Prof. Dr. Sarenur Gökben

A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiency

Metabolic Brain Disease, 2017

DOI 10.1007/s11011-017-9984-5 PMID 28281033 27 citations (Europe PMC) Source : OpenAlex

A rare cause of brachial plexopathy after vaccination: Hereditary neuralgic amyotrophy

European Journal of Paediatric Neurology, 2017

DOI 10.1016/j.ejpn.2017.04.887 Source : OpenAlex

The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome

Scientific Reports, 2017

DOI 10.1038/s41598-017-11620-3 PMID 28947817 28 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

The Effect of Vagal Nerve Stimulation on the Quality of Life in Pediatric Cases

The Journal of Pediatric Research, 2017

DOI 10.4274/jpr.43434 1 citation (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Risk factors for epilepsy in cases with cerebral palsy: A retrospective study

European Journal of Paediatric Neurology, 2017

DOI 10.1016/j.ejpn.2017.04.1171 2 citations (OpenAlex) Source : OpenAlex

PRUNE1: a disease-causing gene for secondary microcephaly

Brain, 2017

DOI 10.1093/brain/awx197 PMID 28969376 12 citations (OpenAlex) Source : OpenAlex

A practical approach to the nutritional management of children with neurologic disorders

European Journal of Paediatric Neurology, 2017

DOI 10.1016/j.ejpn.2017.04.1073 Source : OpenAlex

Polyneuropathy After Gastric By-pass Surgery

The Journal of Pediatric Research, 2017

DOI 10.4274/jpr.96658 Texte intégral en libre accèsSource : OpenAlex

Beyin Felcinde Oral Tedaviler

2017

Source : OpenAlex

Excellent response to deep brain stimulation in a young girl with GNAO1-related progressive choreoathetosis

Child s Nervous System, 2016

DOI 10.1007/s00381-016-3139-6 PMID 27278281 46 citations (OpenAlex) Source : OpenAlex

Targeted next generation sequencing: the diagnostic value in early-onset epileptic encephalopathy

Acta Neurologica Belgica, 2016

DOI 10.1007/s13760-016-0709-z PMID 27734276 40 citations (OpenAlex) Source : OpenAlex

Evaluation of ten prognostic factors affecting the outcome of West syndrome

Acta Neurologica Belgica, 2016

DOI 10.1007/s13760-016-0611-8 PMID 26850102 15 citations (OpenAlex) Source : OpenAlex

Molecular Genetic Analysis of Survival Motor Neuron Gene in 460 Turkish Cases with Suspicious Spinal Muscular Atrophy Disease.

Iranian journal of child neurology., 2016

DOI 10.22037/ijcn.v10i4.10943 PMID 27843464 5 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Yenidoğanda Status Epileptikus

Turkiye Klinikleri Neurology - Special Topics, 2016

Source : OpenAlex

The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorder

Brain and Development, 2015

DOI 10.1016/j.braindev.2015.06.004 PMID 26126837 28 citations (OpenAlex) Source : OpenAlex

Different Neurologic Aspects of Nutritional B 12 Deficiency in Infancy

Journal of Child Neurology, 2015

DOI 10.1177/0883073815601497 PMID 26310585 17 citations (OpenAlex) Source : OpenAlex

Mitochondrial Membrane Protein–Associated Neurodegeneration

Pediatric Neurology, 2015

DOI 10.1016/j.pediatrneurol.2015.06.012 PMID 26231266 8 citations (OpenAlex) Source : OpenAlex

Ictal urinary urge: localization and lateralization value in a pediatric case

Child s Nervous System, 2015

DOI 10.1007/s00381-015-2816-1 PMID 26206115 6 citations (OpenAlex) Source : OpenAlex

Quality of Life in Childhood Epilepsy: The Role of an Education Program on the Disease

The Journal of Pediatric Research, 2015

DOI 10.4274/jpr.77486 6 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Turkish cases of early infantile epileptic encephalopathy: two novel mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene

The Turkish Journal of Pediatrics, 2015

DOI 10.24953/turkjpediatr.2015.1236 PMID 26701947 2 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Seizures due to high dose camphor ingestion

Türk Pediatri Arşivi, 2015

DOI 10.5152/turkpediatriars.2015.1360 PMID 26884696 4 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Optic disc drusen mimicking papilledema in an infant with Joubert syndrome.

PubMed, 2015

PMID 26043505 5 citations (OpenAlex) Source : OpenAlex

Landau-Kleffner Syndrome: Case Report

The Journal of Pediatric Research, 2015

DOI 10.4274/jpr.74745 2 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Comparison Between Simultaneously Recorded Amplitude Integrated Electroencephalography and Standard Electroencephalography in Neonates with Acute Brain Injury

The Journal of Pediatric Research, 2015

DOI 10.4274/jpr.07279 1 citation (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

PP12.8 – 2541: A case of mitochondrial membrane protein associated neurodegeneration due to a novel mutation

European Journal of Paediatric Neurology, 2015

DOI 10.1016/s1090-3798(15)30263-4 Source : OpenAlex

A Neurobrucellosis Case Presenting with Bilateral Facial Nerve Palsy and Peripheral Neuropathy

Turkiye Klinikleri Journal of Pediatrics, 2015

DOI 10.5336/pediatr.2014-41269 Texte intégral en libre accèsSource : OpenAlex

Aicardi Syndrome: A Rare Neurological Disease: Case Report

Turkiye Klinikleri Journal of Pediatrics, 2015

DOI 10.5336/pediatr.2014-43077 Texte intégral en libre accèsSource : OpenAlex

A CASE OF MACROCEPHALY-CAPILLARY MALFORMATION SYNDROME PRESENTING WITH HOT WATER EPILEPSY.

