| The efficacy, tolerability and safety of levetiracetam therapy in a pediatric population H Tekgül, P Gencpinar, D Çavuşoğlu, NO Dündar Seizure 36, 16-21, 2016 | 50 | 2016 |
| Faecal calprotectin levels in children with Henoch–Schönlein purpura: is this a new marker for gastrointestinal involvement? A Kanik, M Baran, FD Ince, O Cebeci, M Bozkurt, D Cavusoglu, K Eliacik, ... European Journal of Gastroenterology & Hepatology 27 (3), 254-258, 2015 | 22 | 2015 |
| Efficacy of low-dose corticosteroid therapy versus high-dose corticosteroid therapy in Bell’s palsy in children P Arican, NO Dundar, P Gencpinar, D Cavusoglu Journal of child neurology 32 (1), 72-75, 2017 | 20 | 2017 |
| Levetiracetam monotherapy for the treatment of infants with epilepsy P Arican, P Gencpinar, D Cavusoglu, NO Dundar Seizure 56, 73-77, 2018 | 19 | 2018 |
| Clinical and genetic features of congenital myasthenic syndromes due to CHAT mutations: case report and literature review P Arican, P Gencpinar, D Cavusoglu, NO Dundar Neuropediatrics 49 (04), 283-288, 2018 | 14 | 2018 |
| Various neurological symptoms with vitamin B12 deficiency and posttreatment evaluation P Arıcan, O Bozkurt, D Cavusoglu, P Gencpınar, S Haspolat, O Duman, ... Journal of Pediatric Neurosciences 15 (4), 365-369, 2020 | 11 | 2020 |
| Comparison of the neurocognitive outcomes in term infants treated with levetiracetam and phenobarbital monotherapy for neonatal clinical seizures P Arican, NO Dundar, NM Atasever, MA Inal, P Gencpinar, D Cavusoglu, ... Seizure 80, 71-74, 2020 | 10 | 2020 |
| Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation P Arican, NO Dundar, D Cavusoglu, TR Ozdemır, P Gencpinar Child's Nervous System 33, 677-680, 2017 | 9 | 2017 |
| Chromosomal microarray analysis in children with unexplained developmental delay/intellectual disability P Arican, NO Dundar, B Ozyilmaz, D Cavusoglu, P Gencpinar, ... Journal of Pediatric Genetics 8 (01), 001-009, 2019 | 8 | 2019 |
| Febrile infection-related epilepsy syndrome (FIRES) treated with immunomodulation in an 8-year-old boy and review of the literature C Alparslan, F Kamit-Can, AB Anıl, N Olgaç-Dündar, D Çavuşoğlu, Z Göç The Turkish Journal of Pediatrics 59 (4), 463-466, 2017 | 8 | 2017 |
| An option to consider for alternating hemiplegia of childhood: aripiprazole NO Dundar, D Cavusoglu, YC Kaplan, MO Hasturk Clinical neuropharmacology 42 (3), 88-90, 2019 | 7 | 2019 |
| A neurological appearance of celiac disease: is there any associated factor? D Cavusoglu, NO Dundar, O Oztekin, P Arican, P Gencpinar, M Baran Pediatric Emergency Care 37 (6), 303-307, 2021 | 6 | 2021 |
| A De Novo Xp11. 23 duplication in a girl with a severe phenotype: expanding the clinical spectrum P Arican, D Cavusoglu, P Gencpinar, B Ozyilmaz, TR Ozdemir, ... Journal of Pediatric Genetics 7 (02), 074-077, 2018 | 6 | 2018 |
| The first pediatric case of leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL) from Turkey D Çavuşoğlu, N Olgaç-Dündar, Ö Öztekin, TR Özdemir, P Arıcan, ... The Turkish Journal of Pediatrics 60 (2), 216-220, 2018 | 5 | 2018 |
| Kronik nörolojik hastalıklı çocuk sahibi olan annelerin ruhsal belirti düzeylerinin ve baş edebilme becerilerinin incelenmesi P Arıcan, H Yalçın, Ş Demir, M Ünlü, Ö Bezgin, D Çavuşoğlu, P Gençpınar, ... İzmir Katip Çelebi Üniversitesi Sağlık Bilimleri Fakültesi Dergisi 2 (2), 7-11, 2017 | 5 | 2017 |
| Nonketotic hyperglycinemia: novel mutation in the aminomethyl transferase gene. Case report P Gencpinar, D Çavuşoğlu, Ö Özbeyler, ÖÖ Kaya, F Baydan, NO Dundar Arch Argent Pediatr 114 (3), e142-146, 2016 | 5 | 2016 |
| Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study S Bozkaya-Yilmaz, E Karadag-Oncel, N Olgac-Dundar, P Gencpinar, ... European Journal of Pediatrics, 1-9, 2022 | 4 | 2022 |
| An unusual cause of cavitating leukoencephalopathy: ethylmalonic encephalopathy D Cavusoglu, BO Hismi, NO Dundar, O Oztekin, A Koc, E Canda, P Arican, ... Acta Neurologica Belgica 118, 309-312, 2018 | 4 | 2018 |
| An occult cause of infantile spasms: Vitamin B12 deficiency. A case report and review of literature. P Arican, NO Dundar, D Cavusoglu, G Gungor, P Gencpinar Neurology Asia 21 (3), 2016 | 3 | 2016 |
| Re-examining the characteristics of pediatric multiple sclerosis in the era of antibody-associated demyelinating syndromes Ü Yılmaz, K Gücüyener, M Yavuz, İ Öncel, M Canpolat, S Saltık, O Ünver, ... European Journal of Paediatric Neurology 41, 8-18, 2022 | 2 | 2022 |
