Ayşe Tana Aslan
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View article: Fibrosing interstitial lung disease in childhood: prevalence and disease trajectories
Fibrosing interstitial lung disease in childhood: prevalence and disease trajectories Open
Background Pulmonary fibrosis is of critical importance in childhood interstitial lung disease (chILD), yet fibrosis prevalence, impact on the clinical progression, and survival have not been systematically evaluated. Methods Data were ext…
View article: The relationship between inspiratory area under the curve in spirometry and sleep apnea in children
The relationship between inspiratory area under the curve in spirometry and sleep apnea in children Open
View article: Clinical Characteristics and Risk Factors of Patients With Cystic Fibrosis-Related Diabetes and Pre-diabetes: Cohort of Cystic Fibrosis Registry of Türkiye
Clinical Characteristics and Risk Factors of Patients With Cystic Fibrosis-Related Diabetes and Pre-diabetes: Cohort of Cystic Fibrosis Registry of Türkiye Open
View article: Bronchiectasis in Children: A Comparative Analysis of Cystic Fibrosis and Non-Cystic Fibrosis Etiologies Using the Bhalla Score
Bronchiectasis in Children: A Comparative Analysis of Cystic Fibrosis and Non-Cystic Fibrosis Etiologies Using the Bhalla Score Open
The results underscore distinct clinical trajectories between CF and non-CF BE in children. Improvements in CF patients suggest the effectiveness of structured clinical management, whereas inconsistent outcomes in non-CF patients point to …
View article: Current Status of Cystic Fibrosis in Türkiye: Data from the National Registry
Current Status of Cystic Fibrosis in Türkiye: Data from the National Registry Open
The CFRT report provides a valuable resource showing the clinical and laboratory data of patients with CF in the country.
View article: Impact of Modulator Therapy on the Chronic Colonization of Lower Respiratory Tract Pathogens in Children: Data From Cystic Fibrosis Registry of Turkey
Impact of Modulator Therapy on the Chronic Colonization of Lower Respiratory Tract Pathogens in Children: Data From Cystic Fibrosis Registry of Turkey Open
Background Modulators have revolutionized cystic fibrosis (CF) management, but their effects on respiratory pathogens remain unclear. This study evaluated changes in lower respiratory tract pathogen detection after modulator therapy in chi…
View article: Tuberculosis in children and adolescents using biological agents: a nationwide cohort study from Turkey
Tuberculosis in children and adolescents using biological agents: a nationwide cohort study from Turkey Open
The low frequency of TB may be due to effective TB screening before and during the therapy. The age of diagnosis was older, pulmonary and extrapulmonary TB involvement was more common in children using biological agents, which may be relat…
View article: Acute Bronchiolitis To Pediatric Inpatient Clinic In Patients Under 2 Years Old, Installed with Diagnosis Investigation of the Relationship of Bronchiolitis and Asthma
Acute Bronchiolitis To Pediatric Inpatient Clinic In Patients Under 2 Years Old, Installed with Diagnosis Investigation of the Relationship of Bronchiolitis and Asthma Open
Objective: Previously considered a uniform disease, bronchiolitis has been revealed through research as heterogeneous, displaying varied phenotypes and clinical-histopathological differences among patients. Our study aimed to explore disti…
View article: Upper Extremity Exercise Capacity and Muscle Oxygenation in Patients With Primary Ciliary Dyskinesia
Upper Extremity Exercise Capacity and Muscle Oxygenation in Patients With Primary Ciliary Dyskinesia Open
Background and Objectives Patients with primary ciliary dyskinesia (PCD) have a reduction in exercise capacity from the early stages. Although there are studies investigating these patients' lower extremity exercise capacity using various …
View article: Cyclosporine A in children with ABCA3 deficiency
Cyclosporine A in children with ABCA3 deficiency Open
Background Biallelic ATP‐binding cassette subfamily A member 3 (ABCA3) variants can cause interstitial lung disease in children and adults, for which no proven treatments exist. Recent in vitro evidence suggested that cyclosporine A (CsA) …
