Quantitation of cystic fibrosis triple combination therapy, elexacaftor/tezacaftor/ivacaftor, in human plasma and cellular lysate.
暂无分享,去创建一个
E. Acosta | J. Guimbellot | Kevin J. Ryan | Justin D. Anderson | Alexander E. Dowell | C. Kerstner-Wood | Zhongyu Liu | Kedria Reed-Walker
[1] C. Mingora,et al. A case report of CFTR modulator administration via carrier mother to treat meconium ileus in a F508del homozygous fetus. , 2022, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[2] B. Collins,et al. Drug exposure to infants born to mothers taking Elexacaftor, Tezacaftor, and Ivacaftor. , 2021, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[3] J. Beekman,et al. Breast development in a 7 year old girl with CF treated with ivacaftor: An indication for personalized dosing? , 2021, Journal of Cystic Fibrosis.
[4] S. Verbanck,et al. A case of self-limited drug induced liver injury under treatment with elexacaftor/tezacaftor/ivacaftor: When it is worth taking the risk. , 2021, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[5] R. Kuhn,et al. CFTR modulator drug desensitization: Preserving the hope of long term improvement , 2021, Pediatric pulmonology.
[6] D. Kay,et al. Normal pancreatic function and false-negative CF newborn screen in a child born to a mother taking CFTR modulator therapy during pregnancy. , 2021, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[7] B. Quon,et al. Real-World Safety of CFTR Modulators in the Treatment of Cystic Fibrosis: A Systematic Review , 2020, Journal of clinical medicine.
[8] E. Schneider-Futschik,et al. Multiple Reaction Monitoring Mass Spectrometry for the Drug Monitoring of Ivacaftor, Tezacaftor, and Elexacaftor Treatment Response in Cystic Fibrosis: A High-Throughput Method. , 2020, ACS pharmacology & translational science.
[9] J. Taylor-Cousar. CFTR Modulators: Impact on Fertility, Pregnancy, and Lactation in Women with Cystic Fibrosis , 2020, Journal of clinical medicine.
[10] R. Dezube,et al. Biliary disease and cholecystectomy after initiation of elexacaftor/ivacaftor/tezacaftor in adults with cystic fibrosis. , 2020, Journal of Cystic Fibrosis.
[11] S. Rotolo,et al. Testicular pain following initiation of elexacaftor/tezacaftor/ivacaftor in males with cystic fibrosis. , 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[12] E. Acosta,et al. Variable cellular ivacaftor concentrations in people with cystic fibrosis on modulator therapy. , 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[13] M. Duno,et al. Individual pharmacokinetic variation leads to underdosing of ciprofloxacin in some cystic fibrosis patients , 2017, Pediatric pulmonology.
[14] Xiaohong Huang,et al. Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR. , 2015, The New England journal of medicine.
[15] G. Jürgens,et al. Pharmacokinetic variability of clarithromycin and differences in CYP3A4 activity in patients with cystic fibrosis. , 2014, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.
[16] E. Acosta,et al. A sensitive HPLC-MS/MS method for the determination of dolutegravir in human plasma. , 2014, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
[17] S. Noel,et al. Cystic fibrosis: insight into CFTR pathophysiology and pharmacotherapy. , 2012, Clinical biochemistry.
[18] J. Treluyer,et al. Drug Disposition in Cystic Fibrosis , 1998, Clinical pharmacokinetics.
[19] W. Jusko,et al. Altered prednisolone pharmacokinetics in patients with cystic fibrosis. , 1992, The Journal of pediatrics.
[20] R. Parsons,et al. Absorption of two antibacterial drugs, cephalexin and co-trimoxazole, in malabsorption syndromes. , 1975, Journal of Antimicrobial Chemotherapy.