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Sie sind hier: Respirationstrakt » Zystische Fibrose 29. März 2020
Zystische Fibrose
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Kardiovaskuläre Erkrankungen
Muskuloskelettale Erkrankungen
Allergische Rhinitis - Pollinosis
Interstitielle Pneumopathien
Schlaf- Apnoe-Syndrom
Zystische Fibrose
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Newborn Screening for Cystic Fibrosis in Mersin Province: Yearly Assessment of the National Program.
Turk Thorac J
Özdemir A, Do.
PMID: 32202999 [PubMed]

Vitamin D Deficiency and Radiological Findings in Adult Non-Cystic Fibrosis Bronchiectasis.
Turk Thorac J
Niksarl, K, Bilici D, Yi, Uysal MA, Çamsar.
PMID: 32202997 [PubMed]

Impact of CFTR modulator use on outcomes in people with severe cystic fibrosis lung disease.
Eur Respir Rev
Shteinberg M, Taylor-Cousar JL.
PMID: 32198216 [PubMed - in process]

Antibiotic treatment for Stenotrophomonas maltophilia in people with cystic fibrosis.
Cochrane Database Syst Rev
Amin R, Jahnke N, Waters V.
PMID: 32189337 [PubMed - in process]

Genetic diagnosis in practice: From cystic fibrosis to CFTR-related disorders.
Arch Pediatr
Pagin A, Sermet-Gaudelus I, Burgel PR.
PMID: 32172933 [PubMed - in process]

Current and future diagnosis of cystic fibrosis: Performance and limitations.
Arch Pediatr
Bienvenu T, Nguyen-Khoa T.
PMID: 32172931 [PubMed - in process]

Adults with cystic fibrosis: spiritual coping with lifelong disease.
J Health Care Chaplain
Grossoehme DH, Cole AG, Lewis K, Stamper SM, Teeters A, Joseph PM.
PMID: 32172686 [PubMed - as supplied by publisher]

Meta-analysis Reveals Potential Influence of Oxidative Stress on the Airway Microbiomes of Cystic Fibrosis Patients.
Genomics Proteomics Bioinformatics
Shi X, Gao Z, Lin Q, Zhao L, Ma Q, Kang Y, Yu J.
PMID: 32171662 [PubMed - as supplied by publisher]

Update on SLC6A14 in lung and gastrointestinal physiology and physiopathology: focus on cystic fibrosis.
Cell Mol Life Sci
Ruffin M, Mercier J, Calmel C, Mésinèle J, Bigot J, Sutanto EN, Kicic A, Corvol H, Guillot L.
PMID: 32166393 [PubMed - as supplied by publisher]

Health-related quality-of-life in children with cystic fibrosis aged 5-years and associations with health outcomes.
J Cyst Fibros
Cheney J, Vidmar S, Gailer N, Wainwright C, Douglas TA, Australasian Cystic Fibrosis Bronchoalveolar Lavage (ACFBAL) study group..
PMID: 32165156 [PubMed - as supplied by publisher]

Lung T1 mapping magnetic resonance imaging in the assessment of pulmonary disease in children with cystic fibrosis: a pilot study.
Pediatr Radiol
Neemuchwala F, Ghadimi Mahani M, Pang Y, Lee E, Johnson TD, Galbán CJ, Fortuna AB, Sanchez-Jacob R, Flask CA, Nasr SZ.
PMID: 32162080 [PubMed - as supplied by publisher]

CFTR Modulators: The Changing Face of Cystic Fibrosis in the Era of Precision Medicine.
Front Pharmacol
Lopes-Pacheco M.
PMID: 32153386 [PubMed]

Author Correction: A randomised controlled trial of rosuvastatin for the prevention of aminoglycoside-induced kidney toxicity in children with cystic fibrosis.
Sci Rep
McWilliam SJ, Rosala-Hallas A, Jones AP, Shaw V, Greenhalf W, Jaki T, Smyth AR, Smyth RL, Pirmohamed M.
PMID: 32152372 [PubMed - in process]

[Family support upon immediate cystic fibrosis announcement].
Rev Infirm
Kirszenbaum M, Dupont S.
PMID: 32146957 [PubMed - indexed for MEDLINE]

Sleep disorders in cystic fibrosis: A systematic review and meta-analysis.
Sleep Med Rev
Reiter J, Gileles-Hillel A, Cohen-Cymberknoh M, Rosen D, Kerem E, Gozal D, Forno E.
PMID: 32145647 [PubMed - as supplied by publisher]

Changes in the parent cystic fibrosis questionnaire-revised (CFQ-R) with respiratory symptoms in preschool children with cystic fibrosis.
J Cyst Fibros
Perrem L, Stanojevic S, Shaw M, Davis S, Retsch-Bogart G, Ratjen F.
PMID: 32139196 [PubMed - as supplied by publisher]

Aetiological agents for pulmonary exacerbations in children with cystic fibrosis: An observational study from a tertiary care centre in northern India.
Indian J Med Res
Arvind B, Medigeshi GR, Kapil A, Xess I, Singh U, Lodha R, Kabra SK.
PMID: 32134016 [PubMed - in process]

Predictive value of computed tomography scoring systems evolution in adults with cystic fibrosis.
Eur Radiol
Zorzo C, Caballero P, Diab L, Pastor MT, Gómez-Punter RM, Girón RM.
PMID: 32128619 [PubMed - as supplied by publisher]

Changes in the R-region interactions depend on phosphorylation and contribute to PKA and PKC regulation of the cystic fibrosis transmembrane conductance regulator chloride channel.
FASEB Bioadv
Poroca DR, Amer N, Li A, Hanrahan JW, Chappe VM.
PMID: 32123855 [PubMed]

Finding the relevance of antimicrobial stewardship for cystic fibrosis.
J Cyst Fibros
Cogen JD, Kahl BC, Maples H, McColley SA, Roberts JA, Winthrop KL, Morris AM, Holmes A, Flume PA, VanDevanter DR, Waters V, Muhlebach MS, Elborn JS, Saiman L, Bell SC, Antimicrobial Resistance International Working Group in Cystic Fibrosis..
PMID: 32122785 [PubMed - as supplied by publisher]

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