Kothari Sonam

Bengaluru, KA, India

Last Updated: 09/26/2026

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Found 14 publications

Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?

Mitochondrial leukoencephalopathies: A border zone between acquired and inherited white matter disorders in children?

Journal: Multiple sclerosis and related disorders

Published: August 24, 2017

Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations.

Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations.

Journal: Clinical neurology and neurosurgery

Published: August 16, 2017

Reply to Letter to the Editor: Hearing impairment in m.3243A>G carriers requires comprehensive work- and follow-up.

Reply to Letter to the Editor: Hearing impairment in m.3243A>G carriers requires comprehensive work- and follow-up.

Journal: Clinical neurology and neurosurgery

Published: August 26, 2016

Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India.

Mitochondrial oxidative phosphorylation disorders in children: Phenotypic, genotypic and biochemical correlations in 85 patients from South India.

Journal: Mitochondrion

Published: July 23, 2016

Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India.

Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India.

Journal: Mitochondrion

Published: October 26, 2015

Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south India.

Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: A study from south India.

Journal: Mitochondrion

Published: May 31, 2015

Clinical and Neuroimaging Features in Two Children with Mutations in the Mitochondrial ND5 Gene.

Clinical and Neuroimaging Features in Two Children with Mutations in the Mitochondrial ND5 Gene.

Journal: Neuropediatrics

Published: May 15, 2015

Speech-Language and swallowing manifestations and rehabilitation in an 11-year-old girl with MELAS syndrome.

Speech-Language and swallowing manifestations and rehabilitation in an 11-year-old girl with MELAS syndrome.

Journal: Journal of pediatric neurosciences

Published: April 17, 2015

Palatal Tremor in POLG-Associated Ataxia.

Palatal Tremor in POLG-Associated Ataxia.

Journal: Movement disorders clinical practice

Published: January 17, 2015

Mitochondrial myopathy, cardiomyopathy, and pontine signal changes in an adult patient with isolated complex II deficiency.

Mitochondrial myopathy, cardiomyopathy, and pontine signal changes in an adult patient with isolated complex II deficiency.

Journal: Journal of clinical neuromuscular disease

Published: November 22, 2014

Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome.

Audiological manifestations in mitochondrial encephalomyopathy lactic acidosis and stroke like episodes (MELAS) syndrome.

Journal: Clinical neurology and neurosurgery

Published: October 16, 2014

Bilateral hypertrophic olivary nucleus degeneration on magnetic resonance imaging in children with Leigh and Leigh-like syndrome.

Bilateral hypertrophic olivary nucleus degeneration on magnetic resonance imaging in children with Leigh and Leigh-like syndrome.

Journal: The British journal of radiology

Published: January 29, 2014

Showing 1-12 of 14

Last Updated: 09/26/2026