부산대학교 도서관

Ginghina, C.; Stoian, I.; Popescu, B. A.; Serban, M.; Arsenescu, I.; Popa, A.; Ghiorghiu, I.; Ionascu, R.; Coman, I.; Apetrei, E.

European Journal of Echocardiography; 2003, Vol. 4 Issue suppl_1, pS69-S69, 1p

Apetrei, Irina Mirela; Apetrei, Constantin

FOOD RESEARCH INTERNATIONAL; DEC 2013, 54 2, p2075-p2082, 8p.

Apetrei, C.; Knight, A. E. W.; Chasovskikh, E.; Jochnowitz, E. B.; Ding, H.; Maier, J. P.

Journal of Chemical Physics; 8/14/2009, Vol. 131 Issue 6, p064305, 7p, 4 Charts, 5 Graphs

Gherasim, D.; Apetrei, E.; Moise, B.

In: Revista Romana de Cardiologie. (Revista Romana de Cardiologie, 2014, 24(4):278-285)

Apetrei, Irina Mirela; Luz Rodriguez-Mendez, Maria; Apetrei, Constantin; de Saja, Jose A.

IEEE SENSORS JOURNAL; JUL 2013, 13 7, p2548-p2554, 7p.

Massier M; Department of Genetics, Reims University Hospital, Reims, France.; Doco-Fenzy M; Department of Genetics, Reims University Hospital, Reims, France.; Department of Genetics, Nantes University Hospital, Nantes, France.; Egloff M; Department of Genetics, Poitiers University Hospital, Poitiers, France.; University of Poitiers, INSERM, LNEC, Department of Genetics, Poitiers University Hospital, Poitiers, France.; Le Guillou X; Department of Genetics, Poitiers University Hospital, Poitiers, France.; University of Poitiers, CNRS, LMA, Department of Genetics, Poitiers University Hospital, Poitiers, France.; Le Guyader G; Department of Genetics, Poitiers University Hospital, Poitiers, France.; Redon S; Department of Genetics, Brest University Hospital, Brest, France.; Intellectual Disability Reference Center, Department of Pediatrics, Brest University Hospital, Brest, France.; University of Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Benech C; University of Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Le Millier K; Department of Genetics, Brest University Hospital, Brest, France.; Uguen K; Department of Genetics, Brest University Hospital, Brest, France.; Intellectual Disability Reference Center, Department of Pediatrics, Brest University Hospital, Brest, France.; University of Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Ropars J; Intellectual Disability Reference Center, Department of Pediatrics, Brest University Hospital, Brest, France.; Sacaze E; Intellectual Disability Reference Center, Department of Pediatrics, Brest University Hospital, Brest, France.; Audebert-Bellanger S; Department of Genetics, Brest University Hospital, Brest, France.; Intellectual Disability Reference Center, Department of Pediatrics, Brest University Hospital, Brest, France.; Apetrei A; University of Normandy, UNICAEN, RU7450 BioTARGen, Caen University Hospital, Department of Genetics, Reference Center for Developmental Disorders and Malformative Syndromes, Anddi-Rares Network, Caen, France.; Molin A; University of Normandy, UNICAEN, RU7450 BioTARGen, Caen University Hospital, Department of Genetics, Reference Center for Developmental Disorders and Malformative Syndromes, Anddi-Rares Network, Caen, France.; Gruchy N; University of Normandy, UNICAEN, RU7450 BioTARGen, Caen University Hospital, Department of Genetics, Reference Center for Developmental Disorders and Malformative Syndromes, Anddi-Rares Network, Caen, France.; Vincent-Devulder A; University of Normandy, UNICAEN, RU7450 BioTARGen, Caen University Hospital, Department of Genetics, Reference Center for Developmental Disorders and Malformative Syndromes, Anddi-Rares Network, Caen, France.; Spodenkiewicz M; Department of Genetics, Le Reunion University Hospital, St-Pierre, France.; Jacquin C; Department of Genetics, Reims University Hospital, Reims, France.; Loron G; Department of Neonatal Medicine and Pediatric Intensive Care, University of Reims Champagne-Ardenne, CReSTIC, Reims University Hospital, Reims, France.; Thibaud