Yildiran A - Search Results

1

Could familial Mediterranean fever gene mutations be related to PFAPA syndrome?

Celiksoy MH, Ogur G, Yaman E, Abur U, Fazla S, Sancak R, Yildiran A. Celiksoy MH, et al. Among authors: yildiran a. Pediatr Allergy Immunol. 2016 Feb;27(1):78-82. doi: 10.1111/pai.12490. Epub 2015 Oct 20. Pediatr Allergy Immunol. 2016. PMID: 26360812

2

Haemoperfusion may be useful in phenprobamate and polypharmacy intoxication of paediatric patients.

Tasdemir HA, Yildiran A, Islek I, Sancak R, Dilber C. Tasdemir HA, et al. Among authors: yildiran a. Nephrol Dial Transplant. 2002 May;17(5):941. doi: 10.1093/ndt/17.5.941. Nephrol Dial Transplant. 2002. PMID: 11981094 No abstract available.

3

Hemophagocytic bone marrow aplasia with plasma cells in a RAG2-deficient SCID case after a nonconditioned transplantation from a fully matched sibling.

Yildiran A, Fişgin T, Güner SN, Kiliç M, Sancak R, Özyürek E, Albayrak D, Duru F. Yildiran A, et al. J Pediatr Hematol Oncol. 2013 Nov;35(8):e335-7. doi: 10.1097/MPH.0b013e31827e8448. J Pediatr Hematol Oncol. 2013. PMID: 23389499

4

Pulmonary hypoplasia presenting with recurrent wheezing in an infant.

Çeliksoy MH, Tander B, Aşılıoğlu N, Barış YS, Yıldıran A. Çeliksoy MH, et al. Among authors: yildiran a. Clin Respir J. 2015 Oct;9(4):497-500. doi: 10.1111/crj.12158. Epub 2014 May 27. Clin Respir J. 2015. PMID: 24798948

5

Novel NLRP12 mutations associated with intestinal amyloidosis in a patient diagnosed with common variable immunodeficiency.

Borte S, Celiksoy MH, Menzel V, Ozkaya O, Ozen FZ, Hammarström L, Yildiran A. Borte S, et al. Among authors: yildiran a. Clin Immunol. 2014 Oct;154(2):105-11. doi: 10.1016/j.clim.2014.07.003. Epub 2014 Jul 23. Clin Immunol. 2014. PMID: 25064839

6

Comparison of major lymphocyte subpopulations and recent thymic emigrants in patients with ataxia telangiectasia and age-matched healthy groups.

Celiksoy MH, Topal E, Yıldıran A. Celiksoy MH, et al. Among authors: yildiran a. Allergol Immunopathol (Madr). 2015 Sep-Oct;43(5):477-81. doi: 10.1016/j.aller.2014.06.007. Epub 2014 Nov 8. Allergol Immunopathol (Madr). 2015. PMID: 25456532

7

c.761C>T Mutation Linked Hyper IgM Syndrome Presenting with Hypertransaminasemia and Arthritis.

Celiksoy MH, Borte S, İkincioğulları A, Bilgici MC, Karagöz F, Kalaycı AG, Yıldıran A. Celiksoy MH, et al. Among authors: yildiran a. Turk J Haematol. 2014 Dec 5;31(4):420-1. doi: 10.4274/tjh.2014.0081. Turk J Haematol. 2014. PMID: 25541662 Free PMC article. No abstract available.

8

A comparison of B cell subsets in primary immune deficiencies that progress with antibody deficiency and age-matched healthy children.

Celiksoy MH, Yildiran A. Celiksoy MH, et al. Among authors: yildiran a. Allergol Immunopathol (Madr). 2016 Jul-Aug;44(4):331-40. doi: 10.1016/j.aller.2015.11.003. Epub 2016 Mar 11. Allergol Immunopathol (Madr). 2016. PMID: 26976550

9

Vesicourethral reflux-induced renal failure in a patient with ICF syndrome due to a novel DNMT3B mutation.

Kutluğ S, Ogur G, Yilmaz A, Thijssen PE, Abur U, Yildiran A. Kutluğ S, et al. Among authors: yildiran a. Am J Med Genet A. 2016 Dec;170(12):3253-3257. doi: 10.1002/ajmg.a.37866. Epub 2016 Sep 8. Am J Med Genet A. 2016. PMID: 27604394

10

The role of active B cells in allergen immunotherapy.

Celiksoy MH, Sancak R, Yildiran A. Celiksoy MH, et al. Among authors: yildiran a. Allergol Immunopathol (Madr). 2017 Sep-Oct;45(5):439-444. doi: 10.1016/j.aller.2016.10.017. Epub 2017 Feb 21. Allergol Immunopathol (Madr). 2017. PMID: 28236542

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