Mohandas K. Nair

Kozhikode, KL, India

Last Updated: 09/26/2026

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Found 15 publications

Subtle Clinical Clues for Early Diagnosis of Lethal ORAI1 Deficiency in Infants.

Subtle Clinical Clues for Early Diagnosis of Lethal ORAI1 Deficiency in Infants.

Journal: Indian journal of pediatrics
Published: November 04, 2025

Consensus Statement of the Neurodevelopmental Pediatrics Chapter of Indian Academy of Pediatrics (IAP) on the Management of Children With Down Syndrome.

Consensus Statement of the Neurodevelopmental Pediatrics Chapter of Indian Academy of Pediatrics (IAP) on the Management of Children With Down Syndrome.

Journal: Indian pediatrics
Published: February 23, 2023

Clinical, radiological and molecular studies in 24 individuals with Dyggve-Melchior-Clausen dysplasia and Smith-McCort dysplasia from India.

Clinical, radiological and molecular studies in 24 individuals with Dyggve-Melchior-Clausen dysplasia and Smith-McCort dysplasia from India.

Journal: Journal of medical genetics
Published: July 22, 2021

Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India.

Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India.

Journal: Human immunology
Published: June 11, 2021

Hypothermia for moderate or severe neonatal encephalopathy in low-income and middle-income countries (HELIX): a randomised controlled trial in India, Sri Lanka, and Bangladesh.

Hypothermia for moderate or severe neonatal encephalopathy in low-income and middle-income countries (HELIX): a randomised controlled trial in India, Sri Lanka, and Bangladesh.

Journal: The Lancet. Global health
Published: February 15, 2021

Identification and characterization of 30 novel pathogenic variations in 69 unrelated Indian patients with Mucolipidosis Type II and Type III.

Identification and characterization of 30 novel pathogenic variations in 69 unrelated Indian patients with Mucolipidosis Type II and Type III.

Journal: Journal of human genetics
Published: April 10, 2020

Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patients.

Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patients.

Journal: Journal of neurology
Published: January 21, 2019

Hypothermia for encephalopathy in low-income and middle-income countries: feasibility of whole-body cooling using a low-cost servo-controlled device.

Hypothermia for encephalopathy in low-income and middle-income countries: feasibility of whole-body cooling using a low-cost servo-controlled device.

Journal: BMJ paediatrics open
Published: December 18, 2017

Hypothermia for encephalopathy in low and middle-income countries (HELIX): study protocol for a randomised controlled trial.

Hypothermia for encephalopathy in low and middle-income countries (HELIX): study protocol for a randomised controlled trial.

Journal: Trials
Published: March 24, 2017

Pycnodysostosis: Novel Variants in CTSK and Occurrence of Giant Cell Tumor.

Pycnodysostosis: Novel Variants in CTSK and Occurrence of Giant Cell Tumor.

Journal: Journal of pediatric genetics
Published: February 24, 2017

Concept of Health Care Counseling for Pediatricians.

Concept of Health Care Counseling for Pediatricians.

Journal: Indian pediatrics
Published: November 28, 2016

Erratum to: Glutaric Acidemia Type 1-Clinico-Molecular Profile and Novel Mutations in GCDH Gene in Indian Patients.

Erratum to: Glutaric Acidemia Type 1-Clinico-Molecular Profile and Novel Mutations in GCDH Gene in Indian Patients.

Journal: JIMD reports
Published: August 08, 2014
Showing 1-12 of 15

Last Updated: 09/26/2026