about
Cystic fibrosis chronic rhinosinusitis: a comprehensive reviewBackground and EpidemiologyRectal forceps biopsy procedure in cystic fibrosis: technical aspects and patients perspective for clinical trials feasibility.Classic respiratory disease but atypical diagnostic testing distinguishes adult presentation of cystic fibrosis.Diagnostic contribution of molecular analysis of the cystic fibrosis transmembrane conductance regulator gene in patients suspected of having mild or atypical cystic fibrosis.Effects of gender and age at diagnosis on disease progression in long-term survivors of cystic fibrosis.Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendationsMeasurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis.Genotype-phenotype correlation in cystic fibrosis patients bearing [H939R;H949L] alleleNovel personalized therapies for cystic fibrosis: treating the basic defect in all patients.Prenatal screening of Cystic Fibrosis: a single centre experience.Cystic fibrosis: terminology and diagnostic algorithmsDetection of Airway Colonization by Aspergillus fumigatus by Use of Electronic Nose Technology in Patients with Cystic Fibrosis.Hereditary pancreatitis for the endoscopistExpanded genetic screening panel for the Ashkenazi Jewish population.Diagnostic CFTR mutation analysis.Clinical approach to the diagnosis and treatment of cystic fibrosis and CFTR-related disorders.A salty cause of cough in a 24-year-old man.Phenotypic and genetic characterization of patients with features of "nonclassic" forms of cystic fibrosisBrazilian guidelines for the diagnosis and treatment of cystic fibrosis.Evaluation of the intestinal current measurement method as a diagnostic test for cystic fibrosis.Lumacaftor/ivacaftor, a novel agent for the treatment of cystic fibrosis patients who are homozygous for the F580del CFTR mutation.Role of CFTR mutation analysis in the diagnostic algorithm for cystic fibrosis.Early activation of sperm by HCO(3) (-) is regulated hormonally in the murine uterus.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
Nonclassic cystic fibrosis and CFTR-related diseases.
@ast
Nonclassic cystic fibrosis and CFTR-related diseases.
@en
type
label
Nonclassic cystic fibrosis and CFTR-related diseases.
@ast
Nonclassic cystic fibrosis and CFTR-related diseases.
@en
prefLabel
Nonclassic cystic fibrosis and CFTR-related diseases.
@ast
Nonclassic cystic fibrosis and CFTR-related diseases.
@en
P1476
Nonclassic cystic fibrosis and CFTR-related diseases.
@en
P304
P356
10.1097/00063198-200311000-00009
P577
2003-11-01T00:00:00Z