부산대학교 도서관

Benezit Dictionary of Artists, 2011

Vingtième Siècle. Revue d'histoire, 2017 Jan 01(133), 173-176.

International Journal of Engineering and Advanced Technology. 11:12-25

Beaux-Arts Magazine. :114-114

Balfroid T; Pediatric Neurology Department, Université Libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), CUB Hôpital Erasme, Brussels, Belgium.; Vuckovic A; Neonatal Intensive Care Department, Université Libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), Hôpital Universitaire Des Enfants Reine Fabiola (HUDERF), Brussels, Belgium.; Janssens M; Neonatal Intensive Care Department, Centre Hospitalier Universitaire Tivoli, La Louvière, Belgium.; Vilain C; Genetic Department, Université Libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), Hôpital Universitaire Des Enfants Reine Fabiola (HUDERF), Brussels, Belgium.; Lederer D; Institut de Pathologie Génétique (IPG), Gosselies, Belgium.; Empain A; Pediatric Metabolic Disorder Department, Université Libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), Hôpital Universitaire Des Enfants Reine Fabiola (HUDERF), Brussels, Belgium.; Aeby A; Pediatric Neurology Department, Université Libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (HUB), CUB Hôpital Erasme, Brussels, Belgium.

Publisher: Wiley Country of Publication: United States NLM ID: 100891853 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1950-6945 (Electronic) Linking ISSN: 12949361 NLM ISO Abbreviation: Epileptic Disord Subsets: MEDLINE; In Process

Aboulnaga, M.; Puma, P.; Elsharkawy, M.

In: Sustainable Mediterranean Construction. (Sustainable Mediterranean Construction, 2021, 2021(14):96-104)

Revue française d'histoire économique. :289-291

Beltran, Alain; Seta, Roberto Della

Studi Storici, 1987 Oct 01. 28(4), 927-941.

Krug, Amelie; Perlot, Pascale; Empain, Aurelie; Vilain, Catheline; Monier, Anne; Tazi, Kaoutar; De Laet, Corinne

Journal of Medical Case Reports. 19(1)

Puma Paola; Aboulnaga Mohsen; Elsharkawy Maryam

IOP Conference Series: Earth and Environmental Science. 863:012009

Revue du Nord. :951-966

Buttice I; Laboratory of hematology, CHU Brugmann LHUB-ULB site Horta 4, Pl Van Gehuchten, 1020 Brussels Belgium.; Demulder A; Laboratory of hematology, CHU Brugmann LHUB-ULB site Horta 4, Pl Van Gehuchten, 1020 Brussels Belgium.; De Laet C; Nutrition and metabolic clinic, CHU Brugmann site Horta 4, Pl Van Gehuchten, 1020 Brussels Belgium.; Empain A; Nutrition and metabolic clinic, CHU Brugmann site Horta 4, Pl Van Gehuchten, 1020 Brussels Belgium.; Rozen L; Laboratory of hematology, CHU Brugmann LHUB-ULB site Horta 4, Pl Van Gehuchten, 1020 Brussels Belgium.

Publisher: John Libbey Eurotext Country of Publication: France NLM ID: 2984690R Publication Model: Print Cited Medium: Internet ISSN: 1950-6112 (Electronic) Linking ISSN: 00033898 NLM ISO Abbreviation: Ann Biol Clin (Paris) Subsets: MEDLINE; In Process

