Pakize Karaoglu
Overview
Explore the profile of Pakize Karaoglu including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
35
Citations
110
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Gursoy S, Yilmaz Uzman C, Erdogan K, Karaoglu P, Sozen Turk T, Yilmaz U, et al.
Pediatr Neurol
. 2025 Feb;
165:43-51.
PMID: 39951932
Background: X-linked intellectual disability (XLID) is a clinically and genetically heterogeneous disorder. In this study, we aimed to describe the clinical and molecular spectrum of patients with XLID. We also...
2.
Sonmez B, Kocabey M, Polat A, Gursoy S, Karaoglu P, Horvath R, et al.
Mol Syndromol
. 2025 Feb;
16(1):61-68.
PMID: 39911178
Introduction: Nemaline myopathy (NEM) is a heterogeneous muscle disease, which usually presents with hypotonia and muscle weakness. Biallelic pathogenic variants of gene cause severe form of NEM (NEM8), which leads...
3.
Direk M, Besen S, Oncel I, Gunbey C, Ozdogan O, Orgun L, et al.
Mult Scler Relat Disord
. 2023 Dec;
81:105149.
PMID: 38096730
Background: Various etiologies may underlie optic neuritis, including autoantibody-mediated disorders described in the last decade. We re-examined demographic, clinical, laboratory features and prognostic factors in pediatric patients with autoimmune optic...
4.
Guzin Y, Yilmaz U, Pekuz S, Karaoglu P, Parlak Ibis I, Kirkgoz H, et al.
Pediatr Int
. 2023 Oct;
65(1):e15650.
PMID: 37817404
Background: Although Guillain-Barré syndrome (GBS) is now the most common cause of acute flaccid paralysis in children, information on the long-term follow-up of GBS is still limited. Identification of prognostic...
5.
Yilmaz D, Teber S, Gultutan P, Yildirim M, Bektas O, Alikilic D, et al.
Mult Scler Relat Disord
. 2023 Sep;
79:104948.
PMID: 37659352
Objectives: To evaluate clinical characteristics, imaging features and etiological profile of Radiologically Isolated Syndrome (RIS) along with clinical and radiological follow-up. Methods: Demographic, clinical and radiological data of patients younger...
6.
Karaoglu P, Tekin H
Neuropediatrics
. 2022 Dec;
54(1):2-5.
PMID: 36564022
Background: We aimed to evaluate the clinical findings and electroencephalographic (EEG) characteristics of patients with juvenile absence epilepsy (JAE) and to determine the factors that predict response to antiseizure medications...
7.
Unalp A, Kose M, Karaoglu P, Guzin Y, Yilmaz U
Turk J Pediatr
. 2022 Sep;
64(4):747-753.
PMID: 36082649
Background: Hypomyelinating leukodystrophy-14 (HLD14) is a rarely seen neurodevelopmental disease caused by homozygous pathogenic ubiquitin-fold modifier 1 gene variants. The disease has an autosomal recessive inheritance. All patients with this...
8.
Unalp A, Kutlu A, Karaoglu P, Yilmaz U, Cakaloz B
Turk Arch Pediatr
. 2022 Jul;
57(3):282-289.
PMID: 35781230
Objective: The aim of this study was to compare sociodemographic characteristics, quality of life, and levels of depression and anxiety of children with epilepsy and their families with a healthy...
9.
Ayar D, Unalp A, Yilmaz U, Bektas M, Karaoglu P, Akcay E, et al.
Epilepsy Behav
. 2022 Jul;
134:108770.
PMID: 35777351
Aim: Due to reactions, such as being ridiculed, blamed, or rejected, children with epilepsy and their families may consider epilepsy as something to be ashamed of, and therefore both the...
10.
Tekin H, Karaoglu P, Bolat E
Neurocirugia (Astur : Engl Ed)
. 2022 Jun;
33(4):190-194.
PMID: 35725220
Primary diffuse leptomeningeal oligodendrogliomatosis is a rare fatal tumor of childhood. Symptoms usually occur when the tumor causes hydrocephalus. Brain magnetic resonance imaging (MRI) may be nearly normal in the...