R Ganesh-Ramaswamy

12A Nageswara Road
Chennai, TN, India

Last Updated: 09/26/2026

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Found 35 publications

An Extremely Rare Cause of Hyperammonemic Encephalopathy in an Infant.

An Extremely Rare Cause of Hyperammonemic Encephalopathy in an Infant.

Journal: Indian journal of pediatrics

Published: June 21, 2023

Serum Zinc and Copper Levels in Children with Type 1 Diabetes Mellitus.

Serum Zinc and Copper Levels in Children with Type 1 Diabetes Mellitus.

Journal: Indian journal of pediatrics

Published: May 19, 2023

Other Causes of Chronic Diarrhea in Children.

Other Causes of Chronic Diarrhea in Children.

Journal: Indian journal of pediatrics

Published: November 29, 2022

Benign Recurrent Intrahepatic Cholestasis - Unravelleing the Paradox.

Benign Recurrent Intrahepatic Cholestasis - Unravelleing the Paradox.

Journal: Indian pediatrics

Published: May 13, 2021

Clinical Spectrum of Monogenic Infantile-Onset Inflammatory Bowel Disease.

Clinical Spectrum of Monogenic Infantile-Onset Inflammatory Bowel Disease.

Journal: Indian journal of pediatrics

Published: May 04, 2021

Chronic Watery Diarrhea in a Toddler: Think Beyond Toddler's Diarrhea.

Chronic Watery Diarrhea in a Toddler: Think Beyond Toddler's Diarrhea.

Journal: Indian journal of pediatrics

Published: November 13, 2020

Acute Devastating Multifocal Cavitating Leukoencephalopathy in a Six-Year-Old Girl due to Missense Mutation in LYRM7 Gene.

Acute Devastating Multifocal Cavitating Leukoencephalopathy in a Six-Year-Old Girl due to Missense Mutation in LYRM7 Gene.

Journal: Pediatric neurology

Published: November 06, 2020

Dual Internal Pancreatic Fistulae Complicating Chronic Pancreatitis.

Dual Internal Pancreatic Fistulae Complicating Chronic Pancreatitis.

Journal: Indian journal of pediatrics

Published: July 09, 2020

Continuous Venovenous Hemodiafilteration for Extremely High Ammonia Levels in Methyl Malonic Acidemia.

Continuous Venovenous Hemodiafilteration for Extremely High Ammonia Levels in Methyl Malonic Acidemia.

Journal: Indian journal of pediatrics

Published: April 22, 2020

Pyruvate Dehydrogenase Complex Deficiency due to a De Novo Heterozygous Mutation in Exon 7 of PDHA 1 Gene Presenting as Isolated Severe Lactic Acidosis in an Infant.

Pyruvate Dehydrogenase Complex Deficiency due to a De Novo Heterozygous Mutation in Exon 7 of PDHA 1 Gene Presenting as Isolated Severe Lactic Acidosis in an Infant.

Journal: Indian journal of pediatrics

Published: January 24, 2020

Correction to: Clinical Spectrum of Inherited Disorders of Metabolism.

Correction to: Clinical Spectrum of Inherited Disorders of Metabolism.

Journal: Indian journal of pediatrics

Published: September 14, 2019

Clinical Spectrum of Inherited Disorders of Metabolism.

Clinical Spectrum of Inherited Disorders of Metabolism.

Journal: Indian journal of pediatrics

Published: July 19, 2018

Showing 1-12 of 35

Last Updated: 09/26/2026