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

অনুযায়ী Caglayan, Ahmet Okay, Gumus, Hakan, Kato, Mitsuhiro
প্রকাশিত 2010

Intracranial hemorrhages and late hemorrhagic disease associated cholestatic liver disease

অনুযায়ী Per, Hüseyin, Arslan, Duran, Gümüş, Hakan, Çoskun, Abdulhakim, Kumandaş, Sefer
প্রকাশিত 2012

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

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

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

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

Gigantic cerebral hydatid cysts in childhood

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

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

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

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

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

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

অনুযায়ী 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
প্রকাশিত Cerebellum (2019)

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

অনুযায়ী 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
প্রকাশিত Magn Reson Med Sci (2017)

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

অনুযায়ী 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.
প্রকাশিত Ann Neurol (2018)

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

অনুযায়ী 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
প্রকাশিত Neuron (2014)