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Neurology India|November 23, 2006
Perspectives towards predictive testing in Huntington diseaseS M Nagaraja, Sanjeev Jain, Uday B MuthaneParkinsonism & Related Disorders|January 22, 2013
Prevalence and profile of Restless Legs Syndrome in Parkinson's disease and other neurodegenerative disorders: a case-control studyKetaki Bhalsing, K Suresh, Uday B Muthane, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 29, 2006
Direct costs of managing Parkinson's disease in India: concerns in a developing countryMona Ragothaman, Shyla T Govindappa, Rohini Rattihalli, et al.Journal of Medical Genetics|February 12, 2016
Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile ParkinsonismSumedha Sudhaman, Kameshwar Prasad, Madhuri Behari, et al.Journal of Child Neurology|June 4, 2009
Biotin-responsive basal ganglia disease: a treatable and reversible neurological disorder of childhoodP S Bindu, M L Noone, A Nalini, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 4, 2005
Validity of a modified Parkinson's disease screening questionnaire in India: effects of literacy of participants and medical training of screeners and implications for screening efforts in developing countriesNagaraja Sarangmath, Rohini Rattihalli, Mona Ragothaman, et al.Neurobiology of Aging|June 4, 2013
VPS35 and EIF4G1 mutations are rare in Parkinson's disease among IndiansSumedha Sudhaman, Madhuri Behari, Shyla T Govindappa, et al.Journal of Medical Genetics|April 9, 2016
Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypesSumedha Sudhaman, Uday B Muthane, Madhuri Behari, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 30, 2009
Are current recommendations to diagnose orthostatic hypotension in Parkinson's disease satisfactory?Jenny Jamnadas-Khoda, Suma Koshy, Christopher J Mathias, et al.Parkinsonism & Related Disorders|September 5, 2016
Early Onset Parkinson's disease due to DJ1 mutations: An Indian studyMasoom M Abbas, Shyla T Govindappa, Sumedha Sudhaman, et al.Pageof 3