요약정보
Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients.
- Resource Type
- Academic Journal
- Authors
- Bessis D; Department of Dermatology, Saint-Eloi Hospital, University of Montpellier, Montpellier, France.; French National Reference Centre for Rare Diseases of the Skin and Mucous Membranes of Genetic Origin (MAGEC), University hospital of Montpellier, Montpellier, France.; INSERM U1058, Montpellier, France.; Bursztejn AC; Department of Dermatology, Brabois Hospital, University of Nancy, Nancy, France.; Morice-Picard F; French National Reference Centre for Rare Diseases of the Skin and Mucous Membranes of Genetic Origin (MAGEC), University hospital of Montpellier, Montpellier, France.; Department of Paediatric Dermatology, Pellegrin University Hospital of Bordeaux, Bordeaux, France.; Capri Y; Department of Clinical Genetics, Robert-Debré Hospital, Paris, France.; French National Reference Centre for Developmental Anomalies and Malformative Syndromes - Ile de France, Robert-Debré Hospital, AP-HP, Paris, France.; Barbarot S; Department of Dermatology, Hotel Dieu Hospital, University of Nantes, Nantes, France.; Aubert H; Department of Dermatology, Hotel Dieu Hospital, University of Nantes, Nantes, France.; Bodet D; Department of Paediatric Haematology-Immunology-Oncology, Caen Normandie Hospital and University of Caen, Caen, France.; Bourrat E; French National Reference Centre for Rare Diseases of the Skin and Mucous Membranes of Genetic Origin (MAGEC), University hospital of Montpellier, Montpellier, France.; Department of Paediatric Dermatology, Robert-Debré Hospital, AP-HP, Paris, France.; Chiaverini C; French National Reference Centre for Rare Diseases of the Skin and Mucous Membranes of Genetic Origin (MAGEC), University hospital of Montpellier, Montpellier, France.; Department of Dermatology, l'Archet 2 Hospital, University of Nice, Nice, France.; Poujade L; Department of Dermatology, Saint-Eloi Hospital, University of Montpellier, Montpellier, France.; French National Reference Centre for Rare Diseases of the Skin and Mucous Membranes of Genetic Origin (MAGEC), University hospital of Montpellier, Montpellier, France.; Willems M; Department of Clinical Genetics, Arnaud de Villeneuve Hospital, University of Montpellier, Montpellier, France.; French National Reference Centre for Developmental Anomalies - and Malformative Syndromes Sud Ouest Occitanie, University hospital of Montpellier, Montpellier, France.; Rouanet J; Department of Dermatology, d'Estaing Hospital and University Hospital of Clermont-Ferrand, Clermont-Ferrand, France.; Dompmartin-Blanchère A; Department of Dermatology, Caen Normandie Hospital and University of Caen, Caen, France.; Geneviève D; Department of Clinical Genetics, Arnaud de Villeneuve Hospital, University of Montpellier, Montpellier, France.; French National Reference Centre for Developmental Anomalies - and Malformative Syndromes Sud Ouest Occitanie, University hospital of Montpellier, Montpellier, France.; Gerard M; Department of Clinical Genetics, Caen Normandie Hospital and University of Caen, Caen, France.; Ginglinger E; Department of Clinical Genetics, Émile Muller Hospital, Mulhouse, France.; Hadj-Rabia S; French National Reference Centre for Rare Diseases of the Skin and Mucous Membranes of Genetic Origin (MAGEC), University hospital of Montpellier, Montpellier, France.; Department of Paediatric Dermatology, Necker-Enfants Malades Hospital, AP-HP, Paris, France.; Martin L; French National Reference Centre for Rare Diseases of the Skin and Mucous Membranes of Genetic Origin (MAGEC), University hospital of Montpellier, Montpellier, France.; Department of Dermatology, Angers Hospital University, Angers, France.; Mazereeuw-Hautier J; French National Reference Centre for Rare Diseases of the Skin and Mucous Membranes of Genetic Origin (MAGEC), University hospital of Montpellier, Montpellier, France.; Department of Dermatology, Larrey Hospital, University of Toulouse, Toulouse, France.; Bibas N; Department of Dermatology, Larrey Hospital, University of Toulouse, Toulouse, France.; Molinari N; Department of Statistics, La Colombière Hospital and University of Montpellier, Montpellier, France.; Herman F; Department of Statistics, La Colombière Hospital and University of Montpellier, Montpellier, France.; Phan A; Department of Paediatric Dermatology, Femme-Mère-Enfant Hospital-HCL, University of Lyon, Lyon, France.; Rod J; Department of Paediatric Surgery, Caen Normandie Hospital and University of Caen, Caen, France.; Roger H; Doctor's Office, Clermont-Ferrand, France.; Sigaudy S; French National Reference Centre for Developmental Anomalies and Malformative Syndromes - Ile de France, Robert-Debré Hospital, AP-HP, Paris, France.; Department of Clinical Genetics, La Timone Hospital, AP-HM and University of Marseille, Marseille, France.; Ziegler A; Department of Clinical Genetics, Hospital and University of Angers, Angers, France.; Vial Y; French National Reference Centre for Developmental Anomalies and Malformative Syndromes - Ile de France, Robert-Debré Hospital, AP-HP, Paris, France.; Department of Molecular Genetics, Robert-Debré Hospital, AP-HP, Paris, France.; Verloes A; Department of Clinical Genetics, Robert-Debré Hospital, Paris, France.; French National Reference Centre for Developmental Anomalies and Malformative Syndromes - Ile de France, Robert-Debré Hospital, AP-HP, Paris, France.; Cavé H; French National Reference Centre for Developmental Anomalies and Malformative Syndromes - Ile de France, Robert-Debré Hospital, AP-HP, Paris, France.; Department of Molecular Genetics, Robert-Debré Hospital, AP-HP, Paris, France.; Lacombe D; Department of Clinical Genetics, Pellegrin University Hospital of Bordeaux, Bordeaux, France.; French National Reference Centre for Developmental Anomalies - and Malformative Syndromes SOOR, University Hospital of Bordeaux, Bordeaux, France.; INSERM U1211, Bordeaux, France.
- Source
- Publisher:
Wiley-Blackwell Country of Publication: England NLM ID: 9216037 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-3083 (Electronic) Linking ISSN:09269959 NLM ISO Abbreviation: J Eur Acad Dermatol Venereol Subsets: MEDLINE - Subject
- Language
- English