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Home use of interdental cleaning devices, in addition to toothbrushing, for preventing and controlling periodontal diseases and dental caries

Cochrane database of systematic reviews, 2019-04, Vol.4 (4), p.CD012018

2019

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Fetal Physiologically Based Pharmacokinetic Models: Systems Information on the Growth and Composition of Fetal Organs

Clinical pharmacokinetics, 2019-02, Vol.58 (2), p.235-262

2019

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Anatomical, Physiological and Metabolic Changes with Gestational Age during Normal Pregnancy: A Database for Parameters Required in Physiologically Based Pharmacokinetic Modelling

Clinical pharmacokinetics, 2012-06, Vol.51 (6), p.365-396

2012

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Fetal Physiologically Based Pharmacokinetic Models: Systems Information on Fetal Blood Components and Binding Proteins

Clinical pharmacokinetics, 2020-05, Vol.59 (5), p.629-642

2020

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Research methods challenges: A case study of preparedness in The Bahamas

Jamba, 2024, Vol.16 (1), p.1565-1565

2024

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A Preterm Physiologically Based Pharmacokinetic Model. Part I: Physiological Parameters and Model Building

Clinical pharmacokinetics, 2020-04, Vol.59 (4), p.485-500

2020

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Preterm Physiologically Based Pharmacokinetic Model. Part II: Applications of the Model to Predict Drug Pharmacokinetics in the Preterm Population

Clinical pharmacokinetics, 2020-04, Vol.59 (4), p.501-518

2020

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Prediction of Pediatric Pharmacokinetics for CYP3A4 Metabolized Drugs: Comparison of the Performance of Two Hepatic Ontogeny Within a Physiologically Based Pharmacokinetic Model

Journal of clinical pharmacology, 2024-09, Vol.64 (9), p.1083-1094

2024

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Directing Stem Cell Fate: The Synthetic Natural Product Connection

Chemical reviews, 2017-09, Vol.117 (18), p.12052-12086

2017

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Fetal Physiologically Based Pharmacokinetic Models: Systems Information on Fetal Cardiac Output and Its Distribution to Different Organs during Development

Clinical pharmacokinetics, 2021-06, Vol.60 (6), p.741-757

2021

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A Re-evaluation and Validation of Ontogeny Functions for Cytochrome P450 1A2 and 3A4 Based on In Vivo Data

Clinical pharmacokinetics, 2014-07, Vol.53 (7), p.625-636

2014

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Development and Verification of a Japanese Pediatric Physiologically based Pharmacokinetic Model with Emphasis on Drugs Eliminated by Cytochrome P450 or Renal Excretion

Journal of clinical pharmacology, 2023-10, Vol.63 (10), p.1156-1168

2023

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Resurgence in the use of physiologically based pharmacokinetic models in pediatric clinical pharmacology: parallel shift in incorporating the knowledge of biological elements and increased applicability to drug development and clinical practice

Pediatric anesthesia, 2011-03, Vol.21 (3), p.291-301

2011

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Physiologically-based pharmacokinetic models for children: Starting to reach maturation?

Pharmacology & therapeutics (Oxford), 2020-07, Vol.211, p.107541, Article 107541

2020

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Another Step Toward Qualification of Pediatric Physiologically Based Pharmacokinetic Models to Facilitate Inclusivity and Diversity in Pediatric Clinical Studies

Clinical pharmacology and therapeutics, 2023-03, Vol.113 (3), p.735-745

2023

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Physiologically Based Pharmacokinetic Modeling and Allometric Scaling in Pediatric Drug Development: Where Do We Draw the Line?

Journal of clinical pharmacology, 2021-06, Vol.61 (S1), p.S83-S93

2021

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Increasing application of pediatric physiologically based pharmacokinetic models across academic and industry organizations

CPT: pharmacometrics and systems pharmacology, 2022-03, Vol.11 (3), p.373-383

2022

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Incorporation and Performance Verification of Hepatic Portal Blood Flow Shunting in Minimal and Full PBPK Models of Liver Cirrhosis

Clinical pharmacology and therapeutics, 2023-12, Vol.114 (6), p.1264-1273

2023

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Prediction of the clearance of eleven drugs and associated variability in neonates, infants and children

Clinical pharmacokinetics, 2006-01, Vol.45 (9), p.931-956

2006

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Predictive Performance of Physiologically Based Pharmacokinetic (PBPK) Modeling of Drugs Extensively Metabolized by Major Cytochrome P450s in Children

