Uluslararası hakemli dergilerde yayınlanan makaleler (SCI,SSCI,Arts and Humanities)

1. Tekgül H., Polat M., Kitiş Ö., Serdaroğlu G., Tosun A., Terlemez S., Kütükçüler N., Erşahin Y., Gökben S. (2005). T-Cell subsets and interleukin-6 response in Rasmussen’s encephalitis. Pediatric Neurology, 33, 39–45.
2. Tekgül H., Polat M., Tosun A., Serdaroğlu G., Kütükçüler N., Gökben S. (2006). Cerebrospinal fluid interleukin-6 levels in patients with West syndrome. Brain & Development, 28, 19–23.
3. Tekgül H., Serdaroğlu G., Karapınar B., Polat M., Yurtsever S., Tosun A., Çoker M., Gökben S. (2006). Vigabatrin caused rapidly progressive deterioration in two cases with early myoclonic encephalopathy associated with nonketotic hyperglycinemia. Journal of Child Neurology, 21, 82–84.
4. Polat M., Tosun A., Ay Y., Ozer E., Serdaroğlu G., Aydoğdu S., Gökben S., Tekgül H. (2006). Central core disease: Atypical case with respiratory insufficiency in an intensive care unit. Journal of Child Neurology, 21, 173–174.
5. Tosun A., Serdaroğlu G., Aslan M.T., Polat M., Akalın T., Tekgül H., Gökben S. (2006). Severe juvenile dermatomyositis: Two patients complicated with extra musculocutaneous involvement. Rheumatology International, 26, 1040–1043.
6. Kitiş Ö., Tekgül H., Erdemir G., Polat M., Serdaroğlu G., Tosun A., Çoker M., Gökben S. (2006). Identification of axonal involvement in Hallervorden–Spatz disease with magnetic resonance spectroscopy. Journal of Neuroradiology, 33, 129–132.
7. Polat M., Tekgül H., Kılınçer A., Tosun A., Terlemez S., Serdaroğlu G., Uludağ B., Gökben S. (2006). Electrodiagnostic patterns approach for childhood polyneuropathies. Pediatric Neurology, 35, 11–17.
8. Akıncı G., Polat M., Tosun A., Serdaroğlu G., Gökben S., Tekgül H. (2007). Miller Fisher syndrome: A case with pattern of pure sensory polyneuropathy concomitant with anti-GQ1B antibody. Turkish Journal of Pediatrics, 49, 109–112.
9. Cakır D., Tosun A., Polat M., Celebisoy N., Gökben S., Aydoğdu S., Yağcı R.V., Tekgül H. (2007). Subclinical neurological abnormalities in children with celiac disease receiving a gluten-free diet. Journal of Pediatric Gastroenterology and Nutrition, 45, 366–369.
10. Polat M., Tosun A., Serdaroğlu G., Cağlayan E., Karapınar B., Gökben S., Tekgül H. (2007). Chronic inflammatory demyelinating polyradiculopathy: An atypical pediatric case complicated with phrenic nerve palsy. Turkish Journal of Pediatrics, 49, 210–214.
11. Gökben S., Tosun A., Bayram N., Serdaroğlu G., Polat M., Kavaklı K., Tekgül H. (2007). Arterial ischemic stroke in childhood: Risk factors and outcome in old versus new era. Journal of Child Neurology, 22, 1204–1208.
12. Türkmen M., Eliaçik K., Temoçin K., Savk E., Tosun A., Dikicioğlu E. (2007). A rare cause of neonatal seizure: Incontinentia pigmenti. Turkish Journal of Pediatrics, 49, 327–330.
13. İşler A., Başbakkal Z., Serdaroğlu G., Tosun A., Polat M., Gökben S., Tekgül H. (2008). Semiologic seizure classification: The effectiveness of a modular education program for health professionals in pediatrics. Epilepsy & Behavior, 13, 387–390.
14. Tosun A., Gökcen S., Özbaran B., Serdaroğlu G., Polat M., Tekgül H., Gökben S. (2008). The effect of depression on academic achievement in children with epilepsy. Epilepsy & Behavior, 13, 494–498.
15. Serdaroğlu G., Alpman A., Tosun A., Pehlivan S., Özkınay F., Tekgül H., Gökben S. (2009). Febrile seizures: Interleukin-1β and interleukin-1 receptor antagonist polymorphisms. Pediatric Neurology, 40(2), 113–116.
16. Tosun A., Serdaroğlu G., Polat M., Tekgül H., Gökben S. (2009). The evaluation of the cases with acute disseminated encephalomyelitis. Indian Journal of Pediatrics, 76, 547–550.
17. Çeçen E., Uygur Ö., Tosun A. (2009). Severe central nervous and respiratory system depression after sedation with chloral hydrate: A case report. Turkish Journal of Pediatrics, 51, 497–499.
18. Yılmaz A., Gökben S., Serdaroğlu G., Polat M., Tosun A., Tekgül H., Solak U., Kesikci H. (2009). Neuropsychologic impairment in children with Rolandic epilepsy. Pediatric Neurology, 41, 359–363.
19. Tosun A., Koturoğlu G., Serdaroğlu G., Polat M., Kurugöl Z., Gökben S., Tekgül H. (2010). Ratios of nine risk factors in children with recurrent febrile seizures. Pediatric Neurology, 43, 177–182.
20. Girişgen I., Tosun A., Sönmez F., Özsunar Y. (2010). Recurrent and atypical posterior reversible encephalopathy syndrome in a child with peritoneal dialysis. Turkish Journal of Pediatrics, 52, 416–419.
21. Saz E.U., Karapınar B., Özçetin M., Polat M., Tosun A., Serdaroğlu G., Gökben S., Tekgül H. (2011). Convulsive status epilepticus in children: Etiology, treatment protocol and outcome. Seizure, 20, 115–118.
22. Tosun A., Aral Y.Z., Çeçen E., Aydoğdu A., Çetinkaya Çakmak B. (2011). Involuntary movement in infants during vitamin B12 treatment. Turkish Journal of Hematology, 28, 317–322.
23. Polat M., Gökben S., Tosun A., Serdaroğlu G., Tekgül H. (2012). Neurocognitive evaluation in children with occipital lobe epilepsy. Seizure, 21(4), 241–244.
24. Tosun A., Gökben S., Serdaroğlu G., Polat M., Tekgül H. (2013). Changing views of cerebral palsy over 35 years: The experience of a center. Turkish Journal of Pediatrics, 55(1), 8–15.
25. Tekgül H., Polat M., Tosun A., Serdaroğlu G., Gökben S. (2013). Electrophysiologic assessment of spasticity in children using H-reflex. Turkish Journal of Pediatrics, 55(5), 519–523.
26. Tosun A., Dursun Ş., Akyıldız U.O., Oktay S., Tataroğlu C. (2015). Acute motor-sensory axonal neuropathy with hyperreflexia in Guillain–Barré syndrome. Journal of Child Neurology, 30(5), 637–640.
27. Tosun A., Kurtgöz S., Dursun S., Bozkurt G. (2014). A case of Ehlers–Danlos syndrome type VIA with a novel PLOD1 gene mutation. Pediatric Neurology, 51(4), 566–569.
28. Eryılmaz A., Başal Y., Tosun A., Omurlu I.K., Başak S. (2015). The neutrophil to lymphocyte ratios of our pediatric patients with Bell's palsy. International Journal of Pediatric Otorhinolaryngology, 79(12), 2374–2377. doi:10.1016/j.ijporl.2015.10.047
29. Tosun A., Erişen Karaca S., Ünüvar T., Yürekli Y., Yenisey C., Omurlu I.K. (2017). Bone mineral density and vitamin D status in children with epilepsy, cerebral palsy, and cerebral palsy with epilepsy. Child’s Nervous System, 33(1), 153–158. doi:10.1007/s00381-016-3258-0
30. Yış U., Becker K., Hız A.S., Uyanık G., Bayram E., Haliloğlu V.G., Polat A.İ., Ayanoğlu M., Okur T.D., Tosun A.F., Aktan G., Keskin Yılmaz S., Topaloğlu H.A., Anlar F.B., Çırak S., Engel A. (2017). Genetic landscape of congenital myasthenic syndromes from Turkey: Novel mutations and clinical insights. Journal of Child Neurology, 32(8), 759–765.
31. Yılmaz Ü., Anlar B., Gücüyener K.; Turkish Pediatric Multiple Sclerosis Study Group. (2017). Characteristics of pediatric multiple sclerosis: The Turkish pediatric multiple sclerosis database. European Journal of Paediatric Neurology, 21(6), 864–872. doi:10.1016/j.ejpn.2017.06.002
