Ramaswamy Ganesh (Ganesh Ramaswamy, R Ganesh)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 10

Top Topics

Clostridium Difficile

Top Venues

Indian journal of pediatrics

Journal of paediatrics and child health

This page only lists publications with an associated author ORCID identifier.

Publications

Ramaswamy Ganesh, B S Ezhilmathi, Malathi Sathiyasekaran
Cholestatic jaundice in an infant: A twist in the diagnosis. Journal of paediatrics and child health (2024)
Ramaswamy Ganesh, B S Ezhilmathi, Malathi Sathiyasekaran
Cholestatic jaundice in an infant: A twist in the diagnosis. Journal of paediatrics and child health 60 (7) (2024)
Ramaswamy Ganesh, B Meenakshi
Serum Zinc and Copper Levels in Children with Type 1 Diabetes Mellitus. Indian journal of pediatrics (2023)
Ramaswamy Ganesh, R Karthik Narayanan
An Extremely Rare Cause of Hyperammonemic Encephalopathy in an Infant. Indian journal of pediatrics (2023)
Malathi Sathiyasekaran, Ramaswamy Ganesh, Suresh Natarajan
Other Causes of Chronic Diarrhea in Children. Indian journal of pediatrics (2023)
Ramaswamy Ganesh, Malathi Sathiyasekeran, Sankaranarayanan Srinivas, R Karthik Narayanan
Clinical Spectrum of Monogenic Infantile-Onset Inflammatory Bowel Disease. Indian journal of pediatrics 89 (5) (2022)
Ramaswamy Ganesh, Malathi Sathiyasekeran
Chronic Watery Diarrhea in a Toddler: Think Beyond Toddler's Diarrhea. Indian journal of pediatrics 88 (6) (2021)
Ramaswamy Ganesh, Shobana Rajendran, S Arunkumar, R Karthik Narayanan, Rahul Yadav
Continuous Venovenous Hemodiafilteration for Extremely High Ammonia Levels in Methyl Malonic Acidemia. Indian journal of pediatrics 88 (3) (2020)
Ramaswamy Ganesh, Malathi Sathiyasekeran, N Suresh, G Padmapriya, Nataraj Palaniappan, Karthik Narayanan R
Dual Internal Pancreatic Fistulae Complicating Chronic Pancreatitis. Indian journal of pediatrics 88 (3) (2020)
Ramaswamy Ganesh, Natarajan Suresh, B Vasuki, Karthik Narayanan
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. Indian journal of pediatrics 88 (1) (2020)