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Congenital myotonia: a review of twenty cases and a new splice-site mutation in the CLCN1 gene.
Turk J Pediatr. 2020;62(3):450-460. doi: 10.24953/turkjped.2020.03.012.
Turk J Pediatr. 2020.
PMID: 32558419
Free article.
Review.
Ophthalmic, systemic, and genetic characteristics of patients with Wolfram syndrome.
Ustaoglu M, Onder F, Karapapak M, Taslidere H, Guven D.
Ustaoglu M, et al. Among authors: taslidere h.
Eur J Ophthalmol. 2020 Sep;30(5):1099-1105. doi: 10.1177/1120672119842489. Epub 2019 Apr 7.
Eur J Ophthalmol. 2020.
PMID: 30957632
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The relationship between ACTN3 R577X gene polymorphism and physical performance in amateur soccer players and sedentary individuals.
Koku FE, Karamızrak SO, Çiftçi AS, Taşlıdere H, Durmaz B, Çoğulu Ö.
Koku FE, et al. Among authors: taslidere h.
Biol Sport. 2019 Mar;36(1):9-16. doi: 10.5114/biolsport.2018.78900. Epub 2018 Oct 5.
Biol Sport. 2019.
PMID: 30899134
Free PMC article.
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Determination of Lymphocyte Cytokinesis-Block Micronucleus Values in Apparently Healthy Children by means of Age and Sex.
Durmaz B, Taslidere H, Koturoglu G, Gunduz C, Orman M, Cogulu O.
Durmaz B, et al. Among authors: taslidere h.
Biomed Res Int. 2019 Dec 25;2019:8729561. doi: 10.1155/2019/8729561. eCollection 2019.
Biomed Res Int. 2019.
PMID: 31950057
Free PMC article.
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Investigation of miRNA and cytokine expressions in latent tuberculosis infection and active tuberculosis.
Çavuşoğlu C, Çoğulu Ö, Durmaz A, Cengisiz Z, Yılmaz FF, Taşbakan MS, Taşbakan M, Gündüz C, Biçmen C, Karaman O, Taşlıdere H, Akın H, Akarca T, Dereli Ş.
Çavuşoğlu C, et al. Among authors: taslidere h.
Turk J Med Sci. 2022 Jun;52(3):649-657. doi: 10.55730/1300-0144.5357. Epub 2022 Jun 16.
Turk J Med Sci. 2022.
PMID: 36326316
Free PMC article.
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