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Hilmican Ulman

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Articles

Transient hypogammaglobulinemia of infancy and unclassified syndromic immunodeficiencies are highly common in oesophageal atresia patients

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By Deniz Caglar, Zafer Dokumcu, Hilmican Ulman, Ayşe Aygün
| Wiley Online Library Verified
CONFLICT OF INTEREST STATEMENT None. This research did not receive any specific grant from funding agencies in the public, commercial or not-for-profit sectors. REFERENCES 1, , , et al. Oesophageal atresia. Nat Rev Dis Prim. 2019; 5: 26. doi:10.1038/s41572-019-0077-0 2, , , et al. VACTERL anomalies in patients with esophageal atresia: an updated delineation of the spectrum and review of the literature. Pediatr Surg Int. 2007; 23: 309-313. doi:10.1007/s00383-007-1891-0 3, , .
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