학술논문


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'학술논문' 에서 검색결과 523건 | 목록 1~20
Conference
European Journal of Human Genetics
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
Institut de Recerca Germans Trias i Pujol (IGTP)
Academic Journal
Bermejo-Guerrero L; Neuromuscular Disorders Unit, Department of Neurology, Hospital Universitario 12 de Octubre, Madrid, Spain.; Mitochondrial and Neuromuscular Disorders Research Group, '12 de Octubre' Hospital Research Institute (imas12), Madrid, Spain.; Restrepo-Vera JL; Neuromuscular Disorders Unit, Department of Neurology, Hospital Universitario Vall d'Hebron, Barcelona, Spain.; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; Research Group on Neuromuscular and Mitochondrial Diseases, Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Spain.; Martin-Jimenez P; Neuromuscular Disorders Unit, Department of Neurology, Hospital Universitario 12 de Octubre, Madrid, Spain.; Universidad Complutense, Madrid, Spain.; Navarro-Riquelme M; Mitochondrial and Neuromuscular Disorders Research Group, '12 de Octubre' Hospital Research Institute (imas12), Madrid, Spain.; Mitochondrial Disorders Laboratory, Department of Clinical Biochemistry, Hospital Universitario 12 de Octubre, Madrid, Spain.; Garrido-Moraga R; Mitochondrial and Neuromuscular Disorders Research Group, '12 de Octubre' Hospital Research Institute (imas12), Madrid, Spain.; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; Mitochondrial Disorders Laboratory, Department of Clinical Biochemistry, Hospital Universitario 12 de Octubre, Madrid, Spain.; Ochoa LE; Neuromuscular Disorders Unit, Department of Neurology, Hospital Universitario 12 de Octubre, Madrid, Spain.; González-Quintana A; Mitochondrial and Neuromuscular Disorders Research Group, '12 de Octubre' Hospital Research Institute (imas12), Madrid, Spain.; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; Mitochondrial Disorders Laboratory, Department of Clinical Biochemistry, Hospital Universitario 12 de Octubre, Madrid, Spain.; Hernandez-Lain A; Neuropathology Unit, Department of Pathology, Hospital Universitario 12 de Octubre, Madrid, Spain.; Castillo-Villalba J; Neuroimmunology Research Group, Health Research Institute La Fe (IIS La Fe), Valencia, Spain.; Morís G; Neuromuscular Disorders Unit, Neurology Department, Hospital Universitario Central de Asturias, Spain.; Muelas N; Neuromuscular Disorders Unit, Department of Neurology, Hospital Universitari I Politècnic La Fe, Valencia, Spain.; Neuromuscular and Ataxias Research Group, Health Research Institute La Fe (IIS La Fe), Valencia, Spain.; Department of Medicine, Universitat de València, Spain.; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; García-Arumí E; Department of Clinical and Molecular Genetics, Hospital Vall d'Hebron, Barcelona, Spain.; Universitat Autonoma de Barcelona, Spain.; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; Research Group on Neuromuscular and Mitochondrial Diseases, Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Spain.; González V; Universitat Autonoma de Barcelona, Spain.; Movement Disorders Unit, Neurology Department, Hospital Vall d'Hebron, Barcelona, Spain.; Martínez-Sáez E; Universitat Autonoma de Barcelona, Spain.; Department of Pathology, Hospital Vall d'Hebron, Barcelona, Spain.; Vesperinas A; Neuromuscular Disorders Unit, Neurology Department, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.; Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; Llansó L; Neuromuscular Disorders Unit, Neurology Department, Hospital de la Santa Creu I Sant Pau, Barcelona, Spain.; Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; Juntas-Morales R; Neuromuscular Disorders Unit, Department of Neurology, Hospital Universitario Vall d'Hebron, Barcelona, Spain.; Paradas C; Neuromuscular Disorders Unit, Neurology Department, Hospital Universitario Virgen del Rocío, Sevilla, Spain.; Kapetanovic S; Neuromuscular Disorders Unit, Neurology Department, Hospital Universitario de Basurto, Bilbao, Spain.; NAT-RD Research Group, Biobizkaia Health Research Institute, Barakaldo, Spain; and.; Blázquez A; Mitochondrial and Neuromuscular Disorders Research Group, '12 de Octubre' Hospital Research Institute (imas12), Madrid, Spain.; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; Mitochondrial Disorders Laboratory, Department of Clinical Biochemistry, Hospital Universitario 12 de Octubre, Madrid, Spain.; Martí R; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; Research Group on Neuromuscular and Mitochondrial Diseases, Vall d'Hebron Research Institute, Universitat Autònoma de Barcelona, Spain.; Arenas J; Mitochondrial and Neuromuscular Disorders Research Group, '12 de Octubre' Hospital Research Institute (imas12), Madrid, Spain.; Mitochondrial Disorders Laboratory, Department of Clinical Biochemistry, Hospital Universitario 12 de Octubre, Madrid, Spain.; Martín MA; Mitochondrial and Neuromuscular Disorders Research Group, '12 de Octubre' Hospital Research Institute (imas12), Madrid, Spain.; Department of Genetics, Hospital Universitario 12 de Octubre, Madrid, Spain.; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; Domínguez-González C; Mitochondrial and Neuromuscular Disorders Research Group, '12 de Octubre' Hospital Research Institute (imas12), Madrid, Spain.; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain.; Neuromuscular Disorders Unit, Department of Neurology, Hospital Universitario 12 de Octubre, Madrid, Spain.
