Background: The aim of this study was to assess the clinical features and the genotype characteristics of French patients diagnosed with cystic fibrosis (CF) before their fifth year and who were still alive after 30 years. It is the first descriptive study of 114 CF patients with long survival and follow-up. We compared this subgroup of French CF patients with the overall French CF population and with French adult (> 18 years) CF patients regardless of their age at diagnosis. Methods: Data were obtained from the French CF registry. Results: The 67 men and 47 women studied were 30–59 years old. Some 56% of the patients had ΔF508 homozygous genotype, 90% had a pancreatic insufficiency, and 81% were colonized with Pseudomonas aeruginosa. T...
AbstractCystic fibrosis (CF) is the most common autosomal recessive disease in Caucasians. Although ...
Background: In recent years, patients with cystic fibrosis (CF) conductance regulator (CFTR) variant...
Introduction: Significant phenotypic variation occurs even among patients carrying identical CFTR ge...
To assess the relationship between the genotype and phenotype of adult CF patients we have selected ...
AbstractBackgroundThe lifespan of patients with cystic fibrosis (CF) is increasing significantly. Th...
The members of the Cystic Fibrosis Genotype-Phenotype Consortium are listed in the AppendixBackgroun...
Background: Approximately 5-10% of cystic fibrosis (CF) diagnoses are made during adulthood. These p...
RATIONAL: People with cystic fibrosis carrying residual function (RF) mutations are considered to ha...
Currently, more than 1,000 mutations have been identified in the cystic fibrosis transmembrane regulat...
AbstractBackgroundCystic fibrosis (CF) is the most common inherited disorder in Caucasian population...
AbstractBackgroundCystic fibrosis (CF) spans a wide spectrum. Therefore, benchmarking between regist...
Cystic fibrosis is the most common potentially lethal autosomal recessive, genetic disease associate...
Genetic studies of lung disease in Cystic Fibrosis are faced with the challenge of identifying a sev...
Background: The Reunion Island is a French administrative department located in the Indian Ocean bet...
SummaryBackgroundThe proportion of patients with cystic fibrosis (CF) who are middle-aged is increas...
AbstractCystic fibrosis (CF) is the most common autosomal recessive disease in Caucasians. Although ...
Background: In recent years, patients with cystic fibrosis (CF) conductance regulator (CFTR) variant...
Introduction: Significant phenotypic variation occurs even among patients carrying identical CFTR ge...
To assess the relationship between the genotype and phenotype of adult CF patients we have selected ...
AbstractBackgroundThe lifespan of patients with cystic fibrosis (CF) is increasing significantly. Th...
The members of the Cystic Fibrosis Genotype-Phenotype Consortium are listed in the AppendixBackgroun...
Background: Approximately 5-10% of cystic fibrosis (CF) diagnoses are made during adulthood. These p...
RATIONAL: People with cystic fibrosis carrying residual function (RF) mutations are considered to ha...
Currently, more than 1,000 mutations have been identified in the cystic fibrosis transmembrane regulat...
AbstractBackgroundCystic fibrosis (CF) is the most common inherited disorder in Caucasian population...
AbstractBackgroundCystic fibrosis (CF) spans a wide spectrum. Therefore, benchmarking between regist...
Cystic fibrosis is the most common potentially lethal autosomal recessive, genetic disease associate...
Genetic studies of lung disease in Cystic Fibrosis are faced with the challenge of identifying a sev...
Background: The Reunion Island is a French administrative department located in the Indian Ocean bet...
SummaryBackgroundThe proportion of patients with cystic fibrosis (CF) who are middle-aged is increas...
AbstractCystic fibrosis (CF) is the most common autosomal recessive disease in Caucasians. Although ...
Background: In recent years, patients with cystic fibrosis (CF) conductance regulator (CFTR) variant...
Introduction: Significant phenotypic variation occurs even among patients carrying identical CFTR ge...