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ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome.
Cagdas D, Gur Cetinkaya P, Karaatmaca B, Esenboga S, Tan C, Yılmaz T, Gümüş E, Barış S, Kuşkonmaz B, Ozgur TT, Bali P, Santisteban I, Orhan D, Yüce A, Cetinkaya D, Boztug K, Hershfield M, Sanal O, Tezcan İ. Cagdas D, et al. Among authors: Ozgur TT. J Clin Immunol. 2018 May;38(4):484-493. doi: 10.1007/s10875-018-0496-9. Epub 2018 May 9. J Clin Immunol. 2018. PMID: 29744787
Hereditary C1q deficiency: a new family with C1qA deficiency.
Sun-Tan C, Ozgür TT, Kilinç G, Topaloğlu R, Gököz O, Ersoy-Evans S, Sanal O. Sun-Tan C, et al. Turk J Pediatr. 2010 Mar-Apr;52(2):184-6. Turk J Pediatr. 2010. PMID: 20560256
Additional diverse findings expand the clinical presentation of DOCK8 deficiency.
Sanal O, Jing H, Ozgur T, Ayvaz D, Strauss-Albee DM, Ersoy-Evans S, Tezcan I, Turkkani G, Matthews HF, Haliloglu G, Yuce A, Yalcin B, Gokoz O, Oguz KK, Su HC. Sanal O, et al. J Clin Immunol. 2012 Aug;32(4):698-708. doi: 10.1007/s10875-012-9664-5. Epub 2012 Apr 4. J Clin Immunol. 2012. PMID: 22476911 Free PMC article.
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