Detalhe da pesquisa
1.
[CF Lung Disease - a German S3 Guideline: Pseudomonas aeruginosa]. / S3-Leitlinie: Lungenerkrankung bei Mukoviszidose Pseudomonas aeruginosa.
Pneumologie
; 78(6): 367-399, 2024 Jun.
Artigo
Alemão
| MEDLINE | ID: mdl-38350639
2.
Aryl Hydrocarbon Receptor Agonism Antagonizes the Hypoxia-driven Inflammation in Cystic Fibrosis.
Am J Respir Cell Mol Biol
; 68(3): 288-301, 2023 03.
Artigo
Inglês
| MEDLINE | ID: mdl-36252182
3.
Reference Values Matter: Fewer Patients With Malnutrition Using American Compared to More Recent German Growth Charts.
J Pediatr Gastroenterol Nutr
; 72(6): 912-915, 2021 06 01.
Artigo
Inglês
| MEDLINE | ID: mdl-33633076
4.
[CF Lung Disease - a German S3 Guideline: Pseudomonas aeruginosa]. / Erratum: S3-Leitlinie: Lungenerkrankung bei Mukoviszidose Pseudomonas aeruginosa.
Pneumologie
; 78(6): e2, 2024 Jun.
Artigo
Alemão
| MEDLINE | ID: mdl-38423036
5.
Fecal Calprotectin in Cystic Fibrosis and Its Relation to Disease Parameters: A Longitudinal Analysis for 12 Years.
J Pediatr Gastroenterol Nutr
; 65(4): 438-442, 2017 10.
Artigo
Inglês
| MEDLINE | ID: mdl-28207476
6.
Evaluating patient experience in a cystic fibrosis centre using a disease-specific patient satisfaction questionnaire.
Eur J Pediatr
; 174(11): 1451-60, 2015 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-25944680
7.
Factors associated with FEV1 decline in cystic fibrosis: analysis of the ECFS patient registry.
Eur Respir J
; 43(1): 125-33, 2014 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-23598952
8.
Long-Term Assessment of Antibody Response to COVID-19 Vaccination in People with Cystic Fibrosis and Solid Organ Transplantation.
Vaccines (Basel)
; 12(1)2024 Jan 18.
Artigo
Inglês
| MEDLINE | ID: mdl-38250911
9.
Is There a Difference in Immune Response to SARS-CoV-2 Vaccination between Liver and Lung Transplant Patients with Cystic Fibrosis?
Vaccines (Basel)
; 11(3)2023 Mar 14.
Artigo
Inglês
| MEDLINE | ID: mdl-36992241
10.
Early and sustained improvements of lung clearance index from two to sixteen weeks of elexacaftor/tezacaftor/ivacaftor therapy in patients with cystic fibrosis-a real world study.
Front Pharmacol
; 14: 1125853, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-36969845
11.
Impact of elexacaftor/tezacaftor/ivacaftor on lung function, nutritional status, pulmonary exacerbation frequency and sweat chloride in people with cystic fibrosis: real-world evidence from the German CF Registry.
Lancet Reg Health Eur
; 32: 100690, 2023 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-37554663
12.
Bridging of host-microbiota tryptophan partitioning by the serotonin pathway in fungal pneumonia.
Nat Commun
; 14(1): 5753, 2023 09 16.
Artigo
Inglês
| MEDLINE | ID: mdl-37717018
13.
REAL-world clinical effectiveness of ivacaftor therapy in the first 24 months in two infants with cystic fibrosis and different gating mutations-A case report.
Clin Case Rep
; 10(2): e05364, 2022 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-35154718
14.
Malignancies in patients with cystic fibrosis: a case series.
J Med Case Rep
; 16(1): 27, 2022 Jan 19.
Artigo
Inglês
| MEDLINE | ID: mdl-35042562
15.
Arm muscle area for the longitudinal assessment of nutritional status in paediatric patients with cystic fibrosis - A single centre experience.
J Cyst Fibros
; 21(2): e122-e128, 2022 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34728152
16.
Personalized medicine with drugs targeting the underlying protein defect in cystic fibrosis: is monitoring of treatment response necessary?
Ther Adv Chronic Dis
; 13: 20406223221108627, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-35959505
17.
Ivacaftor Reduces Inflammatory Mediators in Upper Airway Lining Fluid From Cystic Fibrosis Patients With a G551D Mutation: Serial Non-Invasive Home-Based Collection of Upper Airway Lining Fluid.
Front Immunol
; 12: 642180, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34025651
18.
Insights Into Patient Variability During Ivacaftor-Lumacaftor Therapy in Cystic Fibrosis.
Front Pharmacol
; 12: 577263, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34408649
19.
Cystic Fibrosis Newborn Screening in Austria Using PAP and the Numeric Product of PAP and IRT Concentrations as Second-Tier Parameters.
Diagnostics (Basel)
; 11(2)2021 Feb 13.
Artigo
Inglês
| MEDLINE | ID: mdl-33668470
20.
Tezacaftor/ivacaftor in people with cystic fibrosis heterozygous for minimal function CFTR mutations.
J Cyst Fibros
; 19(6): 962-968, 2020 11.
Artigo
Inglês
| MEDLINE | ID: mdl-32546431