부산대학교 도서관

Charollais, A. ; Marret, S. ; Stumpf, M.-H. ; Lemarchand, M. ; Delaporte, B. ; Philip, E. ; Monom-Diverre ; Guillois, B. ; Datin-Dorriere, V. ; Debillon, T. ; Simon, M.-J. ; De Barace, C. ; Pasquet, F. ; Saliba, E. ; Zebhib, R.

In Archives de pédiatrie September 2013 20(9):994-999

Charollais A; LAMOPRESCO research group, University Rouen Hospital, Rouen, France.; Service of Pediatric, MFME University Hospital, Fort de France Martinique, France.; Research center on psychological functions and dysfunctions, EA7475, University of Rouen, Mont Saint-Aignan Cedex, Rouen, France.; Laudenbach V; LAMOPRESCO research group, University Rouen Hospital, Rouen, France.; Service of Pediatric, MFME University Hospital, Fort de France Martinique, France.; Research center on psychological functions and dysfunctions, EA7475, University of Rouen, Mont Saint-Aignan Cedex, Rouen, France.; Stumpf MH; LAMOPRESCO research group, University Rouen Hospital, Rouen, France.; Research center on psychological functions and dysfunctions, EA7475, University of Rouen, Mont Saint-Aignan Cedex, Rouen, France.; Delaporte B; LAMOPRESCO research group, University Rouen Hospital, Rouen, France.; Service of Neonatology and Neonatal intensive Care Charles Nicolle University Hospital, Rouen, Cedex, France.; Datin-Dorriere V; LAMOPRESCO research group, University Rouen Hospital, Rouen, France.; Service of Neonatology and Neonatal intensive Care, Jacques Monod Hospital, Le Havre Cedex, France.; Service of Neonatology and Neonatal intensive Care, Côte de Nacre Caen Normandie University Hospital, Caen Cedex 09, France.; Debillon T; LAMOPRESCO research group, University Rouen Hospital, Rouen, France.; Service of Neonatology and Neonatal intensive Care Charles Nicolle University Hospital, Rouen, Cedex, France.; De Barace C; LAMOPRESCO research group, University Rouen Hospital, Rouen, France.; Neonatal Intensive Care Unit, Grenoble Alpes University Hospital, La Tronche, Grenoble, France.; Flechelles O; LAMOPRESCO research group, University Rouen Hospital, Rouen, France.; Service of Pediatric, MFME University Hospital, Fort de France Martinique, France.; Farmer M; LAMOPRESCO research group, University Rouen Hospital, Rouen, France.; FMSS Sherbrooke University Qβc, Sherbrooke QC, Canada.

Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101550902 Publication Model: eCollection Cited Medium: Print ISSN: 1664-1078 (Print) Linking ISSN: 16641078 NLM ISO Abbreviation: Front Psychol Subsets: PubMed not MEDLINE

A, Le Bihannic; K, Beauvais; A, Busnel; C, de Barace; A, Furby

Archives of Disease in Childhood - Fetal and Neonatal Edition. 97:F106-F109

Bertschy, F. ; Le Gouill, I. ; Bernicot, M.P. ; De Baracé, C. ; Busnel, A. ; Bretaudeau, G. ; Le Guillou, C. ; Millet, P. ; Muller, J.B. ; Pichon, C. ; Pladys, P. ; Robert, H. ; Tréguier, G. ; Sizun, J. ; Duigou, A.-L. ; Roué, J.M.

In Archives de pédiatrie September 2013 20(9):917-920

M A, Dragon-Durey; P, Quartier; V, Frémeaux-Bacchi; J, Blouin; C, de Barace; A M, Prieur; L, Weiss; W H, Fridman

The Journal of Immunology. 166:7612-7616

Le Bihannic, A; Beauvais, K; Busnel, A; de Barace, C; Furby, A

Archives of Disease in Childhood: Fetal and Neonatal Edition. Mar 01, 2012 97(2):F106-F109

Riant, F.; Odent, S.; Cecillon, M.; Pasquier, L.; de Baracé, C.; Carney, M. P.; Tournier-Lasserve, E.