View article: Comparison of refugee patients with cystic fibrosis and their counterpart children from Turkey during the war
Comparison of refugee patients with cystic fibrosis and their counterpart children from Turkey during the war Open
Since the outbreak of the Syrian civil war in 2011, the population of Arab refugees in Turkey has rapidly increased. While cystic fibrosis (CF) is believed to be rare among Arabs, recent studies suggest it is underdiagnosed. This study aim…
View article: An Unusual Presentation of Hydatid Cyst Mimicking Eosinophilic Granulomatosis Polyangiitis in a Child
An Unusual Presentation of Hydatid Cyst Mimicking Eosinophilic Granulomatosis Polyangiitis in a Child Open
View article: Neglected Children with Cystic Fibrosis due to War (Turkey Profile of Refugee Patients)
Neglected Children with Cystic Fibrosis due to War (Turkey Profile of Refugee Patients) Open
Introduction: Since the outbreak of the Syrian civil war in 2011, the population of Arab refugees in Turkey has rapidly increased. While cystic fibrosis (CF) is believed to be rare among Arabs, recent studies suggest it is underdiagnosed. …
View article: Anxiety Levels of Children with Primary Ciliary Dyskinesia and Their Mothers at the Beginning of the COVID-19 Pandemic and Change in the First Year
Anxiety Levels of Children with Primary Ciliary Dyskinesia and Their Mothers at the Beginning of the COVID-19 Pandemic and Change in the First Year Open
We aimed to assess anxiety of children with primary ciliary dyskinesia (PCD) and their primary caregivers at the beginning of Coronavirus disease-2019 (COVID-19) pandemic and change in levels of anxiety in first year with prolongation of p…
View article: Patients with cystic fibrosis who could not receive the CFTR modulator treatment: What did they lose in 1 year?
Patients with cystic fibrosis who could not receive the CFTR modulator treatment: What did they lose in 1 year? Open
Background Cystic fibrosis (CF) is an autosomal recessive disorder caused by CF transmembrane conductance regulator (CFTR) genetic variants. CFTR modulators improve pulmonary function and reduce respiratory infections in CF. This study inv…
View article: P180 Evaluation of clinical features of children with cystic fibrosis and CFSPID in newborn screening programme with IRT/IRT protocol
P180 Evaluation of clinical features of children with cystic fibrosis and CFSPID in newborn screening programme with IRT/IRT protocol Open
View article: P359 “No words for feelings” The factors effecting alexithymia in the patients with cystic fibrosis and their mothers
P359 “No words for feelings” The factors effecting alexithymia in the patients with cystic fibrosis and their mothers Open
View article: Clinical characteristics of patients requiring lung transplantation referral in national cystic fibrosis registry data
Clinical characteristics of patients requiring lung transplantation referral in national cystic fibrosis registry data Open
Background. We aimed to determine the number of cystic fibrosis (CF) patients recorded in the Cystic Fibrosis Registry of Türkiye (CFRT) who were in need of lung transplantation (LT) referral and examine clinical differences between p…
View article: Diffuse alveolar haemorrhage in children: an international multicentre study
Diffuse alveolar haemorrhage in children: an international multicentre study Open
Background Paediatric diffuse alveolar haemorrhage (DAH) is a rare heterogeneous condition with limited knowledge on clinical presentation, treatment and outcome. Methods A retrospective, descriptive multicentre follow-up study initiated f…
View article: ABCA3-related interstitial lung disease beyond infancy
ABCA3-related interstitial lung disease beyond infancy Open
Background The majority of patients with childhood interstitial lung disease (chILD) caused by pathogenic variants in ATP binding cassette subfamily A member 3 (ABCA3) develop severe respiratory insufficiency within their first year of lif…
View article: Pulmonary Embolism in Childhood: A Multicenter Experience from Turkey
Pulmonary Embolism in Childhood: A Multicenter Experience from Turkey Open
The Wells scoring system seems insufficient to diagnose pulmonary embolism in children and should be improved by adding new parameters. ISPAT may be more common in children with congenital heart disease and systemic disease.
View article: Evaluation of Children with Congenital Lung Malformations Who Were Diagnosed in The Prenatal and Postnatal Period
Evaluation of Children with Congenital Lung Malformations Who Were Diagnosed in The Prenatal and Postnatal Period Open
Amaç: Çalışmamızda prenatal ve postnatal dönemde tanı alan konjenital akciğer malformasyonu olan hastaların klinik özelliklerini karşılaştırmayı amaçladık. Gereç ve Yöntemler: 2007-2021 yılları arasında Çocuk Göğüs Hastalıkları Bölümü’nde …
View article: Psychological status of mothers of children with cystic fibrosis and primary ciliary dyskinesia
Psychological status of mothers of children with cystic fibrosis and primary ciliary dyskinesia Open
Objectives: We aimed to investigate depression, burnout, attitude, and burden of caregivers of children with cystic fibrosis (CF), and especially caregivers of children with primary ciliary dyskinesia (PCD) due to limited number of studies…
View article: The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey
The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey Open
Using sequencing and Multiplex Ligation-dependent Probe Amplification methods, the identification of seven new mutations that were not previously reported in the literature contributes to a better understanding of the heterogeneous nature …
View article: IPG volume 33 issue 10 Cover and Back matter
IPG volume 33 issue 10 Cover and Back matter Open
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View article: Review of Complications of Operated Esophageal Atresia and Tracheoesophageal Fistula Patients
Review of Complications of Operated Esophageal Atresia and Tracheoesophageal Fistula Patients Open
Hospital admissions of the patients with EA and TEF were higher due to GER, recurrent pneumonia, restrictive lung disease, and scoliosis in the follow-up. Pneumonia, hospitalization, stricture in the esophagus, and growth retardation were …
View article: Sleep disturbances in children with cystic fibrosis, primary ciliary dyskinesia and typically developing children during <scp>COVID</scp>‐19 pandemic
Sleep disturbances in children with cystic fibrosis, primary ciliary dyskinesia and typically developing children during <span>COVID</span>‐19 pandemic Open
Aim We aimed to investigate sleep disturbances in children with cystic fibrosis (CF) and primary ciliary dyskinesia (PCD) and typically developing (TD) children during the COVID‐19 pandemic. Methods Primary care givers of children with CF …
View article: Pulmonary <i>Mycobacterium abscessus</i> Infection in an 11-Year-Old Child, Successfully Treated with Inhaled/Parenteral Amikacin: A Case Report and Review of Literature
Pulmonary <i>Mycobacterium abscessus</i> Infection in an 11-Year-Old Child, Successfully Treated with Inhaled/Parenteral Amikacin: A Case Report and Review of Literature Open
Mycobacterium abscessus appears to be increasing cause of pulmonary infection in children with underlying risk factors including cystic fibrosis, chronic lung disease and immunodeficiency syndromes. We present a case of pulmonary M. absces…
View article: Hepatopulmonary Syndrome and Multiple Arteriovenous Fistulas in a Child with Niemann-Pick Disease
Hepatopulmonary Syndrome and Multiple Arteriovenous Fistulas in a Child with Niemann-Pick Disease Open
Background: Niemann-Pick disease (NPD) is caused by abnormal storage of sphingomyelin. NPD may affect the pulmonary system and cause hypoxia. In the present case, both hepatopulmonary syndrome (HPS) and pulmonary arteriovenous fistulas (PA…
View article: Pigeon breeder`s disease as a cause of hypersensitivity pneumonia in children
Pigeon breeder`s disease as a cause of hypersensitivity pneumonia in children Open
Background and Objectives. Hypersensitivity pneumonia is a complex condition due to exposure time, intensity, different clinical presentation, and treatment practices. We aimed to evaluate the patients that were diagnosed with hypersensiti…