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

Year Number of Results
2010 1
2011 1
2013 1
2014 2
2015 3
2016 1
2017 5
2018 7
2019 11
2020 7
2021 3
2022 2
2023 1
2024 3

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39 results

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Page 1
Experiences in the molecular genetic and histopathological evaluation of calpainopathies.
Ozyilmaz B, Kirbiyik O, Ozdemir TR, Ozer OK, Kutbay YB, Erdogan KM, Guvenc MS, Arıkan Ş, Turk TS, Kale MY, Uludag IF, Baydan F, Sertpoyraz F, Gencpinar P, Diniz G. Ozyilmaz B, et al. Among authors: ozdemir tr. Neurogenetics. 2022 Apr;23(2):103-114. doi: 10.1007/s10048-022-00687-4. Epub 2022 Feb 14. Neurogenetics. 2022. PMID: 35157181
Immunodeficiency in a Child with Alström Syndrome.
Ozdemir TR, Karaca NE, Marshall JD, Kutukculer N, Aksu G, Ozgul RK, Ozanturk A, Isik E, Akgun B, Ozdemir HH, Darcan S, Ozkinay F, Cogulu O. Ozdemir TR, et al. Indian J Pediatr. 2018 Oct;85(10):924-926. doi: 10.1007/s12098-018-2740-y. Epub 2018 Aug 28. Indian J Pediatr. 2018. PMID: 30155784 No abstract available.
The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey.
Ozantürk A, Marshall JD, Collin GB, Düzenli S, Marshall RP, Candan Ş, Tos T, Esen İ, Taşkesen M, Çayır A, Öztürk Ş, Üstün İ, Ataman E, Karaca E, Özdemir TR, Erol İ, Eroğlu FK, Torun D, Parıltay E, Yılmaz-Güleç E, Karaca E, Atabek ME, Elçioğlu N, Satman İ, Möller C, Muller J, Naggert JK, Özgül RK. Ozantürk A, et al. Among authors: ozdemir tr. J Hum Genet. 2015 Jan;60(1):1-9. doi: 10.1038/jhg.2014.85. Epub 2014 Oct 9. J Hum Genet. 2015. PMID: 25296579 Free PMC article. Review.
QF-PCR in invasive prenatal diagnosis: a single-center experience in Turkey.
Özer Kaya Ö, Koç A, Özdemir TR, Kirbiyik Ö, Özyilmaz B, Özeren M, Öztekin DC, Taner CE, Kutbay YB. Özer Kaya Ö, et al. Among authors: ozdemir tr. Turk J Med Sci. 2017 Feb 27;47(1):142-147. doi: 10.3906/sag-1511-157. Turk J Med Sci. 2017. PMID: 28263482 Free article.
Fetal HLA-G alleles and their effect on miscarriage.
Koc A, Kirbiyik O, Kutbay YB, Ozyilmaz B, Ozdemir TR, Kaya OO, Kubat G, Koc ZP. Koc A, et al. Among authors: ozdemir tr. Adv Clin Exp Med. 2018 Sep;27(9):1233-1237. doi: 10.17219/acem/69692. Adv Clin Exp Med. 2018. PMID: 29809322 Free article.
Topiramate-Responsive Tremor in a Novel Pathogenic Variant of SPG15 Patient.
Ersen A, Gençpınar P, Arıcan P, Bozkaya Yılmaz S, Aliyeva N, Özdemir TR, Öztekin Ö, Olgaç Dündar N. Ersen A, et al. Among authors: ozdemir tr. Clin Neuropharmacol. 2020 Jul/Aug;43(4):121-122. doi: 10.1097/WNF.0000000000000392. Clin Neuropharmacol. 2020. PMID: 32501858
First-Line Molecular Genetic Evaluation of Autosomal Recessive Non-Syndromic Hearing Loss.
Özyılmaz B, Mercan GC, Kırbıyık Ö, Özdemir TR, Özkara S, Kaya ÖÖ, Kutbay YB, Erdoğan KM, Güvenç MS, Koç A. Özyılmaz B, et al. Among authors: ozdemir tr. Turk Arch Otorhinolaryngol. 2019 Sep;57(3):140-148. doi: 10.5152/tao.2019.4320. Epub 2019 Sep 1. Turk Arch Otorhinolaryngol. 2019. PMID: 31620696 Free PMC article.
39 results