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Leukodystrophy with disorders of sex development due to WT1 mutations.
Souza, Paulo Victor Sgobbi; Badia, Bruno Mattos Lombardi; Silva, Luiz Henrique Libardi; Teixeira, Carlos Alberto Castro; Seneor, Daniel Delgado; Marin, Vitor Dias Gomes Barrios; Farias, Igor Braga; Dias, Renan Braido; Oliveira, Acary Souza Bulle; Pinto, Wladimir Bocca Vieira Rezende.
Affiliation
  • Souza PVS; Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil. Electronic address: paulo.sgobbi@unifesp.br.
  • Badia BML; Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
  • Silva LHL; Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
  • Teixeira CAC; Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
  • Seneor DD; Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
  • Marin VDGB; Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
  • Farias IB; Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
  • Dias RB; Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
  • Oliveira ASB; Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
  • Pinto WBVR; Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil.
J Neurol Sci ; 390: 94-98, 2018 07 15.
Article de En | MEDLINE | ID: mdl-29801916
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Troubles du développement sexuel / Maladies démyélinisantes héréditaires du système nerveux central / Protéines WT1 / Mutation Type d'étude: Diagnostic_studies Limites: Adolescent / Adult / Female / Humans / Male Langue: En Journal: J Neurol Sci Année: 2018 Type de document: Article
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Troubles du développement sexuel / Maladies démyélinisantes héréditaires du système nerveux central / Protéines WT1 / Mutation Type d'étude: Diagnostic_studies Limites: Adolescent / Adult / Female / Humans / Male Langue: En Journal: J Neurol Sci Année: 2018 Type de document: Article