부산대학교 도서관

Mourao J; Department of Child and Adolescent Psychiatry, Assistance Publique-Hôpitaux de Paris, Sorbonne University, Paris, France.; Fabre A; Institut Imagine INSERM U1163 and U1299, Université Paris Cité, Consultation Mobile Régionale de Génétique Fondation Elan Retrouvé, Paris France.; Zamouri I; Department of Child and Adolescent Psychiatry, Assistance Publique-Hôpitaux de Paris, Sorbonne University, Paris, France; Centre de Référence des Maladies Rares à Expression Psychiatrique, Department of Child and Adolescent Psychiatry, Pitié-Salpêtrière University Hospital, Assistance Publique-Hôpitaux de Paris, Sorbonne University, Paris, France.; de Foucaud A; Department of Child and Adolescent Psychiatry, Assistance Publique-Hôpitaux de Paris, Sorbonne University, Paris, France; Centre de Référence des Maladies Rares à Expression Psychiatrique, Department of Child and Adolescent Psychiatry, Pitié-Salpêtrière University Hospital, Assistance Publique-Hôpitaux de Paris, Sorbonne University, Paris, France.; Baud M; Department of Child and Adolescent Psychiatry, Assistance Publique-Hôpitaux de Paris, Sorbonne University, Paris, France.; Brunelle J; Department of Child and Adolescent Psychiatry, Assistance Publique-Hôpitaux de Paris, Sorbonne University, Paris, France.; Munnich A; Institut Imagine, Consultation Mobile Régionale de Génétique Fondation Elan Retrouvé, Paris France.; Boddaert N; Paediatric Radiology Department, AP-HP, Hôpital Necker Enfants Malades, Université Paris cité, Institut Imagine INSERM U1163 and U1299, F-75015 Paris, France.; Cohen D; Department of Child and Adolescent Psychiatry, Assistance Publique-Hôpitaux de Paris, Sorbonne University, Paris, France; Centre de Référence des Maladies Rares à Expression Psychiatrique, Department of Child and Adolescent Psychiatry, Pitié-Salpêtrière University Hospital, Assistance Publique-Hôpitaux de Paris, Sorbonne University, Paris, France; CNRS UMR 7222, Institute for Intelligent Systems and Robotics, Sorbonne University, Paris, France. Electronic address: david.cohen@aphp.fr.

Publisher: Pergamon Press Country of Publication: United States NLM ID: 8709782 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-3379 (Electronic) Linking ISSN: 08914222 NLM ISO Abbreviation: Res Dev Disabil Subsets: MEDLINE

Hashimoto Y; Smurfit Institute of Genetics, Trinity College Dublin, D02 VF25, Dublin, Ireland.; Besmond C; INSERM UMR1163, Institut Imagine, Paris University, F-75015, Paris, France.; Clinical Genetics Department, Necker Hospital, APHP Centre-Paris University, F-75015, Paris, France.; Boddaert N; INSERM UMR1163, Institut Imagine, Paris University, F-75015, Paris, France.; Department of Pediatric Radiology, Hospital Necker Enfants Malades, F-75015, Paris, France.; Munnich A; INSERM UMR1163, Institut Imagine, Paris University, F-75015, Paris, France.; Clinical Genetics Department, Necker Hospital, APHP Centre-Paris University, F-75015, Paris, France.; Campbell M; Smurfit Institute of Genetics, Trinity College Dublin, D02 VF25, Dublin, Ireland.; FutureNeuro, Science Foundation Ireland Research Centre for Chronic and Rare Neurological Diseases, Royal College of Surgeons in Ireland, University of Medicine and Health Sciences, Dublin, Ireland.

Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

Roux CJ; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Dufeu-Berat CM; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Hully M; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Rotig A; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Schiff M; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; De Lonlay P; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Aubart M; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Alison M; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Jaroussie M; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Levy R; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Dangouloff-Ros V; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Barcia G; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Desguerre I; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Munnich A; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Gitiaux C; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.; Boddaert N; From the Departments of Pediatric Radiology (C.-J.R., R.L., V.D.-R., N.B.), Neurology and Metabolism (C.-M.D.-B., M.H., M.S., P.D.L., M. Aubart, I.D., A.M., C.G.), and Genetics (A.R., G.B.), Hôpital Necker-Enfants Malades, AP-HP, Université Paris Cité; IMAGINE Institute INSERM UMR 1163 (C.-J.R., A.R., M.S., M. Aubart, R.L., V.D.-R., G.B., A.M., N.B.), Paris; INSERM Institut Necker-Enfants Malades (P.D.L.), Paris; and Departments of Pediatric Radiology (M. Alison) and Neurology (M.J.), Hospital Robert Debré, Université Paris Cité, France.

