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

Por Caglayan, Ahmet Okay, Gumus, Hakan, Kato, Mitsuhiro
Publicado em 2010

Intracranial hemorrhages and late hemorrhagic disease associated cholestatic liver disease

Por Per, Hüseyin, Arslan, Duran, Gümüş, Hakan, Çoskun, Abdulhakim, Kumandaş, Sefer
Publicado em 2012

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

Por Bayrakli, Fatih, Canpolat, Mehmet, Per, Huseyin, Gumus, Hakan, Kumandas, Sefer, Kartal, Ugur, Balaban, Hatice
Publicado em 2014

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

Por Gül, Ülkü, Kaçar Bayram, Ayşe, Kendirci, Mustafa, Hatipoğlu, Nihal, Okdemir, Deniz, Gümüş, Hakan, Kurtoğlu, Selim
Publicado no J Clin Res Pediatr Endocrinol (2016)

Gigantic cerebral hydatid cysts in childhood

Por Per, Hüseyin, Gümüs, Hakan, Kumandas, Sefer, Tucer, Bülent, Yikilmaz, Ali, Menku, Ahmet, Coskun, Abdulhakim, Kurtsoy, Ali
Publicado no Ann Saudi Med (2007)

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

Por Narin, Figen, Atabek, Mehmet Emre, Karakukcu, Musa, Narin, Nazmi, Kurtoglu, Selim, Gumus, Hakan, Çoksevim, Bekir, Erez, Rusen
Publicado no Ann Saudi Med (2005)

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

Por Bayram, Ayşe Kaçar, Gümüş, Hakan, Arslan, Duran, Özçora, Güldemet Kaya, Kumandaş, Sefer, Karacabey, Neslihan, Canpolat, Mehmet, Per, Hüseyin
Publicado no Turk Pediatri Ars (2016)

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

Por 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
Publicado no Cerebellum (2019)

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

Por 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
Publicado no Magn Reson Med Sci (2017)

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

Por 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.
Publicado no Ann Neurol (2018)

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

Por 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
Publicado no Neuron (2014)