32. Tosun A., Gürbüz Ö.B., Aksu H., Kaynak Türkmen M. (2017). The long-term neurodevelopmental outcomes of infants born full-term with low birth weight. Turkish Journal of Pediatrics, 59(2), 169–175.
33. Öztürk Z., Yılmaz Ü., Konuşkan B., Gücüyener K., Demir E., Anlar B.; Turkish Pediatric Multiple Sclerosis Study Group. (2018). Multiple sclerosis with onset younger than 10 years in Turkey. Neuropediatrics, 49(1), 51–58.
34. Durum Y., Dayanır Özsunar Y., Navaei A.H., Tosun A. (2018). A case presentation of atypical X-linked adrenoleukodystrophy: Initial experience with ASL technique. Current Medical Imaging  14(2), 158–162.
35. Carman K.B., Çalık M., Karal Y., Isikay S., Koçak O., Özçelik A., Yazar A.S., Nuhoğlu C., Sağ C., Kılıç O., Dinleyici M., Lacinel Gürlevik S., Yimenicioglu S., Ekici A., Perk P., Tosun A., Işık I., Yarar C., Arslantaş D., Dinleyici E.C. (2019). Viral etiological causes of febrile seizures for respiratory pathogens (EFES Study). Human Vaccines & Immunotherapeutics, 15(2), 496–502. doi:10.1080/21645515.2018.1506000
36. Turgut Y.B., Tosun A.F., Kıpçak Yüzbaşı B., Tunca H. (2020). Behçet’s disease from rheumatology and neurology perspectives with special reference to children. Journal of Pediatric Neurology, 18, 175–181.
37. Ozbay H.C., Ozbek M., Sevincok D., Tas K., Aksu H., Tosun A. (2020). Autism spectrum disorder in a child with Hunter syndrome. Psychiatry and Clinical Psychopharmacology, 30(3), 332–334.
38. Yılmaz Ü., Gücüyener K., Yavuz M., Öncel İ., Canpolat M., Saltık S., Ünver O., Çıtak Kurt A.N., Tosun A., Yılmaz S., Özgör B., Erol İ., Öztoprak Ü., Elitez D.A., Direk M.Ç., Bodur M., Teber S., Anlar B. (2022). Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes. European Journal of Paediatric Neurology, 41, 8–18. doi:10.1016/j.ejpn.2022.08.006
39. Sarıkaya Uzan G., Vural A., Yüksel D., Aksoy E., Öztoprak Ü., Canpolat M., Öztürk S., Yıldırım Ç., Güleç A., Per H., Gümüş H., Okuyaz Ç., Çobanoğulları Direk M., Kömür M., Ünalp A., Yılmaz Ü., Bektaş Ö., Teber S., Aliyeva N., Olgaç Dündar N., Gençpınar P., Gürkaş E., Keskin Yılmaz S., Kanmaz S., Tekgül H., Aksoy A., Öz Tuncer G., Acar Arslan E., Tosun A., Ayanoğlu M., Kızılırmak A.B., Yousefi M., Bodur M., Ünay B., Hız Kurul S., Yiş U. (2023). Pediatric-onset chronic inflammatory demyelinating polyneuropathy: A multicenter study. Pediatric Neurology, 145, 3–10. doi:10.1016/j.pediatrneurol.2023.04.018
40. Ayanoğlu M., Çevik Ö., Erdoğan Ö., Tosun A.F. (2024). TARC and Septin 7 can be better monitoring biomarkers than CX3CL1, sICAM5, and IRF5 in children with seizure-free epilepsy with monotherapy and drug-resistant epilepsy. International Journal of Neuroscience, 134(3), 243–252. doi:10.1080/00207454.2022.2100773
41. Direk M.Ç., Besen Ş., Öncel İ., Günbey C., Özdoğan O., Orgun L.T., Şahin S., Cansu A., Yıldız N., Kanmaz S., Yılmaz S., Tekgül H., Türkdoğan D., Ünver O., Thomas G.Ö., Başıbüyük S., Yılmaz D., Kurt A.N., Gültutan P., Özsoy Ö., Yiş U., Kurul S.H., Güngör S., Özgör B., Karadağ M., Dündar N.O., Gençpınar P., Bildik O., Orak S.A., Kabur Ç.Ç., Kara B., Karaca Ö., Canpolat M., Gümüş H., Per H., Yılmaz Ü., Karaoğlu P., Ersoy Ö., Tosun A., Öztürk S.B., Yüksel D., Atasoy E., Gücüyener K., Yıldırım M., Bektaş Ö., Çavuşoğlu D., Yarar Ç., Güngör O., Mert G.G., Sarıgeçili E., Edizer S., Çetin İ.D., Aydın S., Diler B., Özdemir A.A., Erol İ., Okuyaz Ç., Anlar B. (2024). Optic neuritis in Turkish children and adolescents: A multicenter retrospective study. Multiple Sclerosis and Related Disorders, 81, 105149. doi:10.1016/j.msard.2023.105149
42. Kanmaz S., Tekgül H., Kayılıoğlu H., Ataş Y., Kart P.O., Yıldız N., Gümüş H., Aydın K., Tosun A., Turkish Epistep Consortium. (2024). Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study. Seizure, 123, 17–25. doi:10.1016/j.seizure.2024.09.021
43. Gök M., Öner R., Özgezmez F.T., Aydın E., Tosun A.F., Cullu E. (2025). Reviewing the reliability of revised Melbourne Cerebral Palsy Hip Classification System across different medical specialties. Joint Diseases and Related Surgery, 36(1), 148–154. doi:10.52312/jdrs.2025.2023
44. Günay Ç., Aykol D., Özsoy Ö., Sönmezler E., Hancı Y.S., Kara B., Akkoyunlu Sünnetçi D., Cine N., Deniz A., Özer T., Ölçülü C.B., Yılmaz Ö., Kanmaz S., Yılmaz S., Tekgül H., Yıldız N., Acar Arslan E., Cansu A., Olgaç Dündar N., Kuşgöz F., Didinmez E., Gençpınar P., Aksu Uzunhan T., Ertürk B., Gezdirici A., Ayaz A., Ölmez A., Ayanoğlu M., Tosun A., Topçu Y., Kılıç B., Aydın K., Çağlar E., Ersoy Kosvali Ö., Okuyaz Ç., Besen Ş., Tekin Orgun L., Erol İ., Yüksel D., Sezer A., Atasoy E., Toprak Ü., Güngör S., Özgör B., Karadağ M., Dilber C., Şahinoğlu B., Uyur Yalçın E., Eldes Hacifazlıoğlu N., Yaramiş A., Edem P., Gezici Tekin H., Yılmaz Ü., Ünalp A., Turay S., Biçer D., Gül Mert G., Dokurel Çetin İ., Kirik S., Öztürk G., Karal Y., Sanri A., Aksoy A., Polat M., Özgün N., Soydemir D., Sarıkaya Uzan G., Ülker Üstebay D., Gök A., Yeşilmen M.C., Yiş U., Karakülah G., Bursalı A., Oktay Y., Hız Kurul S. (2023). Shared biological pathways and processes in patients with intellectual disability: A multicenter study. Neuropediatrics, 54(4), 225–238. doi:10.1055/a-2034-8528
45. Kanmaz S., Yılmaz S., Dündar N.O., Aksoy A., Canpolat M., Per H., Erol İ., Gümüş H., Özkale Y., Öztürk S., Toprak D.E., Öncel İ., Özkale M., Ozmansur E.N., Serin H.M., Ersöz G., Besen Ş., Mert G.G., Güleç A., Şahin S., Ölçülü C.B., Selek A., Pekuz S., Başarır G., Günay Ç., Biçer D., Kahraman Z.F., Yüksel D., Karadağ M., Şimşek E., Ünalp A., Yıldız N., Direk M.Ç., Yiş U., Tan H., Havalı C., Değerliyurt A., Güngör M., Hergüner Ö., Oncel E.P., Ünver O., Kumandaş S., Çelik H.A., Özgör B., Cansu A., Atasever A.K., Tosun A., Güngör O., Okuyaz Ç., Edizer S., Hız S., Sarıgeçili E., Kayılıoğlu H., Yazgan C.D., Tuncer G.Ö., Gençpınar P., Yılmaz Ü., Özgür S., Tekgül H., Anlar B. (2025). Acute disseminated encephalomyelitis in children and adolescents: A multicenter retrospective study of relapse and outcome. Journal of Child Neurology. doi:10.1177/08830738251334219
46. Bozkaya-Yılmaz S., Olgaç-Dündar N., Aliyeva N., Ersen A., Gençpınar P., Güngör M., Hız A.S., Yiş U., Sarıkaya-Uzan G., Sarıgeçili E., Kirik S., Erol İ., Besen S., Kayılıoğlu H., Haspolat S., Kipoglu O., Ekici A., Turay S., Tosun A., Ayanoğlu M., Danış A., Hancı F., Kutbay Y.B., Ozyılmaz B., Kara B. (2025). Phenotypic variability in cases with CACNA1A mutation. European Journal of Pediatrics, 184(4), 261. doi:10.1007/s00431-025-06062-3
47. Yiğit Z.M., Dikbaş O.S., Tosun A., Ayanoğlu M., Kıyılıoğlu N., Sair A., Akyıldız U.O., Kutlu G., Bozkurt G. (2025). Charting the genetic landscape of autosomal recessive hereditary spastic paraplegia: A deep dive into 10 exceptionally rare cases. Neurogenetics, 26, 58. doi:10.1007/s10048-025-00841-8
48. Oktay S., Söğütlüler T., Avcil S., Akçanal Şeker C., Öner H., Öztürk H., Tosun A., Özsunar Y. (2025). Using audiovisual intervention to reduce anxiety and improve image quality in pediatric magnetic resonance imaging. Pediatric Radiology, 55, 1582–1590. doi:10.1007/s00247-025-06276-5.