M; Department of Pediatrics, American Memorial Hospital, Reims, France.; Delplancq G; Constitutional Genetics Unit, Versailles Hospital, Le Chesnay, France.; Brisset S; Constitutional Genetics Unit, Versailles Hospital, Le Chesnay, France.; Lesieur-Sebellin M; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Malan V; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Romana S; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Rio M; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Marlin S; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Amiel J; Department of Genomic Medicine of Rare Disorders, Necker Hospital, APHP Center, University Paris Cité, Paris, France.; Marquet V; Department of Cytogenetics, Clinical Genetics and Reproductive Biology, Limoges University Hospital, Limoges, France.; Dauriat B; Department of Cytogenetics, Clinical Genetics and Reproductive Biology, Limoges University Hospital, Limoges, France.; Moradkhani K; Department of Genetics, Nantes University Hospital, Nantes, France.; Mercier S; Department of Genetics, Nantes University Hospital, Nantes, France.; Isidor B; Department of Genetics, Nantes University Hospital, Nantes, France.; Arpin S; Department of Genetics, Tours University Hospital, UMR 1253, iBrain, University of Tours, Inserm, Tours, France.; Pujalte M; Department of Genetics, Hospices Civils de Lyon, Lyon, France.; Jedraszak G; Constitutional Genetic Laboratory, University Hospital of Amiens & UR4666 HEMATIM, University of Picardie Jules Verne, Amiens, France.; Pebrel-Richard C; Cytogenetic Medical Department; UIC Cytogenetics of Rare Diseases and Reproduction (GRUIC ADERGEN), Rare Diseases Reference Center (CRMR): Developmental Anomalies and Malformative Syndromes in the Auvergne Region, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.; Salaun G; Cytogenetic Medical Department; UIC Cytogenetics of Rare Diseases and Reproduction (GRUIC ADERGEN), Rare Diseases Reference Center (CRMR): Developmental Anomalies and Malformative Syndromes in the Auvergne Region, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.; Laffargue F; Department of Medical Genetics, UIC ADDIR (GRIUC ADERGEN), Constitutive Reference Center CLAD South-East: Developmental anomalies and malformative syndromes, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.; Boudjarane J; Medical Genetics Department, Timone Enfants University Hospital, Assistance Publique des Hôpitaux de Marseille, Marseille, France.; Missirian C; Medical Genetics Department, Timone Enfants University Hospital, Assistance Publique des Hôpitaux de Marseille, Marseille, France.; Chelloug N; Department of Medical Genetics, Toulouse University Hospital, Toulouse, France.; Toutain A; Department of Genetics, Tours University Hospital, UMR 1253, iBrain, University of Tours, Inserm, Tours, France.; Chiesa J; Department of Genetics, Nimes, University Hospital, Nimes University Hospital, Nimes, France.; Keren B; Department of Genetics, APHP Sorbonne University, Paris, France.; Mignot C; Department of Genetics, APHP Sorbonne University, Paris, France.; Gouy E; Department of Genetics, Hospices Civils de Lyon, Lyon, France.; Jaillard S; Department of Cytogenetics and Cell Biology, Rennes university hospital, Rennes, France.; Landais E; Department of Genetics, Reims University Hospital, Reims, France.; Poirsier C; Department of Genetics, Reims University Hospital, Reims, 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

ŞERB, Aurel; DEFTA, Costinela-Luminiţa; Magdalena, Nicoleta; APETREI, Marius Cristian

Knowledge Horizons / Orizonturi ale Cunoasterii; 2013, Vol. 5 Issue 2, p55-59, 5p

Apetrei, C.; Apetrei, I. M.; Villanueva, S.; de Saja, J. A.; Gutierrez-Rosales, F.; Rodriguez-Mendez, M. L.

ANALYTICA CHIMICA ACTA; MAR 17 2010, 663 1, p91-p97, 7p.

