Articles with public access mandates - Vikram V HollaLearn more
Not available anywhere: 11
A splice altering variant in NDRG1 gene causes Charcot-Marie-Tooth disease, type 4D
P Pravinbabu, VV Holla, P Phulpagar, N Kamble, M Netravathi, R Yadav, ...
Neurological Sciences 43 (7), 4463-4472, 2022
Mandates: Department of Science & Technology, India
Clinical, imaging and genetic profile of twenty-four patients with pantothenate kinase-associated neurodegeneration (PKAN)-A single centre study from India
N Sriram, VV Holla, R Kumari, N Kamble, J Saini, R Mahale, M Netravathi, ...
Parkinsonism & Related Disorders 111, 105409, 2023
Mandates: Council of Scientific and Industrial Research, India
Deep brain stimulation in dopa-responsive parkinsonism–Look out for red flags
VV Holla, BK Surisetti, S Prasad, K Neeraja, N Kamble, B Muthusamy, ...
Parkinsonism & Related Disorders 110, 2023
Mandates: Department of Biotechnology, India
Spinocerebellar ataxia recessive type 7 due to novel compound heterozygous variants in TPP1: First report from India
VV Holla, S Jha, PK Pal, R Yadav, P Phulpagar, B Muthusamy, ...
Parkinsonism & Related Disorders 94, 117-119, 2022
Mandates: Department of Biotechnology, India
Whole exome sequencing and transcript analysis discover a novel pathogenic splice site mutation in DCAF17 gene underlying Woodhouse‐Sakati syndrome.
R Kumari, VV Holla, P Phulpagar, N Sriram, AG Hegde, S Vengalil, ...
Journal of Neuroendocrinology 34 (10), e13185, 2022
Mandates: Council of Scientific and Industrial Research, India, Wellcome Trust/DBT …
Dysregulated Cerebrospinal Fluid Proteome of Spinocerebellar Ataxia Type 2 and its Clinical Implications
A Stezin, GJ Sathe, A Gajbhiye, S Bharadwaj, V Ghose, A Bellad, PK Malo, ...
Movement Disorders, 2024
Mandates: Wellcome Trust, Michael J Fox Foundation
Movement Disorders in Patients with Subacute Sclerosing Panencephalitis: A Systematic Review
D Garg, S Patel, CS Sankhla, VV Holla, V Paramanandam, PL Kukkle, ...
Movement Disorders Clinical Practice, 2024
Mandates: Michael J Fox Foundation
Novel PANK2 Variant in Asian Indians with Atypical Pantothenate Kinase Associated Neurodegeneration
A Saini, VV Holla, D Kalikavil Puthanveedu, S Mehta, A Elavarasi, ...
Movement Disorders, 2024
Mandates: Department of Biotechnology, India
Clinicogenetic Characterization of Patients with PD and Heterozygous GBA1 Variants in an Indian Cohort
SD Kamath, VV Holla, P Phulpagar, N Kamble, R Yadav, B Muthusamy, ...
Movement Disorders 39 (3), 628-630, 2024
Mandates: Department of Biotechnology, India
Novel CWF19L1 mutations in patients with spinocerebellar ataxia, autosomal recessive 17
P Phulpagar, VV Holla, D Tomar, N Kamble, R Yadav, PK Pal, ...
Journal of Human Genetics 68 (12), 859-866, 2023
Mandates: Department of Science & Technology, India
Loss of function variants in L2HGDH gene causing l-2-hydroxyglutaric aciduria
A Bellad, VV Holla, R Kumari, N Kamble, R Yadav, A Pandey, PK Pal, ...
Acta Neurologica Belgica 123 (6), 2315-2323, 2023
Mandates: Council of Scientific and Industrial Research, India, Department of Science …
Available somewhere: 10
COVID-19 vaccine associated demyelination & its association with MOG antibody
M Netravathi, K Dhamija, M Gupta, A Tamborska, A Nalini, VV Holla, ...
Multiple sclerosis and related disorders 60, 103739, 2022
Mandates: UK Medical Research Council, National Institute for Health Research, UK
PLA2G6-associated neurodegeneration in four different populations-case series and literature review
RH Al-Shaikh, LM Milanowski, VV Holla, K Kurihara, R Yadav, N Kamble, ...
Parkinsonism & Related Disorders 101, 66-74, 2022
Mandates: US Department of Defense, US National Institutes of Health, Michael J Fox …
Astrocytes Differentiated from LRRK2-I1371V Parkinson’s-Disease-Induced Pluripotent Stem Cells Exhibit Similar Yield but Cell-Intrinsic Dysfunction in Glutamate Uptake and …
R Banerjee, A Raj, C Potdar, P Kumar Pal, R Yadav, N Kamble, V Holla, ...
Cells 12 (12), 1592, 2023
Mandates: US National Institutes of Health, Department of Biotechnology, India …
KMT2B-related dystonia in Indian patients with literature review and emphasis on Asian cohort
D Dhar, VV Holla, R Kumari, N Sriram, J Saini, R Yadav, A Pandey, ...
Journal of Movement Disorders 16 (3), 285, 2023
Mandates: US National Institutes of Health
A rare case of ophthalmoplegia with ataxia in genetically proven abetalipoproteinemia
S Gurram, VV Holla, N Sriram, P Phulpagar, S Jha, P Sharma, ...
Movement Disorders Clinical Practice 10 (3), 514, 2023
Mandates: Department of Science & Technology, India
Expanding the phenotypic and genotypic spectrum of DYT-TUBB4A with seven patients from India
D Garg, VV Holla, J Ganguly, R Rajan, A Saini, A Agarwal, ...
Parkinsonism & Related Disorders 124, 107012, 2024
Mandates: Michael J Fox Foundation
Sunglasses as an alternative alleviating agent for secondary Meige’s syndrome: Electrophysiological evidence
S Prasad, VV Holla, PK Pal
Annals of Movement Disorders 7 (1), 32-34, 2024
Mandates: Wellcome Trust/DBT India Alliance
Haplotype analysis at HTT locus in Huntington’s disease patients from India
M Purushottam, S Venkatesh, A Ganesh, B Viswanath, V Holla, N Kamble, ...
Mandates: Department of Science & Technology, India
CLCN2‐Related Leukoencephalopathy in Two Unrelated Patients Due to Novel Variants
VV Holla, P Phulpagar, J Saini, N Kamble, PK Pal, R Yadav, ...
Movement Disorders Clinical Practice 10 (7), 1155, 2023
Mandates: Department of Science & Technology, India
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