- Knowledge, Attitudes and Perceptions of Genetic Testing Among Patients With Movement Disorders, Their Caregivers and Health Care Professionals
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Kamath SD, Holla VV, Kamble N, Mahale RR, Yadav R, Pal PK
- KMID: 2558080
- J Mov Disord.
- 2024 Jul;17(3):336-338.
- doi: 10.14802/jmd.24034
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- Genetically Proven Ataxia With Vitamin E Deficiency With Predominant Cervicobrachial Dystonic Presentation: A Case Report From India
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Holla VV, Gurram S, Kamath SD, Arunachal G, Kamble N, Yadav R, Pal PK
- KMID: 2554698
- J Mov Disord.
- 2024 Apr;17(2):220-222.
- doi: 10.14802/jmd.23227
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- 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
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Gunasekaran A, Holla VV, Phulpagar P, Kamath SD, Kamble N, Yadav R, Muthusamy B, Pal PK
- KMID: 2560199
- J Mov Disord.
- 2024 Oct;17(4):436-441.
- doi: 10.14802/jmd.24157
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... -
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