Umesh D. Kalane

Pune, MH, India

Last Updated: 09/26/2026

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Found 10 publications

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.

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.

Journal: Pediatric neurology
Published: January 06, 2025

Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre.

Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centre.

Journal: Orphanet journal of rare diseases
Published: April 18, 2024

Landscape of genetic infantile epileptic spasms syndrome-A multicenter cohort of 124 children from India.

Landscape of genetic infantile epileptic spasms syndrome-A multicenter cohort of 124 children from India.

Journal: Epilepsia open
Published: March 21, 2023

Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children.

Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children.

Journal: Movement disorders clinical practice
Published: December 25, 2021

Dengue Encephalitis in a Newborn.

Dengue Encephalitis in a Newborn.

Journal: Indian journal of pediatrics
Published: March 30, 2021

Clinical and Electrophysiological Factors Predicting Prolonged Recovery in Children with Guillain-Barré Syndrome.

Clinical and Electrophysiological Factors Predicting Prolonged Recovery in Children with Guillain-Barré Syndrome.

Journal: Indian journal of pediatrics
Published: December 15, 2020

Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1.

Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1.

Journal: Journal of pediatric genetics
Published: May 06, 2020

Rhombencephalosynapsis: A rare cerebellar malformation associated with aqueductal stenosis and obstructive hydrocephalus.

Rhombencephalosynapsis: A rare cerebellar malformation associated with aqueductal stenosis and obstructive hydrocephalus.

Journal: Neurology India
Published: November 15, 2016

First reported case of Charcot Marie Tooth disease type 4C in a child from India with SH3TC2 mutation but absent spinal deformities.

First reported case of Charcot Marie Tooth disease type 4C in a child from India with SH3TC2 mutation but absent spinal deformities.

Journal: Neurology India
Published: June 09, 2015

Expanding the spectrum of HEXA mutations in Indian patients with Tay-Sachs disease.

Expanding the spectrum of HEXA mutations in Indian patients with Tay-Sachs disease.

Journal: Molecular genetics and metabolism reports
Published: August 15, 2014
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Last Updated: 09/26/2026