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Evaluation of Markers of Oxidative Stress, Antioxidant Function and Astrocytic Proliferation in the Striatum and Frontal Cortex of Parkinson’s Disease Brains

Neurochemical research, 2011-08, Vol.36 (8), p.1452-1463

2011

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Are current recommendations to diagnose orthostatic hypotension in Parkinson's disease satisfactory?

Movement disorders, 2009-09, Vol.24 (12), p.1747-1751

2009

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Prevalence and profile of Restless Legs Syndrome in Parkinson's disease and other neurodegenerative disorders: A case-control study

Parkinsonism & related disorders, 2013-04, Vol.19 (4), p.426-430

2013

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Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes

Journal of medical genetics, 2016-08, Vol.53 (8), p.559-566

2016

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Novel and reported variants in Parkinson's disease genes confer high disease burden among Indians

Parkinsonism & related disorders, 2020-09, Vol.78, p.46-52

2020

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Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism

Journal of medical genetics, 2016-07, Vol.53 (7), p.450-456

2016

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South Asian medical cohorts reveal strong founder effects and high rates of homozygosity

Nature communications, 2023-06, Vol.14 (1), p.3377-3377, Article 3377

2023

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Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's disease

Parkinsonism & related disorders, 2021-03, Vol.84, p.61-67

2021

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VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians

Neurobiology of aging, 2013-10, Vol.34 (10), p.2442.e1-2442.e3

2013

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Early Onset Parkinson's disease due to DJ1 mutations: An Indian study

Parkinsonism & related disorders, 2016-11, Vol.32, p.20-24

2016

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Parkinsonism Hyperpyrexia Syndrome following Deep Brain Stimulation

Parkinsonism & related disorders, 2015-10, Vol.21 (10), p.1284-1285

2015

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Secondary parkinsonism with Mumps infection

Parkinsonism & related disorders, 2015-10, Vol.21 (10), p.1288-1289

2015

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Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patients

Neuroscience letters, 2006-12, Vol.409 (2), p.83-88

2006

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Leads from xenobiotic metabolism genes for Parkinson’s disease among north Indians

Pharmacogenetics and genomics, 2011-12, Vol.21 (12), p.790-797

2011

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Role of polymorphisms in dopamine synthesis and metabolism genes and association of DBH haplotypes with Parkinsonʼs disease among North Indians

Pharmacogenetics and genomics, 2010-07, Vol.20 (7), p.435-441

2010

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Exome Sequencing Identifies a Novel Homozygous Missense ATP13A2 Mutation

Movement disorders clinical practice (Hoboken, N.J.), 2017-01, Vol.4 (1), p.132-135

2017

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Direct costs of managing Parkinson's disease in india: Concerns in a developing country

Movement disorders, 2006-10, Vol.21 (10), p.1755-1758

2006

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The "Indian turban trick": A novel sensory trick in blepharospasm

Movement disorders, 2007-07, Vol.22 (10), p.1516-1516

2007

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Embouchure dystonia and tremor in a professional windpipe "Nadaswaram" player

Movement disorders, 2007-10, Vol.22 (14), p.2133-2135

2007

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Parkin mutations in familial and sporadic Parkinson's disease among Indians

Parkinsonism & related disorders, 2006-05, Vol.12 (4), p.239-245

2006

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Elemental mercury poisoning probably causes cortical myoclonus

Movement disorders, 2007-10, Vol.22 (13), p.1964-1968

2007

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Biotin-Responsive Basal Ganglia Disease: A Treatable and Reversible Neurological Disorder of Childhood

Journal of child neurology, 2009-06, Vol.24 (6), p.750-752

2009

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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 countries

Movement disorders, 2005-12, Vol.20 (12), p.1550-1556

2005

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Urogenital symptoms in Parkinson's disease and multiple system atrophy-Parkinsonism: at onset and later

Journal of the Association of Physicians of India, 2010-02, Vol.58, p.86-90

2010

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Evaluation of Markers of Oxidative Stress, Antioxidant Function and Astrocytic Proliferation in the Striatum and Frontal Cortex of Parkinson’s Disease Brains

Are current recommendations to diagnose orthostatic hypotension in Parkinson's disease satisfactory?

Prevalence and profile of Restless Legs Syndrome in Parkinson's disease and other neurodegenerative disorders: A case-control study

Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes

Novel and reported variants in Parkinson's disease genes confer high disease burden among Indians

Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism

South Asian medical cohorts reveal strong founder effects and high rates of homozygosity

Compound heterozygous variants in Wiskott-Aldrich syndrome like (WASL) gene segregating in a family with early onset Parkinson's disease

VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians

Early Onset Parkinson's disease due to DJ1 mutations: An Indian study

Parkinsonism Hyperpyrexia Syndrome following Deep Brain Stimulation

Genome‐Wide Polygenic Score Predicts Large Number of High Risk Individuals in Monogenic Undiagnosed Young Onset Parkinson's Disease Patients from India

Secondary parkinsonism with Mumps infection

Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patients

Leads from xenobiotic metabolism genes for Parkinson’s disease among north Indians

Role of polymorphisms in dopamine synthesis and metabolism genes and association of DBH haplotypes with Parkinsonʼs disease among North Indians

Exome Sequencing Identifies a Novel Homozygous Missense ATP13A2 Mutation

Direct costs of managing Parkinson's disease in india: Concerns in a developing country

The "Indian turban trick": A novel sensory trick in blepharospasm

Embouchure dystonia and tremor in a professional windpipe "Nadaswaram" player

Parkin mutations in familial and sporadic Parkinson's disease among Indians

Elemental mercury poisoning probably causes cortical myoclonus

Biotin-Responsive Basal Ganglia Disease: A Treatable and Reversible Neurological Disorder of Childhood

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 countries

Urogenital symptoms in Parkinson's disease and multiple system atrophy-Parkinsonism: at onset and later

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