Uluslararası diğer hakemli dergilerde yayınlanan makaleler

1. Eryılmaz A., Başal Y., Günel C., Özkul A., Tosun A. (2015). Successful treatment of essential palatal tremor lasting over a long term with a rare application of botulinum toxin in a child. Iranian Journal of Child Neurology, 9(4), 75–77. (ESCI)
2. Anık A., Polat A., Durum Y., Tosun A. (2016). An uncommon cause of Duane syndrome in a child: Wildervanck syndrome. Journal of Pediatric Research, 3(1), 53–55. (ESCI)
3. Anık A., Anık A., Ünüvar T., Tosun A., Dursun S., Akcan A.B., Durum Y., Kaynak Türkmen M. (2016). Cystic encephalomalacia and infantile spasm as a complication of transient and mild hyperinsulinemic hypoglycemia. Journal of Pediatric Research, 3(2), 129–132. (ESCI)
4. Gürbüz Ö.B., Aksu H., Tosun A. (2018). Comorbid obsessive compulsive disorder in a child with tuberous sclerosis complex. Psychiatry and Behavioral Sciences, 8(3), 142–144. (ESCI)
5. Ayanoğlu M., Öztürk S., Tosun A. (2022). Assessment of the knowledge levels and attitudes of physicians regarding the management of acute seizures in pediatric patients. Journal of Pediatric Research, 9(4), 320–330. (ESCI)
6. Ayanoğlu M., Sönmez F., Tosun A., Yılmaz D. (2021). Ophthalmoplegia in the Acute Phase of Hemolytic Uremic Syndrome: A Case Report. Trends in Pediatrics, 2(1), 47–50.  (ESCI)
7. Carman K.B., Tuncel T., Çalık M., vd. (2019). Aquaporin 4 Gene Polymorphism in Children with Febrile Seizure. Osmangazi Journal of Medicine. doi:10.20515/otd.469491.  (ESCI)
8. Uysal P., Telli M., Turan Y., Eryılmaz A., Durum Y., Tosun A. (2019). An Adolescent with a Suddenly Developed Mask Face (Ani Maske Yüz Gelişen Bir Adolesan). Meandros Medical and Dental Journal, 20, 247–250.  (ESCI)
9. Ayanoğlu M., Tosun A. (2022). Assessment of Serum 25-hydroxyvitamin D Levels at the First Manifestation of Multiple Sclerosis in Children and Adolescents. Trends in Pediatrics. (ESCI)
10. Ayanoğlu M., Kömürlüoğlu Tan A., Çelik E., Çelik S.F., Tosun A. (2022). Assessment of the Association Between Complete Blood Cell Parameters, Levels of Vitamin B12 and Folate, Decreased Iron Storage and Recurrent Vasovagal Syncope Episodes. Meandros Medical and Dental Journal. (ESCI)
11. Çelik E., Güngör Ş., Ayanoğlu M., Tosun A. (2023). Üst Solunum Yolu Enfeksiyonu Olan Ateşli Çocuklarda Ateşli Nöbetin Öngörüsü. Journal of Pediatric Emergency and Intensive Care Medicine. (ESCI)
12. Yiğit Z.M., Savaş R., Erbaş A.M., Bozkurt G., Tosun A. (2025). Tip C Sanfilippo Sendromu ve Tip 1 Wolfram Sendromu Birlikteliği Gösteren Bir Olgu ve Tanıda Yeni Nesil Dizilemenin Rolü. J Dr Behcet Uz Child Hosp, 15(2), 121–125. doi:10.4274/jbuch.galenos.2025.23471. (ESCI)

Uluslararası bilimsel toplantılarda sunulan ve bildiri kitabında basılan bildiriler