Clinical Genetics. Dec 01, 2014 86(6):585-588

Romano, S; Bajolle, F; Valayannopoulos, V; Lyonnet, S; Colomb, V; de Baracé, C; Vouhe, P; Pouard, P; Vuillaumier-Barrot, S; Dupré, T; de Keyzer, Y; Sidi, D; Seta, N; Bonnet, D; de Lonlay, P

Journal of Medical Genetics. Apr 01, 2009 46(4):287-288

El Khattabi L; Cochin Institute, INSERM U1016, Paris, France.; Cytogenetics Department, APHP, Cochin Hospital, Paris Descartes University, Paris, France.; Jaillard S; Cytogenetics and Cell Biology Department, Rennes University Hospital, Rennes, France.; Andrieux J; Medical Genetics Department, Lille Hospital, Lille, France.; Pasquier L; Medical Genetics Department, Rennes University Hospital, Rennes, France.; Perrin L; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France.; Capri Y; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France.; Benmansour A; Pediatrician, Oran, Algeria.; Toutain A; Department of Genetics, Tours University Hospital, Tours, France.; Marcorelles P; Department of Pathology, CHU Brest, France.; Vincent-Delorme C; Department of Genetics, Arras Hospital, Arras, France.; Journel H; Department of Medical Genetics, CHBA, Vannes, France.; Henry C; Cytogenetics and Cell Biology Department, Rennes University Hospital, Rennes, France.; De Barace C; Department of Pediatrics, Saint-Brieuc Hospital, Saint-Brieuc, France.; Devisme L; Department of Anatomy and Cell Pathology, CHRU Lille, France.; Dubourg C; Molecular Genetics Department, Rennes University Hospital, Rennes, France.; UMR 6290, IGDR, Medical School, Rennes, France.; Demurger F; Medical Genetics Department, Rennes University Hospital, Rennes, France.; Lucas J; Cytogenetics and Cell Biology Department, Rennes University Hospital, Rennes, France.; Belaud-Rotureau MA; Cytogenetics and Cell Biology Department, Rennes University Hospital, Rennes, France.; UMR 6290, IGDR, Medical School, Rennes, France.; Amiel J; Department of Genetics, APHP, Necker-Enfants Malades University Hospital, Paris, France.; Malan V; Laboratory of Cytogenetics, APHP, Necker-Enfants Malades Hospital, Paris Descartes University, Paris, France.; De Blois MC; Laboratory of Cytogenetics, APHP, Necker-Enfants Malades Hospital, Paris Descartes University, Paris, France.; De Pontual L; Department of Pediatrics, Jean-Verdier Hospital, APHP, Paris 13 University, Bondy, France.; Lebbar A; Cytogenetics Department, APHP, Cochin Hospital, Paris Descartes University, Paris, France.; Le Dû N; Cytogenetics Department, APHP, Cochin Hospital, Paris Descartes University, Paris, France.; Germain DP; Department of Genetics, Raymond Poincaré University Hospital, Garches, France.; Pinard JM; Department of Neuropediatrics, Raymond Poincaré University Hospital, Garches, France.; Pipiras E; Cytogenetics, APHP, Jean-Verdier University Hospital, Bondy; Paris 13, Sorbonne Paris Cité, UFR SMBH, Bobigny, France; Inserm, U676, Paris, France.; Tabet AC; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France.; Aboura A; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France.; Verloes A; Department of Genetics, APHP-Robert Debré University Hospital, Paris, France.; INSERM U676, and Paris VII-Denis Diderot Medical School, Paris, 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

C. Droitcourt; C. De Barace; S. Odent; F. Le Gall; H. Jouan; P. Toulouse; J. Chevrant-Breton

Annales de Dermatologie et de Vénéréologie. 132:170

Mercier S; Department of Medical Genetics, CHU Nantes, France.; Toutain A; Toussaint A; Raynaud M; de Barace C; Marcorelles P; Pasquier L; Blayau M; Espil C; Parent P; Journel H; Lazaro L; Andoni Urtizberea J; Moerman A; Faivre L; Eymard B; Maincent K; Gherardi R; Chaigne D; Ben Yaou R; Leturcq F; Chelly J; Desguerre I

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.A. Dragon-Durey; P. Quartier; V. Frémeaux-Bacchi; J. Blouin; C. de Barace; A. Prieur; L. Weiss; W.H. Fridman

Immunopharmacology. 49:25

Eseberri Barace, Itziar; Ibáñez Moya, Francisco C.

Academica-e. Repositorio Institucional de la Universidad Pública de Navarra
Universidad Pública de Navarra

Eseberri Barace, Itziar; Ibáñez Moya, Francisco C.

Academica-e. Repositorio Institucional de la Universidad Pública de Navarra
Universidad Pública de Navarra

Eseberri Barace, Itziar; Ibáñez Moya, Francisco C.

