Chavet; H Tevissen; C Perrot; J.J Baudon; F Gold

Archives de Pédiatrie. 7:1085-1087

Parra-Diaz, P.; Monteil, A.; del Pino, I.; Beltran-Corbellini, A.; Spinelli, E.; Calame, D.; Vera-Medialdea, R.; Dieterich, K.; Tevissen, H.; Soliani, L.; Cordelli, D. M.; Waltz, S.; Riley, K.; Kritzer, A.; Caron, E.; Sanchez-Miranda Roman, I.; Gil-Nagel, A.

EPILEPSIA; NOV 2024, 65 p296-p297, 2p. Supplement: 1

Masson J; Service de Génétique, Laboratoire de Cytogénétique Constitutionnelle, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, Bron, France; Lyon Neuroscience Research Center, GENDEV Team, CNRS UMR 5292, INSERM U1028, UCBL1, Bron, France; Université Claude Bernard Lyon 1, France.; Pons L; Service de Génétique, Laboratoire de Cytogénétique Constitutionnelle, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, Bron, France.; Busa T; Service de Génétique, Hôpital de la Timone Enfant, APHM, Marseille, France.; Missirian C; Service de Génétique, Hôpital de la Timone Enfant, APHM, Marseille, France.; Lines M; Division of Metabolics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.; Tevissen H; Centre Hospitalier de Valence, Service de pédiatrie, Valence, France.; Diguet F; Service de Génétique, Laboratoire de Cytogénétique Constitutionnelle, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, Bron, France.; Rollat-Farnier PA; Service de Génétique, Laboratoire de Cytogénétique Constitutionnelle, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, Bron, France.; Lesca G; Service de Génétique, Laboratoire de Cytogénétique Constitutionnelle, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, Bron, France; Lyon Neuroscience Research Center, GENDEV Team, CNRS UMR 5292, INSERM U1028, UCBL1, Bron, France; Université Claude Bernard Lyon 1, France.; Sanlaville D; Service de Génétique, Laboratoire de Cytogénétique Constitutionnelle, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, Bron, France; Lyon Neuroscience Research Center, GENDEV Team, CNRS UMR 5292, INSERM U1028, UCBL1, Bron, France; Université Claude Bernard Lyon 1, France.; Schluth-Bolard C; Service de Génétique, Laboratoire de Cytogénétique Constitutionnelle, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, Bron, France; Lyon Neuroscience Research Center, GENDEV Team, CNRS UMR 5292, INSERM U1028, UCBL1, Bron, France; Université Claude Bernard Lyon 1, France. Electronic address: caroline.schluth-bolard@chru-strasbourg.fr.

Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE

Alqahtani AS; Department of Medical Genetics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; Ministry of Higher Education, Riyadh, Saudi Arabia.; Putoux A; Department of Medical Genetics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; Claude Bernard Lyon 1 University, Lyon, France.; CRNL, CNRS UMR 5292, INSERM U1028, Lyon, France.; Bonnet Dupeyron MN; Department of Medical Genetics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; Department of Genetics, Valence Hospital's Center, Valence, France.; Carneiro M; Department of Neuropediatrics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; Lion-Francois L; Department of Neuropediatrics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; Rossi M; Department of Medical Genetics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; CRNL, CNRS UMR 5292, INSERM U1028, Lyon, France.; Tevissen H; Department of Pediatrics, Valence Hospital's Center, Valence, France.; Schluth Bolard C; Department of Medical Genetics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; Claude Bernard Lyon 1 University, Lyon, France.; CRNL, CNRS UMR 5292, INSERM U1028, Lyon, France.; Labalme A; Department of Medical Genetics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; Lesca G; Department of Medical Genetics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; Claude Bernard Lyon 1 University, Lyon, France.; CRNL, CNRS UMR 5292, INSERM U1028, Lyon, France.; Till M; Department of Medical Genetics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; Edery P; Department of Medical Genetics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; Claude Bernard Lyon 1 University, Lyon, France.; CRNL, CNRS UMR 5292, INSERM U1028, Lyon, France.; Sanlaville D; Department of Medical Genetics, Women Mothers and Children's Hospital, Lyon Hospices Civils, Lyon, France.; Claude Bernard Lyon 1 University, Lyon, France.; CRNL, CNRS UMR 5292, INSERM U1028, Lyon, France.

