Uluslar Arası Bilimsel Makaleler

Efficacy of levetiracetam as first-line therapy for neonatal clinical seizures and neurodevelopmental outcome at 12 months of age. Kanmaz S, Altun Köroğlu Ö, Terek D, Serin HM, Simsek E, Dokurel Cetin İ, Yilmaz S, Yalaz M, Aktan G, Akisu M, Kultursay N, Gokben S, Tekgul H. Acta Neurol Belg. 2020 May 18. doi: 10.1007/s13760-020-01366-7.
 CSF levels of a set of neurotrophic factors (brain-derived neurotrophic factor, nerve growth factor) and neuropeptides (neuropeptide Y, galanin) in epileptic children. Tekgul H, Serin HM, Simsek E, Kanmaz S, Gazeteci H, Azarsiz E, Ozgur S, Yilmaz S, Aktan G, Gokben S.J Clin Neurosci. 2020 ;76:41-45.
Clinical value of a set of neuropeptides in term and preterm neonates with seizures: Brain derived neurotrophic factor, galanin and neuropeptide Y. Tanrıverdi M, Kultursay N, Tekgul H, Sozmen E, Altun Koroglu O, Aktan G, Yalaz M.J Clin Neurosci. 2020;74:168-174. doi: 10.1016/j.jocn.2020.02.01Formun ÜstüFormun Altı
Dropped head related lamin A/C associated congenital muscular dystrophy case; previously defined as emerydreifuss muscular dystrophy. Tekin H, Yılmaz S, Tekgül H, Gökben S, Aktan G.Turk J Pediatr 2020;62(1):130-135. doi: 10.24953/turkjped.2020.01.019.
Sulthiame add-on treatment in children with epileptic encephalopathy with status epilepticus: an efficacy analysis in etiologic subgroups. Kanmaz S, Simsek E, Serin HM, Yilmaz S, Aktan G, Tekgul H, Gokben S. Neurol Sci 2020. doi: 10.1007/s10072-020-04526-y.
A transcranial magnetic stimulation study for the investigation of corticospinal motor pathways in children with cerebral palsy. Tekgul H, Saz U, Yilmaz S, Polat M, Aktan G, Kose T, Kitis O, Gokben S
A rare cause of ischemic stroke in childhood: spontaneous long segment intracranial dissection. Simsek E, Yilmaz S, Oran I, Aktan G, Tekgul H, Gokben S.Childs Nerv Syst 2020. doi: 10.1007/s00381-020-04530-9.
A rare cause of brachial plexopathy: hereditary neuralgic amyotrophy. Serin HM, Yılmaz S, Kanmaz S, Şimşek E, Aktan G, Tekgül H, Gökben S. Turk Pediatri Ars. 2019;54(3):189-191. doi: 10.5152/TurkPediatriArs.2018.5837.
The case of pyridoxine dependent epilepsy misdiagnosed as non-ketotic hyperglycinemia. Gazeteci Tekin H, Demir M, Aktan G, Tekgül H, Gökben S.Turk J Pediatr. 2019;61(4):599-603. doi: 10.24953/turkjped.2019.04.019.
Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey. Yiş U, Diniz G, Hazan F, Daimagüler HS, Baysal BT, Baydan F, Akinci G, Ünalp A, Aktan G, Bayram E, Hiz S, Paketçi C, Okur D, Özer E, Danyeli AE, Polat M, Uyanik G, Çirak S.Acta Myol. 2018;37(3):210-220.
Prevalence and severity of malnutrition in pediatric neurology outpatients with respect to underlying diagnosis and comorbid nutrition and feeding related problems. Tekin H, Tekgül H, Yılmaz S, Arslangiray D, Reyhan H, Serdaroğlu G, Gökben S.Turk J Pediatr 2018;60(6):709-717. doi: 10.24953/turkjped.2018.06.012.
Megalencephalic leukoencephalopathy with subcortical cysts: Characterization of disease variants. Hamilton EMC, Tekturk P, Cialdella F, van Rappard DF, Wolf NI, Yalcinkaya C, Çetinçelik Ü, Rajaee A, Kariminejad A, Paprocka J, Yapici Z, Bošnjak VM, van der Knaap MS; MLC Research Group.Neurology. 2018;90(16):e1395-e1403. doi: 10.1212/WNL.0000000000005334.
Targeted next generation sequencing: the diagnostic value in early-onset epileptic encephalopathy. Gokben S, Onay H, Yilmaz S, Atik T, Serdaroglu G, Tekin H, Ozkinay F. Acta Neurol Belg 2017;117(1):131-138. doi: 10.1007/s13760-016-0709-z.
Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database. Yılmaz Ü, Anlar B, Gücüyener K; Turkish Pediatric Multiple Sclerosis Study Group.Eur J Paediatr Neurol 2017 Nov;21(6):864-872. doi: 10.1016/j.ejpn.2017.06.004.
A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiency. Yilmaz S, Serin M, Canda E, Eraslan C, Tekin H, Ucar SK, Gokben S, Tekgul H, Serdaroglu G.Metab Brain Dis 2017;32(3):675-678. doi: 10.1007/s11011-017-9984-5.
Genetic Landscape of Congenital Myasthenic Syndromes From Turkey: Novel Mutations and Clinical Insights. Yiş U, Becker K, Kurul SH, Uyanik G, Bayram E, Haliloğlu G, Polat Aİ, Ayanoğlu M, Okur D, Tosun AF, Serdaroğlu G, Yilmaz S, Topaloğlu H, Anlar B, Cirak S, Engel AG. J Child Neurol 2017;32(8):759-765. doi: 10.1177/0883073817705252.
