In cystic fibrosis (CF), the respiratory disease is the main factor that influences the outcome
and the prognosis of patients, bacterial infections being responsible for severe …

This study hypothesized that botulinum toxin (Botox) therapy would sustainably reduce
sweat production in axillary hyperhidrosis patients over one year and significantly improve …

The COVID-19 pandemic, caused by the SARS-CoV-2 virus, has had significant impacts on
pulmonary function. This study aimed to comprehensively evaluate pulmonary function and …

Childhood interstitial lung disease (chILD) includes a heterogeneous spectrum of rare
respiratory disorders in children associated with substantial morbi-mortality. Interstitial …

Materials and Methods: In this cross-sectional study, 76 CF children≥ 6 years old registered
in the CF Foundation of Children's Medical Center Hospital, Tehran, Iran, who underwent …

Objectives To analyze the evolution of clinical and anthropometric characteristics of children
and adolescents with cystic fibrosis (CF) over 24 months, including the period of the COVID …

Background: Life expectancy has increased in cystic fibrosis (CF) patients; however, the rate
of mortality is still high, and in a majority of cases, the cause of death is due to respiratory …

In their quasi-physiological study “Ultrasound assessment of the respiratory system using
diaphragm motion-volume indices”, Boussuges et al. matched ultrasounds of the diaphragm …

Background: The Lung Clearance Index (LCI) serves as a non-uniform ventilation index
utilized for monitoring pulmonary function in patients with cystic fibrosis (CF). Lung …

Cystic fibrosis (CF) is a rare, autosomal recessive multiorgan genetic disease. Peripheral
muscle weakness and reduced lung function are prevalent in individuals with CF. Handgrip …