Does extensive genotyping and nasal potential difference testing clarify the diagnosis of cystic fibrosis among patients with single-organ manifestations of cystic fibrosis?

β-Adrenergic Sweat Secretion as a Diagnostic Test for Cystic Fibrosis

(2012) Paul Quinton et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Role of Cystic Fibrosis Transmembrane Conductance Regulator in Patients With Chronic Sinopulmonary Disease

(2012) Tanja Gonska et al.   CHEST

Comparing the American and European diagnostic guidelines for cystic fibrosis: same disease, different language?

(2012) Chee Y Ooi et al.   THORAX

Recommendations for the classification of diseases as CFTR-related disorders

(2011) C. Bombieri et al.   Journal of Cystic Fibrosis

Effects of Gender and Age at Diagnosis on Disease Progression in Long-term Survivors of Cystic Fibrosis

(2010) Jerry A. Nick et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Do commonin silicotools predict the clinical consequences of amino-acid substitutions in the CFTR gene?

(2010) R Dorfman et al.   CLINICAL GENETICS

Type of CFTR Mutation Determines Risk of Pancreatitis in Patients With Cystic Fibrosis

(2010) Chee Y. Ooi et al.   GASTROENTEROLOGY

Deletion of CFTR Translation Start Site Reveals Functional Isoforms of the Protein in CF Patients

(2009) Anabela S. Ramalho et al.   CELLULAR PHYSIOLOGY AND BIOCHEMISTRY

Diagnosis of Cystic Fibrosis by Sweat Testing: Age-Specific Reference Intervals

(2008) Avantika Mishra et al.   JOURNAL OF PEDIATRICS

Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults: Cystic Fibrosis Foundation Consensus Report

(2008) Philip M. Farrell et al.   JOURNAL OF PEDIATRICS