Prof. Dr. Gül Aktan

Prof. Dr. Gül Aktan

Çocuk Nörolojisi - İzmir

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Mansuroğlu Mah. 1593/1 sok. No:6 Lider Centrio C Blok D:77 Bayraklı İzmir

Prof. Dr. Gül Aktan Muayenehanesi

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Prof. Dr. Gül Aktan Hakkında

Prof. Dr. Gül Aktan Kimdir?

Prof.Dr. Gül Aktan, 1990 yılında Ege Üniversitesi Tıp Fakültesinden mezun olmuştur. Çocuk Sağlığı ve Hastalıkları ihtisasını 1995 yılında İzm...

  • Daha Fazla
    • İlgilendiği Hastalıklar
    Tedaviler
    • 3 saatlik video-EEG
    • Aktivasyonlu EEG
    • Bebek ve çocukların nörolojik gelişim takibi
    • Eeg(Elektroensefalografi)
    • Tümünü Göster
    Ödüller
    • Türkiye Çocuk Nörolojisi Derneği, Mayıs 2011; Poster Bildiri Birincilik Ödülü
    • Ulusal Çocuk Nörolojisi Kongresi, Poster Bildiri Ödülü (Üçüncülük) , Eylül 2013; Akut Beyin Hasarlı Yenidoğanlarda Eş Zamanlı Amplitüd EEG Ve Konvansiyonel EEG’nin Karşılaştırılması
    • Türkiye Çocuk Nöroloji Derneği, Mayıs 2015; Poster Bildiri Üçüncülük Ödülü
    • Tümünü Göster
    Yabancı Diller
    • İngilizce
    Yayınlar
    • PERİVENTRİKÜLER LÖKOMALAZİLİ OLGULARDA MANYETİK REZONANS GÖRÜNTÜLEME BULGULARI İLE KLİNİK BULGULARIN KARŞILAŞTIRILMASI-2002
    • PEDİATRİK TÜMÖRLERDE TANIDA GECİKME SÜRESİ-1999
    • ULUSLARARASI YAYIMLANAN BİLİMSEL MAKALELER
    • 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.
    • 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.
    • 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.
    • 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
    • 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.
    • 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 02186.x.
    • 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.
    • 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:
    • 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: .
    • 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.
    • 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.
    • 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.
    • 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 .
    • 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 .
    • 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/
    • 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.
    • 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 .
    • Bone mineral status in pediatric outpatients on antiepileptic drug monotherapy. Tekgul H, Serdaroglu G, Huseyinov A. J Child Neurol 2006;21:411—414; DOI .
    • 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.
    • 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: .
    • 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.
    • 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 .
    • 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.
    • 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.
    • 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.
    • 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 .
    • 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.
    • 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 .
    • 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 .
    • 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: 009-0069-2.
    • 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: 1234083.
    • Reversibility of Cytotoxic Edema in Tacrolimus Leukoencephalopathy. Yilmaz S, Gokben S, Arikan C, Calli C, Serdaroglu G. Pediatr Neurol 2010;43:359-62.
    • 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.
    • 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 .
    • 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 .
    • 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 –
    • 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 .
    • 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.
    • 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.
    • 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 .
    • 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 .
    • Use of Buspirone and Fluoxetine for Breathing Problems in Rett Syndrome. Gökben S, Akyol Ardıç U, Serdaroğlu G. Pediatr Neurol 2012;46: 192-4.
    • 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 .
    • 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.
    • 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.
    • 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: 248561.
    • 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 .
    • 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: .139266.
    • 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 .
    • 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.
    • 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.
    • 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.
    • 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.
    • 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.
    • 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 .
    • 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.
    • 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: 016-0611-8.
    • 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.
    • 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.
    • 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: 016-3139-6.
    • 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 .
    • 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: 017-9984-5.
    • 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 .
    • 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: 016-0709-z.
    • 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): doi: 10.1212/WNL .
    • 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 .
    • 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.
    • 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 .
    • 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.
    • 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: .
    • 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
    • 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: 020-04526-y.
    • 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 .
    • 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.2020.02.01
    • 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.
    • 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: .

    Değerlendirmeler

    Değerlendir

    Hizmetler

    İlgilendiği Hastalıklar
    • Epilepsi
    • Ateşli Havale
    • Dirençli Epilepsi
    • Baş Ağrıları
    • Migren
    • Nöropati
    • Serebral Palsi
    • Beyin Hastalıkları
    • Bayılma
    • Havale
    • Hidrosefali
    • Tuberoskleroz
    • Gelişim Bozuklukları
    • Omurilik Felci
    • Menenjit
    • Optik nöropati
    • Baş Dönmesi
    • Başını dik tutamama, gevşek bebek (Hipotonik bebek)
    • Epilepsi Nöbeti
    • Konuşmada gecikme
    • Yürümede gecikme, parmak ucunda yürüme
    • West Sendromu (İnfantil Spazm)
    • Ateşli ve ateşsiz havale
    • Baş Titremesi (Titubasyon)
    • Çocukluk Çağı Migreni
    • Denge sorunları (Ataksi)
    • Sert bebek (Hipertonik bebek)
    • Yüz Felci
    • Ağlarken nefes tutma (Katılma nöbeti)
    • Kol ve bacaklarda uyuşma, his kusurları
    • Uyurgezerlik
    • Gözlerde Titreme (Nistagmuş)
    • Ellerde titreme (Tremor)
    Tedaviler
    • 3 saatlik video-EEG
    • Aktivasyonlu EEG
    • Bebek ve çocukların nörolojik gelişim takibi
    • Eeg(Elektroensefalografi)
    • Epilepsi Tedavisi
    • Erken doğan bebeklerin veya riskli doğan bebeklerin nörolojik gelişim takibi
    • Normal Randevu
    • Riskli bebek takibi
    • Uyanık EEG
    • Uyanık ve uyku EEG
    • Uyku EEG

    Prof. Dr. Gül Aktan Hakkında

    Prof. Dr. Gül Aktan Kimdir?

    Prof.Dr. Gül Aktan, 1990 yılında Ege Üniversitesi Tıp Fakültesinden mezun olmuştur. Çocuk Sağlığı ve Hastalıkları ihtisasını 1995 yılında İzm...

    Daha Fazla
    İlgilendiği Hastalıklar
    Tedaviler
    • 3 saatlik video-EEG
    • Aktivasyonlu EEG
    • Bebek ve çocukların nörolojik gelişim takibi
    • Eeg(Elektroensefalografi)
    • Tümünü Göster
    Ödüller
    • Türkiye Çocuk Nörolojisi Derneği, Mayıs 2011; Poster Bildiri Birincilik Ödülü
    • Ulusal Çocuk Nörolojisi Kongresi, Poster Bildiri Ödülü (Üçüncülük) , Eylül 2013; Akut Beyin Hasarlı Yenidoğanlarda Eş Zamanlı Amplitüd EEG Ve Konvansiyonel EEG’nin Karşılaştırılması
    • Türkiye Çocuk Nöroloji Derneği, Mayıs 2015; Poster Bildiri Üçüncülük Ödülü
    • Tümünü Göster
    Yabancı Diller
    • İngilizce
    Yayınlar
    • PERİVENTRİKÜLER LÖKOMALAZİLİ OLGULARDA MANYETİK REZONANS GÖRÜNTÜLEME BULGULARI İLE KLİNİK BULGULARIN KARŞILAŞTIRILMASI-2002
    • PEDİATRİK TÜMÖRLERDE TANIDA GECİKME SÜRESİ-1999
    • ULUSLARARASI YAYIMLANAN BİLİMSEL MAKALELER
    • 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.
    • 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.
    • 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.
    • 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
    • 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.
    • 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 02186.x.
    • 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.
    • 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:
    • 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: .
    • 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.
    • 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.
    • 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.
    • 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 .
    • 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 .
    • 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/
    • 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.
    • 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 .
    • Bone mineral status in pediatric outpatients on antiepileptic drug monotherapy. Tekgul H, Serdaroglu G, Huseyinov A. J Child Neurol 2006;21:411—414; DOI .
    • 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.
    • 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: .
    • 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.
    • 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 .
    • 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.
    • 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.
    • 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.
    • 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 .
    • 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.
    • 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 .
    • 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 .
    • 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: 009-0069-2.
    • 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: 1234083.
    • Reversibility of Cytotoxic Edema in Tacrolimus Leukoencephalopathy. Yilmaz S, Gokben S, Arikan C, Calli C, Serdaroglu G. Pediatr Neurol 2010;43:359-62.
    • 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.
    • 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 .
    • 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 .
    • 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 –
    • 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 .
    • 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.
    • 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.
    • 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 .
    • 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 .
    • Use of Buspirone and Fluoxetine for Breathing Problems in Rett Syndrome. Gökben S, Akyol Ardıç U, Serdaroğlu G. Pediatr Neurol 2012;46: 192-4.
    • 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 .
    • 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.
    • 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.
    • 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: 248561.
    • 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 .
    • 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: .139266.
    • 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 .
    • 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.
    • 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.
    • 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.
    • 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.
    • 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.
    • 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 .
    • 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.
    • 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: 016-0611-8.
    • 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.
    • 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.
    • 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: 016-3139-6.
    • 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 .
    • 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: 017-9984-5.
    • 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 .
    • 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: 016-0709-z.
    • 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): doi: 10.1212/WNL .
    • 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 .
    • 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.
    • 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 .
    • 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.
    • 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: .
    • 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
    • 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: 020-04526-y.
    • 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 .
    • 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.2020.02.01
    • 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.
    • 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: .

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