Babylakshmi Muthusamy
Overview
Explore the profile of Babylakshmi Muthusamy including associated specialties, affiliations and a list of published articles.
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60
Citations
2492
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Recent Articles
1.
Rath S, Holla V, Phulpagar P, Kamath S, Kamble N, Muthusamy B, et al.
Parkinsonism Relat Disord
. 2025 Feb;
132:107299.
PMID: 39904175
No abstract available.
2.
Holla V, Dhar D, Phulpagar P, Samim M, Kamath S, Kamble N, et al.
Can J Neurol Sci
. 2025 Jan;
1-30.
PMID: 39817443
No abstract available.
3.
Kumari R, Holla V, Sriram N, Kamble N, Asranna A, Saini J, et al.
Eur J Hum Genet
. 2025 Jan;
PMID: 39755877
Mitochondrial membrane protein-associated neurodegeneration (MPAN) is a rare neurodegenerative disorder characterized by spastic paraplegia, parkinsonism and psychiatric and/or behavioral symptoms caused by variants in gene encoding chromosome-19 open reading frame-12...
4.
Kamath S, Phulpagar P, Holla V, Kamble N, Yadav R, Muthusamy B, et al.
Parkinsonism Relat Disord
. 2024 Oct;
129:107157.
PMID: 39378566
Introduction: Indian Parkinson's Disease (PD) patients are severely underrepresented in terms of genetic studies and little is known about the frequency of variants and their impact on motor and nonmotor...
5.
Gunasekaran A, Holla V, Phulpagar P, Kamath S, Kamble N, Yadav R, et al.
J Mov Disord
. 2024 Sep;
17(4):436-441.
PMID: 39294919
Objective: Recessive variants in the PINK1 gene are known causes of early-onset Parkinson's disease (EOPD). To describe the clinical features and genetic profiles of patients with PINK1-related Parkinson's disease (PARK-PINK1)...
6.
Raval M, Holla V, Kamble N, Arunachal G, Muthusamy B, Saini J, et al.
J Mov Disord
. 2024 Aug;
17(4):430-435.
PMID: 39198013
Objective: In this study, we describe the clinical and investigative profiles of 7 cases of autosomal-recessive spastic ataxia of Charlevoix-Saguenay (ARSACS). Methods: We performed a retrospective chart review of genetically...
7.
Holla V, Samim M, Kumari R, Dhar D, Phulpagar P, Sriram N, et al.
Tremor Other Hyperkinet Mov (N Y)
. 2024 Aug;
14:41.
PMID: 39184971
Background: Despite being the second most common type of neurodegeneration with brain iron accumulation, there is limited literature on -associated neurodegeneration (PLAN) within the Asian ethnicity, particularly in the Indian...
8.
Kamble N, Holla V, Katragadda P, Muthusamy B, Pal P
Mov Disord Clin Pract
. 2024 Jun;
11(10):1295-1297.
PMID: 38934208
No abstract available.
9.
Garg D, Holla V, Ganguly J, Rajan R, Saini A, Agarwal A, et al.
Parkinsonism Relat Disord
. 2024 May;
124:107012.
PMID: 38762926
Background: Variants in the TUBB4A gene are associated with dystonia (DYT-TUBB4A), Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum (H-ABC) and spastic paraplegia. Phenotypes intermediate to these three broad...
10.
Saini A, Holla V, Puthanveedu D, Mehta S, Elavarasi A, Pillai K, et al.
Mov Disord
. 2024 Mar;
39(5):920-923.
PMID: 38506547
No abstract available.