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Almala Pinar Ergenekon

Explore the profile of Almala Pinar Ergenekon including associated specialties, affiliations and a list of published articles. Areas
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Articles 21
Citations 48
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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.
Yanaz M, Unal F, Hepkaya E, Yazan H, Oksay S, Kostereli E, et al.
Thorac Res Pract . 2025 Feb; 26(1):25-31. PMID: 39930731
Objective: The aims of this multi-center study were to describe the characteristics of children receiving long-term home mechanical ventilation (HMV) in İstanbul and to compare the patients receiving non-invasive and...
3.
Selcuk Balci M, Gokdemir Y, Erdem Eralp E, Ergenekon A, Yilmaz Yegit C, Yanaz M, et al.
Pediatr Pulmonol . 2025 Feb; 60(2):e27506. PMID: 39898696
Background: CF R.I.S.E is a program that helps people with Cystic Fibrosis (pwCF) transition from pediatric to adult care. In 2022, we adapted it to CF S.O.B.E in Turkish during...
4.
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...
5.
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...
6.
Selcuk Balci M, Gokdemir Y, Erdem Eralp E, Ergenekon A, Yilmaz Yegit C, Yanaz M, et al.
Pediatr Pulmonol . 2024 Sep; 59(12):3483-3490. PMID: 39221873
Background: Cystic fibrosis (CF) patients have a limited life expectancy, but significant medical advances now highlight the need for successful transition programs from pediatric to adult care. The goal of...
7.
Bilgin G, Unal F, Yanaz M, Baskan A, Uzuner S, Ayhan Y, et al.
Pediatr Pulmonol . 2023 Nov; 59(2):331-341. PMID: 37983721
Materials And Methods: We included 32 caregivers (31 children) who had received standardized training a year ago and administered the same theoretical and practical tests 1 year after training completion....
8.
Yanaz M, Yilmaz Yegit C, Gulieva A, Kalyoncu M, Selcuk M, Uzunoglu B, et al.
J Cyst Fibros . 2023 Sep; 23(2):329-333. PMID: 37748990
Background: We aimed to investigate the effect of the use of electronic home spirometry in children with cystic fibrosis (CF) on 1-year FEV (% predicted, pp) change. Methods: This is...
9.
Kalyoncu M, Namli N, Yilmaz Yegit C, Yanaz M, Gulieva A, Ergenekon A, et al.
Sleep Breath . 2023 Sep; 28(1):331-337. PMID: 37733254
Purpose: Sleep-disordered breathing (SDB) is a disease defined by breathing or breathing irregularities while asleep. The current study examines the association between results of polysomnography (PSG) and the Pediatric Sleep...
10.
Ergenekon A, Gokdemir Y, Ersu R
J Clin Med . 2023 Aug; 12(15). PMID: 37568423
Obstructive sleep apnea (OSA) is characterized by recurrent complete or partial obstruction of the upper airway. The prevalence is 1-4% in children aged between 2 and 8 years and rising...