Two female siblings with West syndrome: Familial idiopathic West syndrome with genetic susceptibility and variable phenotypic expression

由 Caglayan, Ahmet Okay, Gumus, Hakan, Kato, Mitsuhiro
出版 2010

Intracranial hemorrhages and late hemorrhagic disease associated cholestatic liver disease

由 Per, Hüseyin, Arslan, Duran, Gümüş, Hakan, Çoskun, Abdulhakim, Kumandaş, Sefer
出版 2012

A Family with Mental Retardation, Epilepsy and Cerebellar Hypoplasia Showing Linkage to Chromosome 20p11.21-q11.23

由 Bayrakli, Fatih, Canpolat, Mehmet, Per, Huseyin, Gumus, Hakan, Kumandas, Sefer, Kartal, Ugur, Balaban, Hatice
出版 2014

Pseudotumour Cerebri Presentation in a Child Under the Gonadotropin-Releasing Hormone Agonist Treatment

由 Gül, Ülkü, Kaçar Bayram, Ayşe, Kendirci, Mustafa, Hatipoğlu, Nihal, Okdemir, Deniz, Gümüş, Hakan, Kurtoğlu, Selim
發表在 J Clin Res Pediatr Endocrinol (2016)

Gigantic cerebral hydatid cysts in childhood

由 Per, Hüseyin, Gümüs, Hakan, Kumandas, Sefer, Tucer, Bülent, Yikilmaz, Ali, Menku, Ahmet, Coskun, Abdulhakim, Kurtsoy, Ali
發表在 Ann Saudi Med (2007)

The association of plasma homocysteine levels with serum leptin and apolipoprotein B levels in childhood obesity

由 Narin, Figen, Atabek, Mehmet Emre, Karakukcu, Musa, Narin, Nazmi, Kurtoglu, Selim, Gumus, Hakan, Çoksevim, Bekir, Erez, Rusen
發表在 Ann Saudi Med (2005)

Neurological features and management of Wilson disease in children: an evaluation of 12 cases

由 Bayram, Ayşe Kaçar, Gümüş, Hakan, Arslan, Duran, Özçora, Güldemet Kaya, Kumandaş, Sefer, Karacabey, Neslihan, Canpolat, Mehmet, Per, Hüseyin
發表在 Turk Pediatri Ars (2016)

COQ4 mutation leads to childhood-onset ataxia improved by CoQ1O administration

由 Caglayan, Ahmet Okay, Gumus, Hakan, Sandford, Erin, Kubisiak, Thomas L., Ma, Qianyi, Ozel, A. Bilge, Per, Huseyin, Li, Jun Z., Shakkottai, Vikram G., Burmeister, Margit
發表在 Cerebellum (2019)

Magnetic Susceptibility Changes in the Basal Ganglia and Brain Stem of Patients with Wilson’s Disease: Evaluation with Quantitative Susceptibility Mapping

由 Doganay, Selim, Gumus, Kazim, Koc, Gonca, Bayram, Ayse Kacar, Dogan, Mehmet Sait, Arslan, Duran, Gumus, Hakan, Gorkem, Sureyya Burcu, Ciraci, Saliha, Serin, Halil Ibrahim, Coskun, Abdulhakim
發表在 Magn Reson Med Sci (2017)

Loss of protocadherin-12 leads to Diencephalic-Mesencephalic Junction Dysplasia syndrome

由 Guemez-Gamboa, Alicia, Çağlayan, Ahmet Okay, Stanley, Valentina, Gregor, Anne, Zaki, Maha, Saleem, Sahar N., Musaev, Damir, McEvoy-Venneri, Jennifer, Belandres, Denice, Akizu, Naiara, Silhavy, Jennifer L., Schroth, Jana, Rosti, Rasim Ozgur, Copeland, Brett, Lewis, Steven M., Fang, Rebecca, Issa, Mahmoud Y., Per, Huseyin, Gumus, Hakan, Bayram, Ayse Kacar, Kumandas, Sefer, Akgumus, Gozde Tugce, Erson-Omay, Emine Z., Yasuno, Katsuhito, Bilguvar, Kaya, Gali, Heimer, Pillar, Nir, Shomron, Noam, Weissglas-Volkov, Daphna, Porat, Yuval, Einhorn, Yaron, Gabriel, Stacey, Ben-Zeev, Bruria, Gunel, Murat, Gleeson, Joseph G.
發表在 Ann Neurol (2018)

MUTATIONS IN KATNB1 CAUSE COMPLEX CEREBRAL MALFORMATIONS BY DISRUPTING ASYMMETRICALLY DIVIDING NEURAL PROGENITORS

由 Mishra-Gorur, Ketu, Çağlayan, Ahmet Okay, Schaffer, Ashleigh E., Chabu, Chiswili, Henegariu, Octavian, Vonhoff, Fernando, Akgümüş, Gözde Tuğce, Nishimura, Sayoko, Han, Wenqi, Tu, Shu, Baran, Burcin, Gumus, Hakan, Dilber, Cengiz, Zaki, Maha S., Hossni, Heba AA, Rivière, Jean-Baptiste, Kayserili, Hülya, Spencer, Emily G., Rosti, Rasim O., Schroth, Jana, Per, Hüseyin, Cağlar, Caner, Cağlar, Cagri, Dölen, Duygu, Baranoski, Jacob F., Kumandaş, Sefer, Minja, Frank J., Erson-Omay, E. Zeynep, Mane, Shrikant M., Lifton, Richard P., Xu, Tian, Keshishian, Haig, Dobyns, William B, Chi, Neil C., Šestan, Nenad, Louvi, Angeliki, Bilgüvar, Kaya, Yasuno, Katsuhito, Gleeson, Joseph G., Günel, Murat
發表在 Neuron (2014)