Publications by authors named "Umesh Kalane"

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Validation and Modified Application of the 2023 International Expert Consensus Criteria for Diagnosing Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease Among Children With Acquired Demyelination in Resource-Limited Regions.
Vishal Sondhi, Neelu Desai, Lokesh Lingappa, Vrajesh Udani, Naveen Sankhyan, Umesh Kalane

Pediatr Neurol· November 2025

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Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre.
Jayesh Sheth, Aadhira Nair, Frenny Sheth, Manali Ajagekar, Tejasvi Dhondekar, Umesh Kalane

Orphanet J Rare Dis· August 2024

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Landscape of genetic infantile epileptic spasms syndrome-A multicenter cohort of 124 children from India.
Balamurugan Nagarajan, Vykuntaraju K Gowda, Sangeetha Yoganathan, Indar Kumar Sharawat, Kavita Srivastava, Umesh Kalane

Epilepsia Open· December 2023

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Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children.
Divyani Garg, Sangeetha Yoganathan, Uzma Shamim, Kshitij Mankad, Parveen Gulati, Umesh Kalane

Mov Disord Clin Pract· October 2022

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Clinical and Electrophysiological Factors Predicting Prolonged Recovery in Children with Guillain-Barré Syndrome.
Ekta Agarwal, Ankita Bhagat, Kavita Srivastava, Bina Thakore, Sujit Jagtap, Umesh Kalane

Indian J Pediatr· May 2022

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Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1.
Parag M Tamhankar, Lakshmi Vasudevan, Pratima Kondurkar, Sarfaraj Niazi, Rita Christopher, Umesh Kalane

J Pediatr Genet· September 2021

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Dengue Encephalitis in a Newborn.
Shilpa U Kalane, Asha N Gokhale, Umesh D Kalane

Indian J Pediatr· July 2021

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Rhombencephalosynapsis: A rare cerebellar malformation associated with aqueductal stenosis and obstructive hydrocephalus.
Umesh Kalane, Ashish Atre

Neurol India· November 2018

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First reported case of Charcot Marie Tooth disease type 4C in a child from India with SH3TC2 mutation but absent spinal deformities.
Umesh Dinkar Kalane, Chaitanya Datar, Anita Mahadevan

Neurol India· January 2015

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Expanding the spectrum of mutations in Indian patients with Tay-Sachs disease.
Jayesh Sheth, Mehul Mistri, Chaitanya Datar, Umesh Kalane, Shekhar Patil

Mol Genet Metab Rep· September 2014

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