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Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment.
Gök V, Erdem Ş, Haliloğlu Y, Bişgin A, Belkaya S, Başaran KE, Canatan MF, Özcan A, Yılmaz E, Acıpayam C, Karakükcü M, Canatan H, Per H, Patıroğlu T, Eken A, Ünal E. Gök V, et al. Among authors: yilmaz e. Genes Immun. 2023 Feb;24(1):12-20. doi: 10.1038/s41435-022-00191-7. Epub 2022 Dec 15. Genes Immun. 2023. PMID: 36517554
X-linked severe combined immunodeficiency due to a novel mutation complicated with hemophagocytic lymphohistiocytosis and presented with invagination: A case report.
Patiroglu T, Haluk Akar H, van den Burg M, Unal E, Akyildiz BN, Tekerek NU, Yilmaz E. Patiroglu T, et al. Among authors: yilmaz e. Eur J Microbiol Immunol (Bp). 2014 Sep;4(3):174-6. doi: 10.1556/EUJMI-D-14-00019. Epub 2014 Sep 11. Eur J Microbiol Immunol (Bp). 2014. PMID: 25215194 Free PMC article.
Biliary Rhabdomyosarcoma in an Infant Male With Neurofibromatosis Type 1.
Alhashem F, Yilmaz E, Ozdemir MA, Deniz K, Yikilmaz A, Patiroglu T, Karakukcu M, Unal E. Alhashem F, et al. Among authors: yilmaz e. J Pediatr Hematol Oncol. 2019 Jan;41(1):e24-e26. doi: 10.1097/MPH.0000000000001163. J Pediatr Hematol Oncol. 2019. PMID: 29683957
Novel Mutations in RASGRP1 are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma.
Somekh I, Marquardt B, Liu Y, Rohlfs M, Hollizeck S, Karakukcu M, Unal E, Yilmaz E, Patiroglu T, Cansever M, Frizinsky S, Vishnvenska-Dai V, Rechavi E, Stauber T, Simon AJ, Lev A, Klein C, Kotlarz D, Somech R. Somekh I, et al. Among authors: yilmaz e. J Clin Immunol. 2018 Aug;38(6):699-710. doi: 10.1007/s10875-018-0533-8. Epub 2018 Jul 20. J Clin Immunol. 2018. PMID: 30030704
1,807 results