Ceren Ayca Yildiz
Overview
Explore the profile of Ceren Ayca Yildiz including associated specialties, affiliations and a list of published articles.
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5
Citations
4
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Recent Articles
1.
Uzunoglu B, Selcuk Balci M, Kalyoncu M, Karabulut S, Metin Cakar N, Yildiz C, et al.
Pediatr Pulmonol
. 2025 Mar;
60(3):e71037.
PMID: 40062574
Background: Although modulator therapies have proven effective in cystic fibrosis (CF) access is limited due to reimbursement issues in Turkey. We aimed to examine anxiety and depression levels of people...
2.
Metin Cakar N, Karabulut S, Yuksel Kalyoncu M, Selcuk Balci M, Yildiz C, Kocaman D, et al.
J Cyst Fibros
. 2024 Nov;
PMID: 39516142
Background: Our study aimed to identify the social domains that pose the greatest barriers to managing and supporting pwCF, particularly in relation to income levels. Methods: To identify associations between...
3.
Yildiz C, Selcuk Balci M, Karabulut S, Baser Z, Kalyoncu M, Metin Cakar N, et al.
Pediatr Pulmonol
. 2024 Sep;
59(12):3540-3549.
PMID: 39291770
Backgrounds: Genetic variants in CF transmembrane conductance regulator (CFTR) gene causes cystic fibrosis (CF), a prevalent autosomal recessive disorder. More than 2000 variants in CFTR have been described as disease...
4.
Yildiz C, Selcuk Balci M, Karabulut S, Baser Z, Yuksel Kalyoncu M, Metin Cakar N, et al.
Pediatr Pulmonol
. 2024 Jul;
59(12):3250-3259.
PMID: 39031495
Background: Cystic fibrosis (CF) is an autosomal recessive disease caused by variants of CFTR gene. Over 2000 variants have been identified, and new drugs called CFTR modulators have been developed...
5.
Bozlak S, Alkaya D, Kasap B, Yuksel Ulker A, Yildiz C, Altindag V, et al.
Turk Arch Pediatr
. 2023 Mar;
58(2):182-188.
PMID: 36856356
Objective: Williams syndrome is caused by a microdeletion at 7q11.23 and is characterized by a distinctive face, cardiovascular disease, and intellectual disability with a specific cognitive and behavioral profile. This...
6.
Mollaoglu E, Alkaya D, Yildiz C, Kasap B, Tuysuz B
Clin Genet
. 2022 Dec;
103(5):574-579.
PMID: 36504352
Acromesomelic dysplasias (AMD) are a group of skeletal dysplasia characterized by shortening of the middle and distal segments of the limbs. Recently, biallelic PRKG2 variants have been reported to cause...