Atıf İçin Kopyala
KASAP CÜCEOĞLU M., ŞENER S., BATU AKAL E. D., Akca U. K., Demir S., Sag E., ...Daha Fazla
SEMINARS IN ARTHRITIS AND RHEUMATISM, cilt.51, sa.3, ss.559-564, 2021 (SCI-Expanded)
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Yayın Türü:
Makale / Derleme
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Cilt numarası:
51
Sayı:
3
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Basım Tarihi:
2021
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Doi Numarası:
10.1016/j.semarthrit.2021.04.009
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Dergi Adı:
SEMINARS IN ARTHRITIS AND RHEUMATISM
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Derginin Tarandığı İndeksler:
Science Citation Index Expanded (SCI-EXPANDED), Scopus, CINAHL, EMBASE, MEDLINE
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Sayfa Sayıları:
ss.559-564
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Anahtar Kelimeler:
Polyarteritis nodosa, Deficiency of adenosine deaminase 2, Systematic review, Child, immunosuppressants, Biological therapies, Outcome measures, Vasculitis, ADENOSINE-DEAMINASE 2, PHENOTYPIC VARIABILITY, PEDIATRIC VASCULITIS, ADA2 DEFICIENCY, CASE SERIES, CHILDREN, DISEASE, MUTATIONS, GENOTYPE, CLASSIFICATION
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Eskişehir Osmangazi Üniversitesi Adresli:
Hayır
Özet
Background: Diagnosis of childhood polyarteritis nodosa (PAN) has become challenging after the definition of deficiency of adenosine deaminase 2 (DADA2). We aimed to define the differential features of pediatric PAN and DADA2 patients in our center and in the literature.