Atilla Ersen
Overview
Explore the profile of Atilla Ersen including associated specialties, affiliations and a list of published articles.
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Articles
22
Citations
84
Followers
0
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Recent Articles
1.
Bildik O, Dundar N, Basarir G, Ersen A, Bozkaya Yilmaz S, Kusgoz F, et al.
Pediatr Neurol
. 2023 Jun;
145:148-153.
PMID: 37369146
Background: We aimed to analyze pediatric patients with coronavirus disease 2019 (COVID-19) with a diverse spectrum of neurological manifestations in a single center since neurological involvement in children is still...
2.
Bozkaya-Yilmaz S, Karadag-Oncel E, Olgac-Dundar N, Gencpinar P, Sarioglu B, Arican P, et al.
Eur J Pediatr
. 2021 Aug;
181(1):383-391.
PMID: 34355277
Children with chronic neurological diseases, including cerebral palsy (CP), are especially susceptible to vaccine-preventable infections and face an increased risk of severe respiratory infections and decompensation of their disease. This...
3.
Ersen A, Gencpinar P, Arican P, Bozkaya Yilmaz S, Aliyeva N, Ozdemir T, et al.
Clin Neuropharmacol
. 2020 Jun;
43(4):121-122.
PMID: 32501858
Hereditary spastic paraplegia (HSP) is group of a rare neurodegenerative disorder with both genetically and clinically diverse neurologic features. Indeed, disease progression is varying greatly within the different forms and...
4.
Arican P, Oztekin O, Cavusoglu D, Bozkaya Yilmaz S, Ersen A, Dundar N, et al.
Turk J Pediatr
. 2020 May;
62(2):343-346.
PMID: 32419431
Background: Hypertrophic olivary degeneration (HOD) is a rare degenerative disorder that is thought to occur subsequent to a disruption of the dentate-rubro-olivary pathway. Case: We report a pediatric case of...
5.
Arican P, Gencpinar P, Kirbiyik O, Bozkaya Yilmaz S, Ersen A, Oztekin O, et al.
Pediatr Neurol
. 2019 Jun;
99:55-59.
PMID: 31201073
Background: We explored the clinical and molecular characteristics of molybdenum cofactor deficiency due to MOCS2 muations. Methods: We summarize the genetic and clinical findings of previously reported patients with a...
6.
Onal H, Kutlu E, Aydin B, Ersen A, Topal N, Adal E, et al.
J Pediatr Endocrinol Metab
. 2019 Jun;
32(7):683-687.
PMID: 31199773
Objective To investigate the relationship between brain masculinization and retinal thickness in children with congenital adrenal hyperplasia (CAH). Methods Forty-five patients with CAH aged between 4 and 18 years and...
7.
Onal H, Ersen A, Gemici H, Adal E, Guler S, Sander S, et al.
J Clin Res Pediatr Endocrinol
. 2018 Mar;
10(4):391-394.
PMID: 29513222
Spontaneous intracranial hypotension (SIH) is a rare and potentially serious condition in childhood. Cerebrospinal fluid (CSF) volume depletion is thought to be the main causative feature for intracranial hypotension and...
8.
Onal Z, Balkaya S, Ersen A, Mutlu N, Onal H, Adal E
J Pediatr Endocrinol Metab
. 2017 Mar;
30(5):551-555.
PMID: 28350538
Background: In this study we evaluated whether vitamin B12 deficiency affects neonatal screening (NS) for congenital hypothyroidism (CH). Methods: A cross-sectional study conducted from 2010 to 2011. A total of...
9.
Onal Z, Ersen A, Bayramoglu E, Kazanci S, Onal H, Adal E
J Pediatr Endocrinol Metab
. 2016 Sep;
29(9):1013-7.
PMID: 27658137
Background: Type 1 diabetes mellitus (T1DM) is speculated to have an impaired immunological response to vaccines. This paper aimed to investigate the presence of specific antibodies against hepatitis B virus...
10.
Adal E, Onal Z, Ersen A, Yalcin K, Onal H, Aydin A
J Clin Res Pediatr Endocrinol
. 2015 Mar;
7(1):57-62.
PMID: 25800477
Objective: Considering the ever increasing population of diabetic adolescents and the association of the disease with psychosocial problems throughout its course, depression and/or anxiety and social support from parents are...