1. Türkmen, M, A. Tosun, AR Odabaşı, F. Sönmez, A. Bıçkıcı ve G. İnan. (2003). “Pregnancy Outcome in a Renal Recipient Treated with Tacrolimus”, I^st Congress of Union of Mediterranean Neonatal Societies (UMENS) and XII^th National Congress of Neonatology, 147, İstanbul. 
2. Türkmen, M., A. Aydoğdu, A. Tosun, E. Güngör ve G. İnan. (2003). “Transcutaneous Bilurubin Measurement: Correlation with Total Serum Biluribin and Visual Assessment of The Skin for Jaundice”, I^st Congress of Union of Mediterranean Neonatal Societies (UMENS) and XII^th National Congress of Neonatology,41, İstanbul.
3. Gökben, S., M. Polat, H. Tekgül, A. Tosun, G. Serdaroğlu ve N. Kütükçüler. (2005). “Cerebrospinal fluid Interleukin-6 Levels in Patients with West Syndrome”, 26^th International Epilepsy Congress, Epilepsia, Paris,Vol. 46, Suppl. 6, 392, Wıley-Blackwell,
4. Tekgül, H., B. Karapınar, M. Özçetin, E.U. Saz, M. Polat, A. Tosun, G. Serdaroğlu ve S. Gökben. (2005). “Effectiveness of Midazolam in the Treatment of Paediatric Status Epilepticus in an Intensive Care Unit”, 26^th International Epilepsy Congress, Epilepsia, Paris, Vol. 46, Suppl. 6, 409, Wıley-Blackwell.
5. Tosun, A., G. Serdaroğlu, M. Polat, H. Tekgül ve S. Gökben. (2005). “The evaluation of the cases with acute disseminated encephalomyelitis”, 6^th European Paediatric Neurology Society, EPNS Congress, European Journal of Paediatric Neurology, Göteborg, Vol. 9, 219-220, Elsevier.
6. Tekgül, H., U.E. Saz, M. Polat, A. Tosun, G. Serdaroğlu, Ö. Kitis, B. Uludağ ve S. Gökben. (2005). “Evaluation of corticospinal system maturation and plasticity with transcranial magnetic stimulation in children”, 6^th European Paediatric Neurology Society, EPNS Congress, European Journal of Paediatric Neurology, Göteborg, Vol. 9, 186-187, Elsevier, 2005.
7. Polat, M., A. Tosun, G. Serdaroğlu, S. Gökben ve H. Tekgül. (2005). “Electrodiagnostic pattern approach for childhood polyneuropathies”, 6^th European Paediatric Neurology Society, EPNS Congress, European Journal of Paediatric Neurology, Göteborg, Vol. 9, 226, Elsevier.
8. Serdaroğlu, G., M. Polat, A. Tosun, H. Tekgül ve S. Gökben. (2005). “Two cases with acute necrotizing encephalopathy”, 6^th European Paediatric Neurology Society, EPNS Congress,  European Journal of Paediatric Neurology, Göteborg Vol. 9, 214, Elsevier.
9. Gökben, S., A. Tosun, M. Polat, G. Serdaroğlu ve H. Tekgül (2005). “The evaluation of the patients with idiopathic childhood occipital epilepsies”, 6^th European Paediatric Neurology Society, EPNS Congress, , European Journal of Paediatric Neurology, Göteborg Vol. 9, 204, Elsevier.
10. İşler, A., Z. Bakkaloğlu, G. Serdaroğlu, A. Tosun, M. Polat, S. Gökben, H. Tekgül. (2007). “The effectiveness semiologic seizure classification on health professionals in pediatrics”, Seventh European Paediatric Neurology Society EPNS Congress, European Journal of Paediatric Neurology, Kusadası, Vol. 11, Suppl.1, 60-61, Elsevier.
11. Tosun, A., M.Polat, G. Serdaroğlu, H. Tekgül, S. Gökben.(2007). “Evaluation of patients with cerebral palsy”, Seventh European Paediatric Neurology Society EPNS Congress, European Journal of Paediatric Neurology, Kusadası, Vol. 11, Suppl.1, 46, Elsevier.
12. Polat, M., S. Gökben, G. Serdaroğlu, A. Tosun, H.Tekgül.(2007). “Neuropsychological evaluation in patients with benign childhood epilepsy, with occipital paroxysms”, Seventh European Paediatric Neurology Society EPNS Congress, European Journal of Paediatric Neurology, Kusadası, Vol. 11, Suppl.1, 26, Elsevier.
13. Saz, E.U., H. Tekgül, G. Serdaroğlu, A.Tosun, M. Polat, E. Çağlayan, S. Aydoğdu, S. Mir ve S. Gökben. (2007), “Acute seizures in a pediatric emergency unit: etiologic profils and outcome”, Seventh European Paediatric Neurology Society EPNS Congress, European Journal of Paediatric Neurology, Kusadası, Vol. 11, Suppl.1, 98, Elsevier.
14. Ay, Y., G. Serdaroğlu, A. Tosun, M. Polat, H. Tekgül ve S. Gökben. (2007). “Neuropsychological impairment in children with rolandic epilepsy”, Seventh European Paediatric Neurology Society EPNS Congress, European Journal of Paediatric Neurology, Kusadası, Vol. 11, Suppl.1, 62, Elsevier.
15. Tosun, A., G. Serdaroğlu, M. Polat, H. Tekgül ve S. Gökben. (2008). “Malignant migrating partial seizures in infancy; additional three cases from Turkish population”, 8^th European Congress on Epileptology, SEP 21-25, 2008 Berlin, Germany  Source: EPILEPSIA   Volume: 50   Pages: 207-207    Suppl.4  
16. Türkmen, M., A. Aydoğdu, Ö. Uygur, A.R. Odabaşı, H. Yüksel ve A. Tosun. (2008). “Neonatal complications in infants born to diabetic mothers”, 1st UENPS Congress Global Neonatology and Perinatalogy, Early Human Development, Roma, Vol. 84, S16, Elsevier.
17. Türkmen, M., A. Tosun, C. Yılmaz, Y. Özsunar, A. Aydoğdu, ve B.Ç. Çakmak. (2008). “Evaluation of neonates with hypoxic ischemic encephalopathy in an intensive care unit”, 1st UENPS Congress Global Neonatology and Perinatalogy, Early Human Development, Roma, Vol. 84, S15, Elsevier.
18. Uslu M, Sendur N, Savk E, Karaman G, Tosun A, Tataroglu C. (2012). Phacomatosis Pigmentokeratotica with Musculuskelatal Abnormality: A Case Report. 11^th ESPD Congress, Istanbul, Turkey European Journal of Pediatric Dermatology. Volume:22; Page:78, Supplement:1.
19. Tosun A, Erisen S, Unuvar T, Dursun S. (2013). Assesment of bone mineral density disorders in children with cerebral palsy and epilepsy. 10^th European Pediatric Neurology Society Congress, Brussels, Belgium, 25-28 Sep 2013. European Journal of Paediatric Neurology. 17 S, S:54, Elsevier.
20.  Tosun A, Kurtgoz S, Dursun S, Keskin E.(2013). A case of Ehlers Danlos Syndrome Type VI Awith novel PLOD 1 gene mutation. 10^th European Pediatric Neurology Society Congress, Brussels, Belgium, 25-28 Sep 2013. European Journal of Paediatric Neurology. 17 S, S: 117, Elsevier.
21. Berkit Karatas I, Turan Y, Sendur Ö.F, Tosun A, Kahvecioglu F, Bayraktar K, Omurlu Kurt I.(2014). The effect of the physical therapy and rehabilitationpractıceson the functional state in patients with cerebral palsy. World congress for Neurorehabilitation. Istanbul, Turkey, page:379.
22.  Anık A, Anık A, Ünüvar T, Tosun A, Dursun Ş, Akcan AB, Kaynak Türkmen M.(2015). Cystic Encephalomalacia and Infantile Spasm as a Complication of Transient and Mild Hyperinsulinemic Hypoglycemia. ESPE 2015 (Özet Bildiri/Poster)(Yayın No:6643719)
23. Kaynak Türkmen M, Çolak D, Tosun A, Dayanır Y, Aksu H. (2016). Neurodevelopmental outcome of infants with Exchange transfusion. Eur J Pediatr.EAPS Congress.
24. Tosun A, Kıpçak Yüzbaşı B, Akyol A. (2016).  Clinical findings of tuberous sclerosis patients in Menderes region.  12th European Congress on Epileptology (Özet Bildiri/Poster)(Yayın No:3175588)
25. Tosun A, Bulut Y, Kaya Ş, Kıpçak Yüzbaşı B. (2016).  A case of Fischer Bickerstaff Syndrome overlapped by Guillain  barre Syndrome.  14th International Child Neurology Congress (Özet Bildiri/Poster)(Yayın No:3175458)
26. Tosun A, Edizsoy Oktay S, Dursun Ş, Aksu H, Özsunar Dayanır Y, Kıpçak Yuzbaşı B, Kaynak Türkmen M. (2016).  Long term neurodevelopmental outcoms very low birth weight infants.  14th International Child Neurology Congress (Özet Bildiri/Poster)(Yayın No:3113462)
27. Can E, Kıpçak Yüzbası B, Anık A, Ünüvar T, Tataroglu C, Çil E, Sendur N, Tosun A. (2017). Severe hypercalcemıa due to subcutaneous fat necrosıs successfully treated wıth pamıdronate ın an ınfant wıth hypoxıc-ıschemıc encephalopathy. 10th International Joint Meeting of Pediatric Endocrinology.
28. Yıs Uluç, Becker Krıstıen,Hız Ayse Semra,Uyanık Gökhan,Bayram Erhan, Halıloglu Vıldan Göknur, Polat Ayse İpek, Ayanoglu Müge, Okur Tuncay Derya,Tosun Ayse, Aktan Gül, Keskın Yılmaz Sanem, Topaloglu Haluk Aydın, Anlar Fatma Banu, Çırak Sebahattin, Engel Andrew. (2017). Genetic Landscape Of Congenital Myasthenic Syndromes From Turkey: Novel Mutations And Clinical Insights.22nd Internatıonal Congress Of The WMS.
29. Akyol A, Tosun A, Özkul A,Kıpçak Yüzbası B.Akyol Gürses A. (2017). Neurofibromatosis type 1 and epilepsy in Aydin province. 32nd Internatonal Epilepsy Congress.
30. Akyol A,Özkul A,Tosun A, Sendur N. (2017). Stevens-Johnson syndrome prevalence due to antiepileptic drug therapy at Aydın provience. 32 nd International epilepsy congress.
31. Can E, Kıpçak Yüzbaşı B, Anık A, Ünüvar T, Çil E, Şendur N, Tosun A.(2017). Severe hypercalcemia due to subcutaneous fat necrosis successfully treated with pamidronate in an infant with hypoxic-ischemıc encephalopathy. 10th International Joint Meeting of Pediatric Endocrinology.  (Özet Bildiri/Poster)(Yayın No:6643554)
32. Yılmaz D, Kıpçak Yüzbaşı B, Can E, Can A, Sönmez F, Tosun A. (2018). Anti –CASPR2 positive SLE case with autoimmune encephalitis clinic. 4 th Congress of Mediterranean Kidney Society.Mostar April 2018.

