Baydan F - Search Results

1

Clinical and genetic characterization of PYROXD1-related myopathy patients from Turkey.

Daimagüler HS, Akpulat U, Özdemir Ö, Yis U, Güngör S, Talim B, Diniz G, Baydan F, Thiele H, Altmüller J, Nürnberg P, Cirak S. Daimagüler HS, et al. Among authors: baydan f. Am J Med Genet A. 2021 Jun;185(6):1678-1690. doi: 10.1002/ajmg.a.62148. Epub 2021 Mar 10. Am J Med Genet A. 2021. PMID: 33694278

2

Importance of Skin Changes in the Differential Diagnosis of Congenital Muscular Dystrophies.

Yis U, Baydan F, Karakaya M, Hız Kurul S, Cirak S. Yis U, et al. Among authors: baydan f. Biomed Res Int. 2016;2016:3128735. doi: 10.1155/2016/3128735. Epub 2016 Mar 31. Biomed Res Int. 2016. PMID: 27123443 Free PMC article.

3

Occipital cortex dysgenesis with white matter changes due to mutations in Laminin a2.

Yiş U, Dixit V, Işıkay S, Karakaya M, Baydan F, Diniz G, Polat İ, Hız-Kurul S, Çırak S. Yiş U, et al. Among authors: baydan f. Turk J Pediatr. 2017;59(3):338-341. doi: 10.24953/turkjped.2017.03.018. Turk J Pediatr. 2017. PMID: 29376585 Free article.

4

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.

5

Impact of next-generation sequencing panels in the evaluation of limb-girdle muscular dystrophies.

Özyilmaz B, Kirbiyik Ö, Özdemir TR, Kaya Özer Ö, Kutbay YB, Erdogan KM, Güvenç MS, Kale MY, Gazeteci H, Kiliç B, Sertpoyraz F, Diniz G, Baydan F, Gençpinar P, Dündar NO, Yiş U. Özyilmaz B, et al. Among authors: baydan f. Ann Hum Genet. 2019 Sep;83(5):331-347. doi: 10.1111/ahg.12319. Epub 2019 May 7. Ann Hum Genet. 2019. PMID: 31066050

6

Dihydropyridine Receptor Congenital Myopathy In A Consangineous Turkish Family.

Yiş U, Hiz S, Güneş S, Diniz G, Baydan F, Töpf A, Sonmezler E, Lochmüller H, Horvath R, Oktay Y. Yiş U, et al. Among authors: baydan f. J Neuromuscul Dis. 2019;6(3):377-384. doi: 10.3233/JND-190383. J Neuromuscul Dis. 2019. PMID: 31227654 Free PMC article.

7

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

8

Nonketotic hyperglycinemia: novel mutation in the aminomethyl transferase gene. Case report.

Gencpinar P, Çavuşoğlu D, Özbeyler Ö, Kaya ÖÖ, Baydan F, Olgac Dundar N. Gencpinar P, et al. Among authors: baydan f. Arch Argent Pediatr. 2016 Jun 1;114(3):e142-6. doi: 10.5546/aap.2016.eng.e142. Epub 2016 Jun 1. Arch Argent Pediatr. 2016. PMID: 27164344 Free article. English, Spanish.

9

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.

10

Patients with cerebrotendinous xanthomatosis diagnosed with diverse multisystem involvement.

Kısa PT, Yildirim GK, Hismi BO, Dorum S, Kusbeci OY, Topak A, Baydan F, Celik FND, Gorukmez O, Gulten ZA, Ekici A, Ozkan S, Yaman A, Arslan N. Kısa PT, et al. Among authors: baydan f. Metab Brain Dis. 2021 Aug;36(6):1201-1211. doi: 10.1007/s11011-021-00714-7. Epub 2021 Mar 11. Metab Brain Dis. 2021. PMID: 33704661

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