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Expanding the phenotypic and genotypic spectrum of DYT-TUBB4A with seven patients from India.
Garg D, Holla VV, Ganguly J, Rajan R, Saini A, Agarwal A, Radhakrishnan DM, Basu P, Mondal B, Dhar D, Kamble N, Yadav R, Muthusamy B, Kumar H, Srivastava AK, Pal PK. Garg D, et al. Among authors: radhakrishnan dm. Parkinsonism Relat Disord. 2024 May 16;124:107012. doi: 10.1016/j.parkreldis.2024.107012. Online ahead of print. Parkinsonism Relat Disord. 2024. PMID: 38762926
Primary Coenzyme Q10 Deficiency-4 Causing Young Onset Ataxia-Dystonia.
Radhakrishnan DM, Saini A, Fatima S, Gupta A, Vishnu VY, Singh MB, Bhatia R, Srivastva MVP, Srivastava AK, Rajan R. Radhakrishnan DM, et al. Mov Disord Clin Pract. 2024 Apr;11(4):438-440. doi: 10.1002/mdc3.13950. Epub 2023 Dec 17. Mov Disord Clin Pract. 2024. PMID: 38556906 No abstract available.
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: radhakrishnan dm. Mov Disord. 2024 May;39(5):920-923. doi: 10.1002/mds.29737. Epub 2024 Mar 20. Mov Disord. 2024. PMID: 38506547 No abstract available.
The role of susceptibility-weighted imaging & contrast-enhanced MRI in the diagnosis of primary CNS vasculitis: a large case series.
Agarwal S, Sebastian LJD, Gaikwad S, Srivastava MVP, Sharma MC, Singh M, Bhatia R, Agarwal A, Sharma J, Dash D, Goyal V, Srivastava AK, Tripathi M, Suri V, Singh MB, Sarkar C, Suri A, Singh RK, Vibha D, Pandit AK, Rajan R, Gupta A, Elavarasi A, Radhakrishnan DM, Das A, Tandon V, Doddamani R, Upadhyay A, Vishnu VY, Garg A. Agarwal S, et al. Among authors: radhakrishnan dm. Sci Rep. 2024 Feb 27;14(1):4718. doi: 10.1038/s41598-024-55222-2. Sci Rep. 2024. PMID: 38413676 Free PMC article.
151 results