Kotan, D., İskender, C., Özoğuz Erimiş, A., Başak, A.N., 'A Turkish Family with a Familial ALS-positive UBQLN2-S3401 Mutation', Archives of Neuropsychiatry, 53, 3, 283-285, 2016. Dil Türkçe
Genç, G., Apaydın, H., Gündüz, A., Poyraz, Ç., Oğuz, S., Yağcı, S., Canaz, H., Aydın, S., Gündoğdu-Eken, A., Başak, A.N., Ertan, S., 'Successful Treatment of Juvenile Parkinsonism with Bilateral Subthalamic Deep Brain Stimulation in a 14-year-old Patient with Parkin Gene Mutation', Parkinsonism & Related Disorders, 24, 137-138, 2016. Dil Türkçe
Erol, A.M., Kılıç, A.K., Çelik, A., Çelik, C., Başak, A.N, 'Brait-Fahn-Schwarz disease: Parkinson's Disease and Amyotrophic Lateral Sclerosis Complex', ACTA Neurologica Belgica, 116, 3, 401-403, 2016. Dil Türkçe
Furman, A., Çoraman, E., Bilgin, R.,”Bats and tourism: A response to Paksuz & Özkan”, Oryx, 46, 3, 330-330, 2012. Dil Türkçe
Deymeer, F., Matur, Z., Poyraz, M., Battaloğlu, E., Oflazer-Serdaroğlu, P., Parman, Y., “Nerve conduction studies in Charcot-Marie-Tooth disease in a cohort from Turkey reply”, Muscle & Nerve, 46, 2, 296-296, 2012. Dil Türkçe
Tüysüz, B., Tolun, A., Yıldırım, Y., “Response to kouwenberg Et Al. recognizable phenotype with common occurrence of microcephaly, psychomotor retardation, but no spontaneous bone fractures in ARCL2B due to PYCR1 mutations”, American Journal of Medical Genetics Part A, 155A, 9, 2333-2334, 2011 Dil Türkçe
Tüysüz, B., Tolun, A., Yıldırım, Y., “Response to Kouwenberg et al. ~Recognizable phenotype with common occurrence of microcephaly, psychomotor retardation, but no spontaneous bone fractures in arcl2b due to pycr1 mutations~”, American Journal of Medical Genetics Part A, 155A, 9, 2333-2334, 2011. Dil Türkçe
Berber, E., Rimoldi, V., Usluer, S., Aksu, S., Pekçelen, Y., Çağlayan, S.H., Duga, S., “Characterization of the genetic basis of FXI deficiency in two Turkish patients”, Haemophilia, 16, 3, 564-566, 2010. Dil Türkçe
Parman, Y., Çiftçi, F., Poyraz, M., Halefoğlu, A.M., Öge, A.E., Eraksoy, M., Saruhan-Direskeneli, G., Deymeer, F., Battaloğlu, E., “X Linked Charcot Marie Tooth Disease and Multiple Sclerosis”, Journal of Neurology, 254, 7, 953-955, 2007. Dil Türkçe
