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Sie sind hier: Respirationstrakt » Zystische Fibrose 19. Januar 2021
Zystische Fibrose
Erweiterte Suche
Kardiovaskuläre Erkrankungen
Muskuloskelettale Erkrankungen
Allergische Rhinitis - Pollinosis
Interstitielle Pneumopathien
Schlaf- Apnoe-Syndrom
Zystische Fibrose
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Designing the GALAXY study: Partnering with the cystic fibrosis community to optimize assessment of gastrointestinal symptoms.
J Cyst Fibros
Freeman AJ, Sathe M, Aliaj E, Borowitz D, Fogarty B, Goss CH, Freedman S, Heltshe SL, Khan U, Riva D, Roman C, Romasco M, Schwarzenberg SJ, Ufret-Vincenty CA, Moshiree B.
PMID: 33451899 [PubMed - as supplied by publisher]

Antibiotics in Adult Cystic Fibrosis Patients: A Review of Population Pharmacokinetic Analyses.
Clin Pharmacokinet
El Hassani M, Caissy JA, Marsot A.
PMID: 33447944 [PubMed - as supplied by publisher]

Towards human translation of lentiviral airway gene delivery for cystic fibrosis: A one-month CFTR and reporter gene study in marmosets.
Hum Gene Ther
Farrow NR, Cmielewski P, Delhove J, Rout-Pitt N, Vaughan L, Kuchel T, Christou C, Finnie J, Smith M, Knight E, Donnelley M, Parsons D.
PMID: 33446042 [PubMed - as supplied by publisher]

Exercise as a substitute for traditional airway clearance in cystic fibrosis: a systematic review.
Ward N, Morrow S, Stiller K, Holland AE.
PMID: 33443204 [PubMed - as supplied by publisher]

The impact of liver disease on mortality in cystic fibrosis - a systematic review protocol.
HRB Open Res
Sasame A, Connolly L, Fitzpatrick E, Stokes D, Bourke B, Rowland M.
PMID: 33305166 [PubMed]

PMID: 33439587 [PubMed]

Epidemiologic Study of Cystic Fibrosis: 25 years of observational research.
Pediatr Pulmonol
Konstan MW, Pasta DJ, VanDevanter DR, Wagener JS, Morgan WJ, Scientific Advisory Group and the Investigators and Coordinators of ESCF..
PMID: 33434406 [PubMed - as supplied by publisher]

Exhaled volatile organic compounds detect pulmonary exacerbations early in children with Cystic Fibrosis: results of a one-year observational pilot study.
J Breath Res
van Horck M, Smolinska A, Wesseling G, de Winter-de Groot KM, de Vreede I, Winkens B, Jöbsis Q, Dallinga J, Dompeling E, van Schooten FJ.
PMID: 33429373 [PubMed - as supplied by publisher]

Assessment of Distinct Electrophysiological Parameters in Rectal Biopsies for the Choice of the Best Diagnosis/Prognosis Biomarkers for Cystic Fibrosis.
Front Physiol
Silva IAL, Duarte A, Marson FAL, Centeio R, Dou, Kunzelmann K, Amaral MD.
PMID: 33424627 [PubMed]

The modified shuttle test as a predictor of risk for hospitalization in youths with cystic fibrosis: A two-year follow-up study: Modified shuttle test as a predictor of hospitalization.
J Cyst Fibros
Donadio MVF, Vendrusculo FM, Campos NE, Becker NA, de Almeida IS, Queiroz KCV, Leite LR, Aquino ES.
PMID: 33422453 [PubMed - as supplied by publisher]

Implementation of microbiota analysis in clinical trials for cystic fibrosis lung infection: Experience from the OligoG phase 2b clinical trials.
J Microbiol Methods
Weiser R, Rye PD, Mahenthiralingam E.
PMID: 33421446 [PubMed - as supplied by publisher]

Effect of Expiratory Muscle Training on Peak Cough Flow in Children and Adolescents with Cystic Fibrosis: A Randomized Controlled Trial.
Pediatr Pulmonol
Emirza C, Aslan GK, Kilinc AA, Cokugras H.
PMID: 33421333 [PubMed - as supplied by publisher]

Impaired cholesterol metabolism in the mouse model of cystic fibrosis. A preliminary study.
PLoS One
Amato F, Castaldo A, Castaldo G, Cernera G, Corso G, Ferrari E, Gelzo M, Monzani R, Villella VR, Raia V.
PMID: 33412572 [PubMed - in process]

Positive expiratory pressure (PEP) therapy. What pressures do we achieve in young children with cystic fibrosis? A single-centre study.
BMJ Paediatr Open
Kiernan N, Johnstone B, Anderson P, Stewart R.
PMID: 33409382 [PubMed]

Tribulations and (clinical) trials in cystic fibrosis.
J Cyst Fibros
Cagnina RE, Sawicki GS.
PMID: 33408059 [PubMed - as supplied by publisher]

Pseudomonas aeruginosa associated with severity of non-cystic fibrosis bronchiectasis measured by the modified bronchiectasis severity score (BSI) and the FACED: The US bronchiectasis and NTM Research Registry (BRR) study.
Respir Med
Choate R, Aksamit TR, Mannino D, Addrizzo-Harris D, Barker A, Basavaraj A, Daley CL, Daniels MLA, Eden E, DiMango A, Fennelly K, Griffith DE, Johnson MM, Knowles MR, McShane PJ, Metersky ML, Noone PG, O'Donnell AE, Olivier KN, Salathe MA, Schmid A, Thomashow B, Tino G, Winthrop KL, Stone G.
PMID: 33401148 [PubMed - as supplied by publisher]

Comparison of respiratory pathogen colonization and antimicrobial susceptibility in people with cystic fibrosis bronchiectasis versus non-cystic fibrosis bronchiectasis: a protocol for a systematic review.
Syst Rev
Verma S, Mathew JL, Ray P.
PMID: 33397475 [PubMed - in process]

Optimizations of In Vitro Mucus and Cell Culture Models to Better Predict In Vivo Gene Transfer in Pathological Lung Respiratory Airways: Cystic Fibrosis as an Example.
Ghanem R, Laurent V, Roquefort P, Haute T, Ramel S, Le Gall T, Aubry T, Montier T.
PMID: 33396283 [PubMed]

Development of an intervention to increase adherence to nebuliser treatment in adults with cystic fibrosis: CFHealthHub.
Pilot Feasibility Stud
Arden MA, Hutchings M, Whelan P, Drabble SJ, Beever D, Bradley JM, Hind D, Ainsworth J, Maguire C, Cantrill H, O'Cathain A, Wildman M.
PMID: 33390191 [PubMed]

Psychological distress in adults with and without cystic fibrosis during the COVID-19 lockdown.
J Cyst Fibros
Ciprandi R, Bonati M, Campi R, Pescini R, Castellani C.
PMID: 33384222 [PubMed - as supplied by publisher]

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