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

Year Number of Results
1996 3
1997 1
1998 2
2002 2
2003 2
2004 4
2005 1
2007 1
2008 1
2009 3
2010 1
2011 4
2012 4
2013 3
2014 3
2015 4
2016 3
2017 8
2018 11
2019 15
2020 15
2021 16
2022 13
2023 11
2024 4

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114 results

Results by year

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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.
[Autologous osteochondral transplantation].
Taşkiran E, Ozçelik C. Taşkiran E, et al. Acta Orthop Traumatol Turc. 2007;41 Suppl 2:70-8. Acta Orthop Traumatol Turc. 2007. PMID: 18180587 Free article. Review. Turkish.
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.
A Tribute to Dr. Freddie H. Fu: Remembering A "Good Friend".
Demirhan M, Taşkıran E, Kılıçoğlu Ö, Pınar H. Demirhan M, et al. Among authors: taskiran e. Acta Orthop Traumatol Turc. 2021 Sep;55(5):371-373. doi: 10.5152/j.aott.2021.05.16. Acta Orthop Traumatol Turc. 2021. PMID: 34744031 No abstract available.
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
114 results