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

od Caglayan, Ahmet Okay, Gumus, Hakan, Kato, Mitsuhiro
Izdano 2010

Intracranial hemorrhages and late hemorrhagic disease associated cholestatic liver disease

od Per, Hüseyin, Arslan, Duran, Gümüş, Hakan, Çoskun, Abdulhakim, Kumandaş, Sefer
Izdano 2012

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

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

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

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

Gigantic cerebral hydatid cysts in childhood

od Per, Hüseyin, Gümüs, Hakan, Kumandas, Sefer, Tucer, Bülent, Yikilmaz, Ali, Menku, Ahmet, Coskun, Abdulhakim, Kurtsoy, Ali
izdano v Ann Saudi Med (2007)

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

od Narin, Figen, Atabek, Mehmet Emre, Karakukcu, Musa, Narin, Nazmi, Kurtoglu, Selim, Gumus, Hakan, Çoksevim, Bekir, Erez, Rusen
izdano v Ann Saudi Med (2005)

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

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

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

od 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
izdano v Cerebellum (2019)

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

od 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
izdano v Magn Reson Med Sci (2017)

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

od 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.
izdano v Ann Neurol (2018)

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

od 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
izdano v Neuron (2014)