Volume 12 (2024)
Volume 11 (2023)
Volume 10 (2022)
Volume 9 (2021)
Volume 8 (2020)
Volume 7 (2019)
Volume 6 (2018)
Volume 5 (2017)
Volume 4 (2016)
Volume 3 (2015)
Volume 2 (2014)
Volume 1 (2013)
Keywords = Cystic Fibrosis
Number of Articles: 24
The Effect of Spark Physical Program (Sports, Play and Active Recreation for Kids) on Quality of Life and Spirometry in 6-18-Year-Old Children with Cystic Fibrosis
Volume 11, Issue 5 , May 2023, , Pages 17790-17799
Abstract
Background: The effect of SPARK physical education program on lung function in cystic fibrosis patients is not yet determined. SPARK (Sports, play and active recreation for kids) includes ... Read More
The Effect of Outpatient Management of Cystic Fibrosis Exacerbation on Pulmonary Function Tests: A Clinical Trial
Volume 10, Issue 6 , June 2022, , Pages 16121-16126
Abstract
Background: Cystic fibrosis (CF) is an inherited disease which involves multiple organs including respiratory tract. It results in chronic respiratory signs and symptoms which exacerbate ... Read More
The Relationship between Bone Mineral Density and Serum Vitamin D Levels in Cystic Fibrosis Children
Volume 10, Issue 6 , June 2022, , Pages 16147-16154
Abstract
Background: Cystic fibrosis is a multisystemic disorder. It is the most common autosomal recessive disorder in whites that causes complications such as changes in bone density. Therefore, ... Read More
The effect of Complementary and Alternative Medicines on the symptoms of Cystic Fibrosis patients: A Systematic Review
Volume 10, Issue 4 , April 2022, , Pages 15881-15900
Abstract
Background: Cystic fibrosis (CF) is the most common life-threatening hereditary disease among Caucasian populations. Due to the side effects caused by this disease and the high amount ... Read More
Towards the Validation of the Persian Translation of the Revised Cystic Fibrosis Quality of Life Questionnaire in Adolescents and Adults (CFQ-R 14+)
Volume 10, Issue 1 , January 2022, , Pages 15313-15322
Abstract
Background: the present study aimed to translate the cystic fibrosis questionnaire for adolescents and adults (CFQ-R 14+) into Persian, and assess its validity and reliability.Methods: ... Read More
Towards the Validation of the Persian Version of the Revised Cystic Fibrosis Quality of Life Questionnaire for children and parents (CFQ-R)
Volume 9, Issue 12 , December 2021, , Pages 15003-15014
Abstract
Background: The present study aimed to translate the cystic fibrosis questionnaire-revised (CFQ-R) for children with cystic fibrosis (CF) into Persian and evaluate the reliability and ... Read More
Evaluation of miR-301b and miR-302b Expressions in the Serum of Cystic Fibrosis Patients and their Association with Clinical Scoring System
Volume 9, Issue 11 , November 2021, , Pages 14907-14913
Abstract
Background: Cystic fibrosis (CF) is an autosomal recessive disorder caused by a mutation in CF transmembrane conductance regulator gene (CFTR). Clinical manifestations of the disease ... Read More
Possible Effect and Mechanism of Action of Flaxseed on Cystic Fibrosis Pulmonary Disorder: a Medical Hypothesis
Volume 9, Issue 9 , September 2021, , Pages 14400-14412
Abstract
Background: Cystic fibrosis (CF) as is an inherited disorder that can result in early death. Today, for treating the pulmonary symptoms of CF-related infections and inflammations, antibiotics ... Read More
The Effectiveness of Viktor Frankl's Logo therapy on the Mental Health of Pediatric Patients with Cystic Fibrosis
Volume 9, Issue 6 , June 2021, , Pages 13803-13810
Abstract
Background Individuals with cystic fibrosis (CF) are at high risk of clinically significant anxiety, which can be related to lower treatment adherence and poorer health ... Read More
Investigation the Lifestyle in Patients with Cystic Fibrosis According to Iranian Traditional Medicine
Volume 9, Issue 5 , May 2021, , Pages 13551-13557
Abstract
Respiratory involvement in cystic fibrosis (CF) is one of the most complaints in pulmonary disorders. Though symptomatic treatment of the patients with chemical medications is efficient ... Read More
Diagnostic Value of Changes in Serum Calprotectin Level and Patients' Sputum in Response to Treatment of Cystic Fibrosis Exacerbation in Children
Volume 9, Issue 5 , May 2021, , Pages 13569-13579
Abstract
Background Today few studies have focused on using calprotectin as an effective biomarker for monitoring the exacerbation of pulmonary complications in cystic fibrosis (CF). Thus, the ... Read More
The Effect of Nutritional Consultation on the Level of Malnutrition and Growth Indices in Children with Cystic Fibrosis
Volume 8, Issue 8 , August 2020, , Pages 11793-11801
Abstract
Background: Malnutrition is one of the most common disorders among children with Cystic Fibrosis (CF). The present study aimed to investigate the effect of nutritional consultation ... Read More
Effects of Curcumin Supplementation on Quality of Life of Cystic Fibrosis Patients
Volume 8, Issue 4 , April 2020, , Pages 11169-11176
Abstract
Background: Cystic fibrosis (CF) is one of the most common genetic disorders in children. CF patients are susceptible to chronic lung infections and malabsorption. Although patient ... Read More
Evaluation of Antibiotic Resistance Trend among Cystic Fibrosis Patients: A Single Center Study from 2014-2019
Volume 8, Issue 1 , January 2020, , Pages 10719-10729
Abstract
Background: Antibiotic resistance in Cystic Fibrosis (CF) patients has been a serious issue in their survival. The objective of this study was to investigate the antibiogram trend in ... Read More
Investigating the Effect of TNF α (-863) and TNF α (-308) genes Polymorphism on the Progression of Disease in Patients with Cystic Fibrosis
Volume 7, Issue 11 , November 2019, , Pages 10335-10341
Abstract
Background: Recent studies have shown that the course of cystic fibrosis in patients with this disease differs despite the same mutation in CFTR gene. We aimed to investigate the role ... Read More
Cardiac Involvement in Mild Cystic Fibrosis Lung Involvement Assessed by Tissue‐Doppler Echocardiography
Volume 7, Issue 10 , October 2019, , Pages 10205-10214
Abstract
Background:Cystic Fibrosis (CF) is a systemic disease affecting extra pulmonary dysfunction as a result of CF-related lung disease. Because of lack of enough studies in this field and ... Read More
Cystic Fibrosis Patients Evaluation in the Last Decades in a Referral Center, Tehran-Iran
Volume 7, Issue 8 , August 2019, , Pages 9997-10007
Abstract
Background Cystic fibrosis (CF) is the most prevalent lethal chronic genetic and multivariate disease, widespread in Iranian population. The aim of this study was to evaluate the condition ... Read More
Bone Mineral Density and Cystic Fibrosis: A Review
Volume 7, Issue 7 , July 2019, , Pages 9701-9710
Abstract
Cystic fibrosis (CF) is a common progressive genetic disorder among children which involves lungs, kidneys, intestine and liver. Apart from the significance of genetic factors, various ... Read More
Effects of Coenzyme Q10 Level on Clinical Parameters in Cystic Fibrosis Patients
Volume 7, Issue 4 , April 2019, , Pages 9285-9294
Abstract
Background: Cystic Fibrosis (CF) is a hereditary autosomal recessive genetic disorder that can affect many organs including the lungs and the digestive system. We aimed to assess the ... Read More
Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran
Volume 7, Issue 4 , April 2019, , Pages 9333-9339
Abstract
Background: Cystic fibrosis (CF) is the most common lethal genetic disorder of Cystic Fibrosis Trans-membrane Conductance (CFTR) Regulator gene mutations. We aimed to investigate common ... Read More
Positive Expiratory Pressure (PEP) versus Conventional Chest Physiotherapy in Pediatric Patients with Acute Exacerbation of Cystic Fibrosis
Volume 7, Issue 1 , January 2019, , Pages 8881-8888
Abstract
Background Pulmonary involvement is the main cause of mortality in cystic fibrosis (CF). Airway clearance techniques are non-pharmacological complement options for CF patients. The ... Read More
Identification of Dermatoglyphic Patterns in Parents of Children with Cystic Fibrosis
Volume 6, Issue 3 , March 2018, , Pages 7277-7284
Abstract
Background Dermatoglyphics could assist in the diagnosis of congenital abnormalities. The aim of this study was to identify the dermatoglyphic patterns (finger print pattern type, total ... Read More
Low Bone Mineral Density and Associated Factors in Patients with Cystic Fibrosis: A Cross-Sectional Study
Volume 5, Issue 7 , July 2017, , Pages 5237-5244
Abstract
Background: Failure to maintain bone mass density is a major complication in patients with cystic fibrosis (CF). This study was conducted to evaluate the prevalence of low bone mineral ... Read More
Outcome of Cystic Fibrosis in Patients with Bronchiectasis
Volume 2, Issue 4.1 , October 2014, , Pages 313-318