Prashant Phulpagar

International Technology Park
Bengaluru, KA 560066, India

Last Updated: 09/26/2026

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Found 14 publications

Clinical, Radiological, and Genetic Profiles of Eight Patients with Combined Dystonic Manifestation of Type-III GM1 Gangliosidosis: A Video Case Series from India.

Clinical, Radiological, and Genetic Profiles of Eight Patients with Combined Dystonic Manifestation of Type-III GM1 Gangliosidosis: A Video Case Series from India.

Journal: Tremor and other hyperkinetic movements (New York, N.Y.)
Published: December 08, 2025

Clinical Profile and Genetic Composition of Patients With Juvenile Parkinsonism From a Single Tertiary Care Center in India.

Clinical Profile and Genetic Composition of Patients With Juvenile Parkinsonism From a Single Tertiary Care Center in India.

Journal: Journal of movement disorders
Published: May 13, 2025

PRKN-Gene-Related Parkinsonism: An Experience from a Tertiary Centre and Literature Review of Asian Cohort.

PRKN-Gene-Related Parkinsonism: An Experience from a Tertiary Centre and Literature Review of Asian Cohort.

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: January 16, 2025

Clinico-genetic analysis of patients with LRRK2-related Parkinson's disease from a referral centre in India.

Clinico-genetic analysis of patients with LRRK2-related Parkinson's disease from a referral centre in India.

Journal: Parkinsonism & related disorders
Published: September 11, 2024

Clinico-Genetic Profiles of Seven Patients With PINK1-Related Parkinson's Disease: A Case Series From a Tertiary Care Centre in India and a Review of the Literature.

Clinico-Genetic Profiles of Seven Patients With PINK1-Related Parkinson's Disease: A Case Series From a Tertiary Care Centre in India and a Review of the Literature.

Journal: Journal of movement disorders
Published: July 08, 2024

The Clinical, Radiological and Genetic Spectrum of PLA2G6-Associated Neurodegeneration: An Experience From a Tertiary Center.

The Clinical, Radiological and Genetic Spectrum of PLA2G6-Associated Neurodegeneration: An Experience From a Tertiary Center.

Journal: Tremor and other hyperkinetic movements (New York, N.Y.)
Published: April 05, 2024

Genetic architecture of a single cohort of 230 Indian Parkinson's Disease patients.

Genetic architecture of a single cohort of 230 Indian Parkinson's Disease patients.

Journal: Parkinsonism & related disorders
Published: January 08, 2024

Clinicogenetic Characterization of Patients with PD and Heterozygous GBA1 Variants in an Indian Cohort.

Clinicogenetic Characterization of Patients with PD and Heterozygous GBA1 Variants in an Indian Cohort.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: October 23, 2023

Novel CWF19L1 mutations in patients with spinocerebellar ataxia, autosomal recessive 17.

Novel CWF19L1 mutations in patients with spinocerebellar ataxia, autosomal recessive 17.

Journal: Journal of human genetics
Published: February 02, 2023

CLCN2-Related Leukoencephalopathy in Two Unrelated Patients Due to Novel Variants.

CLCN2-Related Leukoencephalopathy in Two Unrelated Patients Due to Novel Variants.

Journal: Movement disorders clinical practice
Published: December 15, 2022

A Rare Case of Ophthalmoplegia with Ataxia in Genetically Proven Abetalipoproteinemia.

A Rare Case of Ophthalmoplegia with Ataxia in Genetically Proven Abetalipoproteinemia.

Journal: Movement disorders clinical practice
Published: September 16, 2022

A splice altering variant in NDRG1 gene causes Charcot-Marie-Tooth disease, type 4D.

A splice altering variant in NDRG1 gene causes Charcot-Marie-Tooth disease, type 4D.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: November 10, 2021
Showing 1-12 of 14

Last Updated: 09/26/2026