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2020 | 1 |
2021 | 4 |
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Page 1
Parkinsonism, Olivary Hypertrophy and Cerebellar Atrophy with TTC19 Gene Mutation.
Ann Indian Acad Neurol. 2021 Nov-Dec;24(6):991-993. doi: 10.4103/aian.AIAN_625_20. Epub 2021 Apr 16.
Ann Indian Acad Neurol. 2021.
PMID: 35359541
Free PMC article.
No abstract available.
Autosomal Dominant Cerebral Small Vessel Disease in HTRA1 Gene Mutation.
Mahale RR, Agarwal A, Gautam J, Varghese N, Kovoor J, Mailankody P, Padmanabha H, Pavagada M.
Mahale RR, et al. Among authors: kovoor j.
Ann Indian Acad Neurol. 2021 Mar-Apr;24(2):297-299. doi: 10.4103/aian.AIAN_381_20. Epub 2020 Oct 7.
Ann Indian Acad Neurol. 2021.
PMID: 34220097
Free PMC article.
No abstract available.
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Upbeat Nystagmus in Late Onset Cerebellar Ataxia: Think of Anti-Glutamate Decarboxylase 65 Antibody-Associated Cerebellar Ataxia.
Mahale RR, Dutta D, Kovoor J, Mailankody P, Padmanabha H, Mathuranath PS.
Mahale RR, et al. Among authors: kovoor j.
Ann Indian Acad Neurol. 2021 May-Jun;24(3):441-443. doi: 10.4103/aian.AIAN_470_20. Epub 2021 Feb 10.
Ann Indian Acad Neurol. 2021.
PMID: 34447019
Free PMC article.
No abstract available.
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Rapidly Progressive Spastic Paraplegia Due to Hyperhomocysteinemia in Child with MTHFR Gene Mutation and Mitochondrial Complex I Deficiency: A Rare Association.
Mahale RR, Gautam J, Arunachal G, Alappati S, Varghese N, Kovoor J, Mailankody P, Padmanabha H, Pavagada M.
Mahale RR, et al. Among authors: kovoor j.
J Pediatr Neurosci. 2021 Apr-Jun;16(2):153-155. doi: 10.4103/jpn.JPN_96_20. Epub 2021 Jul 12.
J Pediatr Neurosci. 2021.
PMID: 35018185
Free PMC article.
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