PubMed, 2015

PMID 26625665 Source : OpenAlex

P157 – 2542: Movement disorder, periventricular nodular heterotopia and putaminal hyperintensity due to an ARFGEF2 gene mutation

European Journal of Paediatric Neurology, 2015

DOI 10.1016/s1090-3798(15)30470-0 Source : OpenAlex

Mitochondrial Membrane ProteineAssociated Neurodegeneration

2015

Source : OpenAlex

PP01.1 – 2565: Next generation sequencing analysis in neonatal/early epileptic encephalopathy

European Journal of Paediatric Neurology, 2015

DOI 10.1016/s1090-3798(15)30091-x Source : OpenAlex

Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation: clinical and genetic characterization and target for therapy

Brain, 2014

DOI 10.1093/brain/awu026 PMID 24566671 83 citations (Europe PMC) Texte intégral en libre accèsSource : OpenAlex

Clinical characteristics and outcome of children with electrical status epilepticus during slow wave sleep

Journal of Pediatric Neurosciences, 2014

DOI 10.4103/1817-1745.139266 PMID 25250061 34 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Acute Transverse Myelitis Complicating Breakthrough Varicella Infection

The Pediatric Infectious Disease Journal, 2014

DOI 10.1097/inf.0000000000000418 PMID 24853543 14 citations (OpenAlex) Source : OpenAlex

Concomitant Alpha- and Gamma-Sarcoglycan Deficiencies in a Turkish Boy with a Novel Deletion in the Alpha-Sarcoglycan Gene

Case Reports in Genetics, 2014

DOI 10.1155/2014/248561 PMID 25050186 6 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Neurological and developmental outcome of children with neonatal hypoglycemic seizures

Journal of Dr Behcet Uz Children s Hospital, 2014

DOI 10.5222/buchd.2014.037 2 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Psikotik Davranışlar ve İnsomninin Nadir Bir Sebebi: Anti-NMDA Reseptör Ensefaliti

Turkiye Klinikleri Journal of Pediatrics, 2014

Source : OpenAlex

G.P.225

Neuromuscular Disorders, 2014

DOI 10.1016/j.nmd.2014.06.301 Source : OpenAlex

A Rare Presentation of Conversion Disorder: Palpebral Ptosis

The Journal of Pediatric Research, 2014

DOI 10.4274/jpr.03511 Texte intégral en libre accèsSource : OpenAlex

Gastro-Özofageal Hastalık İlişkili Distoni: Sandifer Sendromu

The Journal of Pediatric Research, 2014

DOI 10.4274/jpr.55264 Texte intégral en libre accèsSource : OpenAlex

Lafora Hastalığı Tanılı 12 Türk Olgunun Mutasyon Analizleri 5 Yeni Mutasyonun Tanımlanması

Bursa Uludag University - AVESIS, 2014

Source : OpenAlex

Electrophysiologic assessment of spasticity in children using H-reflex

The Turkish Journal of Pediatrics, 2013

DOI 10.24953/turkjpediatr.2013.1544 PMID 24382533 23 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Changing views of cerebral palsy over 35 years: the experience of a center.

PubMed, 2013

PMID 23692827 15 citations (OpenAlex) Source : OpenAlex

Diagnostic Tools of Early Brain Disturbances in an Asymptomatic Neonate with Maple Syrup Urine Disease

Neuropediatrics, 2013

DOI 10.1055/s-0032-1332741 PMID 23341096 12 citations (OpenAlex) Source : OpenAlex

Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene

Journal of Medical Genetics, 2012

DOI 10.1136/jmedgenet-2012-100859 PMID 22693283 78 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Syncope or seizure? The diagnostic value of synchronous tilt testing and video-EEG monitoring in children with transient loss of consciousness

Epilepsy & Behavior, 2012

DOI 10.1016/j.yebeh.2012.02.006 PMID 22459868 23 citations (OpenAlex) Source : OpenAlex

Use of Buspirone and Fluoxetine for Breathing Problems in Rett Syndrome

Pediatric Neurology, 2012

DOI 10.1016/j.pediatrneurol.2011.12.003 PMID 22353299 33 citations (OpenAlex) Source : OpenAlex

Neurocognitive evaluation in children with occipital lobe epilepsy

Seizure, 2012

DOI 10.1016/j.seizure.2011.12.015 PMID 22265577 8 citations (OpenAlex) Texte intégral en libre accèsSource : OpenAlex

Diagnostic tools of metabolic and structural brain disturbances in neonatal non‐ketotic hyperglycinemia

Pediatrics International, 2012

DOI 10.1111/j.1442-200x.2012.03591.x PMID 23005907 6 citations (OpenAlex) Source : OpenAlex

Early-Onset Acquired Myasthenia Gravis Secondary to Anti–Muscle-Specific Kinase Autoantibodies

Journal of Child Neurology, 2012

DOI 10.1177/0883073812467689 PMID 23234677 2 citations (OpenAlex) Source : OpenAlex