Prashant Phulpagar
5PUBLICATIONS
15CO-AUTHORS
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Publications (5)
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|Feb 16, 2026
Clinical, Radiological, and Genetic Profiles of Eight Patients with Combined Dystonic Manifestation of Type-III GM1 Gangliosidosis: A Video Case Series from India.Subhajit Roy, Cheshta Arora, Vikram V Holla
|Jan 16, 2025
<i>PRKN</i>-Gene-Related Parkinsonism: An Experience from a Tertiary Centre and Literature Review of Asian Cohort.Vikram V Holla, Debjyoti Dhar, Prashant Phulpagar
|Aug 26, 2024
The Clinical, Radiological and Genetic Spectrum of <i>PLA2G6</i>-Associated Neurodegeneration: An Experience From a Tertiary Center.Vikram V Holla, M M Samim, Riyanka Kumari
|Sep 26, 2023
Novel CWF19L1 mutations in patients with spinocerebellar ataxia, autosomal recessive 17.Prashant Phulpagar, Vikram V Holla, Deepti Tomar
|Jul 25, 2022
Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndrome.Riyanka Kumari, Vikram V Holla, Prashant Phulpagar
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Frequent Collaborators
5 joint publications
Babylakshmi Muthusamy
4 joint publications
Vikram V Holla
4 joint publications
Nitish Kamble
4 joint publications
Ravi Yadav
4 joint publications
Pramod Kumar Pal
2 joint publications
Riyanka Kumari
2 joint publications
Neeharika Sriram
2 joint publications
M M Samim
2 joint publications
Debjyoti Dhar
2 joint publications
Shweta Prasad
