부산대학교 도서관

Sofia C; Department of Biomedical Sciences and Morphologic and Functional Imaging, University of Messina, Policlinico 'G. Martino', Via Consolare Valeria 1, 98100, Messina, Italy. carm.sofia@tiscali.it.; Aertsen M; Department of Radiology, University Hospitals Katholieke Universiteit (KU), Louvain, Belgium.; Garel C; Department of Radiology, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Cassart M; Department of Radiology and Fetal Medicine, Iris South Hospitals, Brussels, Belgium.

Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0365332 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1998 (Electronic) Linking ISSN: 03010449 NLM ISO Abbreviation: Pediatr Radiol Subsets: MEDLINE

Guilbaud L; Fetal Medicine Department, Armand Trousseau University Hospital, Spin@ Reference Center, Sorbonne University, Paris, France.; Carreras E; Maternal-Fetal Medicine Unit, Department of Obstetrics, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.; Garel C; Pediatric Radiology Department, Armand Trousseau University Hospital, Sorbonne University, Paris, France.; Maiz N; Maternal-Fetal Medicine Unit, Department of Obstetrics, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.; Dhombres F; Fetal Medicine Department, Armand Trousseau University Hospital, Spin@ Reference Center, Sorbonne University, Paris, France.; Deprest J; Clinical Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium.; Institute of Women's Health, University College London, London, UK.; Jouannic JM; Fetal Medicine Department, Armand Trousseau University Hospital, Spin@ Reference Center, Sorbonne University, Paris, France.

Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE

Sadan OR; Sagol Brain Institute, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel.; Sagol School of Neuroscience, Tel-Aviv University, Tel-Aviv, Israel.; Avisdris N; Sagol Brain Institute, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel.; School of Computer Science and Engineering, The Hebrew University of Jerusalem, Jerusalem, Israel.; Rabinowich A; Sagol Brain Institute, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel.; Department of Radiology, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel.; Faculty of Medical & Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.; Link-Sourani D; Sagol Brain Institute, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel.; Technion Human MRI Research Center, Faculty of Biomedical Engineering, Technion - Israel Institute of Technology, Haifa, Israel.; Krajden Haratz K; Faculty of Medical & Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.; Department of Obstetrics and Gynecology, Lis Hospital for Women, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel.; Garel C; Department of Radiology, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel.; Hiersch L; Faculty of Medical & Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.; Department of Obstetrics and Gynecology, Lis Hospital for Women, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel.; Ben Sira L; Sagol School of Neuroscience, Tel-Aviv University, Tel-Aviv, Israel.; Department of Radiology, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel.; Faculty of Medical & Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.; Ben Bashat D; Sagol Brain Institute, Tel Aviv Sourasky Medical Center, Tel-Aviv, Israel.; Sagol School of Neuroscience, Tel-Aviv University, Tel-Aviv, Israel.; Faculty of Medical & Health Sciences, Tel-Aviv University, Tel-Aviv, Israel.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9105850 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1522-2586 (Electronic) Linking ISSN: 10531807 NLM ISO Abbreviation: J Magn Reson Imaging Subsets: MEDLINE

Chanclud J; Department of Pediatric Radiology, Trousseau Hospital, APHP Sorbonne Université, 26 Avenue du Docteur Arnold Netter, Paris, 75012, France. justine.chanclud@aphp.fr.; Blondiaux E; Department of Pediatric Radiology, Trousseau Hospital, APHP Sorbonne Université, 26 Avenue du Docteur Arnold Netter, Paris, 75012, France.; Garel C; Department of Pediatric Radiology, Trousseau Hospital, APHP Sorbonne Université, 26 Avenue du Docteur Arnold Netter, Paris, 75012, France.

Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0365332 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1998 (Electronic) Linking ISSN: 03010449 NLM ISO Abbreviation: Pediatr Radiol Subsets: PubMed not MEDLINE; MEDLINE

Garel J; Department of Radiology, Sainte-Justine University Hospital, University of Montreal, Montreal, QC, H3T 1C5, Canada. gareljuliette7@gmail.com.; Rossi A; Neuroradiology Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.; Department of Health Sciences (DISSAL), University of Genoa, Genoa, Italy.; Blondiaux E; Department of Radiology, Médecine Sorbonne Université, APHP, DMU DIAMENT, GRC Images, Paris, France.; Cassart M; Department of Radiology and Fetal Medicine, Iris South Hospitals, 63 Rue J. Paquot, 1050, Brussels, Belgium.; Hoffmann C; Department of Radiology, Tel Hashomer Hospital, Chaim Sheba Medical Center, Ramat-Gan, Israel.; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.; Garel C; Department of Radiology, Hôpital d'Enfants Armand-Trousseau, AP-HP, Paris, France.; National Reference Center for Rare Disease: Vertebral and Spinal Cord Anomalies (MAVEM Center), AP-HP, Trousseau Hospital, Paris, France.

Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0365332 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1998 (Electronic) Linking ISSN: 03010449 NLM ISO Abbreviation: Pediatr Radiol Subsets: MEDLINE

Heide S; Department of Genetics and Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Assistance Publique-Hopitaux de Paris, Pitié-Salpêtrière Hospital, Paris, 75013, France, Paris, France solveig.heide@aphp.fr.; Argilli E; Department of Neurology, University of California San Francisco Division of Hospital Medicine, San Francisco, California, USA.; Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, California, USA.; Valence S; Department of Neuropediatry & Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Hopital Armand-Trousseau, Paris, France.; Boutaud L; Genomic medicine of rare diseases, UF MP5, Hopital universitaire Necker-enfants Malades, Assistance Publique Hôpitaux de Paris, Paris, France.; Roux N; Genomic medicine of rare diseases, UF MP5, Hopital universitaire Necker-enfants Malades, Assistance Publique Hôpitaux de Paris, Paris, France.; Mignot C; Department of Genetics and Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Assistance Publique-Hopitaux de Paris, Pitié-Salpêtrière Hospital, Paris, 75013, France, Paris, France.; Nava C; Department of Genetics, Unit of Developmental Genomics, AP-HP.Sorbonne Université, Pitié-Salpêtrière Hospital, Paris, France.; Keren B; Department of Genetics, Unit of Developmental Genomics, AP-HP.Sorbonne Université, Pitié-Salpêtrière Hospital, Paris, France.; Giraudat K; Department of Neuropediatry & Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Hopital Armand-Trousseau, Paris, France.; Faudet A; Department of Genetics and Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Assistance Publique-Hopitaux de Paris, Pitié-Salpêtrière Hospital, Paris, 75013, France, Paris, France.; Gerasimenko A; Department of Genetics and Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Assistance Publique-Hopitaux de Paris, Pitié-Salpêtrière Hospital, Paris, 75013, France, Paris, France.; Garel C; Department of pediatric and prenatal imaging, Armand-Trousseau Hospital, Sorbonne Université, Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.; Blondiaux E; Department of pediatric and prenatal imaging, Armand-Trousseau Hospital, Sorbonne Université, Assistance Publique des Hôpitaux de Paris (AP-HP), Paris, France.; Rastetter A; Paris Brain Institute (ICM Institut du Cerveau), Sorbonne Université, INSERM UMR S 1127, Paris, France.; Grevent D; Radiology Department, Hopital universitaire Necker-enfants Malades, Paris, France.; EA fetus 7328 and LUMIERE Platform, Université de Paris, Paris, France.; Le C; Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, California, USA.; Department of Neurology, University of California, Institute of Human Genetics and Weill Institute for Neurosciences, San Francisco, California, USA.; Mackenzie L; Department of Neuroscience, Washington University in St Louis School of Medicine, St Louis, Missouri, USA.; Richards L; Department of Neuroscience, Washington University in St Louis School of Medicine, St Louis, Missouri, USA.; Queensland Brain Institute, University of Queensland, Brisbane, Queensland, Australia.; Attié-Bitach T; Genomic medicine of rare diseases, UF MP5, Hopital universitaire Necker-enfants Malades, Assistance Publique Hôpitaux de Paris, Paris, France.; Depienne C; Institute of Human Genetics, University Hospital Essen, Universitu Duisburg-Essen, Essen, Germany.; Sherr E; Department of Neurology, University of California San Francisco Division of Hospital Medicine, San Francisco, California, USA.; Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, California, USA.; Héron D; Department of Genetics and Referral Center for Intellectual disabilities of rare causes, AP-HP.Sorbonne Université, Assistance Publique-Hopitaux de Paris, Pitié-Salpêtrière Hospital, Paris, 75013, France, Paris, France.

