Aktuglu-Zeybek AC - Search Results

1

Hereditary Tyrosinemia Type 1 in Turkey.

Aktuglu-Zeybek AC, Kiykim E, Cansever MS. Aktuglu-Zeybek AC, et al. Adv Exp Med Biol. 2017;959:157-172. doi: 10.1007/978-3-319-55780-9_15. Adv Exp Med Biol. 2017. PMID: 28755194 Review.

2

Determination of NTBC in serum samples from patients with hereditary tyrosinemia type I by capillary electrophoresis.

Cansever MS, Aktuğlu-Zeybek AC, Erim FB. Cansever MS, et al. Talanta. 2010 Mar 15;80(5):1846-8. doi: 10.1016/j.talanta.2009.10.032. Epub 2009 Oct 24. Talanta. 2010. PMID: 20152421

3

Differences in the gut microbiota of healthy children and those with type 1 diabetes.

Soyucen E, Gulcan A, Aktuglu-Zeybek AC, Onal H, Kiykim E, Aydin A. Soyucen E, et al. Pediatr Int. 2014 Jun;56(3):336-43. doi: 10.1111/ped.12243. Epub 2014 Jan 29. Pediatr Int. 2014. PMID: 24475780

4

Screening of Free Carnitine and Acylcarnitine Status in Children With Familial Mediterranean Fever.

Kiykim E, Aktuğlu Zeybek AÇ, Barut K, Zübarioğlu T, Cansever MŞ, Alsancak Ş, Kasapçopur Ö. Kiykim E, et al. Arch Rheumatol. 2016 Mar 10;31(2):133-138. doi: 10.5606/ArchRheumatol.2016.5696. eCollection 2016 Jun. Arch Rheumatol. 2016. PMID: 29900937 Free PMC article.

5

Coagulation Disturbances in Patients with Argininemia.

Kiykim E, Zubarioglu T, Cansever MS, Celkan T, Häberle J, Aktuglu Zeybek AC. Kiykim E, et al. Acta Haematol. 2018;140(4):221-225. doi: 10.1159/000493678. Epub 2018 Oct 24. Acta Haematol. 2018. PMID: 30355940 Free article.

6

Multimodal imaging including optical coherence tomography angiography in patients with type B Niemann-Pick disease.

Bolukbasi S, Dogan C, Kiykim E, Cakir A, Erden B, Bayat AH, Elcioglu MN, Aktuglu Zeybek AC. Bolukbasi S, et al. Int Ophthalmol. 2019 Nov;39(11):2545-2552. doi: 10.1007/s10792-019-01102-y. Epub 2019 Apr 11. Int Ophthalmol. 2019. PMID: 30977024

7

Capillary electrophoresis with capacitively coupled contactless conductivity detection for the determination of urinary ethylmalonic acid for the diagnosis of ethylmalonic aciduria.

Özçelik S, Öztekin N, Kıykım E, Cansever MŞ, Aktuğlu-Zeybek AÇ. Özçelik S, et al. J Sep Sci. 2020 Apr;43(7):1365-1371. doi: 10.1002/jssc.201901044. Epub 2020 Feb 9. J Sep Sci. 2020. PMID: 31958360

8

Screening for Fabry Disease in Patients With Juvenile Systemic Lupus Erythematosus.

Kiykim E, Şahİn S, ZubarioĞlu T, Barut K, Adrovic A, Cansever MŞ, AktuĞlu Zeybek AÇ, KasapÇopur Ö. Kiykim E, et al. Arch Rheumatol. 2020 Feb 7;35(1):7-12. doi: 10.5606/ArchRheumatol.2020.7135. eCollection 2020 Mar. Arch Rheumatol. 2020. PMID: 32637914 Free PMC article.

9

Challenges of following patients with inherited metabolic diseases during the COVID-19 outbreak. A cross-sectional online survey study.

Oge Enver E, Hopurcuoglu D, Ahmadzada S, Zubarioglu T, Aktuglu Zeybek AC, Kiykim E. Oge Enver E, et al. J Pediatr Endocrinol Metab. 2020 Nov 12;34(1):103-107. doi: 10.1515/jpem-2020-0441. Print 2021 Jan 27. J Pediatr Endocrinol Metab. 2020. PMID: 33185576 Free article.

10

Reflex Decay Test Can Reveal Ear Involvement in Fabry Disease.

Kiykim E, Kaya M, Dincer MT, Bakir A, Alagoz S, Aktuglu Zeybek A, Gulcicek S, Seyahi N, Trabulus S, Atas A. Kiykim E, et al. Ear Hear. 2021 Sep/Oct;42(5):1351-1357. doi: 10.1097/AUD.0000000000001030. Ear Hear. 2021. PMID: 33758156

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