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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
Course of IL-2-inducible T-cell kinase deficiency in a family: lymphomatoid granulomatosis, lymphoma and allogeneic bone marrow transplantation in one sibling; and death in the other.
Çağdaş D, Erman B, Hanoğlu D, Tavil B, Kuşkonmaz B, Aydın B, Akyüz C, Uçkan D, Sanal Ö, Tezcan I. Çağdaş D, et al. Bone Marrow Transplant. 2017 Jan;52(1):126-129. doi: 10.1038/bmt.2016.185. Epub 2016 Jul 25. Bone Marrow Transplant. 2017. PMID: 27454071 No abstract available.
140 results