Excellent response to deep brain stimulation in a young girl with GNAO1-related progressive choreoathetosis. Yilmaz S, Turhan T, Ceylaner S, Gökben S, Tekgul H, Serdaroglu G. Childs Nerv Syst 2016;32(9):1567-8. doi: 10.1007/s00381-016-3139-6.
The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorder. Yilmaz S, Gokben S, Serdaroglu G, Eraslan C, Mancinic MS, Tekin H, Tekgul H. Brain and Dev 2016;38:124-7.
Different Neurologic Aspects of Nutritional B12 Deficiency in Infancy. Yilmaz S, Serdaroglu G, Tekgul H, Gokben S.J Child Neurol 2016;31(5):565-8. doi: 10.1177/0883073815601497.
PRUNE1: a disease-causing gene for secondary microcephaly. Karakaya M, Yilmaz S, Storbeck M, Hoelker I, Heller R, Serdaroglu G, Gökben S, Yis U, Wirth B. Brain 2017;140(10):e61. doi: 10.1093/brain/awx197.
Evaluation of ten prognostic factors affecting the outcome of West syndrome. Yilmaz S, Tekgul H, Serdaroglu G, Akcay A, Gokben S.Acta Neurol Belg. 2016;116(4):519-527. doi: 10.1007/s13760-016-0611-8.
Seizures due to high dose camphor ingestion. Tekin HG, Gökben S, Serdaroğlu G.Turk Pediatri Ars. 2015;50(4):248-50. doi: 10.5152/TurkPediatriArs.2015.1360.
The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorder. Yilmaz S, Gokben S, Serdaroglu G, Eraslan C, Mancini GM, Tekin H, Tekgul H.Brain Dev. 2016;38(1):124-7. doi: 10.1016/j.braindev.2015.06.004.
Ictal urinary urge: localization and lateralization value in a pediatric case. Yilmaz S, Gokben S, Turhan T, Serdaroglu G, Tekgul H.Childs Nerv Syst. 2015 Dec;31(12):2383-5.
A case of macrocephaly-capıllary malformatıon syndrome presentıng wıth hot water epılepsy. Yilmaz S, Tekin H, Kitis O, Serdaroglu G, Tekgul H, Gokben S.Genet Couns. 2015;26(3):333-7.
Optic disc drusen mimicking papilledema in an infant with Joubert syndrome. Yilmaz S, Biler ED, Solmaz AE, Serdaroglu G, Tekin HG, Gokben S.Genet Couns. 2015;26(1):35-9.
Extreme delta brush activity: Could it be a marker for early diagnosis and prognosis of anti- NMDA (N-methyl-D-aspartate) encephalitis? Tekin HG, Gökben S, Serdaroğlu G.Turk Pediatri Ars. 2019 Mar 1;54(1):61-65. doi: 10.5152/TurkPediatriArs.2018.4628.
Turkish cases of early infantile epileptic encephalopathy: two novel mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene. Gökben S, Serdaroğlu G, Yılmaz S, Bienvenu T, Ceylaner S.Turk J Pediatr. 2015;57(3):272-6.
Early-onset acquired myasthenia gravis secondary to anti-muscle-specific kinase autoantibodies. Yilmaz S, Gokben S, Serdaroglu G, Akcay A.J Child Neurol. 2014;29(1):108-10. doi: 10.1177/0883073812467689.
Clinical characteristics and outcome of children with electrical status epilepticus during slow wave sleep. Yilmaz S, Serdaroglu G, Akcay A, Gokben S. J Pediatr Neurosci. 2014;9(2):105-9. doi: 10.4103/1817-1745.139266.
Histopathological and genetic features of patients with limb girdle muscular dystrophy type 2C. Dınız G, Hazan F, Yildirim HT, Unalp A, Polat M, Serdaroğlu G, Güzel O, Bağ O, Seçıl Y, Ozgönül F, Türe S, Akhan G, Tükün A.Turk Patoloji Derg. 2014;30(2):111-7. doi: 10.5146/tjpath.2014.01239.
Concomitant alpha- and gamma-sarcoglycan deficiencies in a Turkish boy with a novel deletion in the alpha-sarcoglycan gene. Diniz G, Tosun Yildirim H, Gokben S, Serdaroglu G, Hazan F, Yararbas K, Tukun A. Case Rep Genet. 2014;2014:248561. doi: 10.1155/2014/248561.
Changing views of cerebral palsy over 35 years: the experience of a center. Tosun A, Gökben S, Serdaroğlu G, Polat M, Tekgül H.Turk J Pediatr. 2013 Jan-Feb;55(1):8-15.
Electrophysiologic assessment of spasticity in children using H-reflex. Tekgül H, Polat M, Tosun A, Serdaroğlu G, Gökben S.Turk J Pediatr. 2013;55(5):519-23.
Neurocognitive evaluation in children with occipital lobe epilepsy. Polat M, Gokben S, Tosun A, Serdaroglu G, Tekgul H.Seizure. 2012 May;21(4):241-4. doi: 10.1016/j.seizure.2011.12.015.
Use of Buspirone and Fluoxetine for Breathing Problems in Rett Syndrome. Gökben S, Akyol Ardıç U, Serdaroğlu G. Pediatr Neurol 2012;46: 192-4.
