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Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus reportTargeted therapies to improve CFTR function in cystic fibrosisEpidemiology and genetics of cystic fibrosis in Asia: In preparation for the next-generation treatmentsDefective CFTR expression and function are detectable in blood monocytes: development of a new blood test for cystic fibrosisEarly anti-pseudomonal acquisition in young patients with cystic fibrosis: rationale and design of the EPIC clinical trial and observational study'Twenty questions in genetic medicine--an assessment of World Wide Web databases for genetics information at the point of care.Rectal forceps biopsy procedure in cystic fibrosis: technical aspects and patients perspective for clinical trials feasibility.The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practiceNationwide genetic analysis for molecularly unresolved cystic fibrosis patients in a multiethnic society: implications for preconception carrier screening.Diagnostic contribution of molecular analysis of the cystic fibrosis transmembrane conductance regulator gene in patients suspected of having mild or atypical cystic fibrosis.Defining a mutational panel and predicting the prevalence of cystic fibrosis in omanThe K+ channel opener 1-EBIO potentiates residual function of mutant CFTR in rectal biopsies from cystic fibrosis patients.Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendationsAnalysis of cystic fibrosis gene mutations in children with cystic fibrosis and in 964 infertile couples within the region of Basilicata, Italy: a research studyIntestinal current measurement versus nasal potential difference measurements for diagnosis of cystic fibrosis: a case-control study.Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis.Jejunoileal atresia and cystic fibrosis: don't miss itPhenotypic expression of the p.Leu1077Pro CFTR mutation in Sicilian cystic fibrosis patients.Challenging the diagnosis of cystic fibrosis in a patient carrying the 186-8T/C allelic variant in the CF transmembrane conductance regulator geneGenotype-phenotype correlation in cystic fibrosis patients bearing [H939R;H949L] alleleActivated MCTC mast cells infiltrate diseased lung areas in cystic fibrosis and idiopathic pulmonary fibrosis.Ivacaftor in a young boy with the rare gating mutation S549R--use of lung clearance index to track progress: a case report.The cystic fibrosis microbiome in an ecological perspective and its impact in antibiotic therapy.Prevalence and factors associated with nontuberculous mycobacteria in non-cystic fibrosis bronchiectasis: a multicenter observational study.Repeatability and Diagnostic Value of Nasal Potential Difference in a Genetically Admixed Population.Atypical cystic fibrosis: identification in the primary care setting.Detection of Airway Colonization by Aspergillus fumigatus by Use of Electronic Nose Technology in Patients with Cystic Fibrosis.Nasal potential difference measurements to assess CFTR ion channel activity.Novel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis.Evaluation of Serum Adenosine Deaminase in Cystic Fibrosis Patients in an Iranian Referral Hospital.Assessment of serology and spirometry and the combination of both to complement microbiological isolation for earlier detection of Pseudomonas aeruginosa infection in children with cystic fibrosis.Changing epidemiology and clinical issues arising in an ageing cystic fibrosis population.Apoptotic process in cystic fibrosis cells.Molecular testing for cystic fibrosis carrier status practice guidelines: recommendations of the National Society of Genetic Counselors.What can the CF registry tell us about rare CFTR-mutations? A Belgian study.Clinical approach to the diagnosis and treatment of cystic fibrosis and CFTR-related disorders.Cystic fibrosis: a clinical view.A salty cause of cough in a 24-year-old man.Chronic cough with normal sweat chloride: Phenotypic descriptions of two rare cystic fibrosis genotypes.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
Cystic fibrosis: terminology and diagnostic algorithms
@ast
Cystic fibrosis: terminology and diagnostic algorithms
@en
type
label
Cystic fibrosis: terminology and diagnostic algorithms
@ast
Cystic fibrosis: terminology and diagnostic algorithms
@en
prefLabel
Cystic fibrosis: terminology and diagnostic algorithms
@ast
Cystic fibrosis: terminology and diagnostic algorithms
@en
P2093
P2860
P356
P1433
P1476
Cystic fibrosis: terminology and diagnostic algorithms
@en
P2093
C Castellani
Diagnostic Working Group
K De Boeck
M Sinaasappel
M Wilschanski
P2860
P304
P356
10.1136/THX.2005.043539
P407
P577
2005-12-29T00:00:00Z