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Pallidal Deep Brain Stimulation for Monogenic Dystonia: The Effect of Gene on Outcome

Frontiers in neurology, 2021-01, Vol.11, p.630391-630391

2021

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Harnessing Transcriptomics to Decipher Dystonia Pathogenesis

Movement disorders, 2022-05, Vol.37 (5), p.891-891

2022

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Monogenic Parkinson's Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing

Genes, 2022-03, Vol.13 (3), p.471

2022

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Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia

Current neurology and neuroscience reports, 2021-02, Vol.21 (4), p.15-15, Article 15

2021

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Targeting glucocerebrosidase: Reduced enzymatic activity and Parkinson's disease

Movement disorders, 2015-10, Vol.30 (12), p.1620-1620

Raj Kumar, Kishore

2015

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Editorial: Genetics of Paroxysmal Movement Disorders

Frontiers in neurology, 2021-09, Vol.12, p.752000-752000

2021

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Age Cutoff for Early‐Onset Parkinson's Disease: Recommendations from the International Parkinson and Movement Disorder Society Task Force on Early Onset Parkinson's Disease

Movement disorders clinical practice (Hoboken, N.J.), 2022-10, Vol.9 (7), p.869-878

2022

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Mitochondrial Function in Hereditary Spastic Paraplegia: Deficits in SPG7 but Not SPAST Patient-Derived Stem Cells

Frontiers in neuroscience, 2020-08, Vol.14, p.820-820

2020

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Unmet Need in Early-Onset Parkinson’s Disease: Deep Brain Stimulation and Pregnancy

Journal of Parkinson's disease, 2024-09, Vol.14 (6), p.1277-1282

2024

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ADCY5 identified as a novel cause of benign hereditary chorea

Movement disorders, 2015-11, Vol.30 (13), p.1726-1726

2015

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Dystonia Responsive to Dopamine: POLG Mutations Should Be Considered If Sensory Neuropathy Is Present

Journal Of Movement Disorders, 2021, 14(2), , pp.157-160

2021

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Screening study of TUBB4A in isolated dystonia

Parkinsonism & related disorders, 2017-08, Vol.41, p.118-120

2017

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SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies

Movement disorders, 2024-03, Vol.39 (3), p.457-461

2024

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Reply to: Comment to “SCA4 Unravelled After More than 25Years Using Advanced Genomic Technologies”

Movement disorders, 2024-06, Vol.39 (6), p.1078-1078

2024

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Reply to: Comment to “SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies”

Movement disorders, 2024-06, Vol.39 (6), p.1078-1078

2024

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SCA4 Unravelled After More than 25Years Using Advanced Genomic Technologies

Movement disorders, 2024-03, Vol.39 (3), p.457-461

2024

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Reply to: Neurometabolic causes of dystonia: Sepiapterin reductase-deficient dopamine- and serotonin-responsive dystonia-plus syndrome

Journal of the neurological sciences, 2021-06, Vol.425, p.117469-117469, Article 117469

2021

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Targeting glucocerebrosidase: Reduced enzymatic activity and Parkinson's disease: Hot Topics

Movement disorders, 2015-10, Vol.30 (12), p.1620-1620

Raj Kumar, Kishore

2015

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Mutations in Hippocalcin and Autosomal Recessive Dystonia: A Role for Perturbed Calcium Signaling?

Movement disorders, 2015-06, Vol.30 (7), p.911-911

Kumar, Kishore Raj

2015

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Mutations in H ippocalcin and A utosomal R ecessive D ystonia: A R ole for P erturbed C alcium S ignaling?

Movement disorders, 2015-06, Vol.30 (7), p.911-911

Kumar, Kishore Raj

2015

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Clinical characteristics and diagnostic clues to Neurometabolic causes of dystonia

Journal of the neurological sciences, 2020-12, Vol.419, p.117167-117167, Article 117167

2020

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Clinical phenotyping is key to differentiating RFC1-associated neuropathy from immune-mediated neuropathy

Brain communications, 2024, Vol.6 (4), p.fcae212

2024

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Facioscapulohumeral muscular dystrophy type 2: an update on the clinical, genetic, and molecular findings

Neuromuscular disorders : NMD, 2021-11, Vol.31 (11), p.1101-1112

2021

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An Update on the Adult-Onset Hereditary Cerebellar Ataxias: Novel Genetic Causes and New Diagnostic Approaches

Cerebellum (London, England), 2024-05

2024

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Mitigation of Arsenic Concentration in Green Leafy Vegetables viz. Cabbage (Brassica oleracea var. capitata), Spinach (Spinacia oleracea), Cauliflower (Brassica oleracea var. botrytis) through Different Biochemical Washing Techniques

Current Journal of Applied Science and Technology, 2020-04, p.53-58

2020

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Pallidal Deep Brain Stimulation for Monogenic Dystonia: The Effect of Gene on Outcome

Harnessing Transcriptomics to Decipher Dystonia Pathogenesis

Monogenic Parkinson's Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing

Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia

Targeting glucocerebrosidase: Reduced enzymatic activity and Parkinson's disease

Editorial: Genetics of Paroxysmal Movement Disorders

Age Cutoff for Early‐Onset Parkinson's Disease: Recommendations from the International Parkinson and Movement Disorder Society Task Force on Early Onset Parkinson's Disease

Mitochondrial Function in Hereditary Spastic Paraplegia: Deficits in SPG7 but Not SPAST Patient-Derived Stem Cells

Unmet Need in Early-Onset Parkinson’s Disease: Deep Brain Stimulation and Pregnancy

ADCY5 identified as a novel cause of benign hereditary chorea

Dystonia Responsive to Dopamine: POLG Mutations Should Be Considered If Sensory Neuropathy Is Present

Screening study of TUBB4A in isolated dystonia

SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies

Reply to: Comment to “SCA4 Unravelled After More than 25Years Using Advanced Genomic Technologies”

Reply to: Comment to “SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies”

SCA4 Unravelled After More than 25Years Using Advanced Genomic Technologies

Reply to: Neurometabolic causes of dystonia: Sepiapterin reductase-deficient dopamine- and serotonin-responsive dystonia-plus syndrome

Targeting glucocerebrosidase: Reduced enzymatic activity and Parkinson's disease: Hot Topics

Mutations in Hippocalcin and Autosomal Recessive Dystonia: A Role for Perturbed Calcium Signaling?

Mutations in H ippocalcin and A utosomal R ecessive D ystonia: A R ole for P erturbed C alcium S ignaling?

Clinical characteristics and diagnostic clues to Neurometabolic causes of dystonia

Clinical phenotyping is key to differentiating RFC1-associated neuropathy from immune-mediated neuropathy

Facioscapulohumeral muscular dystrophy type 2: an update on the clinical, genetic, and molecular findings

An Update on the Adult-Onset Hereditary Cerebellar Ataxias: Novel Genetic Causes and New Diagnostic Approaches

Mitigation of Arsenic Concentration in Green Leafy Vegetables viz. Cabbage (Brassica oleracea var. capitata), Spinach (Spinacia oleracea), Cauliflower (Brassica oleracea var. botrytis) through Different Biochemical Washing Techniques

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