Academica-e. Repositorio Institucional de la Universidad Pública de Navarra
Universidad Pública de Navarra

S Romano; F Bajolle; V Valayannopoulos; S Lyonnet; V Colomb; C de Baracé; P Vouhe; P Pouard; S Vuillaumier-Barrot; T Dupré; Y de Keyzer; D Sidi; N Seta; D Bonnet; P de Lonlay

Journal of Medical Genetics. 46:287-288

Ventura-Cots, M. (Meritxell); Argemí, J. (Josepmaria); Jones, P.D. (Patricia D.); Lackner, C. (Carolin); Hag, M. (Mohamed) El; Abraldes, J.G. (Juan G.); Alvarado-Tapias, E. (Edilmar); Clemente-Sánchez, A. (Ana); Ravi, S. (Samhita); Alves, A. (Antonio); Alboraie, M. (Mohamed); Altamirano, J. (Jose); Barace, S. (Sergio); Bosques, F. (Francisco); Brown, R. (Robert); Caballeria, J. (Juan); Cabezas, J. (Joaquín); Carvalhana, S. (Sofia); Cortez-Pinto, H. (Helena); Costa, A. (Adilia); Degré, D. (Delphine); Fernández-Carrillo, C. (Carlos); Ganne-Carrie, N. (Nathalie); Garcia-Tsao, G. (Guadalupe); Genesca, J. (Joan); Koskinas, J. (John); Lanthier, N. (Nicolas); Louvet, A. (Alexandre); Lozano, J.J. (Juan J.); Lucey, M.R. (Michael R.)

Dadun. Depósito Académico Digital de la Universidad de Navarra
Universidad de Navarra

M, Rio; A S, Lebre; P, de Lonlay; V, Valayannopoulos; I, Desguerre; J-L, Dufier; D, Grévent; M, Zilbovicius; C, Tréguier; F, Brunelle; C, de Baracé; J, Kaplan; M A, Espinase-Berrod; C, Sainte-Rose; S, Puget; A, Rotig; A, Munnich; N, Boddaert

