Carbamazepine-induced hiccups: A case report von Incecik, Faruk, Herguner, Ozlem M

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Homozygous Mutation in CWF19L1 with Recessive Ataxia Syndrome in a Turkish Child von Incecik, Faruk, Ozcanyuz, Duygu G, Bozdogan, Sevcan T, Herguner, Ozlem M

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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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Hereditary spastic paraplegia type 35 with a novel mutation in fatty acid 2-hydroxylase gene and literature review of the clinical features von Incecik, Faruk, Besen, Seyda, Bozdogan, Sevcan

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D-bifunctional protein deficiency: A case report of a Turkish child von Incecik, Faruk, Mungan, Neslihan

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

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Prognostic significance of failure of the initial antiepileptic drug in children with benign childhood epilepsy with centrotemporal spikes von Incecik, Faruk, Altunbasak, Sakir, Herguner, Ozlem M, Mert, Gulen, Sahan, Duygu

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Acetazolamide-Induced agranulocytosis in a patient with pseudotumor cerebri von Incecik, Faruk, Ozcan, Neslihan, Ozcanyuz, Duygu, Mert, Gulen

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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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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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Spinocerebellar ataxia-21 in a Turkish child von Incecik, Faruk, Herguner, Ozlem, Willems, Patrick, Mungan, Neslihan

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Electroconvulsive therapy for refractory status epilepticus in a child: A case report von Incecik, Faruk, Horoz, Ozden O, Herguner, Ozlem M, Yıldızdas, Dincer, Altunbasak, Sakir

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Factors Affecting Epilepsy Development and Epilepsy Prognosis in Cerebral Palsy von Gul Mert, Gulen, MD, Incecik, Faruk, MD, Altunbasak, Sakir, MD, Herguner, Ozlem, MD, Kurthan Mert, Mustafa, MD, Kiris, Nurcihan, PhD, Unal, Ilker, PhD

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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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Urinary and fecal incontinence during levetiracetam therapy von Incecik, Faruk, Herguner, Ozlem M, Besen, Seyda, Altunbasak, Sakir

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Hereditary Spastic Paraplegia Type 26 with a Novel Mutation in B4GALNT1 Gene and Literature Review of the Clinical Features von Incecık, Faruk, Herguner, Ozlem M, Bozdogan, Sevcan Tug

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MEDNIK syndrome with a frame shift causing mutation in AP1S1 gene and literature review of the clinical features von Incecik, Faruk, Bisgin, Atil, Yılmaz, Mustafa

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Guillain-Barre Syndrome Presenting as Acute Abdomen von Faruk incecik, Ozden O. Horoz, Ozlem M. Herguner, Dincer Yildizdas

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Intravenous levetiracetam in critically ill children von Incecik, Faruk, Horoz, Ozden O, Herguner, Ozlem M, Yıldızdas, Dincer, Besen, Seyda, Tolunay, Ilknur, Altunbasak, Sakir

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