Syncope or seizure? The diagnostic value of synchronous tilt testing and video-EEG monitoring in children with transient loss of consciousness. Yilmaz S, Gökben S, Levent E, Serdaroğlu G, Özyürek R.Epilepsy Behav. 2012;24(1):93-6. doi: 10.1016/j.yebeh.2012.02.006.
Video/EEG recording of myoclonic absences in GLUT1 deficiency syndrome with a hot-spot R126C mutation in the SLC2A1 gene. Gökben S, Yılmaz S, Klepper J, Serdaroğlu G, Tekgül H. Epilepsy Behav. 2011;21(2):200-2. doi: 10.1016/j.yebeh.2011.03.027.
Recurrent Pseudotumor Cerebri in Childhood: A Case of Neuro-Behçet Disease Complicated With Thrombotic Risk Factors. Yilmaz S, Serdaroglu G, Unver H, Akçay A, Tekgul H, Gokben S. J of Child Neurol 2011;26:881-4.
Paroxysmal Dystonia as a Rare Initial Manifestation of Multiple Sclerosis. Yilmaz S, Serdaroglu G, Gokben S, Tekgul H. J Child Neurol 2011;26: 1564-66.
A case of neurobrucellosis presenting with isolated intracranial hypertension. Yilmaz S, Serdaroglu G, Gokben S, Tekgul H.J Child Neurol. 2011 Oct;26(10):1316-8. doi: 10.1177/0883073811402205.
Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation, A Vandersteen, U Yiş, G Serdaroglu… – Orphanet journal of …, 2011 –
Triosephosphate isomerase deficiency: a patient with Val231Met mutation. Serdaroglu G, Aydinok Y, Yilmaz S, Manco L, Ozer E. Pediatr Neurol 2011;44(2):139-42. doi:10.1016/j.pediatrneurol.2010.08.016.
Convulsive status epilepticus in children: etiology, treatment protocol and outcome. Saz EU, Karapinar B, Ozcetin M, Polat M, Tosun A, Serdaroglu G, Gokben S, Tekgul H. Seizure 2011;20(2):115-8. doi: 10.1016/j.seizure.2010.10.034.
Ratios of Nine Risk Factors in Children With Recurrent Febrile Seizures. Tosun A, Koturoglu G, Serdaroglu G, Polat M, Kurugol Z, Gokben S, Tekgul H. Pediatr Neurol 2010;43:177-82.
Reversibility of Cytotoxic Edema in Tacrolimus Leukoencephalopathy. Yilmaz S, Gokben S, Arikan C, Calli C, Serdaroglu G. Pediatr Neurol 2010;43:359-62.
An inherited nonsense R1645X mutation in neuronal sodium channel alpha1-subunit gene in a Turkish patient with severe myoclonic epilepsy of infancy. Gökben S, Berdeli A, Serdaroğlu G. Neuropediatrics. 2009 Apr;40(2):82-4. doi: 10.1055/s-0029-1234083.
Evaluation of the cases with acute disseminated encephalomyelitis. Tosun A, Serdaroglu G, Polat M, Tekgul H, Gokben S.Indian J Pediatr 2009;76(5):547-50. doi: 10.1007/s12098-009-0069-2.
Neuropsychologic impairment in children with rolandic epilepsy. Ay Y, Gokben S, Serdaroglu G, Polat M, Tosun A, Tekgul H, Solak U, Kesikci H.Pediatr Neurol 2009;41(5):359-63. doi:10.1016/j.pediatrneurol.2009.05.013.
Febrile seizures: interleukin 1beta and interleukin-1 receptor antagonist polymorphisms. Serdaroğlu G, Alpman A, Tosun A, Pehlivan S, Ozkinay F, Tekgül H, Gökben S. Pediatr Neurol 2009;40(2):113-6. doi: 10.1016/j.pediatrneurol.2008.10.004.
The effect of depression on academic achievement in children with epilepsy. Tosun A, Gokcen S, Ozbaran B, Serdaroglu G, Polat M, Tekgul H, Gokben S. Epil Behav 2008;13:494-8.
Semiologic seizure classification: the effectiveness of a modular education program for health professionals in pediatrics. Isler A, Basbakkal Z, Serdaroglu G, Tosun A, Polat M, Gokben S, Tekgul H.Epilepsy Behav. 2008 Aug;13(2):387-90. doi: 10.1016/j.yebeh.2008.04.023.
Chronic inflammatory demyelinating polyradiculopathy: an atypical pediatric case complicated with phrenic nerve palsy. Polat M, Tosun A, Serdaroğlu G, Cağlayan E, Karapinar B, Gökben S, Tekgül H.Turk J Pediatr. 2007;49(2):210-4.
Miller Fisher syndrome: a case with pattern of pure sensory polyneuropathy concomitant with anti-GQ1B antibody. Akıncı G, Polat M, Tosun A, Serdaroğlu G, Gökben S, Tekgül H. The Turkish Journal of Pediatrics 2007; 49: 109-112.
Vigabatrin caused rapidly progressive deterioration in two cases with early myoclonic encephalopathy associated with nonketotic hyperglycinemia. Tekgul H, Serdaroğlu G, Karapinar B, Polat M, Yurtsever S, Tosun A, Coker M, Gokben S.J Child Neurol. 2006 Jan;21(1):82-4. doi: 10.1177/08830738060210011801.
Electrodiagnostic pattern approach for childhood polyneuropathies. Polat M, Tekgul H, Kilincer A, Tosun A, Terlemez S, Serdaroglu G, Uludag B, Gokben S.Pediatr Neurol. 2006;35(1):11-7. doi: 10.1016/j.pediatrneurol.2005.11.002.
