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Dermatologic manifestations in paediatric neurofibromatosis type 2: a cross sectional descriptive multicentric study.
Legoupil, S; Bessis, D; Picard, F; Mallet, S; Mazereeuw, J; Phan, A; Dupin-Deguine, D; Kalamarides, M; Chiaverini, C.
Afiliação
  • Legoupil S; Department of Dermatology, CRMRP-Sud, ARCHET 2 Hospital, CHU de Nice, 151 route st Antoine de Ginestière, 06200, Nice, France.
  • Bessis D; Department of Pediatrics, CHU de Nice, Fondation Lenval, Nice, France.
  • Picard F; Department of Dermatology, CHU de Montpellier, Montpellier, France.
  • Mallet S; Department of Dermatology, CHU de Bordeaux, Bordeaux, France.
  • Mazereeuw J; Department of Dermatology, APHM, Timone Enfant de Marseille, Marseille, France.
  • Phan A; Department of Dermatology, CHU de Toulouse, Toulouse, France.
  • Dupin-Deguine D; Department of Pediatric Dermatology, Hospices Civils de Lyon, Lyon, France.
  • Kalamarides M; Department of ENT, CHU de Toulouse, Toulouse, France.
  • Chiaverini C; CNR-NF2, APHP, Pitié-Salpêtrière, Paris, France.
Orphanet J Rare Dis ; 17(1): 242, 2022 06 21.
Article em En | MEDLINE | ID: mdl-35729665
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neurofibromatose 2 / Neurofibromatose 1 / Doenças do Sistema Nervoso / Neurilemoma Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies / Screening_studies Limite: Adolescent / Child / Humans Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neurofibromatose 2 / Neurofibromatose 1 / Doenças do Sistema Nervoso / Neurilemoma Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies / Screening_studies Limite: Adolescent / Child / Humans Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2022 Tipo de documento: Article