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Phulpagar, Prashant
9
results:
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1
Novel CWF19L1 mutations in patients with spinocerebellar at..:
Phulpagar, Prashant
;
Holla, Vikram V.
;
Tomar, Deepti
...
Journal of Human Genetics. 68 (2023) 12 - p. 859-866 , 2023
Link:
https://doi.org/10.1038/..
?
2
Clinicogenetic Characterization of Patients with PD and Het..:
Kamath, Sneha D
;
Holla, Vikram V.
;
Phulpagar, Prashant
...
Movement Disorders. 39 (2023) 3 - p. 628-630 , 2023
Link:
https://doi.org/10.1002/..
?
3
CLCN2‐Related Leukoencephalopathy in Two Unrelated Patients..:
Holla, Vikram V.
;
Phulpagar, Prashant
;
Saini, Jitender
...
Movement Disorders Clinical Practice. 10 (2023) 7 - p. 1155-1158 , 2023
Link:
https://doi.org/10.1002/..
?
4
A splice altering variant in NDRG1 gene causes Charcot-Mari..:
Pravinbabu, Pooja
;
Holla, Vikram V.
;
Phulpagar, Prashant
...
Neurological Sciences. 43 (2022) 7 - p. 4463-4472 , 2022
Link:
https://doi.org/10.1007/..
?
5
Whole exome sequencing and transcript analysis discover a n..:
Kumari, Riyanka
;
Holla, Vikram V.
;
Phulpagar, Prashant
...
Journal of Neuroendocrinology. 34 (2022) 10 - p. , 2022
Link:
https://doi.org/10.1111/..
?
6
Spinocerebellar ataxia recessive type 7 due to novel compou..:
Holla, Vikram V.
;
Jha, Shreyasi
;
Pal, Pramod Kumar
...
Parkinsonism & Related Disorders. 94 (2022) - p. 117-119 , 2022
Link:
https://doi.org/10.1016/..
?
7
A Rare Case of Ophthalmoplegia with Ataxia in Genetically P..:
Gurram, Sandeep
;
Holla, Vikram V.
;
Sriram, Neeharika
...
Movement Disorders Clinical Practice. 10 (2022) 3 - p. 514-517 , 2022
Link:
https://doi.org/10.1002/..
?
8
Effective Visualization and Easy Tracking of Extracellular ..:
Mondal, Abir
;
Ashiq, K. A.
;
Phulpagar, Prashant
..
Biological Procedures Online. 21 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
9
Hydroxyapatite nanorods loaded with parathyroid hormone (PT..:
Dave, Jay R.
;
Dewle, Ankush M.
;
Mhaske, Suhas T.
...
Nanomedicine: Nanotechnology, Biology and Medicine. 15 (2019) 1 - p. 218-230 , 2019
Link:
https://doi.org/10.1016/..
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