Central core disease: atypical case with respiratory insufficiency in an intensive care unit. Polat M, Tosun A, Ay Y, Ozer E, Serdaroglu G, Aydogdu S, Gokben S, Tekgul H.J Child Neurol. 2006;21(2):173-4. doi: 10.1177/08830738060210021301.
Identification of axonal involvement in Hallervorden-Spatz disease with magnetic resonance spectroscopy. Kitis O, Tekgul H, Erdemir G, Polat M, Serdaroglu G, Tosun A, Coker M, Gokben S.J Neuroradiol. 2006;33(2):129-32. doi: 10.1016/s0150-9861(06)77244-3.
Severe juvenile dermatomyositis: two patients complicated with extra musculocutaneous involvement. Tosun A, Serdaroğlu G, Aslan MT, Polat M, Akalın T, Tekgul H, Gökben S. Rheumatology International 2006;26:1040–1043.
Bone mineral status in pediatric outpatients on antiepileptic drug monotherapy. Tekgul H, Serdaroglu G, Huseyinov A. J Child Neurol 2006;21:411—414; DOI 10.2310/7010.2006.00066.
Cerebrospinal fluid interleukin-6 levels in patients with West syndrome. Tekgul H, Polat M, Tosun A, Serdaroglu G, Kutukculer N, Gokben S.Brain Dev 2006;28(1):19-23. doi:10.1016/j.braindev.2005.03.007.
T-Cell Subsets and Interleukin-6 Response in Rasmussen’s Encephalitis. Tekgul, Polat M, Kitis O, Serdaroglu G, Tosun A, Terlemez S, Kutukculer N, Ersahin Y, Gökben S. Pediatr Neurol 2005;33:39-45.
Ring chromosome 20 syndrome with intractable epilepsy. Alpman A, Serdaroglu G, Cogulu O, Tekgul H. Dev Med Child Neurol 2005;47:343-6. doi.org/10.1017/S0012162205000642
Subacute sclerosing panencephalitis: a case with fulminant course after ACTH. Serdaroglu G, Kutlu A, Tekgul H, Tutuncuoglu S.Pediatr Neurol. 2004 Jul;31(1):67-70. doi: 10.1016/j.pediatrneurol.2003.12.019.
Lymphocyte subsets in Bell’s palsy: immune pathogenesis and outcome prediction. Tekgul H, Polat M, Serdaroğlu G, Ikizoğlu T, Yalaz M, Kutukculer N, Gökben S. Pediatr Neurol 2004;31(4):258-60. doi: 10.1016/j.pediatrneurol.2004.05.003.
Correlative value of magnetic resonance imaging for neurodevelopmental outcome in periventricular leukomalacia. Serdaroglu G, Tekgul H, Kitis O, Serdaroglu E, Gökben S. Dev Med Child Neurol 2004; 46:733-9.
Gastroesophageal reflux in children with cerebral palsy: efficacy of cisapride. Bozkurt M, Tutuncuoglu S, Serdaroglu G, Tekgul H, Aydogdu S. J of Child Neurol 2004, 19(12):973-976.
Prognostic correlative values of the late-infancy MRI pattern in term infants with perinatal asphyxia. Tekgul H, Serdaroglu G,Yalman O, Tutuncuoglu S. Pediatr Neurol 2004;31:35-41.
Oxcarbazepine in the treatment of childhood epilepsy. Serdaroglu G, Kurul S, Tutuncuoglu S, Dirik E, Sarioglu B. Pediatr Neurol 2003;28(1):37-41. doi: 10.1016/s0887-8994(02)00467-8.
The use of botulinum toxin type A treatment in children with spasticity. Sarioglu B, Serdaroglu G, Tutuncuoglu S, Ozer EA.Pediatr Neurol. 2003 Oct;29(4):299-301. doi: 10.1016/s0887-8994(03)00269-8
Tension‐type headache in children: A clinical evaluation. Sarioglu B, Erhan E, Serdaroglu G, Gokce Doering B, Erermis S,Tutuncuoglu S. Pediatr Int 2003;45:186-9.
Sodium valproate prophylaxis in childhood migraine. Serdaroglu G, Erhan E, Tekgul H, Oksel F, Erermis S, Uyar M, Tutuncuoglu S.Headache. 2002 ;42(8):819-22. doi: 10.1046/j.1526-4610.2002.02186.x.
Reflex sympathetic dystrophy in childhood. Tekgül H, Serdaroglu G, Uyar M, Tütüncüoglu S. Indian J Pediatr 2002;69(4):359-61. doi: 10.1007/BF02723223.
Dissection of aorta: a pediatric case report. Serdaroğlu G, Levent E, Yurtsever S, Calkavur T, Yünten N, Aydoğdu S.Turk J Pediatr. 2002;44(3):254-7.PMID: 12405441
Landau-Kleffner syndrome beginning with stuttering: case report. Tütüncüoğlu S, Serdaroğlu G, Kadioğlu B.J Child Neurol. 2002 Oct;17(10):785-8. doi: 10.1177/08830738020170101808.
Coagulation abnormalities and acquired von Willebrand’s disease type 1 in children receiving valproic acid. Serdaroglu G, Tütüncüoglu S, Kavakli K, Tekgül H.J Child Neurol. 2002 Jan;17(1):41-3. doi: 10.1177/088307380201700110.
Hemiplegic Migraine With Prolonged Symptoms: Case Report. Serdaroğlu G, Tütüncüoğlu S, Çalli C, Sarioglu B, Korkmaz H. J of Child Neurol 2002;17:80-1.

