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Invasive meningococcal disease in three siblings with hereditary deficiency of the 8(th) component of complement: evidence for the importance of an early diagnosis.
Dellepiane, Rosa Maria; Dell'Era, Laura; Pavesi, Paola; Macor, Paolo; Giordano, Mara; De Maso, Luca; Pietrogrande, Maria Cristina; Cugno, Massimo.
Afiliación
  • Dellepiane RM; Department of Pediatrics, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy. rosamaria.dellepiane@policlinico.mi.it.
  • Dell'Era L; Department of Pediatrics, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
  • Pavesi P; Department of Pediatrics, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
  • Macor P; Department of Life Sciences, University of Trieste, Trieste, Italy.
  • Giordano M; Department of Health Sciences, Laboratory of Genetics, University of Eastern Piedmont and Interdisciplinary Research Center of Autoimmune Diseases, Novara, Italy.
  • De Maso L; Department of Life Sciences, University of Trieste, Trieste, Italy.
  • Pietrogrande MC; Department of Pediatrics, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
  • Cugno M; Department of Pathophysiology and Transplantation, Internal Medicine, University of Milan, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Orphanet J Rare Dis ; 11(1): 64, 2016 05 17.
Article en En | MEDLINE | ID: mdl-27183977
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Complemento C8 / Síndromes de Inmunodeficiencia / Infecciones Meningocócicas Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Complemento C8 / Síndromes de Inmunodeficiencia / Infecciones Meningocócicas Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2016 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido