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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2011 1
2012 3
2013 2
2014 2
2015 1
2016 1
2017 5
2018 6
2019 7
2020 10
2021 13
2022 6
2023 4
2024 2

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51 results

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Page 1
Ophthalmo-acromelic syndrome in an infant.
Ürel-Demir G, Taşkıran EZ, Akgün-Doğan Ö, Şimşek-Kiper PÖ, Utine GE. Ürel-Demir G, et al. Among authors: taskiran ez. Eur J Med Genet. 2019 Jul;62(7):103664. doi: 10.1016/j.ejmg.2019.05.003. Epub 2019 May 5. Eur J Med Genet. 2019. PMID: 31067494 Review.
Clinical and molecular evaluation of 16 patients with Rett syndrome.
Zengin-Akkuş P, Taşkıran EZ, Kabaçam S, Şimşek-Kiper PÖ, Haliloğlu G, Boduroğlu K, Utine GE. Zengin-Akkuş P, et al. Among authors: taskiran ez. Turk J Pediatr. 2018;60(1):1-9. doi: 10.24953/turkjped.2018.01.001. Turk J Pediatr. 2018. PMID: 30102473 Free article.
Neonatal ichthyosis-sclerosing cholangitis syndrome: report of a novel mutation and a review of the literature.
Demir E, Tuna Kirsaçlioğlu C, Saltik-Temizel İN, Ürel-Demir G, Karaosmanoğlu B, Taşkiran EZ, Şimşek-Kiper PÖ, Utine GE, Kuloğlu Z, Kansu A. Demir E, et al. Among authors: taskiran ez. Clin Dysmorphol. 2023 Apr 1;32(2):88-91. doi: 10.1097/MCD.0000000000000451. Epub 2023 Feb 13. Clin Dysmorphol. 2023. PMID: 36779798 Review. No abstract available.
TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasia.
Alanay Y, Ergüner B, Utine E, Haçariz O, Kiper PO, Taşkıran EZ, Perçin F, Uz E, Sağiroğlu MŞ, Yuksel B, Boduroglu K, Akarsu NA. Alanay Y, et al. Among authors: taskiran ez. Am J Med Genet A. 2014 Feb;164A(2):291-304. doi: 10.1002/ajmg.a.36248. Epub 2013 Nov 5. Am J Med Genet A. 2014. PMID: 24194475 Review.
Homozygous Missense Epithelial Cell Adhesion Molecule Variant in a Patient with Congenital Tufting Enteropathy and Literature Review.
Güvenoğlu M, Şimşek-Kiper PÖ, Koşukcu C, Taskiran EZ, Saltık-Temizel İN, Gucer S, Utine E, Boduroğlu K. Güvenoğlu M, et al. Among authors: taskiran ez. Pediatr Gastroenterol Hepatol Nutr. 2022 Nov;25(6):441-452. doi: 10.5223/pghn.2022.25.6.441. Epub 2022 Nov 2. Pediatr Gastroenterol Hepatol Nutr. 2022. PMID: 36451688 Free PMC article. Review.
HERC1 mutations in idiopathic intellectual disability.
Utine GE, Taşkıran EZ, Koşukcu C, Karaosmanoğlu B, Güleray N, Doğan ÖA, Kiper PÖ, Boduroğlu K, Alikaşifoğlu M. Utine GE, et al. Among authors: taskiran ez. Eur J Med Genet. 2017 May;60(5):279-283. doi: 10.1016/j.ejmg.2017.03.007. Epub 2017 Mar 18. Eur J Med Genet. 2017. PMID: 28323226
A lethal and rare cause of arthrogryposis: Glyt1 encephalopathy.
Daşar T, Şimşek-Kiper PÖ, Taşkıran EZ, Çağan M, Özyüncü Ö, Deren Ö, Utine GE, Güçer KŞ, Boduroğlu K. Daşar T, et al. Among authors: taskiran ez. Eur J Med Genet. 2022 Dec;65(12):104631. doi: 10.1016/j.ejmg.2022.104631. Epub 2022 Oct 3. Eur J Med Genet. 2022. PMID: 36195292
CD66b+ monocytes represent a proinflammatory myeloid subpopulation in cancer.
Horzum U, Yoyen-Ermis D, Taskiran EZ, Yilmaz KB, Hamaloglu E, Karakoc D, Esendagli G. Horzum U, et al. Among authors: taskiran ez. Cancer Immunol Immunother. 2021 Jan;70(1):75-87. doi: 10.1007/s00262-020-02656-y. Epub 2020 Jul 6. Cancer Immunol Immunother. 2021. PMID: 32632664
51 results