Detalhe da pesquisa
1.
Neonatal Outcomes of Critical Congenital Heart Defects: A Multicenter Epidemiological Study of Turkish Neonatal Society : Neonatal Outcomes of CCHD.
Pediatr Cardiol
; 45(2): 257-271, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38153547
2.
Evaluation of the Neuroprotective Effect of Pycnogenol in a Hypoxic-Ischemic Brain Injury Model in Newborn Rats.
Am J Perinatol
; 40(6): 612-618, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34044458
3.
Evaluation of syringin's neuroprotective effect in a model of neonatal hypoxic-ischemic brain injury.
Turk J Med Sci
; 53(5): 1312-1320, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38813032
4.
Epilepsy Frequency and Risk Factors Three Years After Neonatal Seizures.
Pediatr Neurol
; 149: 120-126, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37866139
5.
Is respiratory syncytial virus infection more dangerous than COVID 19 in the neonatal period?
J Matern Fetal Neonatal Med
; 35(22): 4398-4403, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-33225779
6.
Evaluation of Sporadic and Familial Cases with Craniofrontonasal Syndrome: A Wide Clinical Spectrum and Identification of a Novel EFNB1 Gene Mutation.
Mol Syndromol
; 12(5): 269-278, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34602953
7.
Ultrasonographic evaluation of the children with candiduria for the fungal ball: Is It necessary?
J Pediatr Urol
; 17(5): 738.e1-738.e5, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34389232
8.
Challenges in the management of an ignored cause of hyperammonemic encephalopathy: pyruvate carboxylase deficiency.
J Pediatr Endocrinol Metab
; 33(4): 569-574, 2020 Apr 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32145058
9.
A rare vascular lesion of newborn: cutis marmorata telangiectatica congenital.
Turk Pediatri Ars
; 54(2): 133-136, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31384150
10.
Abernethy Malformation Type 2 and Biliary Atresia Coexistence: A Rare Cause of Infantile Liver Transplant.
Euroasian J Hepatogastroenterol
; 8(2): 163-166, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30828559
11.
A Different SLC2A1 Gene Mutation in Glut 1 Deficiency Syndrome: c.734A>C.
Balkan Med J
; 34(6): 580-583, 2017 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28443597