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Comparison of the clinical diagnostic criteria and the results of the next-generation sequence gene panel in patients with monogenic systemic autoinflammatory diseases.
Sözeri, Betül; Demir, Ferhat; Sönmez, Hafize Emine; Karadag, Serife Gül; Demirkol, Yasemin Kendir; Dogan, Özlem Akgün; Doganay, Hamdi Levent; Ayaz, Nuray Aktay.
Affiliation
  • Sözeri B; Department of Pediatric Rheumatology, Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
  • Demir F; Department of Pediatric Rheumatology, Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey. drferhat@outlook.com.
  • Sönmez HE; Department of Pediatric Rheumatology, Kanuni Sultan Süleyman Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
  • Karadag SG; Department of Pediatric Rheumatology, Kanuni Sultan Süleyman Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
  • Demirkol YK; Department of Pediatric Genetics, Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
  • Dogan ÖA; Department of Pediatric Genetics, Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
  • Doganay HL; Genomic Laboratory (GLAB), Umraniye Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
  • Ayaz NA; Department of Pediatric Rheumatology, Kanuni Sultan Süleyman Training and Research Hospital, University of Health Sciences, Istanbul, Turkey.
Clin Rheumatol ; 40(6): 2327-2337, 2021 Jun.
Article de En | MEDLINE | ID: mdl-33165748
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Fièvre méditerranéenne familiale / Déficit en mévalonate kinase / Maladies auto-inflammatoires héréditaires / Syndromes périodiques associés à la cryopyrine Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Humans Langue: En Journal: Clin Rheumatol Année: 2021 Type de document: Article Pays d'affiliation: Turquie
Texte intégral
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XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Fièvre méditerranéenne familiale / Déficit en mévalonate kinase / Maladies auto-inflammatoires héréditaires / Syndromes périodiques associés à la cryopyrine Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Humans Langue: En Journal: Clin Rheumatol Année: 2021 Type de document: Article Pays d'affiliation: Turquie