b1.Spectrum of CFTR Gene Mutations in Iranian Azeri Turkish Patients with Cystic Fibrosis
b2.Quality of Life in Cystic Fibrosis Children
b3.Crystallization Test in Diagnosis of Cystic Fibrosis
b4.CYP1B1 Mutation Profile of Iranian Primary Congenital Glaucoma Patients and bAssociated Haplotypes
b5.Treatment for sulfur mustard lung injuries; new therapeutic approaches from acute to chronic phase
b6.Effects of Probiotics on Quality of Life in Children with Cystic Fibrosis; A Randomized Controlled Trial
b7.Predisposing Factors for Nephrolithiasis and Nephrocalcinosis in Cystic Fibrosis
b8.Detecting Common CFTR Mutations by Reverse Dot Blot Hybridization Method in Cystic Fibrosis First Report from Northern Iran
b9.Mutation Analysis of Exons 10 and 17a of CFTR Gene in Patients with Cystic Fibrosis in Kermanshah Province, Western Iran
b10.Drug resistance pattern of Pseudomonas aeruginosa strains isolated from cystic fibrosis patients at Isfahan AL Zahra hospital, Iran (2009-2010)
b11.Clinical and Genetic Features in Patients with Cystic Fibrosis in Southwestern Iran
b12.Recent advances in the treatment of Pseudomonasaeruginosa infections in cystic fibrosis
b13.Analysis of c.3499+200TA(7_56) and D7S523 MicrosatellitesLinked to Cystic Fibrosis Trans membrane Regulator
b14.The Correlation of Brody High Resolution Computed Tomography Scoring System withClinical Status and Pulmonary Function Test inPatients with Cystic Fibrosis
b15.Plasma ghrelin levels in children with cystic fibrosisand healthy children
b16.Variation in plasma leptin levels in young Iranian childrenwith cystic fibrosis
b16.Phenotypic and Genetic Characterization of Carbapenemase and ESBLs Producing Gram-negative Bacteria (GNB) Isolated from Patients with Cystic Fibrosis (CF) in Tehran Hospitals
b17.CD4/CD8 ratio and cytokine levels of the BAL fluid in patients withbronchiectasis caused by sulfur mustard gas inhalation
b18.Screening for Five Mutations Detects 97% of Cystic Fibrosis (CF) Chromosomes and Predicts a Carrier Frequency of 1:29 in theJewish Ashkenazi Population
b19.Comparison of in Vitro Activity of Doripenem versus Old Carbapenems against Pseudomonas Aeruginosa Clinical Isolates from both CF and Burn Patients
b20.Community acquired Pseudomonas pneumonia in an immune competent host
b21.Biodistribution of Amikacin Solid Lipid Nanoparticles after Pulmonary Delivery
b22.Community Genetic Services in Iran
b23.Emergence of Pseudomonas aeruginosa cross-infection in children with cystic fibrosis attending an Iranian referral pediatric center
b24.Concomitant Cryptococcosis and Burkholderia Infection in an Asymptomatic Lung Transplant Patient with Cystic Fibrosis
b25.Utility of Gram Stain in Evaluation of Sputa from Patients with Cystic Fibrosis