Journal of Movement Disorders

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The First Indian Patient With Benign Hereditary Chorea due to a De Novo Mutation in the NKX2-1 Gene: Divyani Garg, Ayush Agarwal, Mohammed Faruq, Achal Kumar Srivastava; J Mov Disord. 2024;17(2):239-241. Published online February 29, 2024; DOI: https://doi.org/10.14802/jmd.23273

Manganism without Parkinsonism: Isolated Unilateral Upper Limb Tremor in a Welder: Shweta Prasad, Uzma Shamim, Akanksha Minj, Mohammed Faruq, Pramod Kumar Pal; J Mov Disord. 2019;12(2):135-137. Published online April 5, 2019; DOI: https://doi.org/10.14802/jmd.18068

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