Meghana N. Sathe

Pediatric Gastroenterology | Pediatrics

5323 Harry Hines Blvd
Dallas, TX 75235

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 46 publications

Corrigendum to "Results of a clinical trial of ANG003, a non-porcine pancreatic enzyme replacement therapy, in people with cystic fibrosis" [Journal of Cystic Fibrosis Original Article Articles in Press July 31, 2025].

Corrigendum to "Results of a clinical trial of ANG003, a non-porcine pancreatic enzyme replacement therapy, in people with cystic fibrosis" [Journal of Cystic Fibrosis Original Article Articles in Press July 31, 2025].

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: December 04, 2025

Study Design Considerations for the Evaluation of Pancreatic Enzyme Replacement Therapy (PERT) Products in People with Cystic Fibrosis: An Update.

Study Design Considerations for the Evaluation of Pancreatic Enzyme Replacement Therapy (PERT) Products in People with Cystic Fibrosis: An Update.

Journal: Clinical therapeutics

Published: November 13, 2025

Implementation of Non-invasive Point of Care Transient Elastography for Evaluation of Liver Disease in Pediatric Populations with Cystic Fibrosis.

Implementation of Non-invasive Point of Care Transient Elastography for Evaluation of Liver Disease in Pediatric Populations with Cystic Fibrosis.

Journal: Journal of visualized experiments : JoVE

Published: September 15, 2025

Results of a clinical trial of ANG003, a non-porcine pancreatic enzyme replacement therapy, in people with cystic fibrosis.

Results of a clinical trial of ANG003, a non-porcine pancreatic enzyme replacement therapy, in people with cystic fibrosis.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: April 07, 2025

Validation of dietary whey protein substrate challenge absorption test as an indicator of proteolysis.

Validation of dietary whey protein substrate challenge absorption test as an indicator of proteolysis.

Journal: PloS one

Published: January 15, 2025

Characterization of Pancreatic Cystosis Phenotype in People With Cystic Fibrosis.

Characterization of Pancreatic Cystosis Phenotype in People With Cystic Fibrosis.

Journal: Pancreas

Published: January 13, 2025

Cystic Fibrosis Learning Network Telehealth Innovation Lab During the COVID-19 Pandemic: Impact on Access to Care, Outcomes, and a New CF Care Model.

Cystic Fibrosis Learning Network Telehealth Innovation Lab During the COVID-19 Pandemic: Impact on Access to Care, Outcomes, and a New CF Care Model.

Journal: Pediatric pulmonology

Published: December 13, 2024

Guiding caregivers of infants with CF in understanding differences in pediatric growth charts.

Guiding caregivers of infants with CF in understanding differences in pediatric growth charts.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: April 02, 2024

Cystic fibrosis hepatobiliary involvement: an update on imaging in diagnosis and monitoring.

Cystic fibrosis hepatobiliary involvement: an update on imaging in diagnosis and monitoring.

Journal: Pediatric radiology

Published: March 04, 2024

Estimating minimal clinically important difference (MCID) for gastrointestinal symptoms in cystic fibrosis.

Estimating minimal clinically important difference (MCID) for gastrointestinal symptoms in cystic fibrosis.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: October 15, 2023

Remote endpoints for clinical trials in cystic fibrosis: Report from the U.S. CF foundation remote endpoints task force.

Remote endpoints for clinical trials in cystic fibrosis: Report from the U.S. CF foundation remote endpoints task force.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: October 11, 2023

Intrahepatic Cholangiolitis in Cystic Fibrosis (ICCF): An Under-Appreciated Cause of Persistent Cholestasis in Infancy.

Intrahepatic Cholangiolitis in Cystic Fibrosis (ICCF): An Under-Appreciated Cause of Persistent Cholestasis in Infancy.

Journal: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society

Published: October 06, 2023

Showing 1-12 of 46

Last Updated: 09/26/2026