학술논문

발행년
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(예 : 2010-2015)
'학술논문' 에서 검색결과 28건 | 목록 1~10
Academic Journal
Bada-Bosch T; Department of Nephrology, Hospital Universitario  12 de Octubre, Madrid, Spain.; Sevillano AM; Department of Nephrology, Hospital Universitario  12 de Octubre, Madrid, Spain.; Sánchez-Calvin MT; Department of Genetics, Hospital Universitario  12 de Octubre, Madrid, Spain.; Palma-Milla C; Department of Genetics, Hospital Universitario  12 de Octubre, Madrid, Spain.; Alba de Cáceres I; Department of Radiology, Hospital Universitario  12 de Octubre, Madrid, Spain.; Díaz-Crespo F; Department of Pathology, Hospital General Universitario, Gregorio Marañón, Madrid, Spain.; Trujillo H; Department of Nephrology, Hospital Universitario  12 de Octubre, Madrid, Spain.; Alonso M; Department of Pathology, Hospital Universitario  12 de Octubre, Madrid, Spain.; Cases-Corona C; Department of Nephrology, Hospital Fundación Alcorcón, Madrid, Spain.; Shabaka A; Department of Nephrology, Hospital Universitario La Paz, Madrid, Spain.; Quesada-Espinosa JF; Department of Genetics, Hospital Universitario  12 de Octubre, Madrid, Spain.; Lezana-Rosales JM; Department of Genetics, Hospital Universitario  12 de Octubre, Madrid, Spain.; Gutiérrez E; Department of Nephrology, Hospital Universitario  12 de Octubre, Madrid, Spain.; Fernández-Juárez G; Department of Nephrology, Hospital Universitario La Paz, Madrid, Spain.; Caravaca-Fontán F; Instituto de Investigación, Hospital Universitario  12 de Octubre, Madrid, Spain.; Praga M; Department of Medicine, Complutense University, Madrid, Spain.; Nephrology Division, Hospital Universitario Quironsalud, Madrid, Spain.
Publisher: Oxford University Press Country of Publication: England NLM ID: 8706402 Publication Model: Print Cited Medium: Internet ISSN: 1460-2385 (Electronic) Linking ISSN: 09310509 NLM ISO Abbreviation: Nephrol Dial Transplant Subsets: MEDLINE
Academic Journal
Reda Del Barrio S; Department of Otolaryngology-Head and Neck Surgery, Hospital Universitario 12 de Octubre, Madrid, Spain. Electronic address: sara.reda@salud.madrid.org.; de Vergas Gutiérrez J; Department of Otolaryngology-Head and Neck Surgery, Hospital Universitario 12 de Octubre, Madrid, Spain.; Quesada-Espinosa JF; Department of Genetics, Hospital Universitario 12 de Octubre, Madrid, Spain.; Sánchez-Calvín MT; Department of Genetics, Hospital Universitario 12 de Octubre, Madrid, Spain.; Gómez-Manjón I; Department of Genetics, Hospital Universitario 12 de Octubre, Madrid, Spain.; Sierra-Tomillo O; Department of Genetics, Hospital Universitario 12 de Octubre, Madrid, Spain.; Juárez-Rufián A; Department of Genetics, Hospital Universitario 12 de Octubre, Madrid, Spain.; García Fernández A; Department of Otolaryngology-Head and Neck Surgery, Hospital Universitario 12 de Octubre, Madrid, Spain.
Publisher: Elsevier España Country of Publication: Spain NLM ID: 101770938 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2173-5735 (Electronic) Linking ISSN: 21735735 NLM ISO Abbreviation: Acta Otorrinolaringol Esp (Engl Ed) Subsets: MEDLINE
Academic Journal
Reda Del Barrio S; Servicio de Otorrinolaringología, Hospital Universitario 12 de Octubre, Madrid, Spain. Electronic address: sara.reda@salud.madrid.org.; García Fernández A; Servicio de Otorrinolaringología, Hospital Universitario 12 de Octubre, Madrid, Spain.; Quesada-Espinosa JF; Servicio de Genética, Hospital Universitario 12 de Octubre, Madrid, Spain.; Sánchez-Calvín MT; Servicio de Genética, Hospital Universitario 12 de Octubre, Madrid, Spain.; Gómez-Manjón I; Servicio de Genética, Hospital Universitario 12 de Octubre, Madrid, Spain.; Sierra-Tomillo O; Servicio de Genética, Hospital Universitario 12 de Octubre, Madrid, Spain.; Juárez-Rufián A; Servicio de Genética, Hospital Universitario 12 de Octubre, Madrid, Spain.; de Vergas Gutiérrez J; Servicio de Otorrinolaringología, Hospital Universitario 12 de Octubre, Madrid, Spain.