Clinical pharmacology and therapeutics, 2018-07, Vol.104 (1), p.188-200

2018

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Fetal Physiologically-Based Pharmacokinetic Models: Systems Information on Fetal Biometry and Gross Composition

Clinical pharmacokinetics, 2018-09, Vol.57 (9), p.1149-1171

2018

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Does “Birth” as an Event Impact Maturation Trajectory of Renal Clearance via Glomerular Filtration? Reexamining Data in Preterm and Full‐Term Neonates by Avoiding the Creatinine Bias

Journal of clinical pharmacology, 2021-02, Vol.61 (2), p.159-171

2021

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Development and Verification of a Full Physiologically Based Pharmacokinetic Model for Sublingual Buprenorphine in Healthy Adult Volunteers that Accounts for Nonlinear Bioavailability

Drug metabolism and disposition, 2024-08, Vol.52 (8), p.785-796

2024

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Total Synthesis of Celastrol, Development of a Platform to Access Celastroid Natural Products

Journal of the American Chemical Society, 2015-09, Vol.137 (37), p.11864-11867

2015

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Authors’ Reply to Völler et al: “Comment on: Preterm Physiologically Based Pharmacokinetic Model, Part I and Part II”

Clinical pharmacokinetics, 2021-05, Vol.60 (5), p.681-683

2021

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Home use of interdental cleaning devices, in addition to toothbrushing, for preventing and controlling periodontal diseases and dental caries

Fetal Physiologically Based Pharmacokinetic Models: Systems Information on the Growth and Composition of Fetal Organs

Anatomical, Physiological and Metabolic Changes with Gestational Age during Normal Pregnancy: A Database for Parameters Required in Physiologically Based Pharmacokinetic Modelling

Fetal Physiologically Based Pharmacokinetic Models: Systems Information on Fetal Blood Components and Binding Proteins

Research methods challenges: A case study of preparedness in The Bahamas

A Preterm Physiologically Based Pharmacokinetic Model. Part I: Physiological Parameters and Model Building

Preterm Physiologically Based Pharmacokinetic Model. Part II: Applications of the Model to Predict Drug Pharmacokinetics in the Preterm Population

Prediction of Pediatric Pharmacokinetics for CYP3A4 Metabolized Drugs: Comparison of the Performance of Two Hepatic Ontogeny Within a Physiologically Based Pharmacokinetic Model

Directing Stem Cell Fate: The Synthetic Natural Product Connection

Fetal Physiologically Based Pharmacokinetic Models: Systems Information on Fetal Cardiac Output and Its Distribution to Different Organs during Development

A Re-evaluation and Validation of Ontogeny Functions for Cytochrome P450 1A2 and 3A4 Based on In Vivo Data

Development and Verification of a Japanese Pediatric Physiologically based Pharmacokinetic Model with Emphasis on Drugs Eliminated by Cytochrome P450 or Renal Excretion

Resurgence in the use of physiologically based pharmacokinetic models in pediatric clinical pharmacology: parallel shift in incorporating the knowledge of biological elements and increased applicability to drug development and clinical practice

Physiologically-based pharmacokinetic models for children: Starting to reach maturation?

Another Step Toward Qualification of Pediatric Physiologically Based Pharmacokinetic Models to Facilitate Inclusivity and Diversity in Pediatric Clinical Studies

Physiologically Based Pharmacokinetic Modeling and Allometric Scaling in Pediatric Drug Development: Where Do We Draw the Line?

Increasing application of pediatric physiologically based pharmacokinetic models across academic and industry organizations

Incorporation and Performance Verification of Hepatic Portal Blood Flow Shunting in Minimal and Full PBPK Models of Liver Cirrhosis

Prediction of the clearance of eleven drugs and associated variability in neonates, infants and children

Predictive Performance of Physiologically Based Pharmacokinetic (PBPK) Modeling of Drugs Extensively Metabolized by Major Cytochrome P450s in Children

Fetal Physiologically-Based Pharmacokinetic Models: Systems Information on Fetal Biometry and Gross Composition

Does “Birth” as an Event Impact Maturation Trajectory of Renal Clearance via Glomerular Filtration? Reexamining Data in Preterm and Full‐Term Neonates by Avoiding the Creatinine Bias

Development and Verification of a Full Physiologically Based Pharmacokinetic Model for Sublingual Buprenorphine in Healthy Adult Volunteers that Accounts for Nonlinear Bioavailability

Total Synthesis of Celastrol, Development of a Platform to Access Celastroid Natural Products

Authors’ Reply to Völler et al: “Comment on: Preterm Physiologically Based Pharmacokinetic Model, Part I and Part II”

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