Ulusal hakemli dergilerde yayınlanan makaleler

1. Gülez P., Kayserili E., Tosun A., Eryılmaz N. (1998). Demir Eksikliği Anemisinde Eritrosit Parametrelerinin Karşılaştırılması. Klinik Bilimler & Doctor, 6, 875–877.
2. Özcan T., Tosun A., İnan G., Yendur G., Özbek E., Can D., Önal H. (2002). Hastanemize Başvuran Zehirlenme Olgularının Değerlendirilmesi. Adnan Menderes Üniversitesi Tıp Fakültesi Dergisi, 3, 5–7.
3. Türkmen M., Tosun A., Odabaşı A.R., Bıçkıcı A., Sönmez F., İnan G. (2003). Pregnancy Outcome in a Renal Transplant Recipient Treated with Tacrolimus. T Klin Jinekol Obst, 13, 138–140.
4. Sönmez F., Tosun A., Semerci N., Akçanal B. (2003). Hematürili Çocuklarda Hiperkalsiüri Sıklığı. Ege Pediatri Bülteni, 10, 27–30.
5. Sönmez F., Tosun A., Acar Ç., Öge Ö., Özeren B., İnan G. (2004). Posterior Üretral Valfe Bağlı Gelişen Kronik Böbrek Yetmezliği Vakası. Nefroloji Dergisi, 13, 39–41.
6. Türkmen M., Aydoğdu S.A., Tosun A., Akdilli A., Helvacı M. (2004). Yenidoğanda Ağır Geçici Hipertansiyon Olgu Sunumu. Adnan Menderes Üniversitesi Tıp Fakültesi Dergisi, 5, 35–37.
7. Türkmen M., Ünüvar T., Tosun A., Aydoğdu A., Ulucan H., Giray Ö. (2005). 22q11 Delesyonu: Bir vaka takdimi. Çocuk Sağlığı ve Hastalıkları Dergisi, 48, 320–323.
8. Sönmez F., Başak S., Tosun A., Ünüvar T., Yıldız M. (2006). Enürezis Nokturnalı Çocuklarda Adenoid Hipertrofisinin Rolü. Ege Pediatri Bülteni, 13, 79–83.
9. Türkmen M., Altıncık A., Acar Ç., Tosun A., Aydoğdu A. (2006). Adnan Menderes Tıp Fakültesi Yenidoğan Yoğunbakım Ünitesinde İzlenen Çok Düşük Doğum Ağırlıklı Bebeklerin Değerlendirilmesi. Adnan Menderes Üniversitesi Tıp Fakültesi Dergisi, 7, 3–6.
10. Ülger Z., Tosun A., Rala S., Serdaroğlu G., Üretmen Ö., Darcan Ş., Tekgül H., Gökben S. (2006). Çocuklarda İdiopatik Orbital Miyozit: Bir vaka takdimi. Çocuk Sağlığı ve Hastalıkları Dergisi, 49, 117–120.
11. Tosun A., Göksoy E., Çeçen E., Aydoğdu A., Aral Y.Z. (2007). Bir Olgu Nedeni ile Nörobruselloz. Ege Pediatri Bülteni, 14, 177–181.
12. Türkmen M., Aydoğdu S.A., Uygur Ö., Odabaşı A.R., Yüksel H., Tosun A. (2008). Diyabetik Anne Bebeklerinin Yenidoğan Dönemi Sorunları. Türkiye Klinikleri J Pediatr, 8–17.
13. Tosun A., Aral Y.Z., Apaydın Ş., Karaman G., Çetin E.D. (2008). Ürtikerya Pigmentosa ve nöbet birlikteliği: Bir vaka takdimi. Çocuk Sağlığı ve Hastalıkları Dergisi, 51, 158–161.
14. Tosun A., Aydoğdu A., Eliaçık K., Çeçen E., Köseoğlu K. (2008). Meningoensefalitli Bir Olguda Düşmeyen Ateş Nedeni: Enfekte Dalak Kisti. Ege Tıp Dergisi, 2, 143–146.
15. Türkmen M., Özkan P., Aydoğdu S.A., Tosun A., Semerci N., Sönmez F. (2008). Yenidoğanlarda torba ve suprapubik aspirasyon yöntemi ile alınan idrar kültürü sonuçlarının karşılaştırılması. Çocuk Sağlığı ve Hastalıkları Dergisi, 51, 193–198.
16. Gökben S., Serdaroğlu G., Polat M., Kitiş Ö., Tosun A., Yüksel H. (2008). Akut Nekrotizan Ensefalopati: İki olgu sunumu. Ege Pediatri Bülteni, 15, 35–38.
17. Türkmen Kaynak M., Tosun A., Özsunar Y., Aydoğdu A., Yılmaz C., Çetinkaya Çakmak B. (2009). Hipoksik İskemik Ensefalopatili Yenidoğanların Klinik, Nörofizyolojik ve Nörogörüntüleme Sonuçlarının Değerlendirilmesi. Türkiye Klinikleri J Pediatr, 18(4), 264–271.
18. Tosun A., İnan G., Yendur G., Can D., Ağın H., Özcan T., Gürel F.S. (2009). Üç yıllık Favizm Olgularımızın Değerlendirilmesi. Sağlıklı Yaşam Tarzı Dergisi, 8–15.
19. Tosun A., Çeçen E., Aral Y.Z., Erişen S. (2010). Pediatric Case Report of Topiramate Toxicity. Türkiye Klinikleri J Pediatr, 19, 227–230.
20. Semerci N., Girişken İ., Sönmez F., Tosun A., Ünüvar T., Meteoğlu İ. (2011). Çocukluk Çağı Nadir Bir Nefrotik Sendrom Nedeni: Schimke İmmünoosseoz Displazi. ADÜ Tıp Fakültesi Dergisi, 12, 41–44.
21. İşler A., Başbakkal Z., Tosun A., Tekgül H. (2011). Moleküler Eğitim Modeli ile Epileptik Nöbeti Olan Çocuğa Yaklaşım. Türkiye Klinikleri J Neu, 6, 39–46.
22. Coşkun S., Kurtgöz S., Tosun A., Keskin E., Bozkurt G. (2013). Seckel Sendromlu Bir Olgu. ADÜ Tıp Fakültesi Dergisi, 14(3), 35–37.
23. Akyol A., Özkul A., Tosun A., Şendur A. (2017). Aydın Bölgesi Üniversite Tıp Fakültesi Hastanesinde Antiepileptik Kullanımına Bağlı Stevens–Johnson Sendromu. Epilepsi, 23(1), 25–28.
24. Çalışır H., Sarıkaya Karabudak S., Karataş P., Meşealan İ., Tosun A. (2018). Serebral Palsili Çocuğu Olan Annelerin Aile Yükü ve Umutsuzluk Düzeyleri. Dokuz Eylül Üniversitesi Hemşirelik Fakültesi Elektronik Dergisi  DEUHEFED, 11(2), 147–156.
25. Öncü S., Akdoğan İ., Güven Ö., Akdoğan H.D., Tosun A. (2021). Aydın Adnan Menderes Üniversitesi Tıp Fakültesi Öğrencileri Gözünden Pandemi Döneminde Uzaktan Eğitim. Tıp Eğitimi Dünyası, 85–97.
26. Çolak D., Türkmen M.K., Dayanır Y.Ö., Aksu H., Başak S., Tosun A.F. (2023). Long-term Neurodevelopmental Outcomes of Newborns with High Bilirubin Levels. Haydarpaşa Numune Medical Journal, 63(2), 120–125.

