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Functional Complement Analysis Can Predict Genetic Testing Results and Long-Term Outcome in Patients With Complement Deficiencies.
Blazina, Stefan; Debeljak, Marusa; Kosnik, Mitja; Simcic, Sasa; Stopinsek, Sanja; Markelj, Gasper; Toplak, Natasa; Kopac, Peter; Zakotnik, Breda; Pokorn, Marko; Avcin, Tadej.
Afiliación
  • Blazina S; Department of Allergology, Rheumatology and Clinical Immunology, Children's Hospital Ljubljana, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Debeljak M; Department of Special Laboratory Diagnostics, Children's Hospital Ljubljana, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Kosnik M; University Clinic of Pulmonary and Allergic Diseases Golnik, Golnik, Slovenia.
  • Simcic S; Department of Internal Medicine, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • Stopinsek S; Faculty of Medicine, Institute of Microbiology and Immunology, University of Ljubljana, Ljubljana, Slovenia.
  • Markelj G; Faculty of Medicine, Institute of Microbiology and Immunology, University of Ljubljana, Ljubljana, Slovenia.
  • Toplak N; Department of Allergology, Rheumatology and Clinical Immunology, Children's Hospital Ljubljana, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Kopac P; Department of Allergology, Rheumatology and Clinical Immunology, Children's Hospital Ljubljana, University Medical Centre Ljubljana, Ljubljana, Slovenia.
  • Zakotnik B; Department of Paediatrics, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
  • Pokorn M; University Clinic of Pulmonary and Allergic Diseases Golnik, Golnik, Slovenia.
  • Avcin T; Department of Infectious Diseases, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Front Immunol ; 9: 500, 2018.
Article en En | MEDLINE | ID: mdl-29619023
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Complemento C2 / Complemento C8 / Enfermedades Genéticas Congénitas / Síndromes de Inmunodeficiencia Tipo de estudio: Prevalence_studies / Prognostic_studies Límite: Adolescent / Adult / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Front Immunol Año: 2018 Tipo del documento: Article País de afiliación: Eslovenia
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Complemento C2 / Complemento C8 / Enfermedades Genéticas Congénitas / Síndromes de Inmunodeficiencia Tipo de estudio: Prevalence_studies / Prognostic_studies Límite: Adolescent / Adult / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Front Immunol Año: 2018 Tipo del documento: Article País de afiliación: Eslovenia