Javier
Maynar Moliner
Publikationen, an denen er mitarbeitet Javier Maynar Moliner (18)
2023
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Ceftaroline and Avibactam Removal by Continuous Renal Replacement Therapies: An in vitro Study
Blood Purification, Vol. 52, Núm. 5, pp. 464-473
2022
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Optimization of levetiracetam dosing regimen in critically ill patients with augmented renal clearance: a Monte Carlo simulation study
Journal of Intensive Care, Vol. 10, Núm. 1
2021
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Population pharmacokinetics of levetiracetam and dosing evaluation in critically ill patients with normal or augmented renal function
Pharmaceutics, Vol. 13, Núm. 10
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Quantification of ceftaroline in human plasma using high‐performance liquid chromatography with ultraviolet detection: Application to pharmacokinetic studies
Pharmaceutics, Vol. 13, Núm. 7
2020
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Impact of augmented renal clearance on the pharmacokinetics of linezolid: Advantages of continuous infusion from a pharmacokinetic/pharmacodynamic perspective
International Journal of Infectious Diseases, Vol. 93, pp. 329-338
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Novel population pharmacokinetic model for linezolid in critically ill patients and evaluation of the adequacy of the current dosing recommendation
Pharmaceutics, Vol. 12, Núm. 1
2019
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Pharmacokinetics of linezolid in critically ill patients on continuous renal replacement therapy: Influence of residual renal function on PK/PD target attainment
Journal of Critical Care, Vol. 50, pp. 69-76
2018
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Population pharmacokinetics of daptomycin in critically ill patients
International Journal of Antimicrobial Agents, Vol. 52, Núm. 2, pp. 158-165
2014
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Population pharmacokinetics of piperacillin and tazobactam in critically ill patients undergoing continuous renal replacement therapy: Application to pharmacokinetic/pharmacodynamic analysis
Journal of Antimicrobial Chemotherapy, Vol. 69, Núm. 1, pp. 180-189
2008
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Population pharmacokinetics of meropenem in critically ill patients undergoing continuous renal replacement therapy
Clinical Pharmacokinetics, Vol. 47, Núm. 3, pp. 173-180
2007
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In vitro AN69 and polysulphone membrane permeability to ceftazidime and in vivo pharmacokinetics during continuous renal replacement therapies
Chemotherapy, Vol. 53, Núm. 3, pp. 194-201
2006
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Elimination of piperacillin and tazobactam by renal replacement therapies with AN69 and polysulfone hemofilters: Evaluation of the sieving coefficient
Blood Purification, Vol. 24, Núm. 4, pp. 347-354
2005
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Cefepime and continuous renal replacement therapy (CRRT): In vitro permeability of two CRRT membranes and pharmacokinetics in four critically ill patients
Clinical Therapeutics, Vol. 27, Núm. 5, pp. 599-608
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Determination of ceftazidime and cefepime in plasma and dialysate-ultrafiltrate from patients undergoing continuous veno-venous hemodiafiltration by HPLC
Journal of Pharmaceutical and Biomedical Analysis, Vol. 39, Núm. 5, pp. 996-1005
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In vitro and in vivo evaluation of enoxaparin removal by continuous renal replacement therapies with acrylonitrile and polysulfone membranes
Clinical Therapeutics, Vol. 27, Núm. 9, pp. 1444-1451
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Influence of renal function on the pharmacokinetics of piperacillin/ tazobactam in intensive care unit patients during continuous venovenous hemofiltration
Journal of Clinical Pharmacology, Vol. 45, Núm. 2, pp. 168-176
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Meropenem and continuous renal replacement therapy: In vitro permeability of 2 continuous renal replacement therapy membranes and influence of patient renal function on the pharmacokinetics in critically ill patients
Journal of Clinical Pharmacology, Vol. 45, Núm. 11, pp. 1294-1304
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Quantification and stability of piperacillin and tazobactam in plasma and ultrafiltrate from patients undergoing continuous venovenous hemofiltration by HPLC
Biomedical Chromatography, Vol. 19, Núm. 8, pp. 570-578