Detalhe da pesquisa
1.
Corrigendum to FEV1 Variability Helps Identify Patients with Cystic Fibrosis at Risk of Greater Loss of Lung Function [The Journal of Pediatrics (2016) 116-121].
J Pediatr
; 255: 265, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36653281
2.
Effectiveness of triple therapy with direct-acting antivirals for hepatitis C genotype 1 infection: application of propensity score matching in a national HCV treatment registry.
BMC Health Serv Res
; 17(1): 288, 2017 04 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-28424064
3.
Forced Expiratory Volume in 1 Second Variability Helps Identify Patients with Cystic Fibrosis at Risk of Greater Loss of Lung Function.
J Pediatr
; 169: 116-21.e2, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26388208
4.
Sustained Benefit from ivacaftor demonstrated by combining clinical trial and cystic fibrosis patient registry data.
Am J Respir Crit Care Med
; 192(7): 836-42, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26132840
5.
Improvements in lung function and height among cohorts of 6-year-olds with cystic fibrosis from 1994 to 2012.
J Pediatr
; 165(6): 1091-1097.e2, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25134852
6.
Liver involvement in the Hispanic population of North America with cystic fibrosis.
J Pediatr Gastroenterol Nutr
; 59(4): 476-9, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24897167
7.
Probability of treatment following acute decline in lung function in children with cystic fibrosis is related to baseline pulmonary function.
J Pediatr
; 163(4): 1152-7.e2, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23810128
8.
Patients with Cystic Fibrosis and a G551D or Homozygous F508del Mutation: Similar Lung Function Decline.
Am J Respir Crit Care Med
; 195(12): 1673-1676, 2017 06 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28617084
9.
Lung Function Decline in Cystic Fibrosis: Impact of Data Availability and Modeling Strategies on Clinical Interpretations.
Ann Am Thorac Soc
; 20(7): 958-968, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36884219
10.
Erratum to: Psychometric evaluation of the Cystic Fibrosis Questionnaire-Revised in a national, US sample.
Qual Life Res
; 21(7): 1279-90, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22240933
11.
Psychometric evaluation of the Cystic Fibrosis Questionnaire-Revised in a national sample.
Qual Life Res
; 21(7): 1267-78, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21993695
12.
Rate of Lung Function Decline in People with Cystic Fibrosis Having a Residual Function Gene Mutation.
Pulm Ther
; 8(4): 385-395, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36319933
13.
Benign prostatic hyperplasia evaluation and management by urologists and primary care physicians: practice patterns from the observational BPH registry.
J Urol
; 186(3): 971-6, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21791352
15.
Socioeconomic status and the likelihood of antibiotic treatment for signs and symptoms of pulmonary exacerbation in children with cystic fibrosis.
J Pediatr
; 159(5): 819-824.e1, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21705017
16.
Epidemiologic Study of Cystic Fibrosis: 25 years of observational research.
Pediatr Pulmonol
; 56(5): 823-836, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33434406
17.
Assessing the impact of sodium oxybate treatment on functioning, productivity, and health-related quality of life in patients with narcolepsy: findings from the Nexus Narcolepsy Registry (waves 1-4).
Sleep Med
; 84: 380-388, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34247126
18.
The Nexus Narcolepsy Registry: methodology, study population characteristics, and patterns and predictors of narcolepsy diagnosis.
Sleep Med
; 84: 405-414, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34304148
19.
Long-term safety and efficacy of tezacaftor-ivacaftor in individuals with cystic fibrosis aged 12 years or older who are homozygous or heterozygous for Phe508del CFTR (EXTEND): an open-label extension study.
Lancet Respir Med
; 9(7): 733-746, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33581080
20.
Rapid lung function decline in adults with early-stage cystic fibrosis lung disease.
J Cyst Fibros
; 19(4): 527-533, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31870629