Olcay Unver
Overview
Explore the profile of Olcay Unver including associated specialties, affiliations and a list of published articles.
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Articles
31
Citations
163
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0
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Recent Articles
1.
Akbeyaz I, Unver O, Ozturk G, Ozturk Hismi B, Ayaz A, Aydin K, et al.
J Pediatr Endocrinol Metab
. 2025 Feb;
38(2):196-200.
PMID: 39903824
Objectives: Sepiapterin reductase deficiency (SRD) is a rare dopa-sensitive neurotransmitter disorder caused by autosomal recessive mutations in the sepiapterin reductase gene. The triad of paroxysmal stiffening, oculogyric crises, and hypotonia...
2.
Yilmaz U, Gucuyener K, Yavuz M, Oncel I, Canpolat M, Saltik S, et al.
Eur J Paediatr Neurol
. 2024 Dec;
PMID: 39627061
No abstract available.
3.
Yuksel Kalyoncu M, Gokdemir Y, Yilmaz Yegit C, Yanaz M, Gulieva A, Selcuk M, et al.
Sleep Med
. 2024 Nov;
124:662-668.
PMID: 39531786
Purpose: Duchenne muscular dystrophy (DMD) is a severe, progressive condition characterized by muscle degeneration and weakness, significantly affecting respiratory function. This study aimed to evaluate the presence of sleep-disordered breathing...
4.
Yuksel Kalyoncu M, Gokdemir Y, Yilmaz Yegit C, Yanaz M, Gulieva A, Selcuk M, et al.
Children (Basel)
. 2024 Aug;
11(8).
PMID: 39201929
Background/objectives: Duchenne muscular dystrophy (DMD) is the most prevalent progressive muscular dystrophy, and the guidelines recommend the regular assessment of respiratory muscle function. This study aimed to assess the relationship...
5.
Cavusoglu D, Ozturk G, Turkdogan D, Kurul S, Yis U, Komur M, et al.
Cerebellum
. 2024 Apr;
23(5):1950-1965.
PMID: 38622473
Pontocerebellar hypoplasia (PCH) is a heterogeneous group of neurodegenerative disorders characterized by hypoplasia and degeneration of the cerebellum and pons. We aimed to identify the clinical, laboratory, and imaging findings...
6.
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...
7.
Ergenekon A, Gumus Z, Yilmaz Yegit C, Cenk M, Gulieva A, Kalyoncu M, et al.
Pediatr Pulmonol
. 2023 Mar;
58(6):1697-1702.
PMID: 36856268
Background: The aim of this study was to evaluate the prevalence of anxiety, depression, sleep, and associated factors in caregivers of children with spinal muscular atrophy (SMA). Materials And Methods:...
8.
Unver O, Celik T, Memisoglu A, Buyukbayrak E, Simsek F, Ozturk G, et al.
Neuromuscul Disord
. 2022 Sep;
32(10):e1.
PMID: 36153225
No abstract available.
9.
Yilmaz U, Gucuyener K, Yavuz M, Oncel I, Canpolat M, Saltik S, et al.
Eur J Paediatr Neurol
. 2022 Sep;
41:8-18.
PMID: 36137476
Background: The discovery of anti-myelin oligodendrocyte glycoprotein (MOG)-IgG and anti-aquaporin 4 (AQP4)-IgG and the observation on certain patients previously diagnosed with multiple sclerosis (MS) actually have an antibody-mediated disease mandated...
10.
Ozturk G, Karadag Saygi E, Unver O, Turkdogan D
Turk J Phys Med Rehabil
. 2022 Aug;
68(1):157-158.
PMID: 35949963
No abstract available.