Zobrazeno 1 - 10
of 541
pro vyhledávání: '"Perez Dueñas B"'
Akademický článek
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Autor:
de la Morena-Barrio, M.E., Di Michele, M., Lozano, M.L., Rivera, J., Pérez-Dueñas, B., Altisent, C., Sevivas, T., Vicente, V., Jaeken, J., Freson, K., Corral, J.
Publikováno v:
In Thrombosis Research March 2014 133(3):412-417
Autor:
Sainz Torres, R., Pérez Dueñas, B.
Publikováno v:
In Neurology Perspectives November 2024 4 Supplement 1:142-142
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
García-Cazorla, A., Ortez, C., Pérez-Dueñas, B., Serrano, M., Pineda, M., Campistol, J., Fernández-Álvarez, E.
Publikováno v:
In European Journal of Paediatric Neurology 2011 15(4):295-302
Autor:
Pérez-Dueñas, B., García-Cazorla, A., Pineda, M., Poo, P., Campistol, J., Cusí, V., Schollen, E., Matthijs, G., Grunewald, S., Briones, P., Pérez-Cerdá, C., Artuch, R., Vilaseca, M.A.
Publikováno v:
In European Journal of Paediatric Neurology 2009 13(5):444-451
Autor:
Carrasco E; Hereditary Cancer Genetics Group, Medical Oncology Department, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Department of Pediatrics, Obstetrics and Gynecology, Preventative Medicine and Public Health, Autonomous University of Barcelona, Barcelona, Spain.; Hereditary Cancer Genetics Group, Medical oncology, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Barcelona Hospital Campus, C/ Natzaret, 115-117, 08035, Barcelona, Spain., López-Fernández A; Hereditary Cancer Genetics Group, Medical Oncology Department, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Hereditary Cancer Genetics Group, Medical oncology, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Barcelona Hospital Campus, C/ Natzaret, 115-117, 08035, Barcelona, Spain., Codina-Sola M; Department of Clinical and Molecular Genetics, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Medicine Genetics Group, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA [EU Framework Partnership Agreement ID: 3HP-HP-FPA ERN-01-2016/739516], ERN-ITHACA, Barcelona, Spain., Valenzuela I; Department of Clinical and Molecular Genetics, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Medicine Genetics Group, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA [EU Framework Partnership Agreement ID: 3HP-HP-FPA ERN-01-2016/739516], ERN-ITHACA, Barcelona, Spain., Cueto-González AM; Department of Clinical and Molecular Genetics, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Medicine Genetics Group, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA [EU Framework Partnership Agreement ID: 3HP-HP-FPA ERN-01-2016/739516], ERN-ITHACA, Barcelona, Spain., Villacampa G; Oncology Data Science (ODysSey) Group, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Barcelona Hospital Campus, C/ Natzaret, 115-117, 08035, Barcelona, Spain., Navarro V; Oncology Data Science (ODysSey) Group, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Barcelona Hospital Campus, C/ Natzaret, 115-117, 08035, Barcelona, Spain., Torres-Esquius S; Hereditary Cancer Genetics Group, Medical oncology, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Barcelona Hospital Campus, C/ Natzaret, 115-117, 08035, Barcelona, Spain., Palau D; Department of Clinical and Molecular Genetics, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA [EU Framework Partnership Agreement ID: 3HP-HP-FPA ERN-01-2016/739516], ERN-ITHACA, Barcelona, Spain., Cruellas M; Hereditary Cancer Genetics Group, Medical Oncology Department, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Hereditary Cancer Genetics Group, Medical oncology, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Barcelona Hospital Campus, C/ Natzaret, 115-117, 08035, Barcelona, Spain., Torres M; Hereditary Cancer Genetics Group, Medical Oncology Department, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain., Perez-Dueñas B; Paediatric Neurology Department, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035 Universitat Autónoma de Barcelona, Barcelona, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Barcelona, Spain., Abulí A; Department of Clinical and Molecular Genetics, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Medicine Genetics Group, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA [EU Framework Partnership Agreement ID: 3HP-HP-FPA ERN-01-2016/739516], ERN-ITHACA, Barcelona, Spain., Diez O; Hereditary Cancer Genetics Group, Medical oncology, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Barcelona Hospital Campus, C/ Natzaret, 115-117, 08035, Barcelona, Spain.; Department of Clinical and Molecular Genetics, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA [EU Framework Partnership Agreement ID: 3HP-HP-FPA ERN-01-2016/739516], ERN-ITHACA, Barcelona, Spain., Sábado-Álvarez C; Department of Pediatric Oncology and Hematology, Vall d'Hebron Barcelona Hospital Campus, C/ Natzaret, 115-117, 08035, Barcelona, Spain., García-Arumí E; Department of Clinical and Molecular Genetics, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Medicine Genetics Group, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA [EU Framework Partnership Agreement ID: 3HP-HP-FPA ERN-01-2016/739516], ERN-ITHACA, Barcelona, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, Barcelona, Spain.; Research Group on Neuromuscular and Mitochondrial Disorders, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain., Tizzano EF; Department of Clinical and Molecular Genetics, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Medicine Genetics Group, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Member of the European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability ERN-ITHACA [EU Framework Partnership Agreement ID: 3HP-HP-FPA ERN-01-2016/739516], ERN-ITHACA, Barcelona, Spain., Moreno L; Department of Pediatric Oncology and Hematology, Vall d'Hebron Barcelona Hospital Campus, C/ Natzaret, 115-117, 08035, Barcelona, Spain lucas.moreno@vallhebron.cat.; Childhood Cancer and Blood Disorders Group, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain., Balmaña J; Hereditary Cancer Genetics Group, Medical Oncology Department, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.; Hereditary Cancer Genetics Group, Medical oncology, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Barcelona Hospital Campus, C/ Natzaret, 115-117, 08035, Barcelona, Spain.; Member of the European Reference Network on GENTURIS, ID: HP-ERN-2016 739547, GENTURIS, Barcelona, Spain.
Publikováno v:
Journal of medical genetics [J Med Genet] 2023 Jul; Vol. 60 (7), pp. 685-691. Date of Electronic Publication: 2022 Nov 29.
Autor:
Pringsheim T; Department of Clinical Neurosciences Psychiatry, Pediatrics and Community Health Sciences, University of Calgary Calgary AB Canada., Batla A; Department of Clinical and Movement Neuroscience UCL Queen Square Institute of Neurology London UK., Shalash A; Department of Neurology Faculty of medicine, Ain Shams Univeristy Cairo Egypt., Sahu JK; Pediatric Neurology Unit, Postgraduate Institute of Medical Education and Research Chandigarh India., Cosentino C; Department of Neurodegenerative Diseases Instituto Nacional de Ciencias Neurologicas and School of Medicine, Universidad Nacional Mayor de San Marcos Lima Peru., Ebrahimi-Fakhari D; Department of Neurology Boston Children's Hospital, Harvard Medical School Boston MA USA., Friedman J; Departments of Neurosciences and Pediatrics UC San Diego San Diego CA USA., Lin JP; Children's Neurosciences, Complex Motor Disorders Service (CMDS) Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust (GSTT), and Women and Children's Health Institute Faculty of Life Sciences & Medicine, Kings Health Partners, King's College London London UK., Mink J; Department of Neurology University of Rochester Rochester NY USA., Munchau A; Institute of Systems Motor Science, University of Lübeck Lübeck Germany., Munoz D; Department of Paediatric Neurology San Borja Arriaran Hospital. University of Chile Santiago Chile., Nardocci N; Pediatric Neuroscience Department Fondazione IRCCS Istituto Neurologico 'C Besta' Milan Italy., Perez-Dueñas B; Department of Pediatric Neurology Hospital Universitari Vall d'Hebrón, Universitat Autònoma de Barcelona. Centre for Biomedical Research of Rare Diseases (CIBERER), ISCIII Madrid Spain., Sardar Z; FCPS, Department of Neurology Columbia University Irving Medical Center/New York Presbyterian Hospital New York NY USA., Triki C; Department of child neurology Hedi Chaker Hospital, LR10ES15, Sfax Medical School, University of Sfax Tunisia Sfax Tunisia., Ben-Pazi H; Movement Disorders Clinic, Assuta Ashdod Ahdod Israel., Silveira-Moriyama L; Department of Neurology University of Campinas (UNICAMP) Campinas Brazil., Troncoso-Schifferli M; Department of Paediatric Neurology San Borja Arriaran Hospital. University of Chile Santiago Chile., Hoshino K; Segawa Memorial Neurological Clinic for Children Tokyo Japan., Dale RC; Children's Hospital at Westmead Clinical School, University of Sydney Sydney NSW Australia., Fung VSC; Movement Disorders Unit, Department of Neurology Westmead Hospital & Sydney Medical School, University of Sydney Sydney NSW Australia., Kurian MA; Developmental Neurosciences Zayed Centre for Research into Rare Disease in Children, GOS-Institute of Child Health, UCL London UK., Roze E; Sorbonne University Paris Brain Institute, Assistance Publique-Hôpitaux de Paris, DMU Neurosciences Paris France.
Publikováno v:
Movement disorders clinical practice [Mov Disord Clin Pract] 2023 Apr 04; Vol. 10 (5), pp. 748-755. Date of Electronic Publication: 2023 Apr 04 (Print Publication: 2023).
Autor:
Centen LM; Department of Neurology, University of Groningen, University Medical Center Groningen, PO Box 30001, 9700 RB, Groningen, The Netherlands. l.m.centen@umcg.nl.; Expertise Center Movement Disorders Groningen, University of Groningen, University Medical Centre Groningen, PO Box 30001, 9700 RB, Groningen, The Netherlands. l.m.centen@umcg.nl., Pinter D; Department of Neurology, Medical School, University of Pécs, Rét Utca 2, Pécs, 7623, Hungary., van Egmond ME; Department of Neurology, University of Groningen, University Medical Center Groningen, PO Box 30001, 9700 RB, Groningen, The Netherlands.; Expertise Center Movement Disorders Groningen, University of Groningen, University Medical Centre Groningen, PO Box 30001, 9700 RB, Groningen, The Netherlands., Graessner H; Centre for Rare Diseases and Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen, Calwerstr. 7, 72076, Tübingen, Germany., Kovacs N; Department of Neurology, Medical School, University of Pécs, Rét Utca 2, Pécs, 7623, Hungary., Koy A; Department of Pediatrics, Faculty of Medicine, University Hospital Cologne, University of Cologne, Cologne, Germany., Perez-Dueñas B; Paediatric Neurology Department, Hospital Vall d'Hebron, Barcelona, Spain., Reinhard C; Centre for Rare Diseases and Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen, Calwerstr. 7, 72076, Tübingen, Germany., Tijssen MAJ; Department of Neurology, University of Groningen, University Medical Center Groningen, PO Box 30001, 9700 RB, Groningen, The Netherlands.; Expertise Center Movement Disorders Groningen, University of Groningen, University Medical Centre Groningen, PO Box 30001, 9700 RB, Groningen, The Netherlands., Boesch S; Department of Neurology, Center for Rare Movement Disorders Innsbruck, Medical University of Innsbruck, Innsbruck, Austria.
Publikováno v:
Journal of neurology [J Neurol] 2023 Feb; Vol. 270 (2), pp. 797-809. Date of Electronic Publication: 2022 Oct 06.