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Uluslar Arası Bilimsel Makaleler

Dropped head related lamin A/C associated congenital muscular dystrophy case; previously defined as emerydreifuss muscular dystrophy. Tekin H, Yılmaz S, Tekgül H, Gökben S, Aktan G.Turk J Pediatr 2020;62(1):130-135. doi: 10.24953/turkjped.2020.01.019.

Sulthiame add-on treatment in children with epileptic encephalopathy with status epilepticus: an efficacy analysis in etiologic subgroups. Kanmaz S, Simsek E, Serin HM, Yilmaz S, Aktan G, Tekgul H, Gokben S. Neurol Sci 2020. doi: 10.1007/s10072-020-04526-y.

A transcranial magnetic stimulation study for the investigation of corticospinal motor pathways in children with cerebral palsy. Tekgul H, Saz U, Yilmaz S, Polat M, Aktan G, Kose T, Kitis O, Gokben S

A rare cause of ischemic stroke in childhood: spontaneous long segment intracranial dissection. Simsek E, Yilmaz S, Oran I, Aktan G, Tekgul H, Gokben S.Childs Nerv Syst 2020. doi: 10.1007/s00381-020-04530-9.

A rare cause of brachial plexopathy: hereditary neuralgic amyotrophy. Serin HM, Yılmaz S, Kanmaz S, Şimşek E, Aktan G, Tekgül H, Gökben S. Turk Pediatri Ars. 2019;54(3):189-191. doi: 10.5152/TurkPediatriArs.2018.5837.

The case of pyridoxine dependent epilepsy misdiagnosed as non-ketotic hyperglycinemia. Gazeteci Tekin H, Demir M, Aktan G, Tekgül H, Gökben S.Turk J Pediatr. 2019;61(4):599-603. doi: 10.24953/turkjped.2019.04.019.

Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey. Yiş U, Diniz G, Hazan F, Daimagüler HS, Baysal BT, Baydan F, Akinci G, Ünalp A, Aktan G, Bayram E, Hiz S, Paketçi C, Okur D, Özer E, Danyeli AE, Polat M, Uyanik G, Çirak S.Acta Myol. 2018;37(3):210-220.

Targeted next generation sequencing: the diagnostic value in early-onset epileptic encephalopathy. Gokben S, Onay H, Yilmaz S, Atik T, Serdaroglu G, Tekin H, Ozkinay F. Acta Neurol Belg 2017;117(1):131-138. doi: 10.1007/s13760-016-0709-z.

Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database. Yılmaz Ü, Anlar B, Gücüyener K; Turkish Pediatric Multiple Sclerosis Study Group.Eur J Paediatr Neurol 2017 Nov;21(6):864-872. doi: 10.1016/j.ejpn.2017.06.004.

A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiency. Yilmaz S, Serin M, Canda E, Eraslan C, Tekin H, Ucar SK, Gokben S, Tekgul H, Serdaroglu G.Metab Brain Dis 2017;32(3):675-678. doi: 10.1007/s11011-017-9984-5.

Excellent response to deep brain stimulation in a young girl with GNAO1-related progressive choreoathetosis. Yilmaz S, Turhan T, Ceylaner S, Gökben S, Tekgul H, Serdaroglu G. Childs Nerv Syst 2016;32(9):1567-8. doi: 10.1007/s00381-016-3139-6.

The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorder. Yilmaz S, Gokben S, Serdaroglu G, Eraslan C, Mancinic MS, Tekin H, Tekgul H. Brain and Dev 2016;38:124-7.

Different Neurologic Aspects of Nutritional B12 Deficiency in Infancy. Yilmaz S, Serdaroglu G, Tekgul H, Gokben S.J Child Neurol 2016;31(5):565-8. doi: 10.1177/0883073815601497.

PRUNE1: a disease-causing gene for secondary microcephaly. Karakaya M, Yilmaz S, Storbeck M, Hoelker I, Heller R, Serdaroglu G, Gökben S, Yis U, Wirth B. Brain 2017;140(10):e61. doi: 10.1093/brain/awx197.

Evaluation of ten prognostic factors affecting the outcome of West syndrome. Yilmaz S, Tekgul H, Serdaroglu G, Akcay A, Gokben S.Acta Neurol Belg. 2016;116(4):519-527. doi: 10.1007/s13760-016-0611-8.

Seizures due to high dose camphor ingestion. Tekin HG, Gökben S, Serdaroğlu G.Turk Pediatri Ars. 2015;50(4):248-50. doi: 10.5152/TurkPediatriArs.2015.1360.

The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorder. Yilmaz S, Gokben S, Serdaroglu G, Eraslan C, Mancini GM, Tekin H, Tekgul H.Brain Dev. 2016;38(1):124-7. doi: 10.1016/j.braindev.2015.06.004.

Ictal urinary urge: localization and lateralization value in a pediatric case. Yilmaz S, Gokben S, Turhan T, Serdaroglu G, Tekgul H.Childs Nerv Syst. 2015 Dec;31(12):2383-5.

A case of macrocephaly-capıllary malformatıon syndrome presentıng wıth hot water epılepsy. Yilmaz S, Tekin H, Kitis O, Serdaroglu G, Tekgul H, Gokben S.Genet Couns. 2015;26(3):333-7.

Optic disc drusen mimicking papilledema in an infant with Joubert syndrome. Yilmaz S, Biler ED, Solmaz AE, Serdaroglu G, Tekin HG, Gokben S.Genet Couns. 2015;26(1):35-9.

Extreme delta brush activity: Could it be a marker for early diagnosis and prognosis of anti- NMDA (N-methyl-D-aspartate) encephalitis? Tekin HG, Gökben S, Serdaroğlu G.Turk Pediatri Ars. 2019 Mar 1;54(1):61-65. doi: 10.5152/TurkPediatriArs.2018.4628.

Turkish cases of early infantile epileptic encephalopathy: two novel mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene. Gökben S, Serdaroğlu G, Yılmaz S, Bienvenu T, Ceylaner S.Turk J Pediatr. 2015;57(3):272-6.

Early-onset acquired myasthenia gravis secondary to anti-muscle-specific kinase autoantibodies. Yilmaz S, Gokben S, Serdaroglu G, Akcay A.J Child Neurol. 2014;29(1):108-10. doi: 10.1177/0883073812467689.

Clinical characteristics and outcome of children with electrical status epilepticus during slow wave sleep. Yilmaz S, Serdaroglu G, Akcay A, Gokben S. J Pediatr Neurosci. 2014;9(2):105-9. doi: 10.4103/1817-1745.139266.

Concomitant alpha- and gamma-sarcoglycan deficiencies in a Turkish boy with a novel deletion in the alpha-sarcoglycan gene. Diniz G, Tosun Yildirim H, Gokben S, Serdaroglu G, Hazan F, Yararbas K, Tukun A. Case Rep Genet. 2014;2014:248561. doi: 10.1155/2014/248561.

Changing views of cerebral palsy over 35 years: the experience of a center. Tosun A, Gökben S, Serdaroğlu G, Polat M, Tekgül H.Turk J Pediatr. 2013 Jan-Feb;55(1):8-15.