Publisher: Published for the American Academy of Neurology by Wolters Kluwer Country of Publication: United States NLM ID: 101671068 Publication Model: eCollection Cited Medium: Print ISSN: 2376-7839 (Print) Linking ISSN: 23767839 NLM ISO Abbreviation: Neurol Genet Subsets: PubMed not MEDLINE
Valenzuela I; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain; Autonomous University of Barcelona, Barcelona, Spain.; Codina-Solà M; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Vazquez E; Department of Pediatric Radiology, Hospital Vall d'Hebron, Barcelona, Spain.; Cueto-González A; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Leno-Colorado J; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Lasa-Aranzasti A; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Trujillano L; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Masotto B; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Masas M; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Escobar M; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; García-Arumí E; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Tizzano EF; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.
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; In Process
Academic Journal
Trujillano L; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Valenzuela I; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Costa-Roger M; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Cuscó I; Genetics Department, Institut d'Investigació Biomèdica Sant Pau (IIB SANT PAU), Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.; Fernandez-Alvarez P; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Cueto-González A; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Lasa-Aranzasti A; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Masotto B; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Abulí A; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Codina-Solà M; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Del Campo M; Department of Clinical Pediatrics, University of California, San Diego, California, USA.; Ruiz Moreno JA; Department of Pediatrics, Hospital Costa del Sol, Marbella, Málaga, Spain.; Pardo Domínguez C; Department of Pediatrics, Hospital Costa del Sol, Marbella, Málaga, Spain.; Palma Milla C; Servicio de Genética, Hospital Universitario 12 de Octubre, Madrid, Spain.; UDISGEN (Unidad de Dismorfología y Genética), Hospital Universitario 12 de Octubre, Madrid, Spain.; Pérez de la Fuente R; Servicio de Genética, Hospital Universitario 12 de Octubre, Madrid, Spain.; UDISGEN (Unidad de Dismorfología y Genética), Hospital Universitario 12 de Octubre, Madrid, Spain.; Quesada-Espinosa JF; Servicio de Genética, Hospital Universitario 12 de Octubre, Madrid, Spain.; UDISGEN (Unidad de Dismorfología y Genética), Hospital Universitario 12 de Octubre, Madrid, Spain.; Núñez-Enamorado N; Departamento de Neurología pediátrica, Hospital Universitario 12 de Octubre, Madrid, Spain.; Gener B; Department of Genetics, Cruces University Hospital, Biobizkaia Health Research Institute, Vizcaya, Spain.; Ballesta-Martínez MJ; Sección Genética Médica, Servicio de Pediatría, Hospital Clinico Universitario Virgen