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Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function.
Shahin T, Aschenbrenner D, Cagdas D, Bal SK, Conde CD, Garncarz W, Medgyesi D, Schwerd T, Karaatmaca B, Cetinkaya PG, Esenboga S, Twigg SRF, Cant A, Wilkie AOM, Tezcan I, Uhlig HH, Boztug K. Shahin T, et al. Among authors: cagdas d. Haematologica. 2019 Mar;104(3):609-621. doi: 10.3324/haematol.2018.194233. Epub 2018 Oct 11. Haematologica. 2019. PMID: 30309848 Free PMC article.
Griscelli syndrome type 3-like phenotype with MYO-5A exon-F deletion.
Yılmaz M, Çağdaş D, Grandin V, Altıntaş DU, Tezcan İ, de Saint Basile G, Sanal Ö. Yılmaz M, et al. Among authors: cagdas d. Pediatr Allergy Immunol. 2014 Dec;25(8):817-9. doi: 10.1111/pai.12285. Epub 2014 Oct 31. Pediatr Allergy Immunol. 2014. PMID: 25283056 No abstract available.
Diagnosis: Melanoderma after Hematopoietic Stem Cell Transplantation.
Ünal Ş, Tezcan İ, Güçer Ş, Boyraz MS, Çağdaş D, Uçkan Çetinkaya D. Ünal Ş, et al. Among authors: cagdas d. Turk J Haematol. 2015 Dec;32(4):378-9. doi: 10.4274/tjh.2014.0475. Epub 2015 Apr 27. Turk J Haematol. 2015. PMID: 25912830 Free PMC article. No abstract available.
Detection of parasites in children with chronic diarrhea.
Maçin S, Kaya F, Çağdaş D, Hizarcioglu-Gulsen H, Saltik-Temizel IN, Tezcan İ, Demir H, Ergüven S, Akyön Y. Maçin S, et al. Among authors: cagdas d. Pediatr Int. 2016 Jun;58(6):531-3. doi: 10.1111/ped.12959. Pediatr Int. 2016. PMID: 27322863
118 results