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Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene.
Garaci, Francesco; Marsili, Luisa; Riant, Florence; Marziali, Simone; Cécillon, Michaelle; Pasquarelli, Roberto; Sangiuolo, Federica; Floris, Roberto; Novelli, Giuseppe; Tournier-Lasserve, Elisabeth; Brancati, Francesco.
Afiliação
  • Garaci F; Department of Diagnostic Imaging, Molecular Imaging, Interventional Radiology and Radiotherapy, Policlinico Tor Vergata University Hospital, Italy Department of Biomedicine and Prevention, Tor Vergata University, Italy.
  • Marsili L; Medical Genetics Unit, Policlinico Tor Vergata University Hospital, Italy Department of Biomedicine and Prevention, Tor Vergata University, Italy.
  • Riant F; Service de Génétique Moléculaire Neurovasculaire, Centre de Référence des Maladies Vasculaires Rares du Cerveau et de l'Oeil (CERVCO), France Génétique des Maladies Vasculaires UMR-S1161, Université Paris Diderot, France.
  • Marziali S; Department of Diagnostic Imaging, Molecular Imaging, Interventional Radiology and Radiotherapy, Policlinico Tor Vergata University Hospital, Italy.
  • Cécillon M; Service de Génétique Moléculaire Neurovasculaire, Centre de Référence des Maladies Vasculaires Rares du Cerveau et de l'Oeil (CERVCO), France.
  • Pasquarelli R; Department of Biomedicine and Prevention, Tor Vergata University, Italy.
  • Sangiuolo F; Medical Genetics Unit, Policlinico Tor Vergata University Hospital, Italy Department of Biomedicine and Prevention, Tor Vergata University, Italy.
  • Floris R; Department of Diagnostic Imaging, Molecular Imaging, Interventional Radiology and Radiotherapy, Policlinico Tor Vergata University Hospital, Italy Department of Biomedicine and Prevention, Tor Vergata University, Italy.
  • Novelli G; Medical Genetics Unit, Policlinico Tor Vergata University Hospital, Italy Department of Biomedicine and Prevention, Tor Vergata University, Italy.
  • Tournier-Lasserve E; Service de Génétique Moléculaire Neurovasculaire, Centre de Référence des Maladies Vasculaires Rares du Cerveau et de l'Oeil (CERVCO), France Génétique des Maladies Vasculaires UMR-S1161, Université Paris Diderot, France.
  • Brancati F; Medical Genetics Unit, Policlinico Tor Vergata University Hospital, Italy Department of Medical, Oral and Biotechnological Sciences, Gabriele D'Annunzio University, Italy f.brancati@igenetica.com.
Neuroradiol J ; 28(3): 289-93, 2015 Jun.
Article em En | MEDLINE | ID: mdl-26246098
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Proto-Oncogênicas / Neoplasias do Sistema Nervoso Central / Hemangioma Cavernoso do Sistema Nervoso Central / Proteínas Reguladoras de Apoptose / Proteínas de Membrana / Meningioma / Neoplasias Primárias Múltiplas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
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XML
PubMed Links
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Proto-Oncogênicas / Neoplasias do Sistema Nervoso Central / Hemangioma Cavernoso do Sistema Nervoso Central / Proteínas Reguladoras de Apoptose / Proteínas de Membrana / Meningioma / Neoplasias Primárias Múltiplas Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article