Detalhe da pesquisa
1.
The Assessment and Management of Childhood Masturbation: An Analysis of 90 Cases.
Neuropediatrics
; 55(2): 104-111, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-37827511
2.
Evaluation of chromosomal abnormalities in the postnatal cohort: A single-center study on 14,242 patients.
J Clin Lab Anal
; 38(1-2): e24997, 2024 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-38115218
3.
A retrospective study on the clinical and molecular outcomes of calpainopathy in a Turkish patient cohort.
Turk J Med Sci
; 54(1): 86-98, 2024.
Artigo
Inglês
| MEDLINE | ID: mdl-38812636
4.
Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment.
Genes Immun
; 24(1): 12-20, 2023 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36517554
5.
Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study.
Eur J Pediatr
; 181(1): 383-391, 2022 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-34355277
6.
Evaluation of micronutrient levels in children with cerebral palsy.
Pediatr Int
; 64(1): e15005, 2022 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-34585809
7.
Shuddering attacks in children: A retrospective analysis of 19 cases from a single-center in Turkey.
Epilepsy Behav
; 117: 107827, 2021 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33621812
8.
An analysis of 109 fetuses with prenatal diagnosis of complete agenesis of corpus callosum.
Neurol Sci
; 41(6): 1521-1529, 2020 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-31970575
9.
Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia Syndrome.
Ann Neurol
; 84(5): 638-647, 2018 11.
Artigo
Inglês
| MEDLINE | ID: mdl-30178464
10.
Neutropenia and Increased Mean Corpuscular Volume (MCV) With Abnormal Neurologic Findings: A Case of Cobalamin D Deficiency.
J Pediatr Hematol Oncol
; 41(1): e54-e56, 2019 01.
Artigo
Inglês
| MEDLINE | ID: mdl-29620684
11.
The relationship between the prognosis of children with acute arterial stroke and polymorphisms of CDKN2B, HDAC9, NINJ2, NAA25 genes.
J Thromb Thrombolysis
; 47(4): 578-584, 2019 May.
Artigo
Inglês
| MEDLINE | ID: mdl-30656483
12.
The use of rapamycin in patients with tuberous sclerosis complex: Long-term results.
Epilepsy Behav
; 88: 357-364, 2018 11.
Artigo
Inglês
| MEDLINE | ID: mdl-30305233
13.
The relationship between hematological parameters and prognosis of children with acute ischemic stroke.
Childs Nerv Syst
; 34(4): 655-661, 2018 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29209887
14.
Investigation of attention deficit hyperactivity disorder (ADHD) sub-types in children via EEG frequency domain analysis.
Int J Neurosci
; 128(4): 349-360, 2018 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-28925800
15.
Neurological Manifestations in Familial Mediterranean Fever: Results of 22 Children from a Reference Center in Kayseri, an Urban Area in Central Anatolia, Turkey.
Neuropediatrics
; 48(2): 79-85, 2017 04.
Artigo
Inglês
| MEDLINE | ID: mdl-27656843
16.
Pediatric central nervous system tumors in the first 3 years of life: pre-operative mean platelet volume, neutrophil/lymphocyte count ratio, and white blood cell count correlate with the presence of a central nervous system tumor.
Childs Nerv Syst
; 33(2): 233-238, 2017 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-27942922
17.
Efficiency of a Combination of Pharmacological Treatment and Nondrug Interventions in Childhood Narcolepsy.
Neuropediatrics
; 47(6): 380-387, 2016 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-27564079
18.
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations.
Nature
; 467(7312): 207-10, 2010 Sep 09.
Artigo
Inglês
| MEDLINE | ID: mdl-20729831
19.
Current approaches to the clinical assessment of syncope in pediatric population.
Childs Nerv Syst
; 32(3): 427-36, 2016 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-26732063
20.
Familial moyamoya disease in two Turkish siblings with same polymorphism in RNF213 gene but different clinical features.
Childs Nerv Syst
; 32(3): 569-73, 2016 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-26277359