Pinçon Michel; Pinçon-Charlot Monique

Genèses 28(1):169-170

Donge M; Department of Pediatric Neurology, Kannerklinik Centre Hospitalier du Luxembourg, L-1210 Luxembourg, Luxembourg.; Marie S; Biochemical Genetics and Newborn Screening Laboratory, Department of Laboratory Medicine, Cliniques Universitaires Saint-Luc, UCLouvain, B-1200 Brussels, Belgium.; Pochet A; Louvain Centre for Toxicology and Applied Pharmacology, Institut de Recherche Experimentale et Clinique, UCLouvain, B-1200 Brussels, Belgium.; Marcelis L; Laboratory of Paediatric Research and Newborn Screening, Université Libre de Bruxelles, B-1020 Brussels, Belgium.; Luis G; Biochemical Genetics and Newborn Screening Laboratory, CHU Liege, B-4000 Liege, Belgium.; Boemer F; Biochemical Genetics and Newborn Screening Laboratory, CHU Liege, B-4000 Liege, Belgium.; Prouteau C; Department of Medical Genetics, Angers University Hospital, F-49000 Angers, France.; Mesli S; Department of Biochemistry, Centre Hospitalier Universitaire de Bordeaux, F-33404 Bordeaux, France.; Cuykx M; Clinical Chemistry and Newborn Screening Center, UZ Antwerpen, B-2650 Antwerpen, Belgium.; Nguyen-Khoa T; Laboratoire du Centre Régional de Dépistage Néonatal de l'Ile de France, Hôpital Necker-Enfants Malades, AP-HP Centre Université Paris Cité, 161, rue de Sèvres, F-75015 Paris, France.; INSERM U1151, Institut Necker Enfants Malades, F-75015 Paris, France.; Guénet D; Laboratory of Biochemistry, Normandie Université, UNICAEN, CHU of Caen Normandie, F-14000 Caen, France.; Empain A; Nutrition and Metabolic Clinic, Brussels University Hospital, Academic Children Hospital Queen Fabiola, Université Libre de Bruxelles, B-1020 Brussels, Belgium.; Barth M; Department of Medical Genetics, Angers University Hospital, F-49000 Angers, France.; Dauriat B; Medical Genetics and Cytogenetics Department, Limoges Universitary Hospital, F-87000 Limoges, France.; Laroche-Raynaud C; Centre de Compétence des Maladies Héréditaires du Métabolisme, Centre Hospitalier Universitaire de Limoges, F-87000 Limoges, France.; De Laet C; Nutrition and Metabolic Clinic, Brussels University Hospital, Academic Children Hospital Queen Fabiola, Université Libre de Bruxelles, B-1020 Brussels, Belgium.; Verloo P; Department of Pediatric Neurology, Center for Inherited Metabolic Disorders, University Hospital Ghent, B-9000 Ghent, Belgium.; Jonckheere AI; Centre for Metabolic Diseases, University Hospital Antwerp, University of Antwerp, B-2650 Antwerpen, Belgium.; Schiff M; Reference Center for Inborn Errors of Metabolism, Necker University Hospital, AP-HP Centre Université Paris Cité, Filière G2M, F-75015 Paris, France.; INSERM UMRS_1163, Institut Imagine, F-75015 Paris, France.; Nassogne MC; Department of Pediatric Neurology, Cliniques Universitaires Saint-Luc, UCLouvain, B-1200 Brussels, Belgium.; Institut des Maladies Rares, Cliniques Universitaires Saint-Luc, UCLouvain, B-1200 Brussels, Belgium.; Dewulf JP; Biochemical Genetics and Newborn Screening Laboratory, Department of Laboratory Medicine, Cliniques Universitaires Saint-Luc, UCLouvain, B-1200 Brussels, Belgium.; Louvain Centre for Toxicology and Applied Pharmacology, Institut de Recherche Experimentale et Clinique, UCLouvain, B-1200 Brussels, Belgium.; Institut des Maladies Rares, Cliniques Universitaires Saint-Luc, UCLouvain, B-1200 Brussels, Belgium.

Publisher: MDPI AG Country of Publication: Switzerland NLM ID: 101665400 Publication Model: Electronic Cited Medium: Internet ISSN: 2409-515X (Electronic) Linking ISSN: 2409515X NLM ISO Abbreviation: Int J Neonatal Screen Subsets: PubMed not MEDLINE

Проект Байкал, Vol 21, Iss 82 (2024)

Revue belge de philologie et d'histoire 91(2):543

Adam, Anne‐Sophie; Marcélis, Lionel; Fage, David; Mathieu, Elise; Empain, Aurélie; Dufour, Céline; Cotton, Frédéric; Laet, Corinne