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

Adamsbaum C; Pediatric radiologist, Faculty of Medicine Paris Saclay, France.; Garel C; Trousseau Hospital, APHP, Paris, France.

Publisher: Elsevier Inc Country of Publication: United States NLM ID: 9710011 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-3933 (Electronic) Linking ISSN: 10918531 NLM ISO Abbreviation: J AAPOS Subsets: MEDLINE

Cassart M; Department of Radiology and Fetal Medicine, Iris Hospitals South, 63 Rue J. Paquot, 1050, Brussels, Belgium. marie.cassart@icloud.com.; Garel C; Department of Radiology, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Ulinski T; Pediatric Nephrology Unit, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Freddy Avni E; Department of Medical Imaging, Marie Curie Civil Hospital, Charleroi, Belgium.

Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 0365332 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1998 (Electronic) Linking ISSN: 03010449 NLM ISO Abbreviation: Pediatr Radiol Subsets: MEDLINE

Gras M; Department of Clinical Genetics, APHP Sorbonne Université, University Hospital Pitié Salpêtrière, Paris, France mathilde.gras@aphp.fr.; Heide S; Department of Clinical Genetics, APHP Sorbonne Université, University Hospital Pitié Salpêtrière, Paris, France.; Reference Center for Rare Diseases « Intellectual disabilities of rare causes » Déficiences Intellectuelles de Causes Rares, University Hospital Pitié Salpêtrière, Paris, France.; Doctoral College, Sorbonne University, Paris, France.; Keren B; Department of Clinical Genetics, APHP Sorbonne Université, University Hospital Pitié Salpêtrière, Paris, France.; Valence S; Unit of Pediatric Neurology, APHP Sorbonne Université, Armand-Trousseau Hospital, Paris, France.; Reference Center for Rare Diseases « Intellectual disabilites of rare causes » Déficiences Intellectuelles de Causes Rares, Armand-Trousseau Hospital, Paris, France.; Garel C; Unit of Pediatric Radiology, APHP Sorbonne Université, Armand-Trousseau Hospital, Paris, France.; Whalen S; Department of Clinical Genetics and Reference Center for Rare Diseases « Developmental disorders and syndromes », APHP Sorbonne Université, Armand-Trousseau Hospital, Paris, France.; Jansen AC; Neurogenetics Research Group, Vrije Universiteit Brussel, Brussels, Belgium.; Keymolen K; Clinical Sciences, Research Group Reproduction and Genetics, Centre for Medical Genetics, Universitair Ziekenhuis Brussel (UZ Brussels), Vrije Universiteit Brussel (VUB), Brussels, Belgium.; Stouffs K; Clinical Sciences, Research Group Reproduction and Genetics, Centre for Medical Genetics, Universitair Ziekenhuis Brussel (UZ Brussels), Vrije Universiteit Brussel (VUB), Brussels, Belgium.; Jennesson M; Pediatrics Unit, University Hospital of Reims, American Memorial Hospital, Reims, France.; Poirsier C; UF génétique clinique, Pôle Femme-Parents-Enfants, CHU Reims, Reims, France.; Lesca G; Department of Genetics, Referral Center for Developmental Anomalies and Malformative Syndromes, Centre-est HCL, Hospices Civils de Lyon, Lyon, France.; Depienne C; Institute of Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.; Nava C; Brain Institute, Paris, France.; Rastetter A; Brain Institute, Paris, France.; Curie A; Reference Centre for Rare Diseases « Intellectual disabilities of rare causes », Civil Hospices of Lyon, Lyon, France.; University Lyon 1 Faculty of Medicine Lyon-Est, Lyon, France.; Cuisset L; APHP Centre Université Paris Cité, Service de Médecine Génomique des Maladies de Système et d'Organe, Cochin Hospital, Paris, France.; Des Portes V; Reference Centre for Rare Diseases « Intellectual disabilities of rare causes », Civil Hospices of Lyon, Lyon, France.; University Lyon 1 Faculty of Medicine Lyon-Est, Lyon, France.; Milh M; Department of Neurology Pediatrics, AP-HM, Hôpital de la Timone, Marseille, France.; Charles P; Department of Clinical Genetics, APHP Sorbonne Université, University Hospital Pitié Salpêtrière, Paris, France.; Reference Center for Rare Diseases « Intellectual disabilities of rare causes » Déficiences Intellectuelles de Causes Rares, University Hospital Pitié Salpêtrière, Paris, France.; Mignot C; Department of Clinical Genetics, APHP Sorbonne Université, University Hospital Pitié Salpêtrière, Paris, France.; Reference Center for Rare Diseases « Intellectual disabilities of rare causes » Déficiences Intellectuelles de Causes Rares, University Hospital Pitié Salpêtrière, Paris, France.; Héron D; Department of Clinical Genetics, APHP Sorbonne Université, University Hospital Pitié Salpêtrière, Paris, France.; Reference Center for Rare Diseases « Intellectual disabilities of rare causes » Déficiences Intellectuelles de Causes Rares, University Hospital Pitié Salpêtrière, Paris, France.