Electrophysiologic assessment of spasticity in children using H-reflex. Tekgül H, Polat M, Tosun A, Serdaroğlu G, Gökben S.Turk J Pediatr. 2013;55(5):519-23.

Neurocognitive evaluation in children with occipital lobe epilepsy. Polat M, Gokben S, Tosun A, Serdaroglu G, Tekgul H.Seizure. 2012 May;21(4):241-4. doi: 10.1016/j.seizure.2011.12.015.

Use of Buspirone and Fluoxetine for Breathing Problems in Rett Syndrome. Gökben S, Akyol Ardıç U, Serdaroğlu G. Pediatr Neurol 2012;46: 192-4.

Syncope or seizure? The diagnostic value of synchronous tilt testing and video-EEG monitoring in children with transient loss of consciousness. Yilmaz S, Gökben S, Levent E, Serdaroğlu G, Özyürek R.Epilepsy Behav. 2012;24(1):93-6. doi: 10.1016/j.yebeh.2012.02.006.

Video/EEG recording of myoclonic absences in GLUT1 deficiency syndrome with a hot-spot R126C mutation in the SLC2A1 gene. Gökben S, Yılmaz S, Klepper J, Serdaroğlu G, Tekgül H. Epilepsy Behav. 2011;21(2):200-2. doi: 10.1016/j.yebeh.2011.03.027.

Recurrent Pseudotumor Cerebri in Childhood: A Case of Neuro-Behçet Disease Complicated With Thrombotic Risk Factors. Yilmaz S, Serdaroglu G, Unver H, Akçay A, Tekgul H, Gokben S. J of Child Neurol 2011;26:881-4.

Paroxysmal Dystonia as a Rare Initial Manifestation of Multiple Sclerosis. Yilmaz S, Serdaroglu G, Gokben S, Tekgul H. J Child Neurol 2011;26: 1564-66.

A case of neurobrucellosis presenting with isolated intracranial hypertension. Yilmaz S, Serdaroglu G, Gokben S, Tekgul H.J Child Neurol. 2011 Oct;26(10):1316-8. doi: 10.1177/0883073811402205.

Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation, A Vandersteen, U Yiş, G Serdaroglu… – Orphanet journal of …, 2011 –

Triosephosphate isomerase deficiency: a patient with Val231Met mutation. Serdaroglu G, Aydinok Y, Yilmaz S, Manco L, Ozer E. Pediatr Neurol 2011;44(2):139-42. doi:10.1016/j.pediatrneurol.2010.08.016.

Convulsive status epilepticus in children: etiology, treatment protocol and outcome. Saz EU, Karapinar B, Ozcetin M, Polat M, Tosun A, Serdaroglu G, Gokben S, Tekgul H. Seizure 2011;20(2):115-8. doi: 10.1016/j.seizure.2010.10.034.

Ratios of Nine Risk Factors in Children With Recurrent Febrile Seizures. Tosun A, Koturoglu G, Serdaroglu G, Polat M, Kurugol Z, Gokben S, Tekgul H. Pediatr Neurol 2010;43:177-82.

Reversibility of Cytotoxic Edema in Tacrolimus Leukoencephalopathy. Yilmaz S, Gokben S, Arikan C, Calli C, Serdaroglu G. Pediatr Neurol 2010;43:359-62.

An inherited nonsense R1645X mutation in neuronal sodium channel alpha1-subunit gene in a Turkish patient with severe myoclonic epilepsy of infancy. Gökben S, Berdeli A, Serdaroğlu G. Neuropediatrics. 2009 Apr;40(2):82-4. doi: 10.1055/s-0029-1234083.

Evaluation of the cases with acute disseminated encephalomyelitis. Tosun A, Serdaroglu G, Polat M, Tekgul H, Gokben S.Indian J Pediatr 2009;76(5):547-50. doi: 10.1007/s12098-009-0069-2.

Neuropsychologic impairment in children with rolandic epilepsy. Ay Y, Gokben S, Serdaroglu G, Polat M, Tosun A, Tekgul H, Solak U, Kesikci H.Pediatr Neurol 2009;41(5):359-63. doi:10.1016/j.pediatrneurol.2009.05.013.

Febrile seizures: interleukin 1beta and interleukin-1 receptor antagonist polymorphisms. Serdaroğlu G, Alpman A, Tosun A, Pehlivan S, Ozkinay F, Tekgül H, Gökben S. Pediatr Neurol 2009;40(2):113-6. doi: 10.1016/j.pediatrneurol.2008.10.004.

The effect of depression on academic achievement in children with epilepsy. Tosun A, Gokcen S, Ozbaran B, Serdaroglu G, Polat M, Tekgul H, Gokben S. Epil Behav 2008;13:494-8.

Semiologic seizure classification: the effectiveness of a modular education program for health professionals in pediatrics. Isler A, Basbakkal Z, Serdaroglu G, Tosun A, Polat M, Gokben S, Tekgul H.Epilepsy Behav. 2008 Aug;13(2):387-90. doi: 10.1016/j.yebeh.2008.04.023.

Chronic inflammatory demyelinating polyradiculopathy: an atypical pediatric case complicated with phrenic nerve palsy. Polat M, Tosun A, Serdaroğlu G, Cağlayan E, Karapinar B, Gökben S, Tekgül H.Turk J Pediatr. 2007;49(2):210-4.

Miller Fisher syndrome: a case with pattern of pure sensory polyneuropathy concomitant with anti-GQ1B antibody. Akıncı G, Polat M, Tosun A, Serdaroğlu G, Gökben S, Tekgül H. The Turkish Journal of Pediatrics 2007; 49: 109-112.

Electrodiagnostic pattern approach for childhood polyneuropathies. Polat M, Tekgul H, Kilincer A, Tosun A, Terlemez S, Serdaroglu G, Uludag B, Gokben S.Pediatr Neurol. 2006;35(1):11-7. doi: 10.1016/j.pediatrneurol.2005.11.002.

