Intracranial hemorrhages and late hemorrhagic disease associated cholestatic liver disease

por Per, Hüseyin, Arslan, Duran, Gümüş, Hakan, Çoskun, Abdulhakim, Kumandaş, Sefer
Publicado 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 2014

Evaluation of Two Types of Drug Treatment with QEEG in Children with ADHD

por Aldemir, Ramazan, Demirci, Esra, Bayram, Ayşe Kaçar, Canpolat, Mehmet, Ozmen, Sevgi, Per, Hüseyin, Tokmakci, Mahmut
Publicado 2018

Gigantic cerebral hydatid cysts in childhood

por Per, Hüseyin, Gümüs, Hakan, Kumandas, Sefer, Tucer, Bülent, Yikilmaz, Ali, Menku, Ahmet, Coskun, Abdulhakim, Kurtsoy, Ali
Publicado 2007

Genetic Polymorphism of VKORC1-1639 in Children With Intracranial Hemorrhage Due to Vitamin K Deficiency

por Berber, Uğur, Özdemir, Mehmet Akif, Unal, Ekrem, Taheri, Serpil, Yildiz, Serkan, Bayramov, Keziban Korkmaz, Güler, Yunus, Per, Hüseyin
Publicado 2018

Evaluating the brainstem in children with breath-holding spells

por Ozcora, Gul Demet Kaya, Kumandas, Sefer, Sagiroglu, Ayse, Acer, Niyazi, Doganay, Selim, Yigit, Huseyin, Canpolat, Mehmet, Per, Huseyin, Gumus, Hakan
Publicado 2022

Long-Term Follow-Up of Patients with a Diagnosis of Posterior Reversible Encephalopathy Syndrome

por Canpolat, Mehmet, Demet Kaya Özçora, Gül, Poyrazoğlu, Hakan, Per, Huseyin, Çoşkun, Abdulhakim, Gümüş, Hakan, Arslan, Duran, Ünal, Ekrem, Karakükçü, Musa, Patıroğlu, Türkan, Kumandaş, Sefer
Publicado 2021

Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking

por Wang, Haicui, Kaçar Bayram, Ayşe, Sprute, Rosanne, Ozdemir, Ozkan, Cooper, Emily, Pergande, Matthias, Efthymiou, Stephanie, Nedic, Ivana, Mazaheri, Neda, Stumpfe, Katharina, Azizi Malamiri, Reza, Shariati, Gholamreza, Zeighami, Jawaher, Bayram, Nurettin, Naghibzadeh, Seyed Kianoosh, Tajik, Mohamad, Yaşar, Mehmet, Sami Güven, Ahmet, Bibi, Farah, Sultan, Tipu, Salpietro, Vincenzo, Houlden, Henry, Per, Hüseyin, Galehdari, Hamid, Shalbafan, Bita, Jamshidi, Yalda, Cirak, Sebahattin
Publicado 2019

Whole exome sequencing identifies recessive WDR62 mutations in severe brain malformations

por Bilgüvar, Kaya, Öztürk, Ali Kemal, Louvi, Angeliki, Kwan, Kenneth Y, Choi, Murim, Tatli, Burak, Yalnizoğlu, Dilek, Tüysüz, Beyhan, Çağlayan, Ahmet Okay, Gökben, Sarenur, Kaymakçalan, Hande, Barak, Tanyeri, Bakircioğlu, Mehmet, Yasuno, Katsuhito, Ho, Winson, Sanders, Stephan, Zhu, Ying, Yilmaz, Sanem, Dinçer, Alp, Johnson, Michele H, Bronen, Richard A, Koçer, Naci, Per, Hüseyin, Mane, Shrikant, Pamir, Mehmet Necmettin, Yalçinkaya, Cengiz, Kumandaş, Sefer, Topçu, Meral, Özmen, Meral, Šestan, Nenad, Lifton, Richard P, State, Matthew W, Günel, Murat
Publicado 2010

Biallelic Mutations in the 3’ Exonuclease TOE1 Cause Pontocerebellar Hypoplasia and Uncover a Role in snRNA Processing

por Lardelli, Rea M., Schaffer, Ashleigh E., Eggens, Veerle R.C., Zaki, Maha S., Grainger, Stephanie L., Sathe, Shashank, Van Nostrand, Eric L., Schlachetzki, Zinayida, Rosti, Basak, Akizu, Naiara, Scott, Eric, Heckman, Laura Dean, Rosti, Rasim Ozgur, Dikoglu, Esra, Gregor, Anne, Guemez-Gamboa, Alicia, Musaev, Damir, Mande, Rohit, Widjaja, Ari, Shaw, Tim L., Markmiller, Sebastian, Marin-Valencia, Isaac, Davies, Justin H., de Meirleir, Linda, Kayserili, Hulya, Altunoglu, Umut, Freckmann, Mary Louise, Warwick, Linda, Chitayat, David, Çağlayan, Ahmet Okay, Bilguvar, Kaya, Per, Huseyin, Fagerberg, Christina, Kibaek, Maria, Aldinger, Kimberley A., Manchester, David, Matsumoto, Naomichi, Muramatsu, Kazuhiro, Saitsu, Hirotomo, Shiina, Masaaki, Ogata, Kazuhiro, Foulds, Nicola, Dobyns, William B., Chi, Neil, Traver, David, Spaccini, Luigina, Bova, Stefania Maria, Gabriel, Stacey B., Gunel, Murat, Valente, Enza Maria, Nassogne, Marie-Cecile, Bennett, Eric J., Yeo, Gene W., Baas, Frank, Lykke-Andersen, Jens, Gleeson, Joseph G.
Publicado 2017