Sneha D. Kamath
Bengaluru, KA, India
Last Updated: 09/26/2026
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Found 21 publications
Surgicogenomics in Genetic Parkinson's Disease: A Single-Center Experience From a Tertiary Care Center.
Journal: Journal of movement disorders
Published: April 13, 2025
PRKN-Gene-Related Parkinsonism: An Experience from a Tertiary Centre and Literature Review of Asian Cohort.
Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
Published: January 16, 2025
Infantile-onset choreo-dystonia due to a novel homozygous truncating HPCA variant: A first report from India.
Journal: Parkinsonism & related disorders
Published: November 24, 2024
Dopamine Dysregulation Syndrome Mimicking Ultradian Cycling Bipolar Disorder in Parkinson's Disease.
Dopamine Dysregulation Syndrome Mimicking Ultradian Cycling Bipolar Disorder in Parkinson's Disease.
Journal: Indian journal of psychological medicine
Published: November 15, 2024
Clinico-genetic analysis of patients with LRRK2-related Parkinson's disease from a referral centre in India.
Journal: Parkinsonism & related disorders
Published: September 11, 2024
Clinico-Genetic Profiles of Seven Patients With PINK1-Related Parkinson's Disease: A Case Series From a Tertiary Care Centre in India and a Review of the Literature.
Journal: Journal of movement disorders
Published: July 08, 2024
Knowledge, Attitudes and Perceptions of Genetic Testing Among Patients With Movement Disorders, Their Caregivers and Health Care Professionals.
Journal: Journal of movement disorders
Published: February 10, 2024
Genetic architecture of a single cohort of 230 Indian Parkinson's Disease patients.
Journal: Parkinsonism & related disorders
Published: January 08, 2024
Genetically Proven Ataxia With Vitamin E Deficiency With Predominant Cervicobrachial Dystonic Presentation: A Case Report From India.
Journal: Journal of movement disorders
Published: November 05, 2023
Levodopa-Responsive Isolated Generalized Dystonia in a Patient with Alpha-Mannosidosis Due to a Novel Homozygous MAN2B1 Missense Variant-A Novel Association.
Journal: Movement disorders clinical practice
Published: November 04, 2023
Clinicogenetic Characterization of Patients with PD and Heterozygous GBA1 Variants in an Indian Cohort.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: October 23, 2023
Genetic literacy and attitude towards genetic testing in patients with Parkinson's disease and their caregivers: A review of literature.
Journal: Parkinsonism & related disorders
Published: May 23, 2023
Last Updated: 09/26/2026