Chennakeshava Thunga

Predictors of Progression to Villous Atrophy in Children with Type 1 Diabetes and Potential Celiac Disease.

Journal: Digestive diseases and sciences

Published: June 17, 2026

The Hepatic Histomorphology and Application of Ensemble Transfer Learning in Convolutional Neural Network Models in the Biopsies of Hepatic Langerhans Cell Histiocytosis.

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

Published: June 16, 2026

Fascioliasis Presenting with Eosinophilia, Gastrointestinal Bleed and Biliary Obstruction.

Journal: Indian journal of pediatrics

Published: March 27, 2026

Recurrent Liver Failure due to SCYL1 Deficiency: A Report of 2 Cases and a Review of the Literature.

Journal: Journal of clinical and experimental hepatology

Published: March 03, 2026

An Unusual Cause of Massive Gastrointestinal Bleed in a Girl with Abdominal Tuberculosis.

Journal: Indian pediatrics

Published: January 08, 2026

Surgical management for aberrant bile ducts at porta in children undergoing laparoscopic and robotic excision of choledochal malformations.

Journal: Journal of pediatric surgery

Published: September 29, 2025

Clinical spectrum and genotype-phenotype correlation of ABCB4 mutations in children: Insights from a North Indian cohort.

Journal: World journal of hepatology

Published: August 28, 2025

Liver Dysfunction and Liver Histopathology in Alanyl-tRNA Synthetase 1 (AARS1) Deficiency with a Novel Mutation: A Case Report.

Journal: Fetal and pediatric pathology

Published: July 17, 2025

Clinical and molecular spectrum of genetic hypertriglyceridaemia in North Indian children: a case series.

Journal: Pediatric endocrinology, diabetes, and metabolism

Published: May 12, 2025

Congenital Lactase Deficiency, An Unusual Cause of Infantile Hypercalcemia.

Journal: Indian journal of pediatrics

Published: March 19, 2025

Predictors of Progression to Villous Atrophy in Children with Type 1 Diabetes and Potential Celiac Disease.

Predictors of Progression to Villous Atrophy in Children with Type 1 Diabetes and Potential Celiac Disease.

The Hepatic Histomorphology and Application of Ensemble Transfer Learning in Convolutional Neural Network Models in the Biopsies of Hepatic Langerhans Cell Histiocytosis.

The Hepatic Histomorphology and Application of Ensemble Transfer Learning in Convolutional Neural Network Models in the Biopsies of Hepatic Langerhans Cell Histiocytosis.

Fascioliasis Presenting with Eosinophilia, Gastrointestinal Bleed and Biliary Obstruction.

Fascioliasis Presenting with Eosinophilia, Gastrointestinal Bleed and Biliary Obstruction.

Recurrent Liver Failure due to SCYL1 Deficiency: A Report of 2 Cases and a Review of the Literature.

Recurrent Liver Failure due to SCYL1 Deficiency: A Report of 2 Cases and a Review of the Literature.

An Unusual Cause of Massive Gastrointestinal Bleed in a Girl with Abdominal Tuberculosis.

An Unusual Cause of Massive Gastrointestinal Bleed in a Girl with Abdominal Tuberculosis.

Surgical management for aberrant bile ducts at porta in children undergoing laparoscopic and robotic excision of choledochal malformations.

Surgical management for aberrant bile ducts at porta in children undergoing laparoscopic and robotic excision of choledochal malformations.

Clinical spectrum and genotype-phenotype correlation of ABCB4 mutations in children: Insights from a North Indian cohort.

Clinical spectrum and genotype-phenotype correlation of ABCB4 mutations in children: Insights from a North Indian cohort.

Liver Dysfunction and Liver Histopathology in Alanyl-tRNA Synthetase 1 (AARS1) Deficiency with a Novel Mutation: A Case Report.

Liver Dysfunction and Liver Histopathology in Alanyl-tRNA Synthetase 1 (AARS1) Deficiency with a Novel Mutation: A Case Report.

Clinical and molecular spectrum of genetic hypertriglyceridaemia in North Indian children: a case series.

Clinical and molecular spectrum of genetic hypertriglyceridaemia in North Indian children: a case series.

Congenital Lactase Deficiency, An Unusual Cause of Infantile Hypercalcemia.

Congenital Lactase Deficiency, An Unusual Cause of Infantile Hypercalcemia.

Neoadjuvant Peptide Receptor Radionuclide Therapy in a Rare Case of Pediatric Primary Hepatic Gastrinoma.

Neoadjuvant Peptide Receptor Radionuclide Therapy in a Rare Case of Pediatric Primary Hepatic Gastrinoma.

Carnitine-acylcarnitine translocase deficiency: a case report with autopsy.

Carnitine-acylcarnitine translocase deficiency: a case report with autopsy.