de la Arrixaca, Murcia, Spain.; Brea-Fernández AJ; Grupo de Genómica y Bioinformática, Centro Singular de Investigación en Medicina Molecular y Enfermedades Crónicas (CiMUS), Centro de Investigación Biomédica en Red de Enfermedades Raras del Instituto de Salud Carlos III (CIBERER-ISCIII), Universidade de Santiago de Compostela, Santiago de Compostela, Spain.; Fundación Pública Galega Instituto de Investigación Sanitaria de Santiago de Compostela (FIDIS), Santiago de Compostela, Spain.; Fernández-Prieto M; Grupo de Genómica y Bioinformática, Centro Singular de Investigación en Medicina Molecular y Enfermedades Crónicas (CiMUS), Centro de Investigación Biomédica en Red de Enfermedades Raras del Instituto de Salud Carlos III (CIBERER-ISCIII), Universidade de Santiago de Compostela, Santiago de Compostela, Spain.; Fundación Pública Galega Instituto de Investigación Sanitaria de Santiago de Compostela (FIDIS), Santiago de Compostela, Spain.; Trujillo-Quintero JP; Center for Genomic Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.; Ruiz A; Center for Genomic Medicine, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.; Santos-Simarro F; Unidad de Diagnóstico Molecular y Genética Clínica, Hospital Universitario Son Espases, Idisba, Palma de Mallorca, Spain.; Rosello M; Genetics Unit, Hospital Universitario y Politecnico La Fe, Valencia, Spain.; Orellana C; Genetics Unit, Hospital Universitario y Politecnico La Fe, Valencia, Spain.; Martinez F; Genetics Unit, Hospital Universitario y Politecnico La Fe, Valencia, Spain.; Martinez-Monseny AF; Department of Genetics and Institut de Recerca, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain.; Casas-Alba D; Department of Genetics and Institut de Recerca, Hospital Sant Joan de Déu Barcelona, Barcelona, Spain.; Serrano M; Pediatric Neurology Department, Institut de Recerca, Hospital Sant Joan de Déu, Barcelona, Spain.; Palomares-Bralo M; Clinical Genetics Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, CIBERER, Hospital Universitario La Paz, Madrid, Spain.; Rikeros-Orozco E; Clinical Genetics Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, CIBERER, Hospital Universitario La Paz, Madrid, Spain.; Gómez-Cano MÁ; Clinical Genetics Section, Medical and Molecular Genetics Institute (INGEMM) IdiPaz, CIBERER, Hospital Universitario La Paz, Madrid, Spain.; Tirado-Requero P; Neuropediatric Unit, University Hospital La Paz, Madrid, Spain.; Pié Juste J; Unit of Clinical Genetics and Functional Genomics, Department of Pharmacology-Physiology, School of Medicine, Universidad de Zaragoza, CIBERER-GCV02 and IIS-Aragon, Zaragoza, Spain.; Ramos FJ; Unit of Clinical Genetics and Functional Genomics, Department of Pharmacology-Physiology, School of Medicine, Universidad de Zaragoza, CIBERER-GCV02 and IIS-Aragon, Zaragoza, Spain.; Unit of Clinical Genetics, Service of Paediatrics, University Hospital 'Lozano Blesa', University of Zaragoza Medical School, CIBERER-GCV02 and IIS-Aragon, Zaragoza, Spain.; García-Arumí E; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.; Tizzano EF; Clinical and Molecular Genetics Area, Vall d'Hebron Hospital, Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Barcelona, Spain.
Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Academic Journal
DIABETES
Simó, R, Hernández, C, Porta, M, Bandello, F, Grauslund, J, Harding, S P, Aldington, S J, Egan, C, Frydkjaer-Olsen, U, García-Arumí, J, Gibson, J, Lang, G E, Lattanzio, R, Massin, P, Midena, E, Ponsati, B, Ribeiro, L, Scanlon, P, Lobo, C, Costa, M Â, Cunha-Vaz, J & European Consortium for the Early Treatment of Diabetic Retinopathy (EUROCONDOR) 2019, ' Effects of Topically Administered Neuroprotective Drugs in Early Stages of Diabetic Retinopathy. Results of the EUROCONDOR Clinical Trial ', Diabetes, vol. 68, no. 2, pp. 457-463 . https://doi.org/10.2337/db18-0682
Academic Journal
Fernández-Cancio M; Growth and Development group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.; Antolín M; Department of Clinical and Molecular Genetics and Rare Disease, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Clemente M; Growth and Development group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.; Pediatric Endocrinology Section, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Pediatrics, Obstetrics and Gynecology and Preventive Medicine Department, Universitat Autònoma de Barcelona, Bellaterra, Spain.; Campos-Martorell A; Growth and Development group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Pediatric Endocrinology Section, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Pediatrics, Obstetrics and Gynecology and Preventive Medicine Department, Universitat Autònoma de Barcelona, Bellaterra, Spain.; Mogas E; Growth and Development group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Pediatric Endocrinology Section, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Pediatrics, Obstetrics and Gynecology and Preventive Medicine Department, Universitat Autònoma de Barcelona, Bellaterra, Spain.; Baz-Redón N; Growth and Development group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.; Leno-Colorado J; Department of Clinical and Molecular Genetics and Rare Disease, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Comas-Armangué G; Department of Clinical and Molecular Genetics and Rare Disease, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; García-Arumí E; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.; Department of Clinical and Molecular Genetics and Rare Disease, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Research Group on Neuromuscular and Mitochondrial Diseases, Vall d'Hebron Research Institute, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Soler-Colomer L; Pediatric Endocrinology Section, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; González-Llorens N; Pediatric Endocrinology Section, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Camats-Tarruella N; Growth and Development group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.; Yeste D; Growth and Development group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Centre for Biomedical Network Research on Rare Diseases (CIBERER), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.; Pediatric Endocrinology Section, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Pediatrics, Obstetrics and Gynecology and Preventive Medicine Department, Universitat Autònoma de Barcelona, Bellaterra, Spain.
Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101555782 Publication Model: eCollection Cited Medium: Print ISSN: 1664-2392 (Print) Linking ISSN: 16642392 NLM ISO Abbreviation: Front Endocrinol (Lausanne) Subsets: MEDLINE
Academic Journal
Subirà O; Ophthalmology Department, Hospital Universitari de Vall d'Hebron, Passeig de la Vall d'Hebron, 119, 08035, Barcelona, Spain. olaia.subira@vallhebron.cat.; Català-Mora J; Ophthalmology Department, Hospital de Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.; Ophthalmology Department, Hospital Universitari de Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain.; Unitat de Distròfies Hereditàries de Retina, Hospital Sant Joan de Déu-Hospital Bellvitge, Barcelona, Spain.; Del Prado C; Ophthalmology Department, Hospital de Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.; Unitat de Distròfies Hereditàries de Retina, Hospital Sant Joan de Déu-Hospital Bellvitge, Barcelona, Spain.; Díaz-Cascajosa J; Ophthalmology Department, Hospital de Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.; Unitat de Distròfies Hereditàries de Retina, Hospital Sant Joan de Déu-Hospital Bellvitge, Barcelona, Spain.; Barraso Rodrigo M; Ophthalmology Department, Hospital de Sant Joan de Déu, Esplugues de Llobregat, Barcelona, Spain.; Unitat de Distròfies Hereditàries de Retina, Hospital Sant Joan de Déu-Hospital Bellvitge, Barcelona, Spain.; Cobos E; Ophthalmology Department, Hospital Universitari de Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain.; Unitat de Distròfies Hereditàries de Retina, Hospital Sant Joan de Déu-Hospital Bellvitge, Barcelona, Spain.; Aguilera C; Laboratori Clínic Territorial Metropolitana Sud, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Clinical Genetics Unit, Hospital Universitari de Bellvitge, L'Hospitalet de Llobregat, Spain.; Esteve-Garcia A; Laboratori Clínic Territorial Metropolitana Sud, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Clinical Genetics Unit, Hospital Universitari de Bellvitge, L'Hospitalet de Llobregat, Spain.; García-Arumí J; Ophthalmology Department, Hospital Universitari de Vall d'Hebron, Passeig de la Vall d'Hebron, 119, 08035, Barcelona, Spain.; Instituto de Microcirugía Ocular (IMO), Barcelona, Spain.; Universitat Autònoma de Barcelona, Barcelona, Spain.; Caminal JM; Ophthalmology Department, Hospital Universitari de Bellvitge, L'Hospitalet de Llobregat, Barcelona, Spain.; Unitat de Distròfies Hereditàries de Retina, Hospital Sant Joan de Déu-Hospital Bellvitge, Barcelona, Spain.
Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 8205248 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1435-702X (Electronic) Linking ISSN: 0721832X NLM ISO Abbreviation: Graefes Arch Clin Exp Ophthalmol Subsets: MEDLINE
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