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

Jaillard A; Department of Radiology, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Valence S; Department of Pediatric Neurology, Reference Center for Rare Diseases and Intellectual Deficiencies of Rare Causes, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Vande Perre S; Department of Radiology, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Dhombres F; Fetal Medicine Department, Armand-Trousseau Hospital, APHP, Sorbonne University, GRC-26, Paris, France.; Héron D; Department of Genetics, Division of Medical Genetics, Reference Center for Rare Diseases and Intellectual Deficiencies of Rare Causes, La Pitié-Salpêtrière Hospital, APHP, Sorbonne University, Paris, France.; Billette de Villemeur T; Department of Pediatric Neurology, Reference Center for Rare Diseases and Intellectual Deficiencies of Rare Causes, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Keren B; Department of Genetics, APHP, Sorbonne University, La Pitié-Salpêtrière Hospital, Paris, France.; Afenjar A; Clinical Genetics Unit, Reference Center for Cerebellar Malformations and Congenital Diseases, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Qebibo L; Department of Genetics, Pediatric Neurogenetics Laboratory, Reference Center for Cerebellar Malformations and Congenital Diseases, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Harion M; Department of Pediatric Neurology, Reference Center for Rare Diseases and Intellectual Deficiencies of Rare Causes, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Quenum-Miraillet G; Department of Medical Genetics, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Rodriguez D; Department of Pediatric Neurology, Reference Center for Rare Diseases and Intellectual Deficiencies of Rare Causes, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Jouannic JM; Fetal Medicine Department, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Burglen L; Department of Genetics, Pediatric Neurogenetics Laboratory, Reference Center for Cerebellar Malformations and Congenital Diseases, Armand-Trousseau Hospital, APHP, Sorbonne University, Paris, France.; Developmental Brain Disorders Laboratory, Imagine Institute, Paris, France.; Garel C; Department of Radiology, Reference Center for Cerebellar Malformations and Congenital Diseases, Armand-Trousseau Hospital, APHP, Sorbonne University, INSERM UMR 1163, Paris, France.

Publisher: Wiley Country of Publication: England NLM ID: 8106540 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1097-0223 (Electronic) Linking ISSN: 01973851 NLM ISO Abbreviation: Prenat Diagn Subsets: MEDLINE