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The Journal of the Association of Physicians of India|July 15, 2011
Role of dysautonomic symptoms in distinguishing Parkinson's disease (PD) from multiple system atrophy (MSA-P) within a year of developing motor symptomsMona Ragothaman, Pazhayannur V Swaminath, Nagaraja Sarangmath, et al.
Pharmacogenetics and Genomics|October 22, 2011
Leads from xenobiotic metabolism genes for Parkinson's disease among north IndiansSohan Punia, Mitashree Das, Madhuri Behari, et al.
The Journal of the Association of Physicians of India|July 27, 2010
Urogenital symptoms in Parkinson's disease and multiple system atrophy-Parkinsonism: at onset and laterPazhayannur V Swaminath, Mona Ragothaman, Suma Koshy, et al.
Parkinsonism & Related Disorders|July 25, 2020
Novel and reported variants in Parkinson's disease genes confer high disease burden among IndiansSumeet Kumar, Navneesh Yadav, Sanjay Pandey, et al.
Parkinsonism & Related Disorders|February 11, 2021
Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's diseaseSumeet Kumar, Masoom M Abbas, Shyla T Govindappa, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2006
Melanized nigral neuronal numbers in Nigerian and British individualsUday B Muthane, Yasha T Chickabasaviah, Jasmine Henderson, et al.
Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|April 12, 2008
Primary cardiac cytotoxic T-cell lymphoma presenting with neurological deficits: a case reportAkkihebbal N Deepti, Mohan L Noone, Anita Mahadevan, et al.
Neurochemical Research|April 13, 2011
Evaluation of markers of oxidative stress, antioxidant function and astrocytic proliferation in the striatum and frontal cortex of Parkinson's disease brainsRajeswara Babu Mythri, C Venkateshappa, G Harish, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 22, 2007
Elemental mercury poisoning probably causes cortical myoclonusMona Ragothaman, Girish Kulkarni, Valappil V Ashraf, et al.
Neuroscience Letters|October 21, 2006
Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patientsSohan Punia, Madhuri Behari, Shyla T Govindappa, et al.
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