Prof. Dr. Sarenur Gökben

A Case of Neurobrucellosis Presenting With Isolated Intracranial Hypertension

Journal of Child Neurology, 2011

DOI 10.1177/0883073811402205 PMID 21551370 17 Zitationen (OpenAlex) Quelle: OpenAlex

Video/EEG recording of myoclonic absences in GLUT1 deficiency syndrome with a hot-spot R126C mutation in the SLC2A1 gene

Epilepsy & Behavior, 2011

DOI 10.1016/j.yebeh.2011.03.027 PMID 21546317 18 Zitationen (OpenAlex) Quelle: OpenAlex

Paroxysmal Dystonia as a Rare Initial Manifestation of Multiple Sclerosis

Journal of Child Neurology, 2011

DOI 10.1177/0883073811410882 PMID 21673278 15 Zitationen (OpenAlex) Quelle: OpenAlex

A rare cause of recurrent stroke in childhood: left atrial rhabdomyosarcoma

Acta Paediatrica, 2011

DOI 10.1111/j.1651-2227.2011.02214.x PMID 21352362 3 Zitationen (OpenAlex) Quelle: OpenAlex

Recurrent Pseudotumor Cerebri in Childhood: A Case of Neuro-Behçet Disease Complicated With Thrombotic Risk Factors

Journal of Child Neurology, 2011

DOI 10.1177/0883073810391905 PMID 21498791 5 Zitationen (OpenAlex) Quelle: OpenAlex

P26.1 The diagnostic value of synchronous TILT-Table Test and video-EEG monitoring in sudden loss of conciousness and tonus

European Journal of Paediatric Neurology, 2011

DOI 10.1016/s1090-3798(11)70468-8 Quelle: OpenAlex

Response

Pediatric Neurology, 2011

DOI 10.1016/j.pediatrneurol.2010.11.017 Quelle: OpenAlex

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

Nature, 2010

DOI 10.1038/nature09327 PMID 20729831 499 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Convulsive status epilepticus in children: Etiology, treatment protocol and outcome

Seizure, 2010

DOI 10.1016/j.seizure.2010.10.034 PMID 21195636 50 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Ratios of Nine Risk Factors in Children With Recurrent Febrile Seizures

Pediatric Neurology, 2010

DOI 10.1016/j.pediatrneurol.2010.05.007 PMID 20691939 30 Zitationen (OpenAlex) Quelle: OpenAlex

Multidrug Resistance 1 (MDR1) Gene Polymorphisms in Childhood Drug-Resistant Epilepsy

Journal of Child Neurology, 2010

DOI 10.1177/0883073810368997 PMID 20448249 30 Zitationen (OpenAlex) Quelle: OpenAlex

Reversibility of Cytotoxic Edema in Tacrolimus Leukoencephalopathy

Pediatric Neurology, 2010

DOI 10.1016/j.pediatrneurol.2010.05.021 PMID 20933182 13 Zitationen (OpenAlex) Quelle: OpenAlex

Mutations in CLN7/MFSD8 are a common cause of variant late-infantile neuronal ceroid lipofuscinosis

Brain, 2009

DOI 10.1093/brain/awn366 PMID 19201763 144 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Febrile Seizures: Interleukin 1β and Interleukin-1 Receptor Antagonist Polymorphisms

Pediatric Neurology, 2009

DOI 10.1016/j.pediatrneurol.2008.10.004 PMID 19135625 37 Zitationen (OpenAlex) Quelle: OpenAlex

Neuropsychologic Impairment in Children With Rolandic Epilepsy

Pediatric Neurology, 2009

DOI 10.1016/j.pediatrneurol.2009.05.013 PMID 19818938 52 Zitationen (OpenAlex) Quelle: OpenAlex

Evaluation of the cases with acute disseminated encephalomyelitis

The Indian Journal of Pediatrics, 2009

DOI 10.1007/s12098-009-0069-2 PMID 19390813 16 Zitationen (OpenAlex) Quelle: OpenAlex

Salla disease in Turkish children: severe and conventional type

The Turkish Journal of Pediatrics, 2009

DOI 10.24953/turkjpediatr.2009.2365 PMID 20196397 6 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

An Inherited Nonsense R1645X Mutation in Neuronal Sodium Channel α1-Subunit Gene in a Turkish Patient with Severe Myoclonic Epilepsy of Infancy

Neuropediatrics, 2009

DOI 10.1055/s-0029-1234083 PMID 19809937 4 Zitationen (OpenAlex) Quelle: OpenAlex

P299 Essential tremor? Wilson disease?

