Alternating Hemiplegia of Childhood in a Child Misdiagnosed as Intractable Epilepsy

por Incecık, Faruk, Herguner, Ozlem M.
Publicado 2016

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

por Incecik, Faruk, Herguner, Ozlem M., Altunbasak, Sakir
Publicado 2015

Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Turkish Child

por Incecik, Faruk, Hergüner, Ozlem M., Bisgin, Atil
Publicado 2018

Effect of Levetiracetam Usage on Serum Creatine Phosphokinase Concentration in Patients with Epilepsy

por Incecik, Faruk, Herguner, Ozlem M, Besen, Seyda
Publicado 2020

Mitochondrial Membrane Protein–Associated Neurodegeneration: A Case Series of Six Children

por Incecik, Faruk, Herguner, Ozlem M., Bisgin, Atil
Publicado 2020

Clinical Features and Molecular Genetics of Autosomal Recessive Ataxia in the Turkish Population

por Incecik, Faruk, Herguner, Ozlem M, Mungan, Neslihan O
Publicado 2020

Urinary and fecal incontinence during levetiracetam therapy

por Incecik, Faruk, Herguner, Ozlem M., Besen, Seyda, Altunbasak, Sakir
Publicado 2015

Merosin-negative congenital muscular dystrophy: Report of five cases

por Incecik, Faruk, Herguner, Ozlem M., Ceylaner, Serdar, Altunbasak, Sakir
Publicado 2015

Mitochondrial membrane protein-associated neurodegeneration in a Turkish patient

por Incecik, Faruk, Hergüner, Ozlem M., Besen, Seyda, Ceylaner, Serdar
Publicado 2016

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

por Incecık, Faruk, Herguner, Ozlem M., Rizzo, Wiliam B., Altunbasak, Sakir
Publicado 2013

Spinocerebellar Ataxia-21 in a Turkish Child

por Incecik, Faruk, Herguner, Ozlem M., Willems, Patrick, Mungan, Neslihan O.
Publicado 2018

Risk of recurrence after discontinuation of antiepileptic drug therapy in children with epilepsy

por Incecik, Faruk, Herguner, Ozlem M., Altunbasak, Sakir, Mert, Gulen, Kiris, Nurcihan
Publicado 2014

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

por Incecik, Faruk, Hergüner, Ozlem M., Yıldızdaş, Dincer, Horoz, Ozden, Besen, Seyda
Publicado 2015

Guillain–Barré syndrome with hyperreflexia and bilateral papillitis in a child

por Incecik, Faruk, Herguner, Ozlem M., Besen, Seyda, Yar, Kemal, Altunbasak, Sakir
Publicado 2016

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

por Incecik, Faruk, Horoz, Ozden O., Herguner, Ozlem M., Yıldızdas, Dincer, Altunbasak, Sakir
Publicado 2015

Late-Onset Leigh Syndrome due to NDUFV1 Mutation in a 10-Year-Old Boy Initially Presenting with Ataxia

por Incecik, Faruk, Herguner, Ozlem M., Besen, Seyda, Bozdoğan, Sevcan T., Mungan, Neslihan O.
Publicado 2018

Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child

por Ozcanyuz, Duygu G., Incecik, Faruk, Herguner, Ozlem M., Mungan, Neslihan O., Bozdogan, Sevcan T.
Publicado 2020

Different Clinical Manifestations of Three Prime Repair Exonuclease 1 Mutation: A Case Series

por Incecik, Faruk, Balci, Sibel, Kisla Ekinci, Rabia Miray, Herguner, Ozlem M., Bisgin, Atil, Yilmaz, Mustafa
Publicado 2020

Intravenous levetiracetam in critically ill children

por Incecik, Faruk, Horoz, Ozden O, Herguner, Ozlem M, Yıldızdas, Dincer, Besen, Seyda, Tolunay, Ilknur, Altunbasak, Sakir
Publicado 2016

Neuro-ichthyotic Syndromes: A Case Series

por Incecık, Faruk, Herguner, Ozlem M., Ozbek, Mehmet N., Gungor, Serdal, Yılmaz, Mustafa, Rizzo, Wiliam B., Mert, Gülen G.
Publicado 2018