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SURF1 related Leigh syndrome: Clinical and molecular findings of 16 patients from Turkey.
Kose M, Canda E, Kagnici M, Aykut A, Adebali O, Durmaz A, Bircan A, Diniz G, Eraslan C, Kose E, Ünalp A, Yılmaz Ü, Ozyilmaz B, Özdemir TR, Atik T, Uçar SK, McFarland R, Taylor RW, Brown GK, Çoker M, Özkınay F. Kose M, et al. Among authors: diniz g. Mol Genet Metab Rep. 2020 Oct 23;25:100657. doi: 10.1016/j.ymgmr.2020.100657. eCollection 2020 Dec. Mol Genet Metab Rep. 2020. PMID: 33134083 Free PMC article.
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: diniz g. Neurogenetics. 2022 Apr;23(2):103-114. doi: 10.1007/s10048-022-00687-4. Epub 2022 Feb 14. Neurogenetics. 2022. PMID: 35157181
The relation between distant metastasis and genetic change type in stage IV lung adenocarcinoma patients at diagnosis.
Ermin S, Batum Ö, Saka Güvenç M, Diniz G, Ayrancı A, Erdoğan KM, Yücel N, Yıldırım E, Özdemir TR, Hacar AG, Güldaval F, Koç A, Aydoğdu Z, Balcı G, Özyılmaz B, Akşit Yaşar H, Özer Kaya Ö, Gayaf M, Kırbıyık Ö, Aksel N, Kutbay YB, Ursavaş TN, Karadeniz G, Polat G, Kömürcüoğlu B, Çırak AK, Yılmaz U. Ermin S, et al. Among authors: diniz g. Clin Respir J. 2021 Feb;15(2):196-202. doi: 10.1111/crj.13284. Epub 2020 Oct 12. Clin Respir J. 2021. PMID: 32981210
GNE Myopathy in Turkish Sisters with a Novel Homozygous Mutation.
Diniz G, Secil Y, Ceylaner S, Tokucoglu F, Türe S, Celebisoy M, İncesu TK, Akhan G. Diniz G, et al. Case Rep Neurol Med. 2016;2016:8647645. doi: 10.1155/2016/8647645. Epub 2016 May 19. Case Rep Neurol Med. 2016. PMID: 27298745 Free PMC article.
[Angiomyxoma: always myxoid, sometimes aggressive].
Dınız G, Temır G, Ortaç R. Dınız G, et al. Turk Patoloji Derg. 2012;28(2):162-4. doi: 10.5146/tjpath.2012.01116. Turk Patoloji Derg. 2012. PMID: 22627635 Free article. Turkish.
218 results