Publisher: Elsevier España Country of Publication: Spain NLM ID: 101770938 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2173-5735 (Electronic) Linking ISSN: 21735735 NLM ISO Abbreviation: Acta Otorrinolaringol Esp (Engl Ed) Subsets: MEDLINE
Academic Journal
Rodríguez-García ME; Grupo de Enfermedades Raras, Mitocondriales y Neuromusculares (ERMN). Instituto de Investigación Hospital 12 de Octubre (i + 12), E-28041, Madrid, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), U723, E-28041, Madrid, Spain.; Cotrina-Vinagre FJ; Grupo de Enfermedades Raras, Mitocondriales y Neuromusculares (ERMN). Instituto de Investigación Hospital 12 de Octubre (i + 12), E-28041, Madrid, Spain.; Olson AN; Department of Chemistry and Biochemistry, University of Maryland, College Park, MD, 20742, USA.; Sánchez-Calvin MT; Servicio de Genética, Hospital 12 de Octubre, E-28041, Madrid, Spain.; de Aragón AM; Servicio de Radiología, Hospital 12 de Octubre, E-28041, Madrid, Spain.; de Las Heras RS; Unidad de Neuropediatría, Hospital 12 de Octubre, Madrid, E-28041, Spain.; Dinman JD; Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD, 20742, USA.; de Vries BBA; Department of Human Genetics, Radboud University Medical Center and Donders Institute for Brain, Cognition and Behavior, 6525 GA, Nijmegen, The Netherlands.; Nabais Sá MJ; Centre for Predictive and Preventive Genetics (CGPP) and UnIGENe, Institute for Molecular and Cell Biology (IBMC), i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.; Quijada-Fraile P; Unidad Pediátrica de Enfermedades Raras, Enfermedades Mitocondriales y Metabólicas Hereditarias, Hospital 12 de Octubre, E-28041, Madrid, Spain.; Martínez-Azorín F; Grupo de Enfermedades Raras, Mitocondriales y Neuromusculares (ERMN). Instituto de Investigación Hospital 12 de Octubre (i + 12), E-28041, Madrid, Spain. fmartinez@h12o.es.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), U723, E-28041, Madrid, Spain. fmartinez@h12o.es.
Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1435-232X (Electronic) Linking ISSN: 14345161 NLM ISO Abbreviation: J Hum Genet Subsets: MEDLINE
Rodríguez-García ME; Grupo de Enfermedades Raras, Mitocondriales y Neuromusculares (ERMN). Instituto de Investigación Hospital 12 de Octubre (i + 12), E-28041, Madrid, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), U723, E-28041, Madrid, Spain.; Cotrina-Vinagre FJ; Grupo de Enfermedades Raras, Mitocondriales y Neuromusculares (ERMN). Instituto de Investigación Hospital 12 de Octubre (i + 12), E-28041, Madrid, Spain.; Olson AN; Department of Chemistry and Biochemistry, University of Maryland, College Park, MD, 20742, USA.; Sánchez-Calvin MT; Servicio de Genética, Hospital 12 de Octubre, E-28041, Madrid, Spain.; de Aragón AM; Servicio de Radiología, Hospital 12 de Octubre, E-28041, Madrid, Spain.; de Las Heras RS; Unidad de Neuropediatría, Hospital 12 de Octubre, Madrid, E-28041, Spain.; Dinman JD; Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, MD, 20742, USA.; de Vries BBA; Department of Human Genetics, Radboud University Medical Center and Donders Institute for Brain, Cognition and Behavior, 6525 GA, Nijmegen, The Netherlands.; Nabais Sá MJ; Centre for Predictive and Preventive Genetics (CGPP) and UnIGENe, Institute for Molecular and Cell Biology (IBMC), i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.; Quijada-Fraile P; Unidad Pediátrica de Enfermedades Raras, Enfermedades Mitocondriales y Metabólicas Hereditarias, Hospital 12 de Octubre, E-28041, Madrid, Spain.; Martínez-Azorín F; Grupo de Enfermedades Raras, Mitocondriales y Neuromusculares (ERMN). Instituto de Investigación Hospital 12 de Octubre (i + 12), E-28041, Madrid, Spain. fmartinez@h12o.es.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), U723, E-28041, Madrid, Spain. fmartinez@h12o.es.
Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print Cited Medium: Internet ISSN: 1435-232X (Electronic) Linking ISSN: 14345161 NLM ISO Abbreviation: J Hum Genet Subsets: PubMed not MEDLINE; MEDLINE
Academic Journal
Bellido-Cuéllar S; Epilepsy Unit, Neurology Department, 12 de Octubre University Hospital, Madrid, Spain. Electronic address: sara.bellidi@salu.madrid.org.; Pérez de la Fuente R; Department of Genetics. UDISGEN-Unidad de Dismorfología y Genética, 12 de Octubre University Hospital, Madrid, Spain.; Lezana-Rosales JM; Department of Genetics. UDISGEN-Unidad de Dismorfología y Genética, 12 de Octubre University Hospital, Madrid, Spain.; Sánchez-Calvín MT; Department of Genetics. UDISGEN-Unidad de Dismorfología y Genética, 12 de Octubre University Hospital, Madrid, Spain.; Saiz-Díaz RA; Epilepsy Unit, Neurology Department, 12 de Octubre University Hospital, Madrid, Spain.; González de la Aleja J; Epilepsy Unit, Neurology Department, 12 de Octubre University Hospital, Madrid, Spain.
