학술논문

발행년
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(예 : 2010-2015)
'학술논문' 에서 검색결과 750건 | 목록 1~10
Academic Journal
Borrelli E; Department of Surgical Sciences, University of Turin, Turin, Italy; Department of Ophthalmology, 'City of Health and Science' Hospital, Turin, Italy. Electronic address: borrelli.enrico@yahoo.com.; Bandello F; Vita-Salute San Raffaele University, Milan, Italy; IRCCS San Raffaele Scientific Institute, Milan, Italy.; Boon CJF; Department of Ophthalmology, Amsterdam University Medical Centers, Amsterdam, the Netherlands; Department of Ophthalmology, Leiden University Medical Center, Leiden, the Netherlands.; Carelli V; Dipartimento di Scienze Biomediche e Neuromotorie, Università di Bologna, Bologna, Italy; IRCCS Istituto delle Scienze Neurologiche di Bologna, Programma di Neurogenetica, Bologna, Italy.; Lenaers G; Equipe MitoLab, Unité MitoVasc, INSERM U1083, Université d'Angers, 49933, Angers, France; Service de Neurologie, CHU d'Angers, 49100, Angers, France.; Reibaldi M; Department of Surgical Sciences, University of Turin, Turin, Italy; Department of Ophthalmology, 'City of Health and Science' Hospital, Turin, Italy.; Sadda SR; Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA; Doheny Eye Institute, Los Angeles, CA, USA.; Sadun AA; Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA; Doheny Eye Institute, Los Angeles, CA, USA.; Sarraf D; Department of Ophthalmology, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA; Retinal Disorders and Ophthalmic Genetics Division, Stein Eye Institute, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.; Yu-Wai-Man P; John van Geest Centre for Brain Repair and MRC Mitochondrial Biology Unit, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK; Cambridge Eye Unit, Addenbrooke's Hospital, Cambridge University Hospitals, Cambridge, UK; Moorfields Eye Hospital NHS Foundation Trust, London, UK; Institute of Ophthalmology, University College London, London, UK.; Barboni P; IRCCS San Raffaele Scientific Institute, Milan, Italy; Studio Oculistico d'Azeglio, Bologna, Italy. Electronic address: p.barboni60@gmail.com.
Publisher: Pergamon Country of Publication: England NLM ID: 9431859 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-1635 (Electronic) Linking ISSN: 13509462 NLM ISO Abbreviation: Prog Retin Eye Res Subsets: MEDLINE
Academic Journal
Tessarech M; Department of Medical Genetics, Angers University Hospital, Angers, France; Mitovasc Unit, UMR CNRS 6015 INSERM 1083, University of Angers, Angers, France. Electronic address: marine.tessarech@chu-lille.fr.; Friocourt G; INSERM, Univ Brest, EFS, UMR 1078, GGB, Brest, France.; Marguet F; Univ Rouen Normandie, INSERM U1245 and Rouen University Hospital, Department of Pathology, Rouen, France.; Lecointre M; Univ Rouen Normandie, INSERM U1245 and Rouen University Hospital, Department of Pathology, Rouen, France.; Le Mao M; Mitovasc Unit, UMR CNRS 6015 INSERM 1083, University of Angers, Angers, France.; Díaz RM; Mitovasc Unit, UMR CNRS 6015 INSERM 1083, University of Angers, Angers, France.; Mignot C; Department of Genetics, Center for Rare Causes of Intellectual Disabilities and UPMC Research Group 'Intellectual Disabilities and Autism' Paris, France.; Keren B; Department of Genetics, Center for Rare Causes of Intellectual Disabilities and UPMC Research Group 'Intellectual Disabilities and Autism' Paris, France; Department of Genetics, La Pitié-Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.; Héron B; Sorbonne University, UPMC Univ Paris 06, UMR S 1127, INSERM U 1127, CNRS UMR 7225, ICM, Paris, France; Department of Pediatric Neurology, Reference Center of Lysosomal Diseases, Trousseau Hospital, APHP, GRC ConCer-LD, Sorbonne Universities, UPMC University, Paris, France.; De Bie C; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Van Gassen K; Department of Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.; Loisel D; Department of Radiology, Angers University Hospital, Angers, France.; Delorme B; Department of Radiology, Angers University Hospital, Angers, France.; Syrbe S; Heidelberg University, Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Division of Pediatric Epileptology, Heidelberg, Germany.; Klabunde-Cherwon A; Heidelberg University, Medical Faculty of Heidelberg, Center for Child and Adolescent Medicine, Division of Pediatric Epileptology, Heidelberg, Germany.; Jamra RA; Institute of Human Genetics, University of Leipzig Hospitals and Clinics, Leipzig, Germany.; Wegler M; Institute of Human Genetics, University of Leipzig Hospitals and Clinics, Leipzig, Germany.; Callewaert B; Center for Medical Genetics, Department of Biomolecular Medicine, Gent, Belgium.; Dheedene A; Center for Medical Genetics, Department of Biomolecular Medicine, Gent, Belgium.; Zidane-Marinnes M; Department of Pathology, Angers University Hospital, Angers, France.; Guichet A; Department of Medical Genetics, Angers University Hospital, Angers, France; Mitovasc Unit, UMR CNRS 6015 INSERM 1083, University of Angers, Angers, France.; Bris C; Department of Medical Genetics, Angers University Hospital, Angers, France; Mitovasc Unit, UMR CNRS 6015 INSERM 1083, University of Angers, Angers, France.; Van Bogaert P; Department of Neuropediatrics, Angers University Hospital, Angers, France.; Biquard F; Department of Gynecology, Angers University Hospital, Angers, France.; Lenaers G; Mitovasc Unit, UMR CNRS 6015 INSERM 1083, University of Angers, Angers, France.; Marcorelles P; Department of Pathology, Brest University Hospital, Brest, France.; Ferec C; INSERM, Univ Brest, EFS, UMR 1078, GGB, Brest, France.; Gonzalez B; Univ Rouen Normandie, INSERM U1245 and Rouen University Hospital, Department of Pathology, Rouen, France.; Procaccio V; Department of Medical Genetics, Angers University Hospital, Angers, France; Mitovasc Unit, UMR CNRS 6015 INSERM 1083, University of Angers, Angers, France.; Vitobello A; UFR Des Sciences de Santé, INSERM-Université de Bourgogne UMR1231 GAD (Génétique des Anomalies du Développement), FHU-TRANSLAD, Dijon, France; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Bonneau D; Department of Medical Genetics, Angers University Hospital, Angers, France; Mitovasc Unit, UMR CNRS 6015 INSERM 1083, University of Angers, Angers, France.; Laquerriere A; Univ Rouen Normandie, INSERM U1245 and Rouen University Hospital, Department of Pathology, Rouen, France.; Khiati S; Mitovasc Unit, UMR CNRS 6015 INSERM 1083, University of Angers, Angers, France.; Colin E; Department of Medical Genetics, Angers University Hospital, Angers, France; Mitovasc Unit, UMR CNRS 6015 INSERM 1083, University of Angers, Angers, France. Electronic address: escolin@chu-angers.fr.
Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE
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[검색어] Lenaers, G.
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