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Divyani Garg 7 Articles
Clozapine-Induced Negative Myoclonus Leads to Recurrent Falls: A Case Report
Shiny Joy, Punith Saroja Bylappa, Divyani Garg, Ayush Agarwal, Achal Kumar Srivastava
J Mov Disord. 2025;18(1):99-100.   Published online November 11, 2024
DOI: https://doi.org/10.14802/jmd.24207
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  • Clozapine/escitalopram

    Reactions Weekly.2024; 2038(1): 92.     CrossRef
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
  • 1,229 View
  • 48 Download
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Jaw Opening Myoclonus in Subacute Sclerosing Panencephalitis: A New Phenotypic Observation
Divyani Garg, Vanshika Kakkar, Suvasini Sharma
J Mov Disord. 2024;17(1):106-108.   Published online September 14, 2023
DOI: https://doi.org/10.14802/jmd.23158
  • 2,020 View
  • 118 Download
  • 1 Web of Science
  • 1 Crossref
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  • Movement Disorders in Patients with Subacute Sclerosing Panencephalitis: A Systematic Review
    Divyani Garg, Sahil Patel, Charulata S. Sankhla, Vikram V. Holla, Vijayashankar Paramanandam, Prashanth L. Kukkle, Sanjay Pandey, Susanne A. Schneider, Pramod K. Pal
    Movement Disorders Clinical Practice.2024; 11(7): 770.     CrossRef
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Periodic Jaw-Opening Myoclonus in Subacute Sclerosing Panencephalitis
Divyani Garg, Ashna Kumar, Suvasini Sharma
J Mov Disord. 2023;16(2):210-212.   Published online April 26, 2023
DOI: https://doi.org/10.14802/jmd.23015
  • 1,742 View
  • 54 Download
  • 2 Web of Science
  • 3 Crossref
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  • Jaw Opening Myoclonus in Subacute Sclerosing Panencephalitis: A New Phenotypic Observation
    Divyani Garg, Vanshika Kakkar, Suvasini Sharma
    Journal of Movement Disorders.2024; 17(1): 106.     CrossRef
  • Movement Disorders in Patients with Subacute Sclerosing Panencephalitis: A Systematic Review
    Divyani Garg, Sahil Patel, Charulata S. Sankhla, Vikram V. Holla, Vijayashankar Paramanandam, Prashanth L. Kukkle, Sanjay Pandey, Susanne A. Schneider, Pramod K. Pal
    Movement Disorders Clinical Practice.2024; 11(7): 770.     CrossRef
  • Subacute sclerosing panencephalitis presenting as repeated extension of the neck: A case report
    Ravindra Kumar Garg, Imran Rizvi, Vikas Prabhu, Neeraj Kumar, Hardeep S. Malhotra, Praveen K. Sharma
    Annals of Movement Disorders.2024; 7(2): 138.     CrossRef
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Opsoclonus-Myoclonus Syndrome as a Heralding Feature of Scrub Typhus: An Illustrative Case with a Video Vignette
Divyani Garg, Rajinder K. Dhamija
J Mov Disord. 2022;15(1):80-82.   Published online May 3, 2021
DOI: https://doi.org/10.14802/jmd.20148
  • 5,304 View
  • 173 Download
  • 1 Web of Science
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  • Neurological facets of scrub typhus: A comprehensive narrative review
    Divyani Garg, Abi Manesh
    Annals of Indian Academy of Neurology.2021; 24(6): 849.     CrossRef
Spastic paraplegia 82 in two Asian Indian siblings with PCYT2 mutation
Anil Dash, Farsana Mustafa, Divyani Garg, Sreeja Samineni, Ayush Agarwal, Ajay Garg, Achal Kumar Srivastava
Received December 16, 2024  Accepted January 24, 2025  Published online January 31, 2025  
DOI: https://doi.org/10.14802/jmd.24259    [Accepted]
  • 434 View
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CSF1R-related adult-onset leukoencephalopathy with axonal spheroids: A case series of four Asian Indian patients
Divyani Garg, Abhishek Vaingankar, Anu Gupta, Roopa Rajan, Ajay Garg, Ayush Agarwal, Farsana Mustafa, Divya M Radhakrishnan, Awadh Kishor Pandit, Venugopalan Y Vishnu, Mamta Bhushan Singh, Rohit Bhatia, Achal Kumar Srivastava
Received January 4, 2025  Accepted February 17, 2025  Published online February 17, 2025  
DOI: https://doi.org/10.14802/jmd.25004    [Accepted]
  • 11 View
  • 2 Download
AbstractAbstract PDF
Background
Colony stimulating factor 1 receptor-related leukoencephalopathy (CSF1R-L) is a rare, adult onset leukoencephalopathy. Descriptions from the Indian subcontinent remain limited.
Objective
To report four patients with genetically confirmed CSF1R-L from four Asian Indian families, describing clinical, molecular and radiological features.
Methods
All patients underwent clinical examination, MRI brain, and whole exome sequencing to identify causative variants in CSF1R gene. We also reviewed published Indian cases with CSF1R-L.
Results
Age at enrolment ranged from 34-40 years. Duration of symptoms ranged from 11 months to 2 years. The chief clinical phenotype in three patients was a rapidly evolving cognitive-behavioural syndrome combined with atypical parkinsonism, and asymmetrical spastic tetraparesis in one patient. We identified four different variants (three missense, one inframe deletion). Radiological findings demonstrated white matter involvement, and diffusion restriction involving subcortical white matter and pyramidal tracts.
Conclusions
We expand the literature from India with four new cases of CSF1R-L.

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