Publications by authors named "Lal D V Nair"

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Impact of Developmental Pediatrics-Based Training for Primary School Teachers in Early Identification of Learning Disability.
Samir Dalwai, Jeeson C Unni, Zafar Meenai, Kawaljit S Multani, Nisha Boopathy, Lal D V Nair

Clin Pediatr (Phila)· October 2025

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Consensus Guidelines of the Indian Academy of Pediatrics (IAP)-Neurodevelopmental Pediatrics Chapter on Developmentally Supportive Follow-Up for High-Risk Infants.
Zafar Mahmood Meenai, M K C Nair, Samir Dalwai, Lal D V Nair, Sheffali Gulati

Indian Pediatr· August 2025

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Erratum: Consensus Guidelines of the Indian Academy of Pediatrics (IAP)-Neurodevelopmental Pediatrics Chapter on Developmentally Supportive Follow-Up for High-Risk Infants.
Zafar Mahmood Meenai, M K C Nair, Samir Dalwai, Lal D V Nair, Sheffali Gulati

Indian Pediatr· August 2025

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Obesity with developmental delay in infancy: a rare cause not to miss-pseudohypoparathyroidism.
Anees F M Ahmed, Rine Benson Thobias, Nilavan Thirumavalavan, Santhosh Thangamani, Lal D V Nair

BMJ Case Rep· February 2025

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Synucleins As Biomarkers of Severity in Autism Spectrum Disorder.
Lal D V Nair, Senthil Kumar Sivanesan, Devika S Kumar

Cureus· September 2024

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A Syndrome Affecting All Five Sense Organs: A Rare Congenital Disorder of Kabuki Makeup Syndrome With Multiple Pre-auricular Skin Tags.
Navin Umapathy, Vaanmathi Azhagar Nambi Santhi, Balakrishnan T, Lal D V Nair

Cureus· September 2024

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Microcornea, cerebellar hypoplasia and hyperlax joints-unusual combo in rare Ehlers-Danlos syndrome-musculocontractural type 1.
Navin Umapathy, Balakrishnan Thirugnana Sambanda Moorthy, Vaanmathi Azhagar Nambi Santhi, Lal D V Nair

BMJ Case Rep· June 2024

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An unusual case of Pseudohypoaldosteronism coexisting with cystic fibrosis.
Navin Umapathy, Balakrishnan Thirugnana Sambanda Moorthy, Vaanmathi Azhagar Nambi Santhi, Lal D V Nair

BMJ Case Rep· June 2024

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Extracellular Oxidative Stress Markers in COVID-19 Patients with Diabetes as Co-Morbidity.
Devika Sanil Kumar, Gowtham Hanumanram, Prasanna Karthik Suthakaran, Jagadeesan Mohanan, Lal Devayani Vasudevan Nair

Clin Pract· February 2022

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Epilepsy in KCNH1-related syndromes.
Mario Mastrangelo, Ingrid E Scheffer, Nuria C Bramswig, Lal D V Nair, Candace T Myers

Epileptic Disord· June 2016

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Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome.
Fanny Kortüm, Viviana Caputo, Christiane K Bauer, Lorenzo Stella, Andrea Ciolfi, Lal D V Nair

Nat Genet· June 2015

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The genetic basis of DOORS syndrome: an exome-sequencing study.
Philippe M Campeau, Dalia Kasperaviciute, James T Lu, Lindsay C Burrage, Choel Kim, Lal D V Nair

Lancet Neurol· January 2014

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