Mahale R - Search Results

1

CSF1R Related Leukoencephalopathy - Rare Childhood Presentation of An Autosomal Dominant Microgliopathy!

Sriram N, Padmanabha H, Chandra SR, Mahale R, Nandeesh B, Bhat MD, Christopher R, Gupta M, Udupi GA, Mailankody P, Mathuranath PS. Sriram N, et al. Among authors: mahale r. Ann Indian Acad Neurol. 2022 Mar-Apr;25(2):311-314. doi: 10.4103/aian.aian_418_21. Epub 2021 Nov 10. Ann Indian Acad Neurol. 2022. PMID: 35693676 Free PMC article. No abstract available.

2

Spinocerebellar Ataxia Type 7 Sans Retinal Degeneration: A Phenotypic Variability.

Mahale RR, Mehta A, Miryala A, Srinivasa R. Mahale RR, et al. Ann Indian Acad Neurol. 2017 Oct-Dec;20(4):438-439. doi: 10.4103/aian.AIAN_236_17. Ann Indian Acad Neurol. 2017. PMID: 29184358 Free PMC article. No abstract available.

3

Isolated mitochondrial myopathy due to m.3243A > G mutation in MT-TL1 gene.

Mahale RR, Gautham J, Mailankody P, Padmanabha H, Mathuranath PS. Mahale RR, et al. Acta Neurol Belg. 2022 Aug;122(4):1115-1116. doi: 10.1007/s13760-021-01598-1. Epub 2021 Jan 23. Acta Neurol Belg. 2022. PMID: 33484420 No abstract available.

4

A Rare Case of Ataxia-Telangiectasia-Like Disorder With MRE11 Mutation.

Mahale RR, Reddy N, Mathuranth P, Mailankody P, Padmanabha H, Retnaswami CS. Mahale RR, et al. J Pediatr Neurosci. 2020 Jul-Sep;15(3):283-285. doi: 10.4103/jpn.JPN_152_19. Epub 2020 Nov 6. J Pediatr Neurosci. 2020. PMID: 33531947 Free PMC article.

5

Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK): a cause of progressive myoclonic epilepsy.

Mahale RR, Tiwari R, Arunachal G, Padmanabha H, Mailankody P. Mahale RR, et al. Acta Neurol Belg. 2022 Jun;122(3):801-803. doi: 10.1007/s13760-021-01645-x. Epub 2021 Mar 16. Acta Neurol Belg. 2022. PMID: 33725338 No abstract available.

6

DNAJC6 mutation causing cranial-onset dystonia with tremor dominant levodopa non-responsive parkinsonism: A novel phenotype.

Ray S, Padmanabha H, Mahale R, Mailankody P, Arunachal G. Ray S, et al. Among authors: mahale r. Parkinsonism Relat Disord. 2021 Aug;89:1-3. doi: 10.1016/j.parkreldis.2021.06.013. Epub 2021 Jun 23. Parkinsonism Relat Disord. 2021. PMID: 34175496

7

Stroke-like episodes with cerebellar ataxia as presenting manifestation of adult-onset anti-N-methyl D-aspartate receptor encephalitis: an unusual presentation.

Mahale R, Farsana MK, Mahadevan A, Mukherjee J, Lakshmi V, Sandeep M, Padmanabha H, Mailankody P, Pavagada M. Mahale R, et al. Acta Neurol Belg. 2021 Aug;121(4):1093-1095. doi: 10.1007/s13760-021-01735-w. Epub 2021 Jul 3. Acta Neurol Belg. 2021. PMID: 34216377 No abstract available.

8

Postpartum Optic Neuropathy: Think of Myelin Oligodendrocyte Glycoprotein Immunoglobulin G-Associated Optic Neuritis - Report of Two Cases.

Mahale RR, Varghese N, Mailankody P, Padmanabha H, Mathuranath PS. Mahale RR, et al. Ann Indian Acad Neurol. 2021 Mar-Apr;24(2):282-284. doi: 10.4103/aian.AIAN_317_20. Epub 2020 Jul 22. Ann Indian Acad Neurol. 2021. PMID: 34220089 Free PMC article. No abstract available.

9

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. 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.

10

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. 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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