Publisher: Elsevier Country of Publication: England NLM ID: 9306979 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2688 (Electronic) Linking ISSN: 10591311 NLM ISO Abbreviation: Seizure Subsets: MEDLINE
Academic Journal
Martinez-Cayuelas E; Department of Pediatrics, Hospital Universitario Fundacion Jimenez Diaz, Madrid, Spain.; Blanco-Kelly F; Department of Genetics and Genomics, Hospital Universitario Fundacion Jimenez Diaz (IIS-FJD), Madrid, Spain.; Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain.; Lopez-Grondona F; Department of Genetics and Genomics, Hospital Universitario Fundacion Jimenez Diaz (IIS-FJD), Madrid, Spain.; Swafiri ST; Department of Genetics and Genomics, Hospital Universitario Fundacion Jimenez Diaz (IIS-FJD), Madrid, Spain.; Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain.; Lopez-Rodriguez R; Department of Genetics and Genomics, Hospital Universitario Fundacion Jimenez Diaz (IIS-FJD), Madrid, Spain.; School of Pharmacy, Universidad San Pablo CEU. CEU Universities, Madrid, Spain.; Losada-Del Pozo R; Department of Pediatrics, Hospital Universitario Fundacion Jimenez Diaz, Madrid, Spain.; Mahillo-Fernandez I; Department of Statistics, Hospital Universitario Fundacion Jimenez Diaz (IIS-FJD), Madrid, Spain.; Moreno B; Department of Pediatrics, Hospital Universitario Fundacion Jimenez Diaz, Madrid, Spain.; Rodrigo-Moreno M; Department of Pediatrics, Hospital Universitario Fundacion Jimenez Diaz, Madrid, Spain.; Casas-Alba D; Clinical Genetics and Dysmorphology, Department of Genetic and Molecular Medicine, Pediatric Insitute of Rare Diseases (IPER), Hospital Sant Joan de Deu, Barcelona, Spain.; Lopez-Gonzalez A; Clinical Genetics and Dysmorphology, Department of Genetic and Molecular Medicine, Pediatric Insitute of Rare Diseases (IPER), Hospital Sant Joan de Deu, Barcelona, Spain.; García-Miñaúr S; Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain.; Medical and Molecular Genetics Institute (INGEMM), Hospital Universitario La Paz, Madrid, Spain.; Ángeles Mori M; Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain.; Medical and Molecular Genetics Institute (INGEMM), Hospital Universitario La Paz, Madrid, Spain.; Pacio-Minguez M; Medical and Molecular Genetics Institute (INGEMM), Hospital Universitario La Paz, Madrid, Spain.; Rikeros-Orozco E; Medical and Molecular Genetics Institute (INGEMM), Hospital Universitario La Paz, Madrid, Spain.; Santos-Simarro F; Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain.; Medical and Molecular Genetics Institute (INGEMM), Hospital Universitario La Paz, Madrid, Spain.; Cruz-Rojo J; Dysmorphology and Genetics Unit (UDISGEN), Hospital Universitario 12 de Octubre, Madrid, Spain.; Endocrinology Unit, Department of Pediatrics, Hospital Universitario 12 de Octubre, Madrid, Spain.; Quesada-Espinosa JF; Dysmorphology and Genetics Unit (UDISGEN), Hospital Universitario 12 de Octubre, Madrid, Spain.; Department of Genetics, Hospital Universitario 12 de Octubre, Madrid, Spain.; Sanchez-Calvin MT; Dysmorphology and Genetics Unit (UDISGEN), Hospital Universitario 12 de Octubre, Madrid, Spain.; Department of Genetics, Hospital Universitario 12 de Octubre, Madrid, Spain.; Sanchez-Del Pozo J; Dysmorphology and Genetics Unit (UDISGEN), Hospital Universitario 12 de Octubre, Madrid, Spain.; Endocrinology Unit, Department of Pediatrics, Hospital Universitario 12 de Octubre, Madrid, Spain.; Bernado Fonz R; Pediatric Neurology Unit, Department of Pediatrics, Navarrabiomed Pediatric Neurology Research Group, Hospital Universitario de Navarra, Pamplona, Spain.; Isidoro-Garcia M; Department of Biochemistry, Hospital Universitario de Salamanca. IBSAL Universidad de Salamanca, Salamanca, Spain.; Ruiz-Ayucar I; Department of Pediatrics, Hospital Universitario de Salamanca, Salamanca, Spain.; Alvarez-Mora MI; Department of Biochemistry and Molecular Genetics, IDIBAPS (Institut de Investigacions Biomèdiques August Pi I Sunyer), Hospital Clinic de Barcelona, Barcelona, Spain.; Blanco-Lago R; Pediatric