The survival advantage of patients with cystic fibrosis diagnosed through neonatal screening: evidence from the United States Cystic Fibrosis Foundation registry data.
about
Novel insights into the diagnostic and therapeutic challenges of the CFTR metabolic syndrome/CF screen positive indeterminate diagnosis.Uncovering symptom progression history from disease registry data with application to young cystic fibrosis patients.Measuring and improving respiratory outcomes in cystic fibrosis lung disease: opportunities and challenges to therapyTranslating scientific advances to improved outcomes for children with sickle cell disease: a timely opportunity.Validation and use of a parametric model for projecting cystic fibrosis survivorship beyond observed data: a birth cohort analysisAn automated communication system in a contact registry for persons with rare diseases: scalable tools for identifying and recruiting clinical research participants.Genetic screening.A decision-tree approach to cost comparison of newborn screening strategies for cystic fibrosis.Showing Value in Newborn Screening: Challenges in Quantifying the Effectiveness and Cost-Effectiveness of Early Detection of Phenylketonuria and Cystic Fibrosis.Effects of immediate telephone follow-up with providers on sweat chloride test timing after cystic fibrosis newborn screening identifies a single mutation.The Use of Economic Evaluation to Inform Newborn Screening Policy Decisions: The Washington State Experience.Nutritional considerations in patients with cystic fibrosis.Cystic fibrosis carrier screening effects on birth prevalence and newborn screening.Comprehensive CFTR gene analysis of the French cystic fibrosis screened newborn cohort: implications for diagnosis, genetic counseling, and mutation-specific therapy.Evaluation of the intestinal current measurement method as a diagnostic test for cystic fibrosis.S737F is a new CFTR mutation typical of patients originally from the Tuscany region in Italy.Early diagnosis from newborn screening maximises survival in severe cystic fibrosis.Treatment of pseudomonas and Staphylococcus bronchopulmonary infection in patients with cystic fibrosis.
P2860
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P2860
The survival advantage of patients with cystic fibrosis diagnosed through neonatal screening: evidence from the United States Cystic Fibrosis Foundation registry data.
description
2005 nî lūn-bûn
@nan
2005 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
The survival advantage of pati ...... osis Foundation registry data.
@ast
The survival advantage of pati ...... osis Foundation registry data.
@en
type
label
The survival advantage of pati ...... osis Foundation registry data.
@ast
The survival advantage of pati ...... osis Foundation registry data.
@en
prefLabel
The survival advantage of pati ...... osis Foundation registry data.
@ast
The survival advantage of pati ...... osis Foundation registry data.
@en
P2093
P1476
The survival advantage of pati ...... osis Foundation registry data.
@en
P2093
Huichuan J Lai
Philip M Farrell
P304
P356
10.1016/J.JPEDS.2005.08.014
P407
P433
P577
2005-09-01T00:00:00Z