Neurology. 75:93-93

Schiff M; Reference Center for Inherited Metabolic Diseases, AP-HP, Robert Debré Hospital, University Paris Diderot-Sorbonne Paris Cité, Paris, France.; INSERM U1141, Paris, France.; Roda C; Reference Center for Inherited Metabolic Disease, AP-HP, Necker-Enfants Malades Hospital, IMAGINE Institute affiliate, University Paris Descartes-Sorbonne Paris Cité, Paris, France.; Monin ML; Department of Genetics, Molecular and Cellular Neurogenetics Unit, Reference Center for Intellectual of Rare Causes, AP-HP, GH Pitié-Salpêtrière, Paris, France.; Arion A; Department of Paediatrics, Paediatric Care Unit, Caen Hospital, Caen, France.; Barth M; Hematology Unit, AP-HP, Necker-Enfants Malades Hospital, Paris, France.; UMR INSERM 1176, Le Kremlin-Bicêtre, Paris, France.; Bednarek N; Neonatal Intensive Care Unit, Institute of Alix de Champagne, Reims University Hospital, Reims, France.; Bidet M; Department of Paediatric Endocrinology, Gynaecology, and Diabetology, AP-HP, Necker-Enfants Malades Hospital, IMAGINE Institute affiliate, Paris, France.; Bloch C; Paediatric Unit, Fondation Lenval, Nice, France.; Boddaert N; Department of Paediatric Radiology, AP-HP, Necker-Enfants Malades Hospital, IMAGINE Institute affiliate, Paris, France.; Sorbonne Paris Cité, INSERM U1000, Paris, France.; UMR 1163, Paris, France.; Borgel D; Hematology Unit, AP-HP, Necker-Enfants Malades Hospital, Paris, France.; UMR INSERM 1176, Le Kremlin-Bicêtre, Paris, France.; Brassier A; Reference Center for Inherited Metabolic Disease, AP-HP, Necker-Enfants Malades Hospital, IMAGINE Institute affiliate, University Paris Descartes-Sorbonne Paris Cité, Paris, France.; Brice A; Sorbonne Universités, UPMC Univ Paris 06, UMR S1127, Paris, France.; INSERM U1127, Paris, France.; CNRS UMR7225, Paris, France.; Brain and Spine Institute (ICM), Paris, France.; Bruneel A; Department of Biochemistry, AP-HP, Bichat Hospital, Rouen, France.; Buissonnière R; Pediatric Unit, André Mignot Hospital, Versailles, France.; Chabrol B; Reference Center for Inherited Metabolic Diseases, Timone Enfants University Hospital, Marseille, France.; Chevalier MC; Department of Paediatrics, Le Mans Hospital, Le Mans, France.; Cormier-Daire V; Departement of Genetics, Centre of Reference for Skeletal Dysplas, AP-HP, Necker-Enfants Malades Hospital, Paris, France.; INSERM UMR1163, IMAGINE Institute affiliate, Paris, France.; University Paris Descartes-Sorbonne Paris Cité, Paris, France.; De Barace C; Paediatric Unit, Saint Brieuc Hospital, Saint Brieuc, France.; De Maistre E; Haematological Laboratory, Dijon Hospita, Dijon, France.; De Saint-Martin A; Paediatric Neurology, Department of Pediatrics, University Hospital, Strasbourg, France.; Dorison N; Pediatric Neurology Department and Neurofibromatosis Reference Center, AP-HP, Armand Trousseau Hospital, Paris, France.; Drouin-Garraud V; Medical Genetics Unit, Rouen University Hospital, Rouen, France.; Dupré T; Echenne B; Paediatric Neurology Unit, University of Montpellier I, Montpellier, France.; Edery P; Department of Genetic, Lyon University Hospitals, Neuroscience Research Centre, CNRS UMR5292, INSERM U1028, Lyon, France.; Feillet F; Faculty of Medicine of Nancy, INSERM U954, NGERE-Nutrition, Genetics, and Environmental Risk Exposure, University of Lorraine, Vandoeuvre-lès-Nancy, France.; Fontan I; Department of Dermatology and Paediatric Dermatology, Bordeaux University Hospitals, Bordeaux, France.; Francannet C; Medical Genetics Unit, Clermont-Ferrand Hospital, Clermont-Ferrand, France.; Labarthe F; Department of Paediatric, Tours Regional University Hospitals, Tours, France.; Gitiaux C; Department of Child Neurology, Reference Centre for Neuromuscular Diseases, AP-HP, Necker-Enfants Malades Hospital, Paris, France.; Héron D; GRC Intellectual Disability and Autism, UPMC Univ Paris 6, Paris, France.; Hully M; Reference Center for Inherited Metabolic Disease, AP-HP, Necker-Enfants Malades Hospital, IMAGINE Institute affiliate, University Paris Descartes-Sorbonne Paris Cité, Paris, France.; Lamoureux S; Department of Paediatric, Henri-Duffaut Hospital, Avignon, France.; Martin-Coignard D; Department of Genetic, Le Mans Hospital, Le Mans, France.; Mignot C; Department of Genetics, Molecular and Cellular Neurogenetics Unit, Reference Center for Intellectual of Rare Causes, AP-HP, GH Pitié-Salpêtrière, Paris, France.; Morin G; Department of Genetic, Amiens University Hospital, Amiens, France.; Pascreau T; Hematology Unit, AP-HP, Necker-Enfants Malades Hospital, Paris, France.; UMR INSERM 1176, Le Kremlin-Bicêtre, Paris, France.; Pincemaille O; Department of Paediatrics, Grasse Hospital, France.; Polak M; Department of Paediatric Endocrinology, Gynaecology, and Diabetology, AP-HP, Necker-Enfants Malades Hospital, IMAGINE Institute affiliate, Paris, France.; Roubertie A; Thauvin-Robinet C; Departement of Genetic, Children's Hospital, Dijon, France.; Toutain A; Division of Genetics, Bretonneau Hospital, Tours, France.; Viot G; Department of Gynecology-Obstetrics, Faculty of Medicine, AP-HP, Cochin Hospital, Paris Descartes University‒Sorbonne Paris Cité, Paris, France.; Vuillaumier-Barrot S; Department of Biochemistry, AP-HP, Bichat Hospital, Rouen, France.; Seta N; Department of Biochemistry, AP-HP, Bichat Hospital, Rouen, France.; De Lonlay P; Reference Center for Inherited Metabolic Disease, AP-HP, Necker-Enfants Malades Hospital, IMAGINE Institute affiliate, University Paris Descartes-Sorbonne Paris Cité, Paris, France.

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

Beauvais K; Explorations Fonctionnelles Neurologiques, Hôpital Y. Le Foll, Saint-Brieuc, France.; Cavé-Riant F; De Barace C; Tardieu M; Tournier-Lasserve E; Furby A

Publisher: Karger Country of Publication: Switzerland NLM ID: 0150760 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0014-3022 (Print) Linking ISSN: 00143022 NLM ISO Abbreviation: Eur Neurol Subsets: MEDLINE