European Journal of Paediatric Neurology, 2009

DOI 10.1016/s1090-3798(09)70357-5 Quelle: OpenAlex

P053 Posterior Reversible Encephalopathy Syndrome (PRES) secondary to immunsupressive treatment

European Journal of Paediatric Neurology, 2009

DOI 10.1016/s1090-3798(09)70111-4 Quelle: OpenAlex

P163 A lateralization sign in early childhood: postictal nosewiping phenomenon

European Journal of Paediatric Neurology, 2009

DOI 10.1016/s1090-3798(09)70221-1 Quelle: OpenAlex

P159 The role of video-EEG in differential diagnosis of paroxysmal dystonia and partial seizure

European Journal of Paediatric Neurology, 2009

DOI 10.1016/s1090-3798(09)70217-x Quelle: OpenAlex

P255 Intraventricular interferon-α in subacute sclerosing panencephalitis

European Journal of Paediatric Neurology, 2009

DOI 10.1016/s1090-3798(09)70313-7 Quelle: OpenAlex

Angelman sendromu: bir olgu sunumu

DergiPark (Istanbul University), 2009

DOI 10.19161/etd.73170 Quelle: OpenAlex

The effect of depression on academic achievement in children with epilepsy

Epilepsy & Behavior, 2008

DOI 10.1016/j.yebeh.2008.05.016 PMID 18599356 23 Zitationen (OpenAlex) Quelle: OpenAlex

Semiologic seizure classification: The effectiveness of a modular education program for health professionals in pediatrics

Epilepsy & Behavior, 2008

DOI 10.1016/j.yebeh.2008.04.023 PMID 18524683 9 Zitationen (OpenAlex) Quelle: OpenAlex

İmmün Kökenli Demyelinizan Hastalıklar

Turkiye Klinikleri Journal of Pediatric Sciences, 2008

Quelle: OpenAlex

Iconography : Identification of axonal involvement in Hallervorden-Spatz Disease with magnetic resonance spectroscopy

2008

Quelle: OpenAlex

Subclinical Neurological Abnormalities in Children With Celiac Disease Receiving a Gluten‐free Diet

Journal of Pediatric Gastroenterology and Nutrition, 2007

DOI 10.1097/mpg.0b013e31806907e8 PMID 17873753 51 Zitationen (OpenAlex) Quelle: OpenAlex

Chronic inflammatory demyelinating polyradiculopathy: an atypical pediatric case complicated with phrenic nerve palsy

The Turkish Journal of Pediatrics, 2007

DOI 10.24953/turkjpediatr.2007.2539 PMID 17907525 5 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Arterial Ischemic Stroke in Childhood: Risk Factors and Outcome in Old Versus New Era

Journal of Child Neurology, 2007

DOI 10.1177/0883073807307863 PMID 17940247 11 Zitationen (OpenAlex) Quelle: OpenAlex

Miller Fisher syndrome: a case with pattern of pure sensory polyneuropathy concomitant with anti-GQ1B antibody

The Turkish Journal of Pediatrics, 2007

DOI 10.24953/turkjpediatr.2007.2521 PMID 17479657 3 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

ECP01 Acute seizures in a pediatric emergency unit: etiologic profiles and outcome

European Journal of Paediatric Neurology, 2007

DOI 10.1016/s1090-3798(08)70629-9 1 Zitation (OpenAlex) Quelle: OpenAlex

ESO03 Neuropsychological evaluation in patients with benign childhood epilepsy with occipital paroxysms

