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Page 1
Parkinsonism, Olivary Hypertrophy and Cerebellar Atrophy with TTC19 Gene Mutation.
Mahale RR, Arunachal G, Gautam J, Dutta D, Kovoor J, Mailankody P, Padmanabha H, Mathuranath PS. Mahale RR, et al. Among authors: mailankody p. 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.
Episodic neurological dysfunction in hereditary peripheral neuropathy.
Kulkarni GB, Mailankody P, Isnwara PP, Prasad C, Mustare V. Kulkarni GB, et al. Among authors: mailankody p. Ann Indian Acad Neurol. 2015 Jan-Mar;18(1):111-4. doi: 10.4103/0972-2327.144314. Ann Indian Acad Neurol. 2015. PMID: 25745327 Free PMC article.
'All that waddles is not dystrophy'.
Padmanabha H, Chandra SR, Jagadish A, Arshad F, Mailankody P, Kasinathan A. Padmanabha H, et al. Among authors: mailankody p. J Paediatr Child Health. 2020 Feb;56(2):339-340. doi: 10.1111/jpc.14783. J Paediatr Child Health. 2020. PMID: 32045122 No abstract available.
Macula as a Window to Diagnosis.
Sangeeth TA, Padmanabha H, Santhosh-Kumar R, Chandra SR, Dhar D, Mailankody P, Santosh V. Sangeeth TA, et al. Among authors: mailankody p. J Pediatr. 2021 Apr;231:284-285. doi: 10.1016/j.jpeds.2020.12.017. Epub 2020 Dec 15. J Pediatr. 2021. PMID: 33333116 No abstract available.
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. Among authors: mailankody p. 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.
74 results