Neurology Unit, Department of Pediatrics, Hospital Universitario Central de Asturias, Oviedo, Spain.; De Azua B; Department of Pediatrics, Hospital Son Llàtzer, Palma de Mallorca, Spain.; Eiris J; Department of Pediatric Neurology, Hospital Universitario de Santiago de Compostela, Santiago de Compostela, Spain.; Garcia-Peñas JJ; Pediatric Neurology Unit, Department of Pediatrics, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.; Gil-Fournier B; Department of Genetics, Hospital Universitario de Getafe, Madrid, Spain.; Gomez-Lado C; Department of Pediatric Neurology, Hospital Universitario de Santiago de Compostela, Santiago de Compostela, Spain.; Irazabal N; Department of Pediatrics, Hospital Can Misses, Eivissa, Spain.; Lopez-Gonzalez V; Medical Genetics Unit, Department of Genetics, Hospital Universitario Virgen de la Arrixaca, Murcia, Spain.; Madrigal I; Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain.; Department of Biochemistry and Molecular Genetics, IDIBAPS (Institut de Investigacions Biomèdiques August Pi I Sunyer), Hospital Clinic de Barcelona, Barcelona, Spain.; Malaga I; Pediatric Neurology Unit, Department of Pediatrics, Hospital Universitario Central de Asturias, Oviedo, Spain.; Martinez-Menendez B; Pediatric Neurology Unit, Department of Neurology, Hospital Universitario de Getafe, Madrid, Spain.; Ramiro-Leon S; Department of Genetics, Hospital Universitario de Getafe, Madrid, Spain.; Garcia-Hoyos M; Genetic Diagnosis Service, NIMGenetics Genomics and Medicine, Madrid, Spain.; Prieto-Matos P; Department of Pediatrics, Hospital Universitario de Salamanca, Salamanca, Spain.; Lopez-Pison J; Pediatric Neurology Unit, Department of Pediatrics, Hospital Universitario Miguel Servet, Zaragoza, Spain.; Aguilera-Albesa S; Pediatric Neurology Unit, Department of Pediatrics, Navarrabiomed Pediatric Neurology Research Group, Hospital Universitario de Navarra, Pamplona, Spain.; Alvarez S; Genetic Diagnosis Service, NIMGenetics Genomics and Medicine, Madrid, Spain.; Fernández-Jaén A; Department of Pediatric Neurology, Hospital Universitario Quironsalud Madrid, Madrid, Spain.; Llano-Rivas I; Department of Genetics, Hospital Universitario de Cruces. Biocruces Bizcaia Health Research Institute, Bizcaia, Spain.; Gener-Querol B; Department of Genetics, Hospital Universitario de Cruces. Biocruces Bizcaia Health Research Institute, Bizcaia, Spain.; Ayuso C; Department of Genetics and Genomics, Hospital Universitario Fundacion Jimenez Diaz (IIS-FJD), Madrid, Spain.; Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain.; Arteche-Lopez A; Dysmorphology and Genetics Unit (UDISGEN), Hospital Universitario 12 de Octubre, Madrid, Spain.; Department of Genetics, Hospital Universitario 12 de Octubre, Madrid, Spain.; Palomares-Bralo M; Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain.; Medical and Molecular Genetics Institute (INGEMM), Hospital Universitario La Paz, Madrid, Spain.; Cueto-González A; Department of Clinical and Molecular Genetics, Vall d'Hebron Research Institute, Hospital Universitario Vall d'Hebron, Barcelona, Spain.; Valenzuela I; Department of Clinical and Molecular Genetics, Vall d'Hebron Research Institute, Hospital Universitario Vall d'Hebron, Barcelona, Spain.; Martinez-Monseny A; Clinical Genetics and Dysmorphology, Department of Genetic and Molecular Medicine, Pediatric Insitute of Rare Diseases (IPER), Hospital Sant Joan de Deu, Barcelona, Spain.; Lorda-Sanchez I; Department of Genetics and Genomics, Hospital Universitario Fundacion Jimenez Diaz (IIS-FJD), Madrid, Spain.; Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain.; Almoguera B; Department of Genetics and Genomics, Hospital Universitario Fundacion Jimenez Diaz (IIS-FJD), Madrid, Spain balmoguera@quironsalud.es.; Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain.
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
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[Author] Sanchez-Calvin MT
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