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Pamukkale Üniversitesi Tıp fakültesi Çocuk Nöroloji Bilim Dalı
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Yıl
The levels of vitamin D, vitamin D receptor, homocysteine and complex B vitamin in children with autism spectrum disorders
H Altun, EB Kurutaş, N Şahin, O Güngör, E Fındıklı
Clinical Psychopharmacology and Neuroscience 16 (4), 383, 2018
862018
A multicenter cross-sectional study to evaluate the clinical characteristics and nutritional status of children with cerebral palsy
K Aydin, Y Akbas, B Unay, M Arslan, A Cansu, S Sahin, C Dilber, ...
Clinical nutrition ESPEN 26, 27-34, 2018
572018
Homocysteine, pyridoxine, folate and vitamin B12 levels in children with attention deficit hyperactivity disorder
H Altun, N Sahin, E Belge Kurutas, O Güngör
Psychiatria Danubina 30 (3), 310-316, 2018
442018
An unusual cause of acute renal failure in a newborn: hydrometrocolpos
C Aygun, O Özkaya, S Ayyýldýz, O Güngör, B Mutlu, Ş Küçüködük
Pediatric Nephrology 21 (4), 572-573, 2006
372006
Association between the corrected QT interval and carotid artery intima-media thickness in obese children
A Güven, T Özgen, O Güngör, M Aydın, K Baysal
Journal of Clinical Research in Pediatric Endocrinology 2 (1), 21, 2010
252010
Cerebral atrophy in 21 hypotonic infants with severe vitamin B12 deficiency
C Acıpayam, H Güneş, O Güngör, S Ipek, N Sarışık, NŞ Demir
Journal of paediatrics and child health 56 (5), 751-756, 2020
222020
The effect of antiepileptic drugs on thyroid hormonal function: valproic acid and phenobarbital
O Güngör, AK Özkaya, F Temiz
Acta Neurologica Belgica 120 (3), 615-619, 2020
192020
A compound heterozygous EARS2 mutation associated with mild leukoencephalopathy with thalamus and brainstem involvement and high lactate (LTBL)
O Güngör, AK Özkaya, Y Şahin, G Güngör, C Dilber, K Aydın
Brain and Development 38 (9), 857-861, 2016
152016
A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis
Y Sahin, O Güngör, A Ayaz, G Güngör, B Sahin, K Yaykasli, S Ceylaner
Brain and Development 39 (2), 166-170, 2017
102017
Catalan transform of the k-lucas numbers
E Özkan, M Taştan, O Güngör
Erzincan University Journal of Science and Technology 13 (ÖZEL SAYI I), 145-149, 2020
92020
Acute mercury poisoning in a group of school children
O Güngör, AK Özkaya, S Kirik, T Dalkiran, G Güngör, S Isikay, ...
Pediatric emergency care 35 (10), 696-699, 2019
82019
Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy
Y Sahin, O Güngör, Z Gormez, H Demirci, B Ergüner, G Güngör, C Dilber
Acta Neurologica Belgica 117 (1), 159-167, 2017
82017
Novel mutation in SUCLA2 identified on sequencing analysis
O Güngör, AK Özkaya, G Güngör, K Karaer, C Dilber, K Aydin
Pediatrics International 58 (7), 659-661, 2016
82016
Vanishing white matter disease with different faces
G Güngör, O Güngör, S Çakmaklı, H Maraş Genç, H İnce, G Yeşil, ...
Child's Nervous System 36, 353-361, 2020
72020
Thalamic T2 hypointensity: a diagnostic clue for Tay–Sachs disease
O Güngör, G Güngör, N Yurttutan, C Dilber
Acta Neurologica Belgica 116, 195-197, 2016
62016
Ulcerating molluscum contagiosum in a boy with relapsed acute lymphoblastic leukemia
E Özyürek, N Sentürk, M Kefeli, O Güngör, M Akbalik, F Aydin, T Fisgin, ...
Journal of pediatric hematology/oncology 33 (3), e114-e116, 2011
62011
Çocuklarda Kırım Kongo Kanamalı Ateşi hastalığı. 50
O Güngör, ÖK Eroğlu, A Güven, AG Kalaycı, F Duru
Milli Pediatri kongresi özet kitapçığı, 8-12, 2006
62006
Importance of Streptococci Infections in Childhood Neuropsychiatric Disorders
S Kırık, O Güngör, Y Kırık
Şişli Etfal Hastanesi tıp Bülteni 53 (4), 441, 2019
52019
A new mutation in an infant with Krabbe disease accompanied by enlargement of the optic nerves
O Güngör, G Güngör, AK Özkaya, C Dilber, K Aydın
Acta Neurologica Belgica 117, 319-321, 2017
52017
A case of congenital insensitivity to pain with anhidrosis
AK Özkaya, E Güler, E Arık, AR Namlı, D Cevizli, O Güngör
Turkish Archives of Pediatrics/Türk Pediatri Arşivi 49 (2), 177, 2014
52014
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