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Movement Disorders Clinical Practice|October 17, 2022
Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian ChildrenDivyani Garg, Sangeetha Yoganathan, Uzma Shamim, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|February 26, 2021
Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticityDirk Dressler, Maria Concetta Altavista, Eckart Altenmueller, et al.BMC Medical Education|December 28, 2024
Designing a summative assessment blueprint in community medicine: an expert consensus approach at All India Institute of Medical SciencesPragya Kumar, Neha Chaudhary, Arun Mahadeo Kokane, et al.Elife|August 30, 2022
Activation of targetable inflammatory immune signaling is seen in myelodysplastic syndromes with SF3B1 mutationsGaurav S Choudhary, Andrea Pellagatti, Bogos Agianian, et al.Nature Communications|May 13, 2026
Chromatin rewiring of β-globin and MYC enhancers by TGF-β1 drives defective erythropoiesisSrinivas Aluri, Kimo Bachiashvili, Anjali Budhathoki, et al.Advanced Genetics (Hoboken, N.J.)|January 9, 2023
Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening ToolPooja Sharma, Akhilesh Kumar Sonakar, Nishu Tyagi, et al.Movement Disorders Clinical Practice|November 13, 2024
The Genomic Landscape of Wilson Disease in a Pan India Disease Cohort and Population-Scale DataMukesh Kumar, Srishti Sharma, Sanjay Pandey, et al.Frontiers in Neurology|July 14, 2020
Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease ResearchRoopa Rajan, K P Divya, Rukmini Mridula Kandadai, et al.Pageof 26