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Page 1
Juvenile PLA2G6-Parkinsonism Due to Indian 'Asian' p.R741Q Mutation, and Response to STN DBS.
Mov Disord. 2022 Mar;37(3):657-658. doi: 10.1002/mds.28950. Epub 2022 Feb 3.
Mov Disord. 2022.
PMID: 35113461
No abstract available.
Ictal kissing: Review of literature and report of 5 cases.
Ravat P, Jain N, Thakkar M, Kalika M, Ravat S.
Ravat P, et al.
Epileptic Disord. 2024 Apr 1. doi: 10.1002/epd2.20208. Online ahead of print.
Epileptic Disord. 2024.
PMID: 38558114
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Challenges for low middle-income people with epilepsy during the COVID-19 pandemic: Lessons learnt, call for action.
Shah U, Rajeshree S, Ravat P, Kalika M, Mehta S, Sapre A, Ravat SH.
Shah U, et al. Among authors: ravat p.
Epilepsia Open. 2022 Dec;7(4):665-673. doi: 10.1002/epi4.12646. Epub 2022 Sep 1.
Epilepsia Open. 2022.
PMID: 36005396
Free PMC article.
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Progressive Myoclonic Epilepsy'-like presentation of Cerebrotendinous Xanthomatosis in an Indian Family with A Novel C.646+1G>A Splice Site Mutation.
Desai KM, Kumar P, Ravat PS, Ravat SH, Jain N, Agrawal S, Ansari R.
Desai KM, et al. Among authors: ravat ps.
Epilepsy Behav Rep. 2020 Nov 16;15:100401. doi: 10.1016/j.ebr.2020.100401. eCollection 2021.
Epilepsy Behav Rep. 2020.
PMID: 33458645
Free PMC article.
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