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Page 1
Rationale, design and objectives of ARegPKD, a European ARPKD registry study.
Ebner K, Feldkoetter M, Ariceta G, Bergmann C, Buettner R, Doyon A, Duzova A, Goebel H, Haffner D, Hero B, Hoppe B, Illig T, Jankauskiene A, Klopp N, König J, Litwin M, Mekahli D, Ranchin B, Sander A, Testa S, Weber LT, Wicher D, Yuzbasioglu A, Zerres K, Dötsch J, Schaefer F, Liebau MC; ESCAPE Study Group; GPN Study Group. Ebner K, et al. Among authors: yuzbasioglu a. BMC Nephrol. 2015 Feb 18;16:22. doi: 10.1186/s12882-015-0002-z. BMC Nephrol. 2015. PMID: 25886171 Free PMC article.
Chanarin-Dorfman syndrome: Genotype-Phenotype Correlation.
Nur BG, Gencpinar P, Yuzbasıoglu A, Emre SD, Mihci E. Nur BG, et al. Among authors: yuzbasioglu a. Eur J Med Genet. 2015 Apr;58(4):238-42. doi: 10.1016/j.ejmg.2015.01.011. Epub 2015 Feb 14. Eur J Med Genet. 2015. PMID: 25682902
Chanarin-dorfman syndrome with multi-system involvement in two siblings.
Arslansoyu Çamlar S, Gençpınar P, Makay B, Yüzbaşıoğlu A, Arslan N, Emre Dökmeci S, Anal O, Köse G. Arslansoyu Çamlar S, et al. Among authors: yuzbasioglu a. Turk J Haematol. 2013 Mar;30(1):72-5. doi: 10.4274/tjh.93798. Epub 2013 Mar 5. Turk J Haematol. 2013. PMID: 24385758 Free PMC article.
Genotype and phenotype evaluation of patients with primary ciliary dyskinesia: First results from Turkey.
Emiralioğlu N, Taşkıran EZ, Koşukcu C, Bilgiç E, Atilla P, Kaya B, Günaydın Ö, Yüzbaşıoğlu A, Tuğcu GD, Ademhan D, Eryılmaz Polat S, Gharibzadeh Hızal M, Yalçın E, Doğru D, Kiper N, Alikaşifoğlu M, Özçelik U. Emiralioğlu N, et al. Among authors: yuzbasioglu a. Pediatr Pulmonol. 2020 Feb;55(2):383-393. doi: 10.1002/ppul.24583. Epub 2019 Nov 25. Pediatr Pulmonol. 2020. PMID: 31765523
Novel mutations of the MLC1 gene in Turkish patients.
Yüzbaşioğlu A, Topçu M, Cetin Kocaefe Y, Ozgüç M. Yüzbaşioğlu A, et al. Eur J Med Genet. 2011 May-Jun;54(3):281-3. doi: 10.1016/j.ejmg.2010.11.014. Epub 2010 Dec 9. Eur J Med Genet. 2011. PMID: 21145992
15 results