| Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy C Simons, LD Rash, J Crawford, L Ma, B Cristofori-Armstrong, D Miller, ... Nature genetics 47 (1), 73-77, 2015 | 146 | 2015 |
| Evaluation of malnutrition development risk in hospitalized children OF Beser, FC Cokugras, T Erkan, T Kutlu, RV Yagci, D Ertem, G Yaşöz, ... Nutrition 48, 40-47, 2018 | 106 | 2018 |
| Natural history of vanishing white matter EMC Hamilton, HDW van der Lei, G Vermeulen, JAM Gerver, ... Annals of neurology 84 (2), 274-288, 2018 | 97 | 2018 |
| Relationship between the corpus callosum and neurocognitive disabilities in children with NF-1: diffusion tensor imaging features S Aydin, S Kurtcan, A Alkan, S Guler, M Filiz, TF Yilmaz, TU Sahin, ... Clinical Imaging 40 (6), 1092-1095, 2016 | 30 | 2016 |
| Prognosis and demographic characteristics of SSPE patients in Istanbul, Turkey S Guler, M Kucukkoc, A Iscan Brain and Development 37 (6), 612-617, 2015 | 26 | 2015 |
| The evaluation of physiological and biochemical parameters and the autonomic nervous systems of children with breath-holding spells H Arslan, E Torun, JCU Akkan, S Guler, S Bayraktar Neuropediatrics 45 (04), 212-216, 2014 | 26 | 2014 |
| The value of echocardiography versus cardiac troponin I levels in the early detection of anthracycline cardiotoxicity in childhood acute leukemia: prospective evaluation of a 7 … K Oztarhan, S Guler, B Aktas, M Arslan, Z Salcioglu, G Aydogan Pediatric hematology and oncology 28 (5), 380-394, 2011 | 24 | 2011 |
| Non epileptic paroxysmal events in childhood B Tatlı, S Güler Turkish Archives of Pediatrics/Türk Pediatri Arşivi 52 (2), 59, 2017 | 22 | 2017 |
| Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals K Saida, R Maroofian, T Sengoku, T Mitani, AT Pagnamenta, D Marafi, ... Genetics in Medicine 25 (1), 90-102, 2023 | 16 | 2023 |
| The impact of SARS-CoV2 on the anxiety levels of subjects and on the anxiety and depression levels of their parents TD Dilek, Z Boybay, N Kologlu, O Tin, S Güler, S Saltık Multiple sclerosis and related disorders 47, 102595, 2021 | 15 | 2021 |
| The impact of epilepsy on preschool children and their families M Tanriverdi, FK Mutluay, D Tarakçi, S Güler, A Iscan Epilepsy & Behavior 62, 6-11, 2016 | 14 | 2016 |
| Erken taburcu olan yenidoğanlarda yeniden hastaneye yatış nedenleri ve sonuçları Orijinal Araştırma MA Akın, S Kavuncuoğlu, S Özbek, EY GÖK, F Uysal, S Güler, E Öztürk Türk Pediatri Arşivi 41 (4), 201-207, 2006 | 14 | 2006 |
| Sleep disturbances and serum vitamin D levels in children with autism spectrum disorder S Guler, G Yesil, M Ozdil, B Ekici, H Onal Int J Clin Exp Med 9 (7), 14691-14697, 2016 | 12 | 2016 |
| Endocrinological evaluations of a neurofibromatosis type 1 cohort: is it necessary to evaluate autoimmune thyroiditis in neurofibromatosis type 1? S Güler, G Yeşil, Ö Hasan Balkan Medical Journal 34 (6), 522-526, 2017 | 10 | 2017 |
| Report of a patient with Temple–Baraitser syndrome G Yesil, S Guler, A Yuksel, Y Alanay American Journal of Medical Genetics Part A 164 (3), 848-851, 2014 | 9 | 2014 |
| MRS features during encephalopathic crisis period in 11 years old case with GA-1 S Kurtcan, B Aksu, A Alkan, S Guler, A Iscan Brain and Development 37 (5), 546-551, 2015 | 8 | 2015 |
| Orta ölçekli hayvancılık işletmelerinde yenilenebilir enerji kullanım olanakları ve örnek bir uygulama S Güler Namık Kemal Üniversitesi, 2014 | 7 | 2014 |
| Expanding clinical phenotype of TRAPPC12-related childhood encephalopathy: two cases and review of literature AD Aslanger, E Demiral, S Sonmez-Sahin, S Guler, B Goncu, E Yucesan, ... Neuropediatrics 51 (06), 430-434, 2020 | 6 | 2020 |
| Acquired Chiari I malformation secondary to spontaneous intracranial hypotension syndrome and persistent hypoglycemia: a case report H Önal, A Ersen, H Gemici, E Adal, S Güler, S Sander, S Albayram Journal of Clinical Research in Pediatric Endocrinology 10 (4), 391, 2018 | 6 | 2018 |
| MRI findings in encephalopathy with primary carnitine deficiency: A case report TF Yilmaz, M Atay, H Toprak, S Guler, A Aralasmak, A Alkan Journal of Neuroimaging 25 (2), 325-328, 2015 | 6 | 2015 |
