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Resequencing the complete SNCA locus in Indian patients with Parkinson's disease.
NPJ Parkinsons Dis. 2024 Apr 15;10(1):85. doi: 10.1038/s41531-024-00676-4.
NPJ Parkinsons Dis. 2024.
PMID: 38622158
Free PMC article.
Novel PANK2 Variant in Asian Indians with Atypical Pantothenate Kinase Associated Neurodegeneration.
Saini A, Holla VV, Kalikavil Puthanveedu D, Mehta S, Elavarasi A, Pillai KS, Mohapatra P, Kumari R, Bari S, Singh I, Cherian A, Krishnan S, Radhakrishnan DM, Agarwal A, Garg D, Garg K, Singh M, Garg A, Muthusamy B, Lal V, Kishore A, Pal PK, Srivastava A, Faruq M, Rajan R.
Saini A, et al. Among authors: kalikavil puthanveedu d.
Mov Disord. 2024 Mar 20. doi: 10.1002/mds.29737. Online ahead of print.
Mov Disord. 2024.
PMID: 38506547
No abstract available.
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Deep Brain Stimulation for Parkinson's Disease-the Developing World's Perspective.
Patel K, Kalikavil Puthanveedu D, Vijayaraghavan A, Kesavapisharady K, Sarma G, Sarma SP, Krishnan S.
Patel K, et al. Among authors: kalikavil puthanveedu d.
Mov Disord Clin Pract. 2023 Oct 26;10(12):1750-1758. doi: 10.1002/mdc3.13901. eCollection 2023 Dec.
Mov Disord Clin Pract. 2023.
PMID: 38094655
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PINK-1 Parkinson's Disease Presenting with Dystonic Head Tremor.
Vijayaraghavan A, Subhash PK, Selvaraj P, Kalikavil Puthanveedu D, Krishnan S.
Vijayaraghavan A, et al. Among authors: kalikavil puthanveedu d.
Mov Disord Clin Pract. 2023 Sep 21;10(11):1691-1692. doi: 10.1002/mdc3.13875. eCollection 2023 Nov.
Mov Disord Clin Pract. 2023.
PMID: 37982116
No abstract available.
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Whole exome and targeted gene sequencing to detect pathogenic recessive variants in early onset cerebellar ataxia.
Shakya S, Kumari R, Suroliya V, Tyagi N, Joshi A, Garg A, Singh I, Kalikavil Puthanveedu D, Cherian A, Mukerji M, Srivastava AK, Faruq M.
Shakya S, et al. Among authors: kalikavil puthanveedu d.
Clin Genet. 2019 Dec;96(6):566-574. doi: 10.1111/cge.13625. Epub 2019 Sep 1.
Clin Genet. 2019.
PMID: 31429931
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