Alternating Hemiplegia of Childhood in a Child Misdiagnosed as Intractable Epilepsy

by Faruk Incecık, Ozlem M. Herguner
Published 2016-12-01

Mitochondrial membrane protein–associated neurodegeneration: A case series of six children

by Faruk Incecik, Ozlem M Herguner, Atil Bisgin
Published 2020-01-01

First-drug treatment failures in 42 Turkish children with idiopathic childhood occipital epilepsies

by Faruk Incecik, Ozlem M. Herguner, Sakir Altunbasak
Published 2015-03-01

Epilepsi ve Fasiyal Dismorfizm ile Gelen Trizomi 9 Mozaisizm: Bir Olgu Sunumu

by Faruk İNCECİK, Özlem M HERGÜNER, Gülen MERT, Şakir ALTUNBAŞAK
Published 2014-07-01

Türk Çocuklarında İdiopatik Çocukluk Çağı Oksipital Lob Epilepsisi

by Faruk İNCECİK, Özlem M. HERGÜNER, Gülen MERT, Şakir ALTUNBAŞAK
Published 2015-09-01

Idiopathic Childhood Occipital Lobe Epilepsies in Turkish Children

by Faruk incecik, Ozlem M. Herguner, Gulen Mert, sakir Altunbasak
Published 2015-09-01

Urinary and fecal incontinence during levetiracetam therapy

by Faruk Incecik, Ozlem M Herguner, Seyda Besen, Sakir Altunbasak
Published 2015-01-01

Trisomy 9 Mosaicism Presenting with Epilepsy, and Facial Dysmorphism: A Case Report

by Faruk Incecik, Ozlem M Herguner, Gulen Mert, Sakir Altunbasak
Published 2014-04-01

Neurofibromatosis type 1 and cardiac manifestations

by Faruk İncecik, Özlem M Hergüner, Sevcan Alınç-erdem, Şakir Altunbaşak
Published 2015-12-01

Spinocerebellar ataxia-21 in a Turkish child

by Faruk Incecik, Ozlem M Herguner, Patrick Willems, Neslihan O Mungan
Published 2018-01-01

A Turkish family with Sjögren-Larsson syndrome caused by a novel ALDH3A2 mutation

by Faruk Incecik, Ozlem M Herguner, Wiliam B Rizzo, Sakir Altunbasak
Published 2013-01-01

Guillain-Barre Syndrome Presenting as Acute Abdomen

by Faruk incecik, Ozden O. Horoz, Ozlem M. Herguner, Dincer Yildizdas
Published 2015-09-01

Duchenne Müsküler Distrofi ve Gilbert"s Sendromu Birlikteliği: Bir Olgu Sunumu

by Faruk İNCECİK, Özlem M. HERGÜNER, Gülen MERT, Özden HOROZ, Şakir ALTUNBAŞAK
Published 2013-12-01

Limbic encephalitis with antibodies to glutamic acid decarboxylase presenting with brainstem symptoms

by Faruk Incecik, Ozlem M Hergüner, Dincer Yildizdas, Ozden Horoz, Seyda Besen
Published 2015-01-01

Coexisting Duchenne Muscular Dystrophy and Gilbert’s Syndrome: A Case Report

by Faruk Incecik, Ozlem M. Herguner, Gulen Mert, Ozden Horoz, Sakir Altunbasak
Published 2013-08-01

Electroconvulsive therapy for refractory status epilepticus in a child: A case report

by Faruk Incecik, Ozden O Horoz, Ozlem M Herguner, Dincer Yildizdas, Sakir Altunbasak
Published 2015-01-01

Dysarthria, ataxia, and dystonia associated with COX20 (FAM36A) gene mutation: A case report of a Turkish child

by Duygu G Ozcanyuz, Faruk Incecik, Ozlem M Herguner, Neslihan O Mungan, Sevcan T Bozdogan
Published 2020-01-01

Coexistence of Two Rare Genetic Disorders: Familial Mediterranean Fever and Neurofibromatosis Type 1 in A Child

by Faruk incecik, Ozlem M. Herguner, Seyda Besen, Zeliha Ucar Haytoglu, Mustafa Yilmaz, sakir Altunbasak
Published 2015-03-01

Different clinical manifestations of three prime repair exonuclease 1 mutation: A case series

by Faruk Incecik, Sibel Balci, Rabia Miray Kisla Ekinci, Ozlem M Herguner, Atil Bisgin, Mustafa Yilmaz
Published 2020-01-01

Intravenous levetiracetam in critically ill children

by Faruk Incecik, Ozden O Horoz, Ozlem M Herguner, Dincer Yıldızdas, Seyda Besen, Ilknur Tolunay, Sakir Altunbasak
Published 2016-01-01