Sniya Valsa Sudhakar
Overview
Explore the profile of Sniya Valsa Sudhakar including associated specialties, affiliations and a list of published articles.
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29
Citations
99
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Recent Articles
1.
Avsenik J, Perkovic Benedik M, Benedik M, Rogac M, Biswas A, Sudhakar S, et al.
Neuropediatrics
. 2024 Dec;
PMID: 39740770
We describe a set of monozygotic twins with Glutamate Ionotropic Receptor N-methyl-D-aspartate Type Subunit 2B-related neurodevelopmental disorder (GRIN2B-ND) who exhibited distinct clinical and imaging characteristics due to a de novo...
2.
Pastore L, Sudhakar S, Mankad K, De Vita E, Biswas A, Tisdall M, et al.
Neuroradiology
. 2024 Oct;
PMID: 39441414
Background: Malformations of cortical development (MCDs) in children with focal epilepsy pose significant diagnostic challenges, and a precise radiological diagnosis is crucial for surgical planning. New MRI sequences and the...
3.
Pastore L, De Vita E, Sudhakar S, Lobel U, Mankad K, Biswas A, et al.
Transl Pediatr
. 2024 Oct;
13(9):1617-1633.
PMID: 39399717
Background And Objective: Epilepsy affects approximately 50 million people worldwide, with 30-40% of patients not responding to medication, necessitating alternative therapies such as surgical intervention. However, the accurate localization of...
4.
Kotambail A, Selvam P, Muthusamy K, Thomas M, Sudhakar S, Ghati C, et al.
Eur J Hum Genet
. 2022 Oct;
31(1):73-80.
PMID: 36202930
Mild/juvenile Canavan disease (M/JCD) is less frequently reported in the literature and little is known about its pathogenetic mechanisms. We report a comprehensive investigation into the pathogenetic mechanism of a...
5.
Yoganathan S, Srinivasaraghavan R, Chandran M, Kratz L, Koshy B, Sudhakar S, et al.
Ann Indian Acad Neurol
. 2021 Jul;
24(2):261-264.
PMID: 34220079
No abstract available.
6.
Biswas A, Malhotra M, Mankad K, Carney O, DArco F, Muthusamy K, et al.
Transl Pediatr
. 2021 May;
10(4):1201-1230.
PMID: 34012862
Inborn errors of metabolism (IEM) although individually rare, together constitute a significant proportion of childhood neurological disorders. Majority of these disorders occur due to deficiency of an enzyme in a...
7.
Yoganathan S, Arunachal G, Kratz L, Varman M, Sudhakar S, Oommen S, et al.
Ann Indian Acad Neurol
. 2020 Jul;
23(3):419-421.
PMID: 32606564
No abstract available.
8.
Yoganathan S, Arunachal G, Kratz L, Varman M, Thomas M, Sudhakar S, et al.
Ann Indian Acad Neurol
. 2020 Feb;
23(1):113-117.
PMID: 32055132
Succinic semialdehyde dehydrogenase (SSADH) deficiency is an autosomal recessive disorder of gamma-aminobutyric acid metabolism. Children with SSADH deficiency usually manifest with developmental delay, behavioral symptoms, language dysfunction, seizures, hypotonia, extrapyramidal...
9.
Yoganathan S, Mariappan R, Sudhakar S, Mani S, Mathew V, Thomas M, et al.
Neuropediatrics
. 2019 Sep;
50(6):395-399.
PMID: 31529425
Spontaneous intracranial hypotension (SIH) is an under-diagnosed cause of headache in children and adolescents. SIH results from cerebrospinal fluid (CSF) leak due to breach in the dura mater and the...
10.
Muthusamy K, Sudhakar S, Thomas M, Yoganathan S, Christudass C, Chandran M, et al.
J Clin Imaging Sci
. 2019 Aug;
9:25.
PMID: 31448176
Context: Krabbe disease shows considerable heterogeneity in clinical features and disease progression. Imaging phenotypes are equally heterogeneous but show distinct age-based patterns. It is important for radiologists to be familiar...