JIMD Reports. January 7, 2026, Vol. 67 Issue 1

Panis B; Department of Pediatrics, MosaKids Children's Hospital, Maastricht University Medical Centre, Maastricht, Netherlands.; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; United for Metabolic Diseases (UMD), Amsterdam, Netherlands.; Vos EN; Department of Pediatrics, MosaKids Children's Hospital, Maastricht University Medical Centre, Maastricht, Netherlands.; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; United for Metabolic Diseases (UMD), Amsterdam, Netherlands.; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, Netherlands.; GROW School for Oncology and Reproduction, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, Netherlands.; Barić I; Department of Pediatrics, University Hospital Center Zagreb, Croatia, and School of Medicine, University of Zagreb, Zagreb, Croatia.; Bosch AM; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; United for Metabolic Diseases (UMD), Amsterdam, Netherlands.; Department of Pediatrics, Division of Metabolic Diseases, Emma Children's Hospital, Amsterdam University Medical Center, Amsterdam Gastroenterology Endocrinology Metabolism, Inborn Errors of Metabolism, Amsterdam, Netherlands.; Brouwers MCGJ; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Department of Internal Medicine, Division of Endocrinology and Metabolic Disease, Maastricht University Medical Centre, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, Netherlands.; Burlina A; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Division of Inherited Metabolic Diseases, Reference Centre Expanded Newborn Screening, University Hospital Padova, Padova, Italy.; Cassiman D; Laboratory of Hepatology, Department of Chronic Diseases, Metabolism and Ageing, Faculty of Medicine, KU Leuven, Leuven, Belgium.; Coman DJ; Queensland Children's Hospital, Children's Health Queensland, Brisbane, QLD, Australia.; Couce ML; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Department of Pediatrics, Diagnosis and Treatment Unit of Congenital Metabolic Diseases, University Clinical Hospital of Santiago de Compostela, IDIS-Health Research Institute of Santiago de Compostela, CIBERER, RICORS Instituto Salud Carlos III, Santiago de Compostela, Spain.; Das AM; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Department of Paediatrics, Pediatric Metabolic Medicine, Hannover Medical School, Hannover, Germany.; Demirbas D; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Manton Center for Orphan Disease Research, Boston, MA, United States.; Empain A; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Department of Paediatrics, Metabolic and Nutrition Unit, Division of Endocrinology, Diabetes and Metabolism, University Hospital for Children Queen Fabiola, Bruxelles, Belgium.; Gautschi M; Department of Paediatrics, Institute of Clinical Chemistry, Inselspital, Bern University Hospital, Swiss Reference Centre for Inborn Errors of Metabolism, Site Bern, Division of Pediatric Endocrinology, Diabetes and Metabolism, University of Bern, Bern, Switzerland.; Grafakou O; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; IEM Clinic, Arch Makarios III Hospital, Nicosia, Cyprus.; Grunewald S; Metabolic Unit Great Ormond Street Hospital and Institute for Child Health, University College London, London, United Kingdom.; Kingma SDK; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Centre for Metabolic Diseases, University Hospital Antwerp, University of Antwerp, Antwerp, Belgium.; Knerr I; National Centre for Inherited Metabolic Disorders, Children's Health Ireland at Temple Street, University College Dublin, Dublin, Ireland.; Leão-Teles E; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Reference Centre of Inherited Metabolic Diseases, Centro Hospitalar Universitário São João, Porto, Portugal.; Möslinger D; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Department of Paediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.; Murphy E; Charles Dent Metabolic Unit, National Hospital for Neurology and Neurosurgery (NHNN), London, United Kingdom.; Õunap K; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Genetics and Personalized Medicine Clinic, Faculty of Medicine, Tartu University Hospital, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.; Pané A; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Endocrinology and Nutrition Department, Hospital Clínic de Barcelona, Centro de Investigación Biomédica en Red de la Fisiopatología de la Obesidad y Nutrición (CIBEROBN), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.; Paci S; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Inborn Errors of Metabolism, Clinical Department of Pediatrics, San Paolo Hospital - ASST Santi Paolo e Carlo, University of Milan, Milan, Italy.; Parini R; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Rare Diseases Unit, Department of Internal Medicine, San Gerardo Hospital IRCCS, Monza, Italy.; Rivera IA; iMed.ULisboa-Instituto de Investigação do Medicamento, Faculdade de Farmácia, Universidade de Lisboa, Lisboa, Portugal.; Scholl-Bürgi S; 29 Department of Child and Adolescent Health, Division of Pediatrics I-Inherited Metabolic Disorders, Medical University Innsbruck, Innsbruck, Austria.; Schwartz IVD; Medical Genetics Service, Hospital de Clinicas de Porto Alegre, Porto Alegre, Brazil.; Sdogou T; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Newborn Screening Department, Institute of Child Health, Athens, Greece.; Shakerdi LA; Adult Metabolics/Genetics, National Centre for Inherited Metabolic Disorders, The Mater Misericordiae University Hospital, Dublin, Ireland.; Skouma A; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; Newborn Screening Department, Institute of Child Health, Athens, Greece.; Stepien KM; Salford Royal Organisation, Northern Care Alliance NHS Foundation Trust, Salford, United Kingdom.; Treacy EP; School of Medicine, Trinity College Dublin, National Rare Diseases Office, Mater Misericordiae University Hospital, Dublin, Ireland.; Waisbren S; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Manton Center for Orphan Disease Research, Boston, MA, United States.; Berry GT; Division of Genetics and Genomics, Boston Children's Hospital, Harvard Medical School, Manton Center for Orphan Disease Research, Boston, MA, United States.; Rubio-Gozalbo ME; Department of Pediatrics, MosaKids Children's Hospital, Maastricht University Medical Centre, Maastricht, Netherlands.; European Reference Network for Hereditary Metabolic Disorders (MetabERN) Member, Padova, Italy.; United for Metabolic Diseases (UMD), Amsterdam, Netherlands.; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, Netherlands.; GROW School for Oncology and Reproduction, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, Netherlands.

Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE