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PROF. DR. DİLŞAD TÜRKDOĞAN

Çocuk Nörolojisi Uzmanı
Epilepsi-EEG ve Epilepsi Cerrahisi Uzmanı
Nörofizyoloji Uzmanı
Çocuk Sağlığı Hastalıkları Uzmanı
Uluslararası hakemli dergilerde yayınlanan makaleler
  1. Türkdoğan D, Emre S, Tanman F, Şirin A, Nayır A, Uysal V. Efficiacy of captopril treatment in children with steroid resistant nephrotic syndrome. Acta Paediatrica Japonica 1994;36:658-61.
  2. Çalışkan M, Türkdoğan D, Özmen M, Cantez T, Baslo A, Apak S. Continous muscle fiber activity syndrome. Acta Paediatrica Japonica. 1995;37:94-6.
  3. Türkdoğan S. D, Barutçu ÜB, Karakoç Y, Yalçın E, Önen S. The effects of antiepileptic drugs on serum zinc and copper levels in children. Journal of Basic and Clinical Physiology and Pharmacology 1995;6:265-69.
  4. Yüksel A, Şenocak D, Türkdoğan S.D, Keskin G, Dirican A, Cenani A, Yalçın E. Effects of carbamazepine and valproate on brainstem auditory evoked potentials in epileptic children. Child's Nervous System 1995;11:474-7.
  5. Türkdoğan S.D, Önsel Ç, Altıok E, Uslu İ, Yalçın E. Cerebellar and subcortical blood flow abnormalities in children with partial epilepsy. Brain and Development 1996:18;95-8.
  6. Türkdoğan S.D, Ataklı D, Okan D, Baybaş S, Arpacı B. Serum lipids in epileptic children treated with carbamazepine and valproate. European Journal of Pediatrics 1997;156:565-7.
  7. Ataklı D, Türkdoğan S. D, Atay T, Baybas S, Arpacı B. Misdiagnosis and treatment in juvenile myoclonic epilepsy. Seizure 1998:7:63-6.
  8. Türkdoğan S.D, Özek MM, Şehiraltı V, Kurtkaya Ö, Sav A. Hemimegalencephaly and Hirschsprung’s disease: A unique association. Pediatric Neurology 1998;18:452-455.
  9. Akyüz G, Türkdoğan S. D, Turan B, Canbolat N, Yılmaz I, Us Ö, Kayhan Ö. Sympathetic skin response and RR interval variation in normal Turkish children. Brain and Development 1999;21:99-102.
  10. Türkdoğan S. D, Özek MM, Sav A, Dinçer A, Pamir MN. Serial MRI and MRS studies with unusual findings in Rasmussen’s syndrome. European Radiology 2000;10:962-6.
  11. Türkdoğan S.D, Onat F, Türe U, Pamir N. Phenytoin toxicity with mandibular tremor secondary to intravenous administration. Int J of Clin Pharma and Therap 2002 Jan;40(1):18-9.
  12. Türkdoğan D, Toplan S, Karakoç Y. Lipid peroxidation and antioxidative enzyme activities in childhood epilepsy. J Child Neurology 2002;17:673-6.
  13. Uneri A, Turkdogan D. Evaluation of vestibular functions in children with vertigo attacks. Archieves of Disease in Childhood 2003;88:510-1.
  14. Türkdoğan D, Akyüz G, Us O. Visual and auditory event related potentials in epileptic children: A comparison with normal and abnormal MRI findings. Brain and Development 2003;25: 396-400.
  15. Müslümanoğlu L, Akı S, Türkdoğan D, Us O, Akyüz G. Involvement of sympathetic reflex activity in patients with acute and chronic stroke: a comparison with functional motor capacity. Archieves of Physical Medicine and Rehabilitation 2004;85: 470-3.
  16. Akman I, Ozek E, Kulekci S, Turkdogan D, Cebeci D, Akdas F. Auditory neuropathy in hyperbilirubinemia: is there a correlation between serum bilirubin, neuron-specific enolase levels and auditory neuropathy? Int J Audiol. 2004 Oct;43(9):516-22.
  17. Türkdoğan D, Duchowny M, Resnick T Jayakar P. Subdural EEG patterns in children with Taylor-type cortical dysplasia: comparison with nondysplastic lesions. Journal of Clinical Neurophysiology 2005; 22: 37-42.
  18. Baykan B, Kayrak Ertaş N, Ertaş M, the Epibase group. Comparison of classifications of seizures: A preliminary study with 28 participants and 48 seizures. Epilepsy and Behaviour 2005;6:607-12.
  19. Türkdoğan D, Cagırıcı S, Soylemez D, Sur H, Bilge C, Turk U. Characteristic and overlapping features of migraine and tension-type headache. Headache 2006; 46: 461-8.
  20. Vanmolkot KR, Kors EE, Turk U, Turkdogan D, Keyser A,…… Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine. Eur J Hum Genet. 2006 Mar 15: 1-6.
  21. Dibbens LM, Mullen S, Helbig I, ….Turkdogan D. … Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance. Human Mol Gen 2009:18:3636-3631.
  22. Turkdogan D, Bekiroglu N, Zaimoglu S. A prevelance study of restless legs syndrome in Turkish children. Sleep Medicine 2011;12:315-21.
  23. Yalçın Ö, ……Turkdogan D,…..Çağlayan H. An association analysis for Idiopathic Absence Epilepsy in 2q36 in the Turkish population. Epilepsia 2011; 52:975-83.
  24. EPICURE Consortium, Leu C, .., Turkdogan D, … Sander T. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies. Epilepsia. 2012 Feb;53:308-18.
  25. PRRT2 mutations are the major cause of benign familial infantile seizures (BFIS). Schubert J…Turkdogan D, … Weber YG. Hum Mutat. 2012 May 23.
  26. EPICURE Consortium, Møller RS, .., Turkdogan D, … Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. Epilepsia. 2013 Feb; 54(2) :256-64.
  27. Turkdogan D, Orengul C, Ekinci G, Zaimoglu S. Anti-N-Methyl-D-Aspartate (Anti-NMDA) receptor encephalitis: rapid and sustained clinical improvement with steroid therapystarting in the late phase. J Child Neurology. 2014; 29: 684-687
  28. Zaimoglu S., Turkdogan D, Mazlum B, et al. When is EEG indicated in Attention-Deficit/Hyperactivity Disorder? J Child Neurology. 2015.
  29. Tanrıkulu B, Özen A, Günal DI, Turkdogan D, Bayraklı F, Bayri Y, Dağçınar A, Şeker A. Deep brain stimulation as treatment for dystonic storm in pantothenate kinase-associated neurodegeneration syndrome: case report of a patient with homozygous C.628 2 T > G mutation of the PANK2 gene. Acta Neurochir . 2015 Sep;157(9):1513-7.
  30. Geckinli BB, Aydin H, Karaman A, Delil K, Simsek H, Gokmeydan E, Turkdogan D. Clinical report of a patient with de novo trisomy 12q23.1q24.33. Genet Couns. 2015;26(4):393 400.
  31. Usluer S, Salar S, Arslan M, Yiş U, Kara B, Tektürk P, Baykan B, Meral C, Türkdoğan D, …. Çağlayan SH. SCN1A gene sequencing in 46 Turkish epilepsy patients disclosed 12 novel mutations. Seizure. 2016 Jul;39:34-43
  32. Ünver O, Ekinci G, Kutlubay BI, Gülten T, Güneş S, Hacıfazlıoğlu NE, Türkdoğan D. Evaluation of cases with cerebral thrombosis in children. Turk Pediatri Ars. 2016 51:87-93.
  33. Ünver O, Hacıfazlıoğlu NE, Karatoprak E, Güneş AS, Sağer G, Kutlubay B, Sözen G, Saltık S, Yılmaz K, Kara B, Türkdoğan D. The frequency of late-onset Pompe disease in pediatric patients with limb-girdle muscle weakness and nonspecific hyperCKemia: A multicenter study. Neuromuscul Disord. 2016; 26:796-800
  34. Ünver O, Kutlubay B, Besci T, Ekinci G, Baltacıoğlu F, Türkdoğan D. Transient Splenial Lesion of the Corpus Callosum Related to Migraine with Aura in a Pediatric Patient. Acta Medica 2016;59:64-6.
  35. Şahin S, Türkdoğan D, Hacıfazlıoğlu NE, Yalçın EU, Eksen ZY, Ekinci G. Global aphasia without hemiparesis may be caused by blunt head trauma: An adolescent boy with transient aphasia. J Clin Neurosci. 2017 May;39:84-86
  36. Turkdogan D, Usluer S, Akalin F, Agyuz U, Aslan ES. Familial early in-fantile epileptic encephalopathy and cardiac conduction disorder: A rare cause of SUDEP in infancy. Seizure. 2017;50:171-172.
  37. Aydin K,…. Turkdogan D,..; Turkish Cerebral Palsy Study Group. A multicenter cross-sectional study to evaluate the clinical characteris tics and nutritional status of children with cerebral palsy. Clin Nutr ES PEN. 2018 Aug;26:27-34. doi: 10.1016/j.clnesp.2018.05.002.
  38. Turkdogan D, Turkyilmaz A, Gormez Z, Sager G, Ekinci G. A novel truncating mutation of DOCK7 gene with an early-onset non- encephalopathic epilepsy. Seizure. 2019 Jan 16;66:12-14. doi: 10.1016/j.seizure.2019.01.010.
  39. Turkdogan D, Thomas G, Demirel B. Ketogenic diet as a successful early treatment modality for SCN2A mutation. Brain and Development. 2019;41:389-391.
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