Central core disease: atypical case with respiratory insufficiency in an intensive care unit. Polat M, Tosun A, Ay Y, Ozer E, Serdaroglu G, Aydogdu S, Gokben S, Tekgul H.J Child Neurol. 2006;21(2):173-4. doi: 10.1177/08830738060210021301.

Identification of axonal involvement in Hallervorden-Spatz disease with magnetic resonance spectroscopy. Kitis O, Tekgul H, Erdemir G, Polat M, Serdaroglu G, Tosun A, Coker M, Gokben S.J Neuroradiol. 2006;33(2):129-32. doi: 10.1016/s0150-9861(06)77244-3.

Severe juvenile dermatomyositis: two patients complicated with extra musculocutaneous involvement. Tosun A, Serdaroğlu G, Aslan MT, Polat M, Akalın T, Tekgul H, Gökben S. Rheumatology International 2006;26:1040–1043.

Bone mineral status in pediatric outpatients on antiepileptic drug monotherapy. Tekgul H, Serdaroglu G, Huseyinov A. J Child Neurol 2006;21:411—414; DOI 10.2310/7010.2006.00066.

Cerebrospinal fluid interleukin-6 levels in patients with West syndrome. Tekgul H, Polat M, Tosun A, Serdaroglu G, Kutukculer N, Gokben S.Brain Dev 2006;28(1):19-23. doi:10.1016/j.braindev.2005.03.007.

T-Cell Subsets and Interleukin-6 Response in Rasmussen’s Encephalitis. Tekgul, Polat M, Kitis O, Serdaroglu G, Tosun A, Terlemez S, Kutukculer N, Ersahin Y, Gökben S. Pediatr Neurol 2005;33:39-45.

Ring chromosome 20 syndrome with intractable epilepsy. Alpman A, Serdaroglu G, Cogulu O, Tekgul H. Dev Med Child Neurol 2005;47:343-6. doi.org/10.1017/S0012162205000642

Subacute sclerosing panencephalitis: a case with fulminant course after ACTH. Serdaroglu G, Kutlu A, Tekgul H, Tutuncuoglu S.Pediatr Neurol. 2004 Jul;31(1):67-70. doi: 10.1016/j.pediatrneurol.2003.12.019.

Lymphocyte subsets in Bell’s palsy: immune pathogenesis and outcome prediction. Tekgul H, Polat M, Serdaroğlu G, Ikizoğlu T, Yalaz M, Kutukculer N, Gökben S. Pediatr Neurol 2004;31(4):258-60. doi: 10.1016/j.pediatrneurol.2004.05.003.

Correlative value of magnetic resonance imaging for neurodevelopmental outcome in periventricular leukomalacia. Serdaroglu G, Tekgul H, Kitis O, Serdaroglu E, Gökben S. Dev Med Child Neurol 2004; 46:733-9.

Gastroesophageal reflux in children with cerebral palsy: efficacy of cisapride. Bozkurt M, Tutuncuoglu S, Serdaroglu G, Tekgul H, Aydogdu S. J of Child Neurol 2004, 19(12):973-976.

Prognostic correlative values of the late-infancy MRI pattern in term infants with perinatal asphyxia. Tekgul H, Serdaroglu G,Yalman O, Tutuncuoglu S. Pediatr Neurol 2004;31:35-41.

Oxcarbazepine in the treatment of childhood epilepsy. Serdaroglu G, Kurul S, Tutuncuoglu S, Dirik E, Sarioglu B. Pediatr Neurol 2003;28(1):37-41. doi: 10.1016/s0887-8994(02)00467-8.

The use of botulinum toxin type A treatment in children with spasticity. Sarioglu B, Serdaroglu G, Tutuncuoglu S, Ozer EA.Pediatr Neurol. 2003 Oct;29(4):299-301. doi: 10.1016/s0887-8994(03)00269-8

Tension‐type headache in children: A clinical evaluation. Sarioglu B, Erhan E, Serdaroglu G, Gokce Doering B, Erermis S,Tutuncuoglu S. Pediatr Int 2003;45:186-9.

Sodium valproate prophylaxis in childhood migraine. Serdaroglu G, Erhan E, Tekgul H, Oksel F, Erermis S, Uyar M, Tutuncuoglu S.Headache. 2002 ;42(8):819-22. doi: 10.1046/j.1526-4610.2002.02186.x.

Reflex sympathetic dystrophy in childhood. Tekgül H, Serdaroglu G, Uyar M, Tütüncüoglu S. Indian J Pediatr 2002;69(4):359-61. doi: 10.1007/BF02723223.

Dissection of aorta: a pediatric case report. Serdaroğlu G, Levent E, Yurtsever S, Calkavur T, Yünten N, Aydoğdu S.Turk J Pediatr. 2002;44(3):254-7.PMID: 12405441

Landau-Kleffner syndrome beginning with stuttering: case report. Tütüncüoğlu S, Serdaroğlu G, Kadioğlu B.J Child Neurol. 2002 Oct;17(10):785-8. doi: 10.1177/08830738020170101808.

Coagulation abnormalities and acquired von Willebrand’s disease type 1 in children receiving valproic acid. Serdaroglu G, Tütüncüoglu S, Kavakli K, Tekgül H.J Child Neurol. 2002 Jan;17(1):41-3. doi: 10.1177/088307380201700110.

Hemiplegic Migraine With Prolonged Symptoms: Case Report. Serdaroğlu G, Tütüncüoğlu S, Çalli C, Sarioglu B, Korkmaz H. J of Child Neurol 2002;17:80-1.

Çocuk Nöroloji - EEG Kliniği

Hakkımda

Eserler

İletişim

Dropped head related lamin A/C associated congenital muscular dystrophy case; previously defined as emerydreifuss muscular dystrophy. Tekin H, Yılmaz S, Tekgül H, Gökben S, Aktan G.Turk J Pediatr 2020;62(1):130-135. doi: 10.24953/turkjped.2020.01.019.

