Your browser doesn't support javascript.
loading
Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutation.
Bessis, D; Miquel, J; Bourrat, E; Chiaverini, C; Morice-Picard, F; Abadie, C; Manna, F; Baumann, C; Best, M; Blanchet, P; Bursztejn, A-C; Capri, Y; Coubes, C; Giuliano, F; Guillaumont, S; Hadj-Rabia, S; Jacquemont, M-L; Jeandel, C; Lacombe, D; Mallet, S; Mazereeuw-Hautier, J; Molinari, N; Pallure, V; Pernet, C; Philip, N; Pinson, L; Sarda, P; Sigaudy, S; Vial, Y; Willems, M; Geneviève, D; Verloes, A; Cavé, H.
Affiliation
  • Bessis D; Department of Dermatology, Saint-Eloi Hospital, Competence Centre for Rare Skin Diseases, Montpellier, France.
  • Miquel J; University of Montpellier, Montpellier, France.
  • Bourrat E; INSERM U1058, Montpellier, France.
  • Chiaverini C; Department of Paediatric Dermatology, Femme-Mère-Enfant Hospital, University of South Réunion, Saint-Pierre Réunion, France.
  • Morice-Picard F; Department of Dermatology, University of Rennes, Rennes, France.
  • Abadie C; Department of Paediatric Dermatology, Robert-Debré Hospital, AP-HP, Paris, France.
  • Manna F; Department of Dermatology, L'Archet 2 Hospital, Nice, France.
  • Baumann C; University of Nice, Nice, France.
  • Best M; Department of Paediatric Dermatology, Pellegrin University Hospital of Bordeaux, Bordeaux, France.
  • Blanchet P; Department of Clinical Genetics, Sud Hospital, Rennes, France.
  • Bursztejn AC; University Hospital of Rennes, Rennes, France.
  • Capri Y; University of Montpellier, Montpellier, France.
  • Coubes C; Department of Medical Information, Epidemiological and Clinical Research Unit, La Colombière Hospital, Montpellier, France.
  • Giuliano F; Department of Clinical Genetics, Robert-Debré Hospital, AP-HP, Paris, France.
  • Guillaumont S; University of Paris-Diderot, Paris, France.
  • Hadj-Rabia S; Department of Dermatology, Saint-Eloi Hospital, Competence Centre for Rare Skin Diseases, Montpellier, France.
  • Jacquemont ML; University of Montpellier, Montpellier, France.
  • Jeandel C; Department of Clinical Genetics, Arnaud de Villeneuve Hospital, Montpellier, France.
  • Lacombe D; Department of Dermatology, Brabois Hospital, Nancy, France.
  • Mallet S; University of Nancy, Nancy, France.
  • Mazereeuw-Hautier J; Department of Clinical Genetics, Robert-Debré Hospital, AP-HP, Paris, France.
  • Molinari N; University of Paris-Diderot, Paris, France.
  • Pallure V; Department of Clinical Genetics, Arnaud de Villeneuve Hospital, Montpellier, France.
  • Pernet C; University of Nice, Nice, France.
  • Philip N; Department of Clinical Genetics, L'Archet 2 Hospital, Nice, France.
  • Pinson L; University of Montpellier, Montpellier, France.
  • Sarda P; Department of Paediatric Cardiology, Arnaud de Villeneuve Hospital, Montpellier, France.
  • Sigaudy S; Department of Paediatric Dermatology, Reference Centre for Rare Skin Diseases, Necker-Enfants Malades Hospital, AP-HP, Paris, France.
  • Vial Y; Department of Clinical Genetics, Femme-Mère-Enfant Hospital, University of South Réunion, Saint-Pierre Réunion, France.
  • Willems M; University of Montpellier, Montpellier, France.
  • Geneviève D; Department of Paediatric Endocrinology, Arnaud de Villeneuve Hospital, Montpellier, France.
  • Verloes A; Department of Clinical Genetics, Pellegrin University Hospital of Bordeaux, AP-HP, Paris, France.
  • Cavé H; Department of Dermatology, La Timone Hospital, AP-HM, Marseille, France.
Br J Dermatol ; 180(6): 1438-1448, 2019 06.
Article in En | MEDLINE | ID: mdl-30417923
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Diseases / Protein Tyrosine Phosphatase, Non-Receptor Type 11 / Genetic Association Studies / Noonan Syndrome Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: Br J Dermatol Year: 2019 Document type: Article Affiliation country: Francia Country of publication: Reino Unido
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skin Diseases / Protein Tyrosine Phosphatase, Non-Receptor Type 11 / Genetic Association Studies / Noonan Syndrome Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: Br J Dermatol Year: 2019 Document type: Article Affiliation country: Francia Country of publication: Reino Unido