| Theory of mind and neurodevelopmental disorders of childhood B Korkmaz Pediatric research 69 (8), 101-108, 2011 | 408 | 2011 |
| Neuropsychological functions in idiopathic occipital lobe epilepsy S Gülgönen, V Demirbilek, B Korkmaz, A Dervent, BD Townes Epilepsia 41 (4), 405-411, 2000 | 132 | 2000 |
| Benign rolandic epilepsy: neuropsychological findings E Gündüz, V Demirbilek, B Korkmaz Seizure 8 (4), 246-249, 1999 | 131 | 1999 |
| Functional deficiencies of sulfite oxidase: Differential diagnoses in neonates presenting with intractable seizures and cystic encephalomalacia JO Sass, A Gunduz, CAR Funayama, B Korkmaz, KGD Pinto, B Tuysuz, ... Brain and Development 32 (7), 544-549, 2010 | 79 | 2010 |
| Otizm B Korkmaz Farklı gelişen çocuklar içinde, 81-114, 2003 | 61 | 2003 |
| Food faddism causing vision loss in an autistic child O Uyanik, B Dogangun, L Kayaalp, B Korkmaz, A Dervent CHILD CARE HEALTH AND DEVELOPMENT 32 (5), 601, 2006 | 39 | 2006 |
| Infantile autism: adult outcome. B Korkmaz Seminars in clinical neuropsychiatry 5 (3), 164-170, 2000 | 31 | 2000 |
| Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophy LE Kolb, Z Arlier, C Yalcinkaya, AK Ozturk, JA Moliterno, O Erturk, ... Neurogenetics 11, 319-325, 2010 | 27 | 2010 |
| Migration abnormality in the left cingulate gyrus presenting with autistic disorder B Korkmaz, G Benbir, V Demirbilek Journal of child neurology 21 (7), 600-604, 2006 | 19 | 2006 |
| Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population B Tüysüz, F Bayrakli, ML DiLuna, K Bilguvar, Y Bayri, C Yalcinkaya, ... Neurogenetics 9, 119-125, 2008 | 17 | 2008 |
| A patient with Duchenne muscular dystrophy and autism demonstrates a hemizygous deletion affecting Dystrophin O Erturk, K Bilguvar, B Korkmaz, Y Bayri, F Bayrakli, Z Arlier, AK Ozturk, ... American Journal of Medical Genetics Part A 152 (4), 1039-1042, 2010 | 12 | 2010 |
| Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population B T ys z, F Bayrakli, ML DiLuna, K Bilguvar, Y Bayri, C Yalcinkaya, ... Neurogenetics 9 (2), 119-125, 2008 | 12 | 2008 |
| A study on visual evoked responses in childhood epilepsy with occipital paroxysms V Demirbilek, A Dervent, B Korkmaz, G Erkol, C Yalçinkaya Seizure 9 (4), 270-273, 2000 | 12 | 2000 |
| Four Novel SCN1A Mutations in Turkish Patients With Severe Myoclonic Epilepsy of Infancy (SMEI) Z Arlier, Y Bayri, LE Kolb, O Erturk, AK Ozturk, F Bayrakli, K Bilguvar, ... Journal of child neurology 25 (10), 1265-1268, 2010 | 11 | 2010 |
| Akdeniz Bölgesi Alçak Islah Zonunda (0-400 m) Kızılçam (Pinus brutia Ten.) Döl Denemeleri (4. Yaş Sonuçları) H Öztürk, S Şıklar, M Alan, T Ezen, B Korkmaz, AG Gülbaba, R Sabuncu, ... Orm. Ağçl. ve Toh. Islah Arşt. Enst. Md., Tek. Bül, 2004 | 11 | 2004 |
| Startle and blink reflex in high functioning autism O Erturk, B Korkmaz, G Alev, V Demirbilek, M Kiziltan Neurophysiologie Clinique/Clinical Neurophysiology 46 (3), 189-192, 2016 | 9 | 2016 |
| Diagnostic utility of superb microvascular imaging in depiction of corkscrew collaterals in Buerger's disease OF Nas, SG Kandemirli, B Erdemli Gursel, C Bilgin, B Korkmaz, ... Journal of Clinical Ultrasound 49 (2), 129-134, 2021 | 7 | 2021 |
| Electroclinical survey on benign epilepsy with occipital paroxysms A Dermirbilek Epilepsia 37 (4), 95, 1996 | 3 | 1996 |
| Autism Spectrum Disorders and Language B Korkmaz Austin Journal of Autism & Related Disabilities 1 (1), 1001-1002, 2015 | 2 | 2015 |
| Autism: clinical and neurobiological features, early diagnosis, treatment and some current developments B Korkmaz Turkish Archives of Pediatrics 45 (Supp: 1), 37-44, 2010 | 2 | 2010 |