Yazılan Ulusal Kitaplar veya Kitap Bölümleri

1. Tosun A. (yıl bilinmiyor). Konuşma Bozuklukları. İçinde: Çocuk Nöroloji Kitabı.
2. Tosun A. (2014). Epifiz patolojilerinde klinik. İçinde: Turgut M., Aral Y.Z. (Ed.), Epifiz – Melatonin (s. 121–142). Aydın: Adnan Menderes Üniversitesi Yayınları.
3. Gökben S., Serdaroğlu G., Polat M., Tosun A. (2014). Dil Gelişim Geriliği. İçinde: Türkiye Milli Pediatri Derneği – Türkiye Çocuk Nörolojisi Derneği Ortak Kılavuzu. [Erişim: https://www.millipediatri.org.tr/Custom/Upload/files/kilavuzlar/kilavuz-7.pdf]
4. Gökben S., Serdaroğlu G., Polat M., Tosun A. (2014). Mental Retardasyon. İçinde: Türkiye Milli Pediatri Derneği – Türkiye Çocuk Nörolojisi Derneği Ortak Kılavuzu. [Erişim: https://www.millipediatri.org.tr/Custom/Upload/files/kilavuzlar/kilavuz-7.pdf]
5. Gökben S., Serdaroğlu G., Polat M., Tosun A. (2014). Motor Gelişim Geriliği. İçinde: Türkiye Milli Pediatri Derneği – Türkiye Çocuk Nörolojisi Derneği Ortak Kılavuzu. [Erişim: https://www.millipediatri.org.tr/Custom/Upload/files/kilavuzlar/kilavuz-7.pdf]
6. Tosun A. (2017). Beyin Felcinde Epidemiyoloji. İçinde: Hepgüler S., Gökben S. (Ed.), Beyin Felci (s. 1–3). İstanbul: Nobel Tıp Kitabevleri.
7. Tosun A. (2020). Demiyelinizan Hastalıklar. İçinde: Hasanoğlu E., Bideci A., Düşünsel R., Boduroğlu K. (Ed.), Temel Pediatri. Ankara: Güneş Tıp Kitabevleri.
8. Ayanoğlu M., Tosun A. (2021). Serebrovasküler Hastalıklar. İçinde: İzmir Dr. Behçet Uz Çocuk Hastanesi Pediatri. Ankara: Nobel Tıp Kitabevi.
9. Tosun A. (2022). Pediatride Anamnez Alma. İçinde: Türkmen M.K., Sönmez F.G., Tosun A. (Ed.), Çocuk Sağlığı ve Hastalıklarında Kliniğe Giriş. Ankara: Akademisyen Yayınevi.
10. Tosun A. (2022). Tıp Eğitim Tarihi. İçinde: Türkmen M.K., Sönmez F.G., Tosun A. (Ed.), Çocuk Sağlığı ve Hastalıklarında Kliniğe Giriş. Ankara: Akademisyen Yayınevi.
11. Ayanoğlu M., Tosun A. (2022). Kronik baş ağrısı tanı ve tedavi algoritması. İçinde: Kumandaş S., Canpolat M. (Ed.), Pediatrik Nörolojik Algoritmalar ve İlaç Rehberi.
12. Ayanoğlu M., Tosun A. (2022). Kronik Baş Ağrıları ve Kronik Günlük Baş Ağrısı. İçinde: Kumandaş S., Canpolat M. (Ed.), Temel Pediatrik Nöroloji: Tanı ve Tedavi.
13. Ayanoğlu M., Tosun A. (2023). Climate Change and Neurological Disorders in Children / İklim Değişikliği ve Çocuklarda Nörolojik Hastalıklar. İçinde: Aksu H., Gürbüz Ö.B. (Ed.), Climate Change: Child and Adolescent Health and Mental Health / İklim Değişikliği: Çocuk ve Ergen Sağlığı ve Ruh Sağlığı. Ankara: Türkiye Klinikleri Yayınevi.
14. Aktan G., Tosun A. (2023). Kortikal Displazilerde Genetik Yaklaşım. İçinde: Gökben S., Hız A.S. (Ed.), Çocuk Nörolojisinde Genetik Yaklaşımlar, 4(1), 25–33. Ankara: Türkiye Klinikleri Yayınevi.
15. Tosun A. (Ed.) (2024). Sistemik Hastalıkların Nörolojik Bulguları. Ankara: Türkiye Klinikleri.

7.8 . Bilimsel Toplantılarda Yapılan Konuşmalar

1. Tosun A. (2003). Meme ile ilgili durumlar. Bebek Dostu Hastane Ekipleri Eğitim Programı, Aydın.
2. Tosun A. (2003). Astımda korunma. Dünya Astım Günü, Aydın.
3. Tosun A. (2006). Febril konvülziyonlar. II. Aydın Çocuk Sağlığı ve Hastalıkları Günü, Aydın.
4. Tosun A. (2007). Nonepileptik paroksismal fenomenler. III. Aydın Çocuk Sağlığı ve Hastalıkları Günü, Aydın.
5. Tosun A. (2008). Senkoplu hastaya yaklaşım. IV. Aydın Çocuk Sağlığı ve Hastalıkları Günü, Aydın.
6. Tosun A. (2009). Febril konvülziyonlu hastaya yaklaşım ve West sendromu. Çocukluk Çağında İlk Nöbete Yaklaşım ve Epilepsi, Aydın.
7. Tosun A. (2011). Febril konvülziyona yaklaşım. Epiped Toplantısı, Denizli.
8. Tosun A. (2011). Bilinci kapalı çocuğa yaklaşım. 6. Aydın Çocuk Sağlığı ve Hastalıkları Günü, Aydın.
9. Tosun A. (2011). Ateş ve ateşli havaleye yaklaşım. UNICEF Aydın Şubesi Eğitim Toplantısı, Aydın.
10. Tosun A. (2011). Havale ve bayılmada ilk yardım. Bebek ve Çocukta İlk Yardım, II. UNICEF Aydın Şubesi Günü, Aydın.
11. Tosun A. (2012). Serebral palsi. Aile Eğitim Semineri, Mart, Aydın.
12. Tosun A. (2012). Status epileptikus. 7. Aydın Çocuk Sağlığı ve Hastalıkları Günü, Aydın.
13. Tosun A. (2015). Tüberküloz menenjit. Çocukta Tüberküloz Paneli, Türkiye Milli Pediatri Derneği Aydın Şubesi Eğitim Toplantısı, Aydın, 7 Ocak.
14. Tosun A. (2015). Serebral palsi göründüğü gibi mi? Olgu örnekleriyle ayırıcı tanı tartışması. 17. Ulusal Çocuk Nörolojisi Kongresi, Çeşme, 6–9 Mayıs.
15. Tosun A. (2016). Febril konvülziyonlara güncel yaklaşımlar. 5. PUADER Kongresi, Çeşme.
16. Tosun A. (2016). Epilepsili hastayı değerlendirmek. Pediatrik Epilepsi Hemşireliği Kursu, İzmir.
17. Tosun A. (2016). Nefroloji ile ilgili sorunlar. 18. Ulusal Çocuk Nöroloji Kongresi, Antalya.
18. Tosun A. (2018). Bilinci kapalı hastaya yaklaşım. 20. Ulusal Çocuk Nörolojisi Kongresi.
19. Tosun A. (2019). Çocuklarda baş ağrıları. Malatya Pediatri Okulu.
20. Tosun A. (2019). Yenidoğan konvülziyonlarında tedavi. 21. Ulusal Çocuk Nörolojisi Kongresi.
21. Tosun A. (2020). Çocuklarda serebrovasküler hastalıklar.
22. Tosun A. (2021). Konvülzif status epileptikusta tedavi ve prognoz. Ulusal Çocuk Nöroloji Kongresi.
23. Tosun A. (2022). Nöromüsküler hastalıklarda IVIg. Malatya Pediatri Okulu, Mayıs.
24. Tosun A. (2023). Hipotonik infanta yaklaşım. 3. Büyüyen Çocuk Kongresi, Ekim.