Zhu Z; Department of Internal Medicine, Section of Endocrinology, Yale University School of Medicine, New Haven, Connecticut, USA; Department of Urology, Xiangya Hospital, Central South University, Changsha, Hunan, China.; Bo-Ran Ho B; Department of Internal Medicine, Section of Endocrinology, Yale University School of Medicine, New Haven, Connecticut, USA.; Chen A; Department of Internal Medicine, Section of Endocrinology, Yale University School of Medicine, New Haven, Connecticut, USA; Department of Otolaryngology, Harvard Medical School, Boston, Massachusetts, USA.; Amrhein J; Pediatric Endocrinology and Diabetes, School of Medicine Greenville Campus, University of South Carolina, Greenville, South Carolina, USA.; Apetrei A; Caen University Hospital, Department of Genetics, UR7450 Biotargen, Reference Center for Rare Diseases of Calcium and Phosphate Metabolism, OSCAR Network, Caen, France.; Carpenter TO; Department of Internal Medicine, Section of Endocrinology, Yale University School of Medicine, New Haven, Connecticut, USA.; Lazaretti-Castro M; Division of Endocrinology, Escola Paulista de Medicina-Universidade Federal de Sao Paulo (EPM-UNIFESP), Sao Paulo, Brazil.; Colazo JM; Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.; McCrystal Dahir K; Division of Endocrinology, Program for Metabolic Bone Disorders, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.; Geßner M; Pediatric Nephrology, Children's and Adolescents' Hospital, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.; Gurevich E; Schneider Children's Medical Center of Israel, Pediatric Nephrology Institute, Petach Tikva, Israel; Faculty of Health Sciences, Ben Gurion University of the Negev, Beer Sheva, Israel.; Heier CA; Children's Department, Oslo University Hospital, Oslo, Norway.; Simmons JH; Department of Pediatrics, Division of Endocrinology and Diabetes, Vanderbilt University School of Medicine, Vanderbilt University, Nashville, Tennessee, USA.; Hunley TE; Division of Pediatric Nephrology, Vanderbilt University Medical Center, Monroe Carell Jr Children's Hospital at Vanderbilt, Nashville, Tennessee, USA.; Hoppe B; Division of Pediatric Nephrology, Department of Pediatrics, University of Bonn, Bonn, Germany.; Jacobsen C; Division of Endocrinology, Harvard Medical School, Boston, Massachusetts, USA.; Kouri A; Pediatric Nephrology, University of Minnesota, Minneapolis, Minnesota, USA.; Ma N; Section of Pediatric Endocrinology, Children's Hospital Colorado, Aurora, Colorado, USA; Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA.; Majumdar S; Department of Internal Medicine, Section of Endocrinology, Yale University School of Medicine, New Haven, Connecticut, USA.; Molin A; Caen University Hospital, Department of Genetics, UR7450 Biotargen, Reference Center for Rare Diseases of Calcium and Phosphate Metabolism, OSCAR Network, Caen, France.; Nokoff N; Department of Pediatrics, Section of Endocrinology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.; Ott SM; Department of Medicine, University of Washington, Seattle, Washington, USA.; Peña HG; Department of Pediatrics, Hospital Universitario Central de Asturias (HUCA), Oviedo, Spain.; Santos F; Department of Pediatrics, Hospital Universitario Central de Asturias (HUCA), Oviedo, Spain.; Tebben P; Division of Endocrinology, Diabetes, Metabolism, and Nutrition, Mayo Clinic, Rochester, Minnesota, USA; Division of Pediatric Endocrinology, Mayo Clinic, Rochester, Minnesota, USA.; Topor LS; Division of Pediatric Endocrinology, Hasbro Children's Hospital, Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA.; Deng Y; Yale School of Public Health, New Haven, Connecticut, USA.; Bergwitz C; Department of Internal Medicine, Section of Endocrinology, Yale University School of Medicine, New Haven, Connecticut, USA. Electronic address: clemens.bergwitz@yale.edu.

Publisher: Elsevier Country of Publication: United States NLM ID: 0323470 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1523-1755 (Electronic) Linking ISSN: 00852538 NLM ISO Abbreviation: Kidney Int Subsets: MEDLINE

Buechler, Connor R.; Bailey, Adam L.; Weiler, Andrea M.; Barry, Gabrielle L.; Breitbach, Meghan E.; Stewart, Laurel M.; Jasinska, Anna J.; Freimer, Nelson B.; Apetrei, Cristian; Phillips-Conroy, Jane E.; Jolly, Clifford J.; Rogers, Jeffrey; Friedrich, Thomas C.; O'Connor, David H.

MSphere; Mar/Apr2017, Vol. 2 Issue 2, p1-7, 7p