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

Csigó K; Institute of Psychology, Pázmány Péter Catholic University, Budapest, Hungary.; Psychotherapy Center, Nyírő Gyula National Institute of Psychiatry and Addictions, Budapest, Hungary.; Münnich Á; Department of Behavioural Sciences, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.; Molnár J; Department of Behavioural Sciences, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101545006 Publication Model: eCollection Cited Medium: Print ISSN: 1664-0640 (Print) Linking ISSN: 16640640 NLM ISO Abbreviation: Front Psychiatry Subsets: PubMed not MEDLINE

Mazel B; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Centre de Génétique, FHU TRANSLAD - CHU Dijon Bourgogne, Dijon, France.; Inserm UMR1231 GAD, Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.; Delanne J; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Centre de Génétique, FHU TRANSLAD - CHU Dijon Bourgogne, Dijon, France.; Centre de référence Déficiences Intellectuelles de Causes Rares, CHU Dijon Bourgogne, Dijon, France.; Garde A; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Centre de Génétique, FHU TRANSLAD - CHU Dijon Bourgogne, Dijon, France.; Inserm UMR1231 GAD, Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.; Racine C; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Centre de Génétique, FHU TRANSLAD - CHU Dijon Bourgogne, Dijon, France.; Inserm UMR1231 GAD, Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.; Bruel AL; Inserm UMR1231 GAD, Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.; Laboratoire de Génomique Médicale, Unité Fonctionnelle Innovation en diagnostic génomique, Unité fonctionnelle innovation en diagnostic génomique des maladies rares, CHU Dijon Bourgogne, Dijon, France.; Duffourd Y; Inserm UMR1231 GAD, Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.; Laboratoire de Génomique Médicale, Unité Fonctionnelle Innovation en diagnostic génomique, Unité fonctionnelle innovation en diagnostic génomique des maladies rares, CHU Dijon Bourgogne, Dijon, France.; Lopergolo D; Molecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit, IRCCS Stella Maris Foudation, Pisa, Italy.; Santorelli FM; Molecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit, IRCCS Stella Maris Foudation, Pisa, Italy.; Marchi V; Department of Developmental Neuroscience, Stella Maris Scientific Institute, IRCCS Fondazione Stella Maris Foundation, Pisa, Italy.; Pinto AM; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.; Mencarelli MA; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.; Canitano R; Division of Child and Adolescent Neuropsychiatry, University Hospital of Siena, Siena, Italy.; Valentino F; Medical Genetics Unit, University of Siena, Policlinico Le Scotte, Siena, Italy.; Papa FT; Medical Genetics Unit, University of Siena, Policlinico Le Scotte, Siena, Italy.; Fallerini C; Medical Genetics Unit, University of Siena, Policlinico Le Scotte, Siena, Italy.; Department of Medical Biotechnologies, Med Biotech Hub and Competence Center, University of Siena, Siena, Italy.; Mari F; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.; Medical Genetics Unit, University of Siena, Policlinico Le Scotte, Siena, Italy.; Renieri A; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.; Medical Genetics Unit, University of Siena, Policlinico Le Scotte, Siena, Italy.; Department of Medical Biotechnologies, Med Biotech Hub and Competence Center, University of Siena, Siena, Italy.; Munnich A; Service de Génétique Médicale et Clinique, Hôpital Necker Enfants Malades, Paris, France.; Niclass T; Service de Génétique Clinique, CHU de Poitiers, Poitiers, France.; Le Guyader G; Service de Génétique Clinique, CHU de Poitiers, Poitiers, France.; Thauvin-Robinet C; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Centre de Génétique, FHU TRANSLAD - CHU Dijon Bourgogne, Dijon, France.; Inserm UMR1231 GAD, Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.; Centre de référence Déficiences Intellectuelles de Causes Rares, CHU Dijon Bourgogne, Dijon, France.; Laboratoire de Génomique Médicale, Unité Fonctionnelle Innovation en diagnostic génomique, Unité fonctionnelle innovation en diagnostic génomique des maladies rares, CHU Dijon Bourgogne, Dijon, France.; Philippe C; Inserm UMR1231 GAD, Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.; Laboratoire de Génomique Médicale, Unité Fonctionnelle Innovation en diagnostic génomique, Unité fonctionnelle innovation en diagnostic génomique des maladies rares, CHU Dijon Bourgogne, Dijon, France.; Faivre L; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Centre de Génétique, FHU TRANSLAD - CHU Dijon Bourgogne, Dijon, France.; Inserm UMR1231 GAD, Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235742 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-485X (Electronic) Linking ISSN: 15524841 NLM ISO Abbreviation: Am J Med Genet B Neuropsychiatr Genet Subsets: MEDLINE

Wang HH; Department of Molecular Physiology and Biological Physics, University of Virginia School of Medicine, University of Virginia, Charlottesville, Virginia, USA.; Department of Molecular & Integrative Physiology and.; Lin LL; Department of Molecular Physiology and Biological Physics, University of Virginia School of Medicine, University of Virginia, Charlottesville, Virginia, USA.; Department of Molecular & Integrative Physiology and.; Li ZJ; Department of Molecular Physiology and Biological Physics, University of Virginia School of Medicine, University of Virginia, Charlottesville, Virginia, USA.; Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan, USA.; Wei X; Department of Molecular Physiology and Biological Physics, University of Virginia School of Medicine, University of Virginia, Charlottesville, Virginia, USA.; Department of Molecular & Integrative Physiology and.; Askander O; Hopital Cheik Zaïd, Hopital Universitaire International RABAT, Morocco.; Cappuccio G; Telethon Institute of Genetics and Medicine, Pozzuoli, Italy.; Department of Translational Medicine, University of Naples Federico II, Naples, Italy.; Hashem MO; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Hubert L; Imagine Institute, INSERM UMR1163, Paris, France.; Université Paris Cité, Paris, France.; Munnich A; Imagine Institute, INSERM UMR1163, Paris, France.; Alqahtani M; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Pang Q; Department of Neurosurgery, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.; Burmeister M; Michigan Neuroscience Institute and Departments of Computational Medicine & Bioinformatics, Psychiatry, and Human Genetics, University of Michigan Medical School, Ann Arbor, Michigan, USA.; Lu Y; Department of Molecular & Integrative Physiology and.; Poirier K; Imagine Institute, INSERM UMR1163, Paris, France.; Besmond C; Imagine Institute, INSERM UMR1163, Paris, France.; Sun S; Department of Pharmacology, University of Virginia, Charlottesville, Virginia, USA.; Brunetti-Pierri N; Telethon Institute of Genetics and Medicine, Pozzuoli, Italy.; Department of Translational Medicine, University of Naples Federico II, Naples, Italy.; Scuola Superiore Meridionale (SSM, School of Advanced Studies), Genomics and Experimental Medicine Program, University of Naples Federico II, Naples, Italy.; Alkuraya FS; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.; Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.; Qi L; Department of Molecular Physiology and Biological Physics, University of Virginia School of Medicine, University of Virginia, Charlottesville, Virginia, USA.; Department of Molecular & Integrative Physiology and.; Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan, USA.

Publisher: American Society for Clinical Investigation Country of Publication: United States NLM ID: 7802877 Publication Model: Electronic Cited Medium: Internet ISSN: 1558-8238 (Electronic) Linking ISSN: 00219738 NLM ISO Abbreviation: J Clin Invest Subsets: MEDLINE

Oláh B; Department of Behavioural Sciences, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.; Doctoral School of Health Sciences, University of Debrecen, Debrecen, Hungary.; Münnich Á; Department of Behavioural Sciences, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.; Kósa K; Department of Behavioural Sciences, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.; Doctoral School of Health Sciences, University of Debrecen, Debrecen, Hungary.

