Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience von Bilge, Serap, Mert, Gülen Gül, Hergüner, Özlem, Özcanyüz, Duygu, Bozdoğan, Sevcan Tuğ, Kaya, Ömer, Havalı, Cengiz

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Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients von Gül Mert, Gülen, Özcan, Neslihan, Hergüner, Özlem, Altunbaşak, Şakir, Incecik, Faruk, Bişgin, Atıl, Ceylaner, Serdar

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Neurofibromatosis type 1 and cardiac manifestations von Incecik, Faruk

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Clinical and Genetic Spectrum of Myotonia Congenita in Turkish Children von Tunçer, Gökçen Öz, Sanri, Aslıhan, Aydin, Seren, Hergüner, Özlem M, Özgün, Nezir, Kömür, Mustafa, İçağasioğlu, Dilara F, Toker, Rabia Tütüncü, Yilmaz, Sanem, Arslan, Elif Acar, Güngör, Mesut, Kutluk, Gültekin, Erol, İlknur, Mert, Gülen Gül, Polat, Burçin Gönüllü, Aksoy, Ayşe

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Methylphenidate treatment outcomes and gender differences in attentional deficit and hyperactivity disorder with epilepsy: a follow-up study von Ray, Perihan, Çelik, Gonca, Tahiroğlu, Ayşegül, Gamlı, İpek, Hergüner, Özlem

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Factors affecting epilepsy prognosis in patients with tuberous sclerosis von Gül Mert, Gülen, Altunbaşak, Şakir, Hergüner, Özlem, İncecik, Faruk, Övetti, Hilal Cansever, Özcan, Neslihan, Kuşçu, Duygu, Ünal, İlker

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Pseudotumor Cerebri in a Child With Familial Mediterranean Fever von Incecik, Faruk, Herguner, Ozlem M, Yilmaz, Mustafa, Altunbasak, Sakir

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A Presentation of Lyme Disease: Pseudotumor Cerebri von Şahin, Burcu, İncecik, Faruk, Hergüner, Özlem M, Alabaz, Derya, Beşen, Şeyda

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Four Gaucher disease type II patients with three novel mutations: a single centre experience from Turkey von Bulut, Fatma Derya, Kör, Deniz, Şeker-Yılmaz, Berna, Hergüner, Özlem, Ceylaner, Serdar, Özkınay, Ferda, Kılavuz, Sebile, Önenli-Mungan, Neslihan

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Autosomal-recessive spastic ataxia of Charlevoix-Saguenay: A Turkish child von Incecik, Faruk, Hergüner, Ozlem, Bisgin, Atil

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Limbic encephalitis associated with anti-leucine-rich glioma-inactivated-1 protein antibodies in a child von Incecik, Faruk, Hergüner, Ozlem, Besen, Seyda, Yılmaz, Mustafa, Altunbasak, Sakir

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Fatal glioblastoma multiforme in a child with neurofibromatosis type 1 von Incecik, F, Hergüner, M. Ozlem, Bayram, I, Zorludemir, S, Altunbasak, S

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Dynamic thiol/disulphide homeostasis in children with Duchenne muscular dystrophy von Incecik, Faruk, Avcıoğlu, Gamze, Erel, Özcan, Neşelioğlu, Salim, Hergüner, Ozlem M.

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Mitochondrial membrane protein-associated neurodegeneration in a Turkish patient von Incecik, Faruk, Hergüner, Ozlem, Besen, Seyda, Ceylaner, Serdar

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Prognosis of Patients With Seizures Occurring in the First 2 Years von Altunbaşak, Şakir, Incecik, Faruk, Hergüner, Özlem, Refik Burgut, H.

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Akut Karın ile Gelen Guillain-Barre Sendromu von İncecik, Faruk, Horoz, Özden Özgür, Hergüner, M. Özlem, Yıldızdaş, Dinçer

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Albendazole-induced dystonic reaction: a case report von Incecik, Faruk, Hergüner, Mihriban Ozlem, Ozcan, Kenan, Altunbaşak, Sakir

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Çocuklarda psödotümör serebri: etyoloji, klinik bulgular, prognoz von Gülen GÜL MERT, Neslihan ÖZCAN, Şeyda BEŞEN, Kemal YAR, Özlem HERGÜNER, Faruk İNCECİK, Şakir ALTUNBAŞAK

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Hypokalemic periodic paralysis due to the SCN4A R672H mutation in a Turkish family von Incecik, Faruk, Hergüner, Mihriban Ozlem, Altunbaşak, Sakir, Lehman-Horn, Frank

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Pseudotumor cerebri in children: Etiology, clinical findings, prognosis von Mert,Gülen Gül, Özcan,Neslihan, Beşen,Şeyda, Yar,Kemal, Hergüner,Mihriban Özlem, İncecik,Faruk, Altunbaşak,Şakir

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