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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: baydan f. Neurogenetics. 2022 Apr;23(2):103-114. doi: 10.1007/s10048-022-00687-4. Epub 2022 Feb 14. Neurogenetics. 2022. PMID: 35157181
The relationship between scoliosis and upper extremity functions in patients with Duchenne muscular dystrophy.
Erdinç Gündüz N, Sertpoyraz FM, Dilek B, Şahin E, Baydan F, Tiftikcioglu Bİ, Keskin Pehlivan E, Dikici A, Zorlu Y, Akalın E, Peker Ö. Erdinç Gündüz N, et al. Among authors: baydan f. Turk J Phys Med Rehabil. 2021 Mar 4;67(1):41-47. doi: 10.5606/tftrd.2021.4979. eCollection 2021 Mar. Turk J Phys Med Rehabil. 2021. PMID: 33948542 Free PMC article.
Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey.
Yiş U, Diniz G, Hazan F, Daimagüler HS, Baysal BT, Baydan F, Akinci G, Ünalp A, Aktan G, Bayram E, Hiz S, Paketçi C, Okur D, Özer E, Danyeli AE, Polat M, Uyanik G, Çirak S. Yiş U, et al. Among authors: baydan f. Acta Myol. 2018 Sep 1;37(3):210-220. eCollection 2018 Sep. Acta Myol. 2018. PMID: 30838351 Free PMC article.
13 results