Mathuranath S. Pavagada

Bengaluru, KA, India

Last Updated: 09/26/2026

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Found 12 publications

SLC18A2 associated infantile-onset- parkinsonism-dystonia 2: A novel genotype.

SLC18A2 associated infantile-onset- parkinsonism-dystonia 2: A novel genotype.

Journal: Parkinsonism & related disorders

Published: March 18, 2025

A Rare Disease and a Novel Variant in an Indian patient with Cerebellar Ataxia: A Case of Gordon Holmes Syndrome.

A Rare Disease and a Novel Variant in an Indian patient with Cerebellar Ataxia: A Case of Gordon Holmes Syndrome.

Journal: Annals of Indian Academy of Neurology

Published: January 31, 2025

Late-Onset Presentation of Spastic Paraplegia 3A ( ATL1 -HSP) and Its Rare Occurrence with Multiple Spinal Neurofibromas.

Late-Onset Presentation of Spastic Paraplegia 3A ( ATL1 -HSP) and Its Rare Occurrence with Multiple Spinal Neurofibromas.

Journal: Annals of Indian Academy of Neurology

Published: April 19, 2024

Early-onset levodopa responsive parkinsonism in PPP2R5D mutation.

Early-onset levodopa responsive parkinsonism in PPP2R5D mutation.

Journal: Parkinsonism & related disorders

Published: January 19, 2024

Spastic Ataxia with Sensory Neuropathy Sans Cerebral Leukodystrophy in Probable Adult Polyglucosan Body Disease.

Spastic Ataxia with Sensory Neuropathy Sans Cerebral Leukodystrophy in Probable Adult Polyglucosan Body Disease.

Journal: Annals of Indian Academy of Neurology

Published: August 13, 2023

Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotype.

Late-onset spastic-ataxia due to KIF1C mutation: broadening the SPG 58 phenotype.

Journal: Acta neurologica Belgica

Published: July 20, 2023

Levodopa Non-Responsive Parkinsonism in Tuberculous Cerebral Arteritis: A Rare Occurrence.

Levodopa Non-Responsive Parkinsonism in Tuberculous Cerebral Arteritis: A Rare Occurrence.

Journal: Annals of Indian Academy of Neurology

Published: June 17, 2021

Granulomatous Panuveitis in Multiple Sclerosis: A Rare Occurrence.

Granulomatous Panuveitis in Multiple Sclerosis: A Rare Occurrence.

Journal: Annals of Indian Academy of Neurology

Published: April 25, 2021

Stroke-like episodes with cerebellar ataxia as presenting manifestation of adult-onset anti-N-methyl D-aspartate receptor encephalitis: an unusual presentation.

Stroke-like episodes with cerebellar ataxia as presenting manifestation of adult-onset anti-N-methyl D-aspartate receptor encephalitis: an unusual presentation.

Journal: Acta neurologica Belgica

Published: April 15, 2021

ADCY5-Related Dyskinesia: A Genetic Cause of Early-Onset Chorea-Report of Two Cases and a Novel Mutation.

ADCY5-Related Dyskinesia: A Genetic Cause of Early-Onset Chorea-Report of Two Cases and a Novel Mutation.

Journal: Annals of Indian Academy of Neurology

Published: September 23, 2020

Autosomal Dominant Cerebral Small Vessel Disease in HTRA1 Gene Mutation.

Autosomal Dominant Cerebral Small Vessel Disease in HTRA1 Gene Mutation.

Journal: Annals of Indian Academy of Neurology

Published: May 03, 2020

Rapidly Progressive Spastic Paraplegia Due to Hyperhomocysteinemia in Child with MTHFR Gene Mutation and Mitochondrial Complex I Deficiency: A Rare Association.

Rapidly Progressive Spastic Paraplegia Due to Hyperhomocysteinemia in Child with MTHFR Gene Mutation and Mitochondrial Complex I Deficiency: A Rare Association.

Journal: Journal of pediatric neurosciences

Published: April 24, 2020

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Last Updated: 09/26/2026