Publisher: Taylor & Francis Country of Publication: United States NLM ID: 9806550 Publication Model: Print Cited Medium: Internet ISSN: 1087-2981 (Electronic) Linking ISSN: 10872981 NLM ISO Abbreviation: Med Educ Online Subsets: MEDLINE

Saadi A; Service de neurologie, Etablissement Hospitalier Specialisé de Ben Aknoun, Université Benyoucef Benkhedda, Algiers, Algeria.; Laboratoire de Neurosciences, Service de neurologie, Centre Hospitalo Universitaire Mustapha Bacha, Université Benyoucef Benkhedda Alger, Algiers, Algeria.; Navarro C; INSERM, MMG, Aix Marseille University, Marseille, France.; Neoflow Therapeutics, 61 boulevard des Dames, 13002, Marseille, France.; Ozalp O; Genetic Diagnosis Center, Adana City Training and Research Hospital University of Health Sciences, Adana, Turkey.; Lourenco CM; Neurogenetics Unit-Inborn Errors of Metabolism Clinics, National Reference Center for Rare Diseases, Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto, Brazil.; Department of Specialized Education, Personalized Medicine Area, DLE/Grupo Pardini, Rio de Janeiro, Brazil.; Fayek R; INSERM, MMG, Aix Marseille University, Marseille, France.; Da Silva N; INSERM, MMG, Aix Marseille University, Marseille, France.; Chaouch A; Service de neurophysiologie, Etablissement Hospitalier Specialisé, Algiers, Algeria.; Benahmed M; Service d'anatomo-pathologie, Centre Pierre Marie Curie, Algiers, Algeria.; Kubisch C; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Munnich A; Department of Clinical Genetics, Institut de Recherche Necker Enfants Malades, Paris, France.; Lévy N; INSERM, MMG, Aix Marseille University, Marseille, France.; Department of Medical Genetics, La Timone Hospital, APHM, Marseille, France.; Roll P; INSERM, MMG, Aix Marseille University, Marseille, France.; Cell Biology Laboratory, La Timone Hospital, APHM, Marseille, France.; Pacha LA; Laboratoire de Neurosciences, Service de neurologie, Centre Hospitalo Universitaire Mustapha Bacha, Université Benyoucef Benkhedda Alger, Algiers, Algeria.; Chaouch M; Service de neurologie, Etablissement Hospitalier Specialisé de Ben Aknoun, Université Benyoucef Benkhedda, Algiers, Algeria.; Lessel D; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Institute of Human Genetics, University Hospital of the Paracelsus Medical University Salzburg, Salzburg, Austria.; De Sandre-Giovannoli A; INSERM, MMG, Aix Marseille University, Marseille, France.; Department of Medical Genetics, La Timone Hospital, APHM, Marseille, France.; Biological Resource Center (CRB-TAC), La Timone Hospital, APHM, Marseille, France.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Desguerre I; Departments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.; Aubart M; Departments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.; Hashimoto Y; Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.; Poirier K; INSERM UMR1163, Institut Imagine, Paris University, Paris 75015, France.; Kaminska A; Departments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.; Alison M; Department of Pediatric Radiology, Hospital Robert Debré, Université Paris Cité, Paris F-75015, France.; Boddaert N; Departments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.; INSERM UMR1163, Institut Imagine, Paris University, Paris 75015, France.; Department of Pediatric Radiology, Hospital Necker Enfants Malades, Université Paris Cité, Paris F-75015, France.; Munnich A; Departments of Pediatric Neurology and Medical Genetics, Hospital Necker-Enfants Malades, Université Paris Cité, Paris F-75015, France.; INSERM UMR1163, Institut Imagine, Paris University, Paris 75015, France.; Campbell M; Smurfit Institute of Genetics, Trinity College Dublin, Dublin 2, Ireland.

Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

Durrleman C; Pediatric Neurology Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.; Grevent D; Pediatric Imaging Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.; Lumiere Platform, Université Paris Cité, Paris, France.; Aubart M; Pediatric Neurology Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.; Kossorotoff M; Pediatric Neurology Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.; Roux CJ; Pediatric Imaging Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.; Kaminska A; Neurophysiology Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.; Rio M; Genetic Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.; Barcia G; Genetic Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.; Boddaert N; Pediatric Imaging Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.; Lumiere Platform, Université Paris Cité, Paris, France.; Munnich A; Genetic Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.; Nabbout R; Pediatric Neurology Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.; Desguerre I; Pediatric Neurology Department, Necker Enfants Malades Hospital, APHP, Université Paris Cité, Paris, France.

Publisher: Wiley Country of Publication: England NLM ID: 9506311 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-1331 (Electronic) Linking ISSN: 13515101 NLM ISO Abbreviation: Eur J Neurol Subsets: MEDLINE