Publisher: John Wiley & Sons Country of Publication: United States NLM ID: 101603758 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2324-9269 (Electronic) Linking ISSN: 23249269 NLM ISO Abbreviation: Mol Genet Genomic Med Subsets: MEDLINE

Mortreux J; Département de Génétique Médicale, APHM, CHU Timone Enfants, Marseille, France. jeremie.mortreux@ap-hm.fr.; Busa T; Département de Génétique Médicale, APHM, CHU Timone Enfants, Marseille, France.; Germain DP; Division of Medical Genetics, University of Versailles, 78180, Montigny, France.; CHU Raymond Poincaré (AP-HP), Garches, France.; Nadeau G; UF de génétique chromosomique, Centre hospitalier métropole Savoie, Chambéry, France.; Puechberty J; Département de Génétique Médicale, Maladies rares et Médecine Personnalisée, CHU de Montpellier, France.; Coubes C; Département de Génétique Médicale, Maladies rares et Médecine Personnalisée, CHU de Montpellier, France.; Gatinois V; Laboratoire de Génétique Chromosomique, CHU de Montpellier, France.; Cacciagli P; Aix Marseille Université, GMGF UMR_S 910, Marseille, France.; Duffourd Y; Fédération Hospitalo-Universitaire Médecine Translationnelle et Anomalies du Développement (FHU TRANSLAD), CHU de Dijon et Université de Bourgogne-Franche Comté, Dijon, France.; Equipe d'Accueil 42271, Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.; Pinard JM; Division of Neuropediatrics, CHU Raymond Poincaré (AP-HP), Garches, France.; Tevissen H; Service de pédiatrie, CH de Valence, Valence, France.; Villard L; Aix Marseille Université, GMGF, Inserm, UMR_S 910, Marseille, France.; Sanlaville D; Department of Genetics, Lyon University Hospitals, Lyon, France.; Lyon Neuroscience Research Centre, CNRS UMR5292, Inserm U1028, Lyon, France.; Claude Bernard Lyon I University, Lyon, France.; Philip N; Département de Génétique Médicale, APHM, CHU Timone Enfants, Marseille, France.; Aix Marseille Université, GMGF UMR_S 910, Marseille, France.; Missirian C; Département de Génétique Médicale, APHM, CHU Timone Enfants, Marseille, France.

Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE

M Descostes; E Tevissen

Physics and Chemistry of the Earth, Parts A/B/C. 29:79-90

PSN: Psychiatrie, Sciences Humaines, Neurosciences. January 2004 2(1):43-54

Schluth-Bolard C; Laboratoire de Cytogénétique Constitutionnelle, Service de Génétique, Centre de Biologie et de Pathologie Est, 59, boulevard Pinel, BRON 69677 Cedex, France. caroline.schluth-bolard@chu-lyon.fr; Labalme A; Cordier MP; Till M; Nadeau G; Tevissen H; Lesca G; Boutry-Kryza N; Rossignol S; Rocas D; Dubruc E; Edery P; Sanlaville D

Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

de Montgolfier-Aubron, I; Burglen, L; Chavet, MS; Tevissen, H; Perrot, C; Baudon, JJ; Gold, F

ARCHIVES DE PEDIATRIE; OCT 2000, 7 10, p1085-p1087, 3p.

EVOLUTION PSYCHIATRIQUE; APR-JUN 2005, 70 2, p271-p281, 11p.

Bachet, M.; Schneider, H.; Jauberty, L.; De Windt, L.; De Dieuleveult, C.; Tevissen, E.

In: Industrial and Engineering Chemistry Research. (Industrial and Engineering Chemistry Research, 9 July 2014, 53(27):11096-11106)

PSN-PSYCHIATRIE SCIENCES HUMAINES NEUROSCIENCES; FEB 2008, 6 1, p38-p53, 16p.