Sulthiame add-on treatment in children with epileptic encephalopathy with status epilepticus: an efficacy analysis in etiologic subgroups. Kanmaz S, Simsek E, Serin HM, Yilmaz S, Aktan G, Tekgul H, Gokben S. Neurol Sci 2020. doi: 10.1007/s10072-020-04526-y.

A transcranial magnetic stimulation study for the investigation of corticospinal motor pathways in children with cerebral palsy. Tekgul H, Saz U, Yilmaz S, Polat M, Aktan G, Kose T, Kitis O, Gokben S

A rare cause of ischemic stroke in childhood: spontaneous long segment intracranial dissection. Simsek E, Yilmaz S, Oran I, Aktan G, Tekgul H, Gokben S.Childs Nerv Syst 2020. doi: 10.1007/s00381-020-04530-9.

A rare cause of brachial plexopathy: hereditary neuralgic amyotrophy. Serin HM, Yılmaz S, Kanmaz S, Şimşek E, Aktan G, Tekgül H, Gökben S. Turk Pediatri Ars. 2019;54(3):189-191. doi: 10.5152/TurkPediatriArs.2018.5837.

The case of pyridoxine dependent epilepsy misdiagnosed as non-ketotic hyperglycinemia. Gazeteci Tekin H, Demir M, Aktan G, Tekgül H, Gökben S.Turk J Pediatr. 2019;61(4):599-603. doi: 10.24953/turkjped.2019.04.019.

Childhood onset limb-girdle muscular dystrophies in the Aegean part of Turkey. Yiş U, Diniz G, Hazan F, Daimagüler HS, Baysal BT, Baydan F, Akinci G, Ünalp A, Aktan G, Bayram E, Hiz S, Paketçi C, Okur D, Özer E, Danyeli AE, Polat M, Uyanik G, Çirak S.Acta Myol. 2018;37(3):210-220.

Targeted next generation sequencing: the diagnostic value in early-onset epileptic encephalopathy. Gokben S, Onay H, Yilmaz S, Atik T, Serdaroglu G, Tekin H, Ozkinay F. Acta Neurol Belg 2017;117(1):131-138. doi: 10.1007/s13760-016-0709-z.

A treatable cause of myelopathy and vision loss mimicking neuromyelitis optica spectrum disorder: late-onset biotinidase deficiency. Yilmaz S, Serin M, Canda E, Eraslan C, Tekin H, Ucar SK, Gokben S, Tekgul H, Serdaroglu G.Metab Brain Dis 2017;32(3):675-678. doi: 10.1007/s11011-017-9984-5.

Excellent response to deep brain stimulation in a young girl with GNAO1-related progressive choreoathetosis. Yilmaz S, Turhan T, Ceylaner S, Gökben S, Tekgul H, Serdaroglu G. Childs Nerv Syst 2016;32(9):1567-8. doi: 10.1007/s00381-016-3139-6.

Different Neurologic Aspects of Nutritional B12 Deficiency in Infancy. Yilmaz S, Serdaroglu G, Tekgul H, Gokben S.J Child Neurol 2016;31(5):565-8. doi: 10.1177/0883073815601497.

PRUNE1: a disease-causing gene for secondary microcephaly. Karakaya M, Yilmaz S, Storbeck M, Hoelker I, Heller R, Serdaroglu G, Gökben S, Yis U, Wirth B. Brain 2017;140(10):e61. doi: 10.1093/brain/awx197.

Evaluation of ten prognostic factors affecting the outcome of West syndrome. Yilmaz S, Tekgul H, Serdaroglu G, Akcay A, Gokben S.Acta Neurol Belg. 2016;116(4):519-527. doi: 10.1007/s13760-016-0611-8.

Seizures due to high dose camphor ingestion. Tekin HG, Gökben S, Serdaroğlu G.Turk Pediatri Ars. 2015;50(4):248-50. doi: 10.5152/TurkPediatriArs.2015.1360.

The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorder. Yilmaz S, Gokben S, Serdaroglu G, Eraslan C, Mancini GM, Tekin H, Tekgul H.Brain Dev. 2016;38(1):124-7. doi: 10.1016/j.braindev.2015.06.004.

Ictal urinary urge: localization and lateralization value in a pediatric case. Yilmaz S, Gokben S, Turhan T, Serdaroglu G, Tekgul H.Childs Nerv Syst. 2015 Dec;31(12):2383-5.

A case of macrocephaly-capıllary malformatıon syndrome presentıng wıth hot water epılepsy. Yilmaz S, Tekin H, Kitis O, Serdaroglu G, Tekgul H, Gokben S.Genet Couns. 2015;26(3):333-7.

Optic disc drusen mimicking papilledema in an infant with Joubert syndrome. Yilmaz S, Biler ED, Solmaz AE, Serdaroglu G, Tekin HG, Gokben S.Genet Couns. 2015;26(1):35-9.

Extreme delta brush activity: Could it be a marker for early diagnosis and prognosis of anti- NMDA (N-methyl-D-aspartate) encephalitis? Tekin HG, Gökben S, Serdaroğlu G.Turk Pediatri Ars. 2019 Mar 1;54(1):61-65. doi: 10.5152/TurkPediatriArs.2018.4628.

Turkish cases of early infantile epileptic encephalopathy: two novel mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene. Gökben S, Serdaroğlu G, Yılmaz S, Bienvenu T, Ceylaner S.Turk J Pediatr. 2015;57(3):272-6.

Early-onset acquired myasthenia gravis secondary to anti-muscle-specific kinase autoantibodies. Yilmaz S, Gokben S, Serdaroglu G, Akcay A.J Child Neurol. 2014;29(1):108-10. doi: 10.1177/0883073812467689.