European Journal of Paediatric Neurology, 2007

DOI 10.1016/s1090-3798(08)70340-4 Quelle: OpenAlex

CPP03 Evaluation of patients with cerebral palsy

European Journal of Paediatric Neurology, 2007

DOI 10.1016/s1090-3798(08)70415-x Quelle: OpenAlex

ESP01 The effectiveness of semiologic seizure classification on health professionals in pediatrics

European Journal of Paediatric Neurology, 2007

DOI 10.1016/s1090-3798(08)70475-6 Quelle: OpenAlex

ESP07 Neuropsychological impairment in children with rolandic epilepsy

European Journal of Paediatric Neurology, 2007

DOI 10.1016/s1090-3798(08)70481-1 Quelle: OpenAlex

Bone Mineral Status in Pediatric Outpatients on Antiepileptic Drug Monotherapy

Journal of Child Neurology, 2006

DOI 10.1177/08830738060210050101 PMID 16901447 54 Zitationen (OpenAlex) Quelle: OpenAlex

Vigabatrin Caused Rapidly Progressive Deterioration in Two Cases With Early Myoclonic Encephalopathy Associated With Nonketotic Hyperglycinemia

Journal of Child Neurology, 2006

DOI 10.1177/08830738060210011801 PMID 16551461 35 Zitationen (OpenAlex) Quelle: OpenAlex

Serum Lipid Profile in Children Receiving Anti-epileptic Drug Monotherapy: Is it Atherogenic?

Journal of Pediatric Endocrinology and Metabolism, 2006

DOI 10.1515/jpem.2006.19.9.1151 PMID 17128563 24 Zitationen (OpenAlex) Quelle: OpenAlex

Severe juvenile dermatomyositis: two patients complicated with extra musculocutaneous involvement

Rheumatology International, 2006

DOI 10.1007/s00296-006-0141-4 PMID 16721599 15 Zitationen (OpenAlex) Frei zugänglicher VolltextQuelle: OpenAlex

Electrodiagnostic Pattern Approach for Childhood Polyneuropathies

Pediatric Neurology, 2006

DOI 10.1016/j.pediatrneurol.2005.11.002 PMID 16814079 5 Zitationen (OpenAlex) Quelle: OpenAlex

Central Core Disease: Atypical Case With Respiratory Insufficiency in an Intensive Care Unit

Journal of Child Neurology, 2006

DOI 10.1177/08830738060210021301 PMID 16566888 4 Zitationen (OpenAlex) Quelle: OpenAlex

Identification of axonal involvement in Hallervorden-Spatz disease with magnetic resonance spectroscopy

Journal of Neuroradiology, 2006

DOI 10.1016/s0150-9861(06)77244-3 PMID 16733428 5 Zitationen (OpenAlex) Quelle: OpenAlex

Kore ve Atetoz

Turkiye Klinikleri Pediatric Sciences - Special Topics, 2006

Quelle: OpenAlex

Idiopathic orbital myositis in childhood: a case report

Çocuk Sağlığı ve Hastalıkları Dergisi, 2006

Frei zugänglicher VolltextQuelle: OpenAlex

Ring chromosome 20 syndrome with intractable epilepsy

Developmental Medicine & Child Neurology, 2005

DOI 10.1017/s0012162205000642 PMID 15892377 34 Zitationen (OpenAlex) Quelle: OpenAlex

Cerebrospinal fluid interleukin-6 levels in patients with west syndrome

Brain and Development, 2005

DOI 10.1016/j.braindev.2005.03.007 PMID 15967615 23 Zitationen (OpenAlex) Quelle: OpenAlex

Value of Biochemical Markers for Outcome in Term Infants With Asphyxia

Obstetrical & Gynecological Survey, 2005

DOI 10.1097/01.ogx.0000160566.40938.e6 9 Zitationen (OpenAlex) Quelle: OpenAlex

T-Cell Subsets and Interleukin-6 Response in Rasmussen’s Encephalitis

Pediatric Neurology, 2005

DOI 10.1016/j.pediatrneurol.2005.01.007 PMID 15876522 14 Zitationen (OpenAlex) Quelle: OpenAlex