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Asish Vijayaraghavan

Showing results (1-10 of 47) with videos related to

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Annals of Indian Academy of Neurology|October 10, 2022
Prominent Jaw Closure Dystonia, Awake Bruxism, and Stereotypies in a Patient with Hypoglycemic EncephalopathyAsish Vijayaraghavan, Anjali Chouksey
Movement Disorders Clinical Practice|May 14, 2024
Unraveling Phenotypic Variability in Action Myoclonus with Renal Failure with SCARB2 Mutation in SiblingsLakshmi J Nair, Asish Vijayaraghavan
Annals of Indian Academy of Neurology|December 23, 2022
"Too Much Sugar is Bitter": An Important Cause of Reversible Inferior QuadrantanopiaJithin George, Asish Vijayaraghavan, Chaithanya R Warrier
Journal of Movement Disorders|June 30, 2025
Phenotypic variability in ATP13A2 mutations-First Report of SPG78 from IndiaLakshmi Priya L, Asish Vijayaraghavan, Syam Krishnan
Current Opinion in Neurology|June 27, 2023
Parkinson's disease - genetic causeAjith Cherian, Divya K P, Asish Vijayaraghavan
Annals of Indian Academy of Neurology|January 9, 2025
"Tracing the Lead" - Lead Encephalopathy Mimicking Autoimmune EncephalitisN Manuraj, Asish Vijayaraghavan, Soumya Sundaram, et al.
Neurology India|July 13, 2025
A Rare Stroke Mimic in Acute Lymphocytic LeukemiaKiren G Koshy, Asish Vijayaraghavan, Adarsh A Kumar
Indian Journal of Pediatrics|April 2, 2023
Gyratory Seizures: An Early Clue to Anti-NMDAR EncephalitisAsish Vijayaraghavan, Soumya Sundaram, Sayooja Sachithanandan, et al.
Neurology India|March 12, 2026
Hypertrophic Pachymeningitis Presenting with Cerebral Venous ThrombosisKiren George Koshy, Asish Vijayaraghavan, Adarsh Anil Kumar
Neurology|September 19, 2022
Pearls & Oy-sters: SCA21 Due to <i>TMEM240</i> Variation Presenting as Myoclonus Dystonia SyndromeAjith Cherian, Divya K P, Asish Vijayaraghavan, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Annals of Indian Academy of Neurology|October 10, 2022
Prominent Jaw Closure Dystonia, Awake Bruxism, and Stereotypies in a Patient with Hypoglycemic EncephalopathyAsish Vijayaraghavan, Anjali Chouksey
Movement Disorders Clinical Practice|May 14, 2024
Unraveling Phenotypic Variability in Action Myoclonus with Renal Failure with SCARB2 Mutation in SiblingsLakshmi J Nair, Asish Vijayaraghavan
Annals of Indian Academy of Neurology|December 23, 2022
"Too Much Sugar is Bitter": An Important Cause of Reversible Inferior QuadrantanopiaJithin George, Asish Vijayaraghavan, Chaithanya R Warrier
Journal of Movement Disorders|June 30, 2025
Phenotypic variability in ATP13A2 mutations-First Report of SPG78 from IndiaLakshmi Priya L, Asish Vijayaraghavan, Syam Krishnan
Current Opinion in Neurology|June 27, 2023
Parkinson's disease - genetic causeAjith Cherian, Divya K P, Asish Vijayaraghavan
Annals of Indian Academy of Neurology|January 9, 2025
"Tracing the Lead" - Lead Encephalopathy Mimicking Autoimmune EncephalitisN Manuraj, Asish Vijayaraghavan, Soumya Sundaram, et al.
Neurology India|July 13, 2025
A Rare Stroke Mimic in Acute Lymphocytic LeukemiaKiren G Koshy, Asish Vijayaraghavan, Adarsh A Kumar
Indian Journal of Pediatrics|April 2, 2023
Gyratory Seizures: An Early Clue to Anti-NMDAR EncephalitisAsish Vijayaraghavan, Soumya Sundaram, Sayooja Sachithanandan, et al.
Neurology India|March 12, 2026
Hypertrophic Pachymeningitis Presenting with Cerebral Venous ThrombosisKiren George Koshy, Asish Vijayaraghavan, Adarsh Anil Kumar
Neurology|September 19, 2022
Pearls & Oy-