Reviewing the reliability of revised Melbourne Cerebral Palsy Hip Classification System across different medical specialties

By

Gok, M (Gok, Mustafa) [1] , [2] , [3] ; Oner, R (Oner, Ridvan) [4] ; Ozgezmez, FT (Ozgezmez, Ferit Tufan) [4] ; Aydin, E (Aydin, Elif) [5] ; Tosun, AF (Tosun, Ayse Fahriye) [6] ; Cullu, E (Cullu, Emre) [4]

 (provided by Clarivate) 

Source

JOINT DISEASES AND RELATED SURGERY

Volume

36

Issue

1

Page

148-154

DOI

10.52312/jdrs.2025.2023

Published

2025

Early Access

DEC 2024

Indexed

2024-12-18

Document Type

Review

Abstract

Objectives: The aim of this study was to measure the reliability of the expanded and revised Melbourne Cerebral Palsy Hip Classification System (r-MCPHCS) across different medical specialties. Patients and methods: Anteroposterior pelvic radiographs of a total of 44 patients (20 males, 24 females; median 16.7 years; range, 12 to 32 years) with cerebral palsy (CP) were analyzed between January 2005 and December 2020. Four medical specialists (an orthopedic surgeon, a pediatric neurologist, a radiologist, and a physical medicine and rehabilitation specialist) were included in the study. The time gap between the first and the second assessment was at least three months. The intra- and inter-observer intraclass correlation coefficient (IntraOb. and InterOb. ICCs) were calculated. An ICC of >0.8 was considered excellent fit. Results: The median IntraOb. ICC was found to be 0.93 (range, 0.89 to 0.97), the median InterOb. ICC was found to be 0.88 for the first assessment (A) and 0.93 for the second assessment (B). Both results were interpreted as excellent in terms of compatibility. Conclusion: Our study results suggest that r-MCPHCS is a well-designed, reliable and reproducible scale that is easy to use among different medical specialists.

Keywords

Author Keywords

Cerebral palsyhipreliabilityrevised Melbourne Cerebral Palsy Hip Classification System
 

Keywords Plus

CHILDRENDISPLACEMENTDISLOCATIONRECONSTRUCTIONINTRAOBSERVERSURVEILLANCEPREVENTIONSURGERY

Climate Change and Neurological Disorders in Children

By

Ayanoglu, M (Ayanoglu, Muge) [1] ; Tosun, AF (Tosun, Ayse Fahriye) [1]

Edited by

Aksu, H (Aksu, H)

Source

CLIMATE CHANGE: CHILD AND ADOLESCENT HEALTH AND MENTAL HEALTH

Page

25-29

Published

2023

Indexed

2023-01-01

Document Type

Article; Book Chapter

Abstract

The review article discusses the impact of climate change on pediatric patients with neurological disorders. Climate change, characterized by global warming caused by increasing gases such as CO2, CH4 and N2O, changes in precipitation patterns, and extreme weather events, is caused by increasing greenhouse gas concentrations. These changes are linked to a rise in infectious diseases with neurological disorders. Environmental neurotoxins, exacerbated by climate change, could accelerate neurodegenerative disorders. Malnutrition arising from disrupted agriculture threatens neurodevelopmental health. Elevated environmental temperatures increase the risk of metabolic and neurological abnormalities. The vulnerability of individuals with pre-existing neurological conditions, such as epilepsy and disabilities, has been discussed in details. The need for preventative actions, education, public awareness, and legal frameworks to mitigate climate change's adverse impact on neurological health has been emphasized.

Keywords

Author Keywords

Climate changeglobal warmingnervous system diseaseschild
 

Keywords Plus

ASSOCIATION

TARC and Septin 7 can be better monitoring biomarkers than CX3CL1, sICAM5, and IRF5 in children with seizure-free epilepsy with monotherapy and drug-resistant epilepsy

By

Ayanoglu, M (Ayanoglu, Muge) [1] ; Çevik, Ö (Cevik, Ozge) [2] ; Erdogan, Ö (Erdogan, Omer) [2] ; Tosun, AF (Tosun, Ayse Fahriye) [1]

 (provided by Clarivate) 

Source

INTERNATIONAL JOURNAL OF NEUROSCIENCE

Volume

134

Issue

3

Page

243-252

DOI

10.1080/00207454.2022.2100773

Published

MAR 3 2024

Early Access

JUL 2022

Indexed

2022-08-19

Document Type

Article

Abstract

Aim: To evaluate i) the relationship between epilepsy and inflammation by analyzing the levels of thymus activation-regulated chemokine (TARC), and interferon regulatory factor 5 (IRF5) in healthy controls, patients with epilepsy on monotherapy and polytherapy, ii) the levels of sICAM5, chemokine (c-x3-c motif) ligand 1 (CX3CL1), and septin 7 (SEPT7) which are important in both inflammation and synaptic formation. Methods: Patients who were seizure-free with monotherapy (epilepsy group-1), patients with drug-resistant epilepsy (epilepsy group-2), and healthy controls were included. Demographical data, disease durations, and medications were noted. Measurements were made by commercial ELISA kits. Results: The numbers of epilepsy group-1, epilepsy group-2, and healthy controls were 23, 20, and 21, respectively. TARC levels were significantly lower in healthy controls than in both epilepsy groups. Higher TARC levels than 0.58 pg/ml indicated epilepsy with a sensitivity of 81.8% and specificity of 84.0%. SEPT7 levels were significantly higher in epilepsy group-1 than in those epilepsy group-2. A negative correlation was found between SEPT7 levels and disease duration as is the case for the correlation between SEPT7 and average seizure duration. A positive correlation was found between IRF5 and CX3CL1 levels, SEPT7 and IRF5 levels, and IRF5 and sICAM5 levels. Conclusions: We suggest that TARC is a promising biomarker, even in a heterogeneous epilepsy group not only for drug-resistance epilepsy but also for seizure-free epilepsy with monotherapy. Additionally, drug resistance, longer disease, and longer seizure durations are related to lower levels of SEPT7, which has an essential role in immunological functions and dendritic morphology.

Keywords

Author Keywords

EpilepsyTARCsICAM5CX3CL1Septin 7
 

Keywords Plus

ACTIVATION-REGULATED CHEMOKINESYNAPTIC PLASTICITYHIPPOCAMPAL-NEURONSMESSENGER-RNASRAT-BRAINTELENCEPHALINRECEPTORICAM-5SERUMFRACTALKINE

Genetic Landscape of Congenital Myasthenic Syndromes From Turkey: Novel Mutations and Clinical Insights

By

Yis, U (Yis, Uluc) [1] ; Becker, K (Becker, Kerstin) [2] ; Kurul, SH (Kurul, Semra Hiz) [1] ; Uyanik, G (Uyanik, Goekhan) [3] , [4] ; Bayram, E (Bayram, Erhan) [1] ; Haliloglu, G (Haliloglu, Goknur) [5] ; Polat, AI (Polat, Ayse Ipek) [1] ; Ayanoglu, M (Ayanoglu, Muge) [1] ; Okur, D (Okur, Derya) [1] ; Tosun, AF (Tosun, Ayse Fahriye) [6] ; 

 (provided by Clarivate) 

Source

JOURNAL OF CHILD NEUROLOGY

Volume

32

Issue

8

Page

759-765

DOI

10.1177/0883073817705252

Published

JUL 2017

Indexed

2017-07-01

Document Type

Article

Abstract

Congenital myasthenic syndromes are clinically and genetically heterogeneous disorders of neuromuscular transmission. Most are treatable, but certain subtypes worsen with cholinesterase inhibitors. This underlines the importance of genetic diagnosis. Here, the authors report on cases with genetically proven congenital myasthenic syndromes from Turkey. The authors retrospectively reviewed their experience of all patients with congenital myasthenic syndromes, referred over a 5-year period (2011-2016) to the Child Neurology Department of Dokuz Eylul University, Izmir, Turkey. In addition, PubMed was searched for published cases of genetically proven congenital myasthenic syndromes originating from Turkey. In total, the authors identified 43 (8 new patients, 35 recently published patients) cases. Defects in the acetylcholine receptor (n = 15; 35%) were the most common type, followed by synaptic basal-lamina associated (n = 14; 33%) and presynaptic syndromes (n = 10; 23%). The authors had only 3 cases (7%) who had defects in endplate development. One patient had mutation GFPT1 gene (n = 1; 2%). Knowledge on congenital myasthenic syndromes and related genes in Turkey will lead to prompt diagnosis and treatment of these rare neuromuscular disorders.

Keywords

Author Keywords

congenital myasthenic syndromesgenetic diagnosisTurk
 

Keywords Plus

MISSENSE MUTATION COLQ MUTATIONS DIAGNOSIS SCOLIOSIS

Comorbid Obsessive Compulsive Disorder in a Child with Tuberous Sclerosis Complex

By

Ozgur, BG (Ozgur, Borte Gurbuz) [1] ; Aksu, H (Aksu, Hatice) [2] ; Tosun, AF (Tosun, Ayse Fahriye) [3]

 (provided by Clarivate) 

Source

PSYCHIATRY AND BEHAVIORAL SCIENCES

Volume

8

Issue

3

Page

142-144

DOI

10.5455/PBS.20180612101258

Published

2018

Indexed

2018-01-01

Document Type

Article

Abstract

Tuberous sclerosis complex (TSC) is a genetic disease that mostly affects the brain, skin, kidneys, eyes, heart and lungs. Various neuropsychiatric comorbidities such as mental retardation, mood disorders, anxiety disorders, disruptive/ aggressive behavior disorders, autism spectrum disorders have been reported. In this study, we report a 15-year old case of with an obsessive compulsive disorder and TSC who is the youngest case in the literature. His sexual and religious obsessions first started when he was 10 years old. In this paper, his medical and psychiatric history and treatment management are presented.

Keywords

Author Keywords

Obsessive-compulsive disorder tuberous sclerosis child

Cystic Encephalomalacia and Infantile Spasm as a Complication of Transient and Mild Hyperinsulinemic Hypoglycemia

By

Anik, A (Anik, Ahmet) [1] ; Anik, A (Anik, Ayse) [2] ; Ünüvar, T (Unuvar, Tolga) [1] ; Tosun, AF (Tosun, Ayse Fahriye) [3] ; Dursun, S (Dursun, Siar) [3] ; Akcan, AB (Akcan, Abdullah Baris) [2] ; Durum, Y (Durum, Yasemin) [4] ; Türkmen, MK (Turkmen, Munevver Kaynak) [2]

 (provided by Clarivate) 

Source

JOURNAL OF PEDIATRIC RESEARCH

Volume

3

Issue

2

Page

129-132

DOI

10.4274/jpr.16878

Published

JUN 2016

Indexed

2016-06-01

Document Type

Article

Abstract

Although it is known that hypoglycemia could cause severe negative effects on brain development and also infantile spasm, it has not been reported that transient hyperinsulinemic hypoglycemia, which spontaneously improves over a short time, may cause infantile spasms. Infantile spasm is a disorder of early childhood typically seen in the first year of life, characterized by the occurence of sudden, brief, generally bilateral and symetric motor spasms of the muscles of the trunk, neck and limbs. Infantile spasms are classified as idiopathic or symptomatic. The most common form symptomatic infantile spasms is due to prenatal, perinatal or postnatal insults. A 3140 g, full-term baby was admitted with poor sucking and feeding difficulty on the postnatal second day. The patient was followed-up with the diagnosis of hyperinsulinemic hypoglycemia and intravenous glucose infusion (15 mg/kg/min) was administered, but due to the persistence of hypoglycemia, diazoxide treatment was initiated. Hypoglycemia was not observed under diazoxide treatment and the drug was gradually decreased; treatment was terminated on the 21st day. The patient was continuously normoglycemic during follow-up and admitted with flexor spasms on the 45th day. A modified hypsarrhythmia pattern was detected in the electroencephalography. On cranial magnetic resonance imaging, diffuse cystic encephalomalacia areas were observed in the temporoparietal white and gray matter. The convulsions were not completely controlled with adrenocorticotropic hormone and vigabatrin treatments. Topiramate and valproate were administered, by which convulsions were partially controlled.

Keywords

Author Keywords

Infantile spasm transient hypoglycemia hyperinsulinemia
 

Keywords Plus

NEONATAL HYPOGLYCEMIA IMAGING FINDINGS DAMAGE MRI

An Uncommon Cause of Duane Syndrome in a Child: Wildervanck Syndrome

By

Anik, A (Anik, Ahmet) [1] ; Dursun, S (Dursun, Siar) [2] ; Polat, A (Polat, Ahmet) [3] ; Anik, A (Anik, Ayse) [4] ; Ünüvar, T (Unuvar, Tolga) [1] ; Durum, Y (Durum, Yasemin) [5] ; Tosun, AF (Tosun, Ayse Fahriye) [2]

 (provided by Clarivate) 

Source

JOURNAL OF PEDIATRIC RESEARCH

Volume

3

Issue

1

Page

53-55

DOI

10.4274/jpr.29200

Published

MAR 2016

Indexed

2016-03-01

Document Type

Article

Abstract

Duane syndrome is a congenital eye movement disorder characterized by limitation of abduction and/or adduction accompanied with lid fissure narrowing, and globe retraction in attempted adduction. Duane syndrome is mostly an isolated entity, but systemic anomalies have been reported in 6-10% of patients. Wildervanck syndrome (cervico-oculo-acoustic syndrome) is a very rare disease comprised of the triad of Klippel-Feil deformity (congenitally fused cervical vertebrae), Duane syndrome, and hearing loss. The disorder is limited, or almost completely limited, to females, raising the question of sex-linked dominance with lethality in the hemizygous male. Herein, we describe an adolescent girl who was admitted to our clinic for obesity and diagnosed with Wildervanck syndrome due to bilateral abducens paralysis (Duane syndrome), Klippel-Feil deformity and hearing loss.

Keywords

Author Keywords

Duane syndrome klippel-feil anomaly hearing loss wildervanck syndrome

A Case Presentation of Atypical X-linked Adrenoleukodystrophy: Initial Experience with ASL Technique

By

Durum, Y (Durum, Yasemin) [1] ; Dayanir, YÖ (Dayanir, Yelda Ozsunar) [1] ; Navaei, AH (Navaei, Amir Hossein) [1] ; Tosun, AF (Tosun, Ayse Fahriye) [2]

 (provided by Clarivate) 

Source

CURRENT MEDICAL IMAGING REVIEWS

Volume

14

Issue

1

Page

158-162

DOI

10.2174/1573405613666170504151024

Published

2018

Indexed

2018-03-06

Document Type

Article

Abstract

Background: A 7-year-old boy with an atypical form of X-linked adrenoleukodystrophy is reported, predominantly involving frontal, occipital and temporal lobes, corticospinal tracts and cerebellar lobes.

Methods: The disease has been well documented previously with Magnetic Resonance Imaging (MRI).

Discussion: However, there isn't enough data on Magnetic Resonance Perfusion Imaging (MRPI) and non-contrast Arterial Spin Labeling (ASL) technique in current literature.

Conclusion: We presented initial and follow up MRI and multiphase ASL perfusion MRI findings.

Keywords

Author Keywords

Atypical form adrenoleukodystrophy arterial spin labeling technique Magnetic Resonance Perfusion Imaging (MRPI)multiphase ASL perfusion

1. Türkiye Çocuk Nörolojisi Derneği
2. Türkiye Milli Pediatri Derneği
3. Türk Pediatri Kurumu
4. International Child Neurology Association (ICNA)