Altintas DU - Search Results

1

Hemophagocytic lymphohistiocytosis in children with Griscelli syndrome type 2: genetics, laboratory findings and treatment.

Cay E, Sezer A, Karakulak V, Serbes M, Ozcan D, Bisgin A, Aygunes U, Sasmaz HI, Yucel SP, Toyran T, Altintas DU. Cay E, et al. Among authors: altintas du. Am J Clin Exp Immunol. 2023 Dec 15;12(6):140-152. eCollection 2023. Am J Clin Exp Immunol. 2023. PMID: 38187365 Free PMC article.

2

Congenital mastocytosis associated with neurosensory deafness.

Ina A, Altintaş DU, Yilmaz M, Uğuz A, Tuncer U, Kiroğlu M, Hergüner O, Bicakci K. Ina A, et al. Among authors: altintas du. Pediatr Dermatol. 2007 Jul-Aug;24(4):460-2. doi: 10.1111/j.1525-1470.2007.00489.x. Pediatr Dermatol. 2007. PMID: 17845199 No abstract available.

3

Clinical phenotypes of childhood food allergies based on immune mechanisms: A multicenter study.

Bingol A, Uygun DFK, Akdemir M, Erengin H, Buyuktiryaki B, Sackesen C, Bingol G, Orhan F, Sekerel BE, Arikoglu T, Altintas DU. Bingol A, et al. Among authors: altintas du. Allergy Asthma Proc. 2021 May 1;42(3):e86-e95. doi: 10.2500/aap.2021.42.210005. Allergy Asthma Proc. 2021. PMID: 33980344

4

Squamous Cell Carcinoma With Hyper-IgE Syndrome: A Case Report.

Sasihuseyinoglu AS, Yilmaz M, Altintaş DU, Dogruel D, Serbes M, Uğuz AH, Kiroğlu M. Sasihuseyinoglu AS, et al. Among authors: altintas du. J Pediatr Hematol Oncol. 2018 Aug;40(6):e380-e382. doi: 10.1097/MPH.0000000000000954. J Pediatr Hematol Oncol. 2018. PMID: 28902078

5

A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis.

Kisla Ekinci RM, Balci S, Bisgin A, Altintas DU, Yilmaz M. Kisla Ekinci RM, et al. Among authors: altintas du. Eur J Med Genet. 2017 Dec;60(12):690-694. doi: 10.1016/j.ejmg.2017.09.004. Epub 2017 Sep 13. Eur J Med Genet. 2017. PMID: 28919362

6

Decreased serum vitamin B₁₂ and vitamin D levels affect sleep quality in children with familial Mediterranean fever.

Ekinci RMK, Balci S, Serbes M, Dogruel D, Altintas DU, Yilmaz M. Ekinci RMK, et al. Among authors: altintas du. Rheumatol Int. 2018 Jan;38(1):83-87. doi: 10.1007/s00296-017-3883-2. Epub 2017 Nov 15. Rheumatol Int. 2018. PMID: 29143127

7

The Utility of Next-Generation Sequencing for Primary Immunodeficiency Disorders: Experience from a Clinical Diagnostic Laboratory.

Bisgin A, Boga I, Yilmaz M, Bingol G, Altintas D. Bisgin A, et al. Biomed Res Int. 2018 May 16;2018:9647253. doi: 10.1155/2018/9647253. eCollection 2018. Biomed Res Int. 2018. PMID: 29888287 Free PMC article.

8

Evaluation of high resolution computed tomography findings of cystic fibrosis.

Sasihuseyinoglu AS, Altıntaş DU, Soyupak S, Dogruel D, Yılmaz M, Serbes M, Duyuler G. Sasihuseyinoglu AS, et al. Among authors: altintas du. Korean J Intern Med. 2019 Mar;34(2):335-343. doi: 10.3904/kjim.2017.287. Epub 2018 Jul 6. Korean J Intern Med. 2019. PMID: 29976036 Free PMC article.

9

Clinical and genetic profiles of patients with X-linked agammaglobulinemia from southeast Turkey: Novel mutations in BTK gene.

Doğruel D, Serbes M, Şaşihüseyinoğlu AŞ, Yılmaz M, Altıntaş DU, Bişgin A. Doğruel D, et al. Among authors: altintas du. Allergol Immunopathol (Madr). 2019 Jan-Feb;47(1):24-31. doi: 10.1016/j.aller.2018.03.004. Epub 2018 Jul 30. Allergol Immunopathol (Madr). 2019. PMID: 30072168

10

MEFV gene variants in children with Henoch-Schönlein purpura and association with clinical manifestations: a single-center Mediterranean experience.

Ekinci RMK, Balci S, Bisgin A, Atmis B, Dogruel D, Altintas DU, Yilmaz M. Ekinci RMK, et al. Among authors: altintas du. Postgrad Med. 2019 Jan;131(1):68-72. doi: 10.1080/00325481.2019.1552479. Epub 2018 Dec 12. Postgrad Med. 2019. PMID: 30513227

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