Prashant Phulpagar

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 5

Top Topics

Intellectual Disability

Dna Methylation

Chronic Kidney Disease

Top Venues

Tremor and other hyperkinetic movements (New York, N.Y.)

Journal of neuroendocrinology

Journal of human genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Vikram Venkappayya Holla, Samim Mm, Riyanka Kumari, Debjyoti Dhar, Prashant Phulpagar, Neeharika Sriram, Shweta Prasad, Jitender Saini, Nitish Kamble, Ravi Yadav, Babylakshmi Muthusamy, Pramod Kumar Pal
The Clinical, Radiological and Genetic Spectrum of PLA2G6 -Associated Neurodegeneration: An Experience From a Tertiary Center. Tremor and other hyperkinetic movements (New York, N.Y.) 14 (2024)
Vikram Venkappayya Holla, Samim Mm, Riyanka Kumari, Debjyoti Dhar, Prashant Phulpagar, Neeharika Sriram, Shweta Prasad, Jitender Saini, Nitish Kamble, Ravi Yadav, Babylakshmi Muthusamy, Pramod Kumar Pal
The Clinical, Radiological and Genetic Spectrum of PLA2G6 -Associated Neurodegeneration: An Experience From a Tertiary Center. Tremor and other hyperkinetic movements (New York, N.Y.) 14 (2024)
Vikram Venkappayya Holla, Samim Mm, Riyanka Kumari, Debjyoti Dhar, Prashant Phulpagar, Neeharika Sriram, Shweta Prasad, Jitender Saini, Nitish Kamble, Ravi Yadav, Babylakshmi Muthusamy, Pramod Kumar Pal
The Clinical, Radiological and Genetic Spectrum of PLA2G6 -Associated Neurodegeneration: An Experience From a Tertiary Center. Tremor and other hyperkinetic movements (New York, N.Y.) 14 (2024)
Prashant Phulpagar, Vikram V Holla, Deepti Tomar, Nitish Kamble, Ravi Yadav, Pramod Kumar Pal, Babylakshmi Muthusamy
Novel CWF19L1 mutations in patients with spinocerebellar ataxia, autosomal recessive 17. Journal of human genetics (2023)
Riyanka Kumari, Vikram Venkappayya Holla, Prashant Phulpagar, Neeharika Sriram, Aditya G Hegde, Seena Vengalil, Nitish Kamble, Jitender Saini, Ravi Yadav, Pramod Kumar Pal, Babylakshmi Muthusamy
Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse-Sakati syndrome. Journal of neuroendocrinology 34 (10) (2022)