Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Cañas EG"'
Autor:
Totten V; Kaweah Health System, Visalia, California, USA.; Kayenta Health Center of the Indian Health Service, Kayenta, Arizona, USA., Teixido-Tura G; Department of Cardiology, Hospital Universitari Vall d'Hebron, CIBER-CV, Vall d'Hebron institut de Recerca, Universitat Autònoma de Barcelona, Barcelona, Spain.; Department of Genetics and Genomics, Hospital Universitario Fundacion Jimenez Diaz (IIS-FJD), Madrid, Spain., Lopez-Grondona F; European Reference Network for Rare Multisystemic Vascular Disease (VASCERN), HTAD Rare Disease Working Group, Barcelona, Spain., Fernandez-Alvarez P; Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital. Medicine Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain.; European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Barcelona, Spain., Lasa-Aranzasti A; Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital. Medicine Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain.; European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Barcelona, Spain., Muñoz-Cabello P; Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital. Medicine Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain.; European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Barcelona, Spain., Kosaki R; Division of Medical Genetics, National Center for Child Health and Development, Tokyo, Japan., Tizzano EF; Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital. Medicine Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain.; European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Barcelona, Spain., Dewals W; Pediatric Cardiology Department, Antwerp University Hospital, Edegem, Belgium., Borràs E; Molecular Genetics Unit, Consorci Sanitari de Terrassa, Terrassa, Spain., Cañas EG; Angiology and Vascular Surgery, Hospital Universitari Parc Tauli, Sabadell, Spain., Almoguera B; European Reference Network for Rare Multisystemic Vascular Disease (VASCERN), HTAD Rare Disease Working Group, Barcelona, Spain.; Centro de Investigacion Biomedica en Red de Enfermedades Raras, Instituto de Salud Carlos III, Madrid, Spain., Loeys B; Center for Medical Genetics, Antwerp University Hospital/University of Antwerp, Antwerp, Belgium., Valenzuena I; Department of Clinical and Molecular Genetics, Vall d'Hebron University Hospital. Medicine Genetics Group, Vall d'Hebron Research Institute, Barcelona, Spain irene.valenzuela@vallhebron.cat.; European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability (ERN-ITHACA), Barcelona, Spain.
Publikováno v:
Journal of medical genetics [J Med Genet] 2024 Aug 29; Vol. 61 (9), pp. 870-877. Date of Electronic Publication: 2024 Aug 29.
Autor:
Cañas EG; Department of Vascular Surgery, Parc Tauli University Hospital, Universitat Autonoma de Barcelona, Sabadell, Catalonia., López SF; Department of Vascular Surgery, Parc Tauli University Hospital, Universitat Autonoma de Barcelona, Sabadell, Catalonia., Guevara-Noriega KA; Department of Vascular Surgery, Parc Tauli University Hospital, Universitat Autonoma de Barcelona, Sabadell, Catalonia., Gaibar AG; Department of Vascular Surgery, Parc Tauli University Hospital, Universitat Autonoma de Barcelona, Sabadell, Catalonia.
Publikováno v:
Journal of vascular surgery. Venous and lymphatic disorders [J Vasc Surg Venous Lymphat Disord] 2021 Jan; Vol. 9 (1), pp. 286-287.