Doniparthi V Seshagiri
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Explore the profile of Doniparthi V Seshagiri including associated specialties, affiliations and a list of published articles.
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20
Citations
23
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Recent Articles
1.
Nagappa M, Mondal S, Rajeevan S, Pradeepkumar B, Chalasani V, Dey S, et al.
J Neuroimmunol
. 2025 Feb;
401:578556.
PMID: 39987753
Objectives: Inflammasome plays a significant role in inflammatory responses. The role of inflammasome and its interactions with oxidative stress markers has not been examined in inflammatory neuropathies like Guillain-Barré syndrome...
2.
Sharma S, Mahadevan A, Narayanappa G, Debnath M, Govindaraj P, Shivaram S, et al.
J Neurogenet
. 2024 Jul;
38(2):27-34.
PMID: 38975939
Tropical ataxic neuropathy (TAN) is characterised by ataxic polyneuropathy, degeneration of the posterior columns and pyramidal tracts, optic atrophy, and sensorineural hearing loss. It has been attributed to nutritional/toxic etiologies,...
3.
Viswanathan L, Nagappa M, Seshagiri D, Bharath R, Sinha S
Ann Indian Acad Neurol
. 2024 Mar;
27(1):80-81.
PMID: 38495248
No abstract available.
4.
Viswanathan L, Seshagiri D, Rao S, Neerupaka V, Kulanthaivelu K, Nagappa M, et al.
Ann Indian Acad Neurol
. 2024 Jan;
26(6):1006-1007.
PMID: 38229622
No abstract available.
5.
Viswanathan L, Alapati S, Nagappa M, Mundlamuri R, Kenchaiah R, Asranna A, et al.
J Neurosci Rural Pract
. 2023 Dec;
14(4):603-609.
PMID: 38059254
Objectives: Nearly 40% of pediatric epilepsies have a genetic basis. There is significant phenotypic and genotypic heterogeneity, especially in epilepsy syndromes caused by sodium channelopathies. Sodium channel subunit 1A (SCN1A)-related...
6.
Reddy T, Seshagiri D, Reddy H, Patwardhan A, Joshi T, Shukla D, et al.
Ann Indian Acad Neurol
. 2023 Nov;
26(5):733-741.
PMID: 38022466
Background And Purpose: Cerebral venous thrombosis (CVT) presenting as vision loss is uncommon. Raised intracranial tension in CVT is proposed as one of the mechanisms (13.2%). There are still unknown...
7.
Nagappa M, Sharma S, Govindaraj P, Chickabasaviah Y, Siram R, Shroti A, et al.
Neurol India
. 2023 Nov;
71(5):940-945.
PMID: 37929431
Background: SH3TC2 variations lead to demyelinating recessive Charcot-Marie-Tooth (CMT) disease, which is commonly associated with early-onset scoliosis and cranial neuropathy. Data from Indian ethnicity is limited. Objective: We aim to...
8.
Huddar A, Seshagiri D, Nandeesh B, Kulanthaivelu K, Gorantla P, Kenchaiah R
Can J Neurol Sci
. 2023 May;
51(3):455-457.
PMID: 37203454
No abstract available.
9.
Shivaram S, Nagappa M, Varghese N, Seshagiri D, Duble S, Siddappa S, et al.
Neurol India
. 2022 Nov;
70(5):1931-1941.
PMID: 36352590
Background: Myasthenia gravis (MG) is an immune-mediated disorder of the neuromuscular junction. About 10% are refractory to immunosuppressive therapy. Aims: To analyze the response of patients with generalized MG to...
10.
Viswanathan L, Nagappa M, Seshagiri D, Kulanthaivelu K, Nagarathna S, Sinha S
Ann Indian Acad Neurol
. 2022 Aug;
25(3):489-490.
PMID: 35936637
No abstract available.