The Effect of Outpatient Management of Cystic Fibrosis Exacerbation on Pulmonary Function Tests: A Clinical Trial
1. The Effect of Outpatient Management of Cystic Fibrosis Exacerbation on Pulmonary Function Tests: A Clinical Trial

Seyed Hossein Mirlohi; Alireza Daneshbakhtiar; Mehrnaz Olfat; Roholla Shirzadi; Niloufar Ghanbari; Seyed Javad Sayedi; Tina Loghmani; Mohammadreza Modaresi

Volume 10, Issue 6 , June 2022, , Pages 16121-16126

http://dx.doi.org/10.22038/ijp.2022.62806.4795

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
2. The Relationship between Bone Mineral Density and Serum Vitamin D Levels in Cystic Fibrosis Children

Hossein Saneian; Fariba Haghani; Niloofar Fakhri; Hosseinali Kharazmi; Majid Keivanfar; Mohsen Reisi

Volume 10, Issue 6 , June 2022, , Pages 16147-16154

http://dx.doi.org/10.22038/ijp.2022.63702.4848

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
3. The effect of Complementary and Alternative Medicines on the symptoms of Cystic Fibrosis patients: A Systematic Review

Samira Borhani; Shahpar Kaveh; Saeed Sadr; Rasool Choopani; Habibbolah Haji-Abdolvahab

Volume 10, Issue 4 , April 2022, , Pages 15881-15900

http://dx.doi.org/10.22038/ijp.2021.59806.4652

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+)
4. Towards the Validation of the Persian Translation of the Revised Cystic Fibrosis Quality of Life Questionnaire in Adolescents and Adults (CFQ-R 14+)

Saeedeh talebi; Seyed Javad Sayedi; Golnaz Ranjbar; Majid Khadem Rezaeian; Hanie Barghchi; Mohammad Safarian; hamidreza kianifar

Volume 10, Issue 1 , January 2022, , Pages 15313-15322

http://dx.doi.org/10.22038/ijp.2021.60865.4694

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)
5. Towards the Validation of the Persian Version of the Revised Cystic Fibrosis Quality of Life Questionnaire for children and parents (CFQ-R)

Saeedeh Talebi; Seyed Javad Sayedi; Golnaz Ranjbar; Majid Khadem Rezaeian; Hanie Bbarghchi; golnaz Kazemi sefat; Mohammad Safarian; Hamidreza Kianifar

Volume 9, Issue 12 , December 2021, , Pages 15003-15014

http://dx.doi.org/10.22038/ijp.2021.61497.4731

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
6. Evaluation of miR-301b and miR-302b Expressions in the Serum of Cystic Fibrosis Patients and their Association with Clinical Scoring System

Nasrin Jalalimanesh; Jalaledin Ghanavi; Maryam Hassanzad; Poopak Farnia; Seyed Javad Sayedi; Ali Akbar Velayati

Volume 9, Issue 11 , November 2021, , Pages 14907-14913

http://dx.doi.org/10.22038/ijp.2021.60598.4683

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
7. Possible Effect and Mechanism of Action of Flaxseed on Cystic Fibrosis Pulmonary Disorder: a Medical Hypothesis

Hanieh Tahermohammadi; Shahpar Kaveh; Saeed Sadr

Volume 9, Issue 9 , September 2021, , Pages 14400-14412

http://dx.doi.org/10.22038/ijp.2020.53208.4218

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
8. The Effectiveness of Viktor Frankl's Logo therapy on the Mental Health of Pediatric Patients with Cystic Fibrosis

Sepideh Nematollah; Maryam Zadahmad; Mohammad Reza Javadani; Mahin Ghaheri; Javad Seyed Jafari; Sara Moussavi

Volume 9, Issue 6 , June 2021, , Pages 13803-13810

http://dx.doi.org/10.22038/ijp.2021.56871.4455

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
9. Investigation the Lifestyle in Patients with Cystic Fibrosis According to Iranian Traditional Medicine

Saeed Sadr; Hanieh Tahermohammadi; Shahpar Kaveh

Volume 9, Issue 5 , May 2021, , Pages 13551-13557

http://dx.doi.org/10.22038/ijp.2020.51785.4122

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
10. Diagnostic Value of Changes in Serum Calprotectin Level and Patients' Sputum in Response to Treatment of Cystic Fibrosis Exacerbation in Children

Nemat Bilan; Farinaz Amirikar; Sina Raeisi

Volume 9, Issue 5 , May 2021, , Pages 13569-13579

http://dx.doi.org/10.22038/ijp.2020.51898.4130

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
11. The Effect of Nutritional Consultation on the Level of Malnutrition and Growth Indices in Children with Cystic Fibrosis

Naghi Dara; Farid Imanzadeh; Seyed Ramin Madani; Saleheh Tajalli; Pejman Rohani; Amirhossein Hosseini; Parastoo Ashtigoo; Sayeh Hatefi; Zahra Fazeli Farsani; Mahmoud Hajipour; Katayoun Khatami; Ali Akbar Sayyari; Beheshteh Olang

Volume 8, Issue 8 , August 2020, , Pages 11793-11801

http://dx.doi.org/10.22038/ijp.2020.44424.3680

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
12. Effects of Curcumin Supplementation on Quality of Life of Cystic Fibrosis Patients

Mandana Rafeey; Zeinab Nikniaz; Fatemeh FarshiRadvar; Ziba Sameni; Elnaz Faramarzi

Volume 8, Issue 4 , April 2020, , Pages 11169-11176

http://dx.doi.org/10.22038/ijp.2019.42990.3602

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
13. Evaluation of Antibiotic Resistance Trend among Cystic Fibrosis Patients: A Single Center Study from 2014-2019

Maryam Hassanzad; Elham Sadati; Fariba Ghorbani; Hosseinali Ghaffaripour; Poopak Farnia; Mihan Porabdollah; Noushin Baghaei; Habib Emami; Ali Akbar Velayati

Volume 8, Issue 1 , January 2020, , Pages 10719-10729

http://dx.doi.org/10.22038/ijp.2019.41725.3517

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
14. Investigating the Effect of TNF α (-863) and TNF α (-308) genes Polymorphism on the Progression of Disease in Patients with Cystic Fibrosis

Maryam Hassanzad; Golnaz Hajiesmail; Poopak Farnia; Jalaledin Ghanavi; Ghamartaj Khanbabayi; Mohammad Feshangchi-Bonab; Ehsan Razeghi; Ali Akbar Velayati

Volume 7, Issue 11 , November 2019, , Pages 10335-10341

http://dx.doi.org/10.22038/ijp.2019.41707.3513

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
15. Cardiac Involvement in Mild Cystic Fibrosis Lung Involvement Assessed by Tissue‐Doppler Echocardiography

Mehdi Ghaderian; Majid Keivanfar; Shiva Barani Beiranvand; Mohsen Reisi

Volume 7, Issue 10 , October 2019, , Pages 10205-10214

http://dx.doi.org/10.22038/ijp.2019.41556.3502

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
16. Cystic Fibrosis Patients Evaluation in the Last Decades in a Referral Center, Tehran-Iran

Maryam Hassanzad; Masoumeh Ansari; Ali Valinejadi; Seyed Javad Sayedi; Ali Akbar Velayati

Volume 7, Issue 8 , August 2019, , Pages 9997-10007

http://dx.doi.org/10.22038/ijp.2019.40329.3416

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
17. Bone Mineral Density and Cystic Fibrosis: A Review

Maryam Hassanzad; Poopak Farnia; Ali Akbar Samadani; Seyed Javad Sayedi; Ali Akbar Velayati

Volume 7, Issue 7 , July 2019, , Pages 9701-9710

http://dx.doi.org/10.22038/ijp.2019.38975.3325

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
18. Effects of Coenzyme Q10 Level on Clinical Parameters in Cystic Fibrosis Patients

Hassan Mozaffari Khosravi; Mohammad Ali Hojjati Kermani; Maryam Hassanzad; Mansour Rezaie; Sabereh Tashayoie-Nejad; Seyed Javad Sayedi; Ali Akbar Velayati

Volume 7, Issue 4 , April 2019, , Pages 9285-9294

http://dx.doi.org/10.22038/ijp.2018.36053.3145

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
19. Prevalence of Cystic Fibrosis Trans-membrane Conductance Regulator Gene common mutations in children with cystic fibrosis in Isfahan, Iran

Mohsen Reisi; Mahdiyeh Behnam; Seyed Javad Sayedi; Farzaneh Salimi; Pegah Kargar; Mansoor Salehi; Hossein Saneian; Iman Kashani; Roya Kelishadi

Volume 7, Issue 4 , April 2019, , Pages 9333-9339

http://dx.doi.org/10.22038/ijp.2018.36309.3168

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
20. Positive Expiratory Pressure (PEP) versus Conventional Chest Physiotherapy in Pediatric Patients with Acute Exacerbation of Cystic Fibrosis

Masoumeh Ghasempour; Nemat Bilan; Mohammadamin Rezazadehsaatlou

Volume 7, Issue 1 , January 2019, , Pages 8881-8888

http://dx.doi.org/10.22038/ijp.2018.34187.3019

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
21. Identification of Dermatoglyphic Patterns in Parents of Children with Cystic Fibrosis

Hamid Reza Kianifar; Atefeh Ezzati; Seyed Ali Jafari; Mohammad Ali Kiani; Hamid Ahanchian; Hasan Karami; Ezzat Khodashenas; Arezoo Jahanbin

Volume 6, Issue 3 , March 2018, , Pages 7277-7284

http://dx.doi.org/10.22038/ijp.2017.25219.2141

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
22. Low Bone Mineral Density and Associated Factors in Patients with Cystic Fibrosis: A Cross-Sectional Study

Abdolhamid Jafari Nodoushan; Soheila Khalilzadeh; Azam Golzar; Maryam Hassanzad; Seyed Javad Sayedi; Aliakbar Velayati

Volume 5, Issue 7 , July 2017, , Pages 5237-5244

http://dx.doi.org/10.22038/ijp.2017.23618.1989

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
23. Outcome of Cystic Fibrosis in Patients with Bronchiectasis

Nemat Bilan; Mitra Agakhani; Mahmood Goldost

Volume 2, Issue 4.1 , October 2014, , Pages 313-318

http://dx.doi.org/10.22038/ijp.2014.3299

Abstract
  Introduction: Bronchiectasis is a common problem in children especially under 5 years. Early diagnosis of disease and its causes could be useful in early treatment and preventing probable ...  Read More