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The VASCERN-VASCA working group diagnostic and management pathways for severe and/or rare infantile hemangiomas.
Diociaiuti, Andrea; Baselga, Eulalia; Boon, Laurence M; Dompmartin, Anne; Dvorakova, Veronika; El Hachem, May; Gasparella, Paolo; Haxhija, Emir; Ghaffarpour, Nader; Kyrklund, Kristiina; Irvine, Alan D; Kapp, Friedrich G; Rößler, Jochen; Salminen, Päivi; van den Bosch, Caroline; van der Vleuten, Carine; Kool, Leo Schultze; Vikkula, Miikka.
Afiliación
  • Diociaiuti A; Dermatology Unit and Genodermatosis Unit, Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Piazza Sant'Onofrio 4, 00165, Rome, Italy. Electronic address: andrea.diociaiuti@opbg.net.
  • Baselga E; Pediatric Dermatology, Hospital Sant Joan de Deu, Barcelona, Spain.
  • Boon LM; Center for Vascular Anomalies, Division of Plastic Surgery, University Clinics Saint-Luc, University of Louvain, VASCERN VASCA European Reference Centre, Brussels, Belgium.
  • Dompmartin A; Department of Dermatology, Université de Caen Basse Normandie, CHU Caen, Caen, France.
  • Dvorakova V; Paediatric Dermatology, Children's Health Ireland, (y)Clinical Medicine, Trinity College Dublin, Ireland.
  • El Hachem M; Dermatology Unit and Genodermatosis Unit, Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Piazza Sant'Onofrio 4, 00165, Rome, Italy.
  • Gasparella P; Department of Paediatric and Adolescent Surgery, Medical University of Graz, Graz, Austria.
  • Haxhija E; Department of Paediatric and Adolescent Surgery, Medical University of Graz, Graz, Austria.
  • Ghaffarpour N; Department of Plastic- and Craniofacial Surgery, Karolinska University Hospital, Stockholm, Sweden.
  • Kyrklund K; Department of Pediatric Surgery, HUS Rare Disease Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
  • Irvine AD; Paediatric Dermatology, Children's Health Ireland, (y)Clinical Medicine, Trinity College Dublin, Ireland.
  • Kapp FG; Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, 79106, Freiburg, Germany.
  • Rößler J; Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, 79106, Freiburg, Germany; Division of Pediatric Hematology and Oncology, Department of Pediatrics, Inselspital, Bern
  • Salminen P; Department of Pediatric Surgery, HUS Rare Disease Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.
  • van den Bosch C; Hevas, Patient Organisation for Vascular Anomalies, the Netherlands.
  • van der Vleuten C; Department of Dermatology, Radboudumc Expertise Center for Haemangiomas and Congenital Vascular Malformations Nijmegen Hecovan, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Kool LS; Department of Radiology, Radboudumc Expertise Center for Haemangiomas and Congenital Vascular Malformations Nijmegen Hecovan, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Vikkula M; Center for Vascular Anomalies, Division of Plastic Surgery, University Clinics Saint-Luc, University of Louvain, VASCERN VASCA European Reference Centre, Brussels, Belgium; Human Molecular Genetics, de Duve Institute, University of Louvain, Brussels, Belgium.
Eur J Med Genet ; 65(6): 104517, 2022 Jun.
Article en En | MEDLINE | ID: mdl-35487416
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Enfermedades Vasculares / Hemangioma Tipo de estudio: Diagnostic_studies / Qualitative_research Límite: Humans / Infant País/Región como asunto: Europa Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Enfermedades Vasculares / Hemangioma Tipo de estudio: Diagnostic_studies / Qualitative_research Límite: Humans / Infant País/Región como asunto: Europa Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article