Deepti A. Kewalramani

Chennai, TN, India

Last Updated: 09/26/2026

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Found 8 publications

Child Neurology: Expanding the LGI1 Spectrum: Homozygous Loss-of-Function Variant in an Infant With Epileptic Encephalopathy.

Child Neurology: Expanding the LGI1 Spectrum: Homozygous Loss-of-Function Variant in an Infant With Epileptic Encephalopathy.

Journal: Neurology
Published: May 18, 2026

Ketogenic Diet for Refractory Epilepsy in a Male Infant with CDKL5 Deficiency Disorder.

Ketogenic Diet for Refractory Epilepsy in a Male Infant with CDKL5 Deficiency Disorder.

Journal: Indian journal of pediatrics
Published: July 24, 2025

Chronic granulomatous herpes simplex encephalitis in a child with digeorge syndrome- expanding the spectrum of herpes-associated neurological disease.

Chronic granulomatous herpes simplex encephalitis in a child with digeorge syndrome- expanding the spectrum of herpes-associated neurological disease.

Journal: BMC infectious diseases
Published: February 12, 2025

A case of carbonic anhydrase type VA deficiency presenting as West syndrome in an infant with a novel mutation in the CA-VA gene.

A case of carbonic anhydrase type VA deficiency presenting as West syndrome in an infant with a novel mutation in the CA-VA gene.

Journal: Epilepsy & behavior reports
Published: August 01, 2022

Favorable response to classic ketogenic diet in a child with anti-GAD 65 antibody mediated super refractory status epilepticus.

Favorable response to classic ketogenic diet in a child with anti-GAD 65 antibody mediated super refractory status epilepticus.

Journal: Epilepsy & behavior reports
Published: March 06, 2022

Guillain-Barré Syndrome with Preserved Reflexes in a Child after COVID-19 Infection.

Guillain-Barré Syndrome with Preserved Reflexes in a Child after COVID-19 Infection.

Journal: Indian journal of pediatrics
Published: March 06, 2021

Genetic Epilepsy Syndrome with Classic Dysmorphism.

Genetic Epilepsy Syndrome with Classic Dysmorphism.

Journal: Indian journal of pediatrics
Published: December 03, 2020

Cavitating leukodystrophy as a manifestation of cerebral involvement in MFN2 neuropathy.

Cavitating leukodystrophy as a manifestation of cerebral involvement in MFN2 neuropathy.

Journal: Neurology
Published: June 12, 2020
Showing 1-8 of 8

Last Updated: 09/26/2026