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

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

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Neurologic findings of nutritional vitamin B12 deficiency in children von Incecik, Faruk, Hergüner, M Ozlem, Altunbaşak, Sakir, Leblebisatan, Göksel

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Peripheral facial nerve palsy in children: clinical manifestations, treatment and prognosis von Bilge, Serap, Mert, Gülen Gül, Hergüner, M Özlem, İncecik, Faruk, Sürmelioğlu, Özgür, Bilen, Sevcan, Yılmaz, Levent

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Mitochondrial membrane protein-associated neurodegeneration: A case series of six children von Incecik, Faruk, Herguner, Ozlem, Bisgin, Atil

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Limbic encephalitis with antibodies to glutamic acid decarboxylase presenting with brainstem symptoms von Incecik, Faruk, Hergüner, Ozlem M, Yıldızdaş, Dincer, Horoz, Ozden, Besen, Seyda

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Clinical Characteristics of 10 Patients With Continuous Spikes and Waves During Slow Sleep Syndrome von HERGIINER, M. Ozlem, INCECIK, Faruk, ALTUNBASAK, Sakir, KIRIS, Nurcihan

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Guillain–Barré syndrome in children von Incecik, Faruk, Ozlem Hergüner, M., Altunbasak, Sakir

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Dysarthria, ataxia, and dystonia associated with COX20 (FAM36A) gene mutation: A case report of a Turkish child von Ozcanyuz, Duygu, Incecik, Faruk, Herguner, Ozlem, Mungan, Neslihan, Bozdogan, Sevcan

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Patients with acute, fulminant form of SSPE von Hergüner, M Ozlem, Altunbaşak, Sakir, Baytok, Vildan

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A rare form of Guillain-Barré syndrome: pharyngeal-cervical-brachial variant von Hergüner, M Ozlem, Tepe, Tugay, Altunbaşak, Sakir, Baytok, Vildan

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Neurofibromatosis type 1 and cardiac manifestations von Incecik, Faruk

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Giant axonal disease: Report of eight cases von Incecik, Faruk, Herguner, Ozlem M, Ceylaner, Serdar, Zorludemir, Suzan, Altunbasak, Sakir

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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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First-drug treatment failures in children with typical absence epilepsy von Incecik, Faruk, Altunbasak, Sakir, Herguner, Ozlem M

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Different clinical manifestations of three prime repair exonuclease 1 mutation: A case series von Incecik, Faruk, Balci, Sibel, Kisla Ekinci, Rabia, Herguner, Ozlem, Bisgin, Atil, Yilmaz, Mustafa

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Acute myeloid leukemia in a child with segmental neurofibromatosis von Incecik, Faruk, Hergüner, Ozlem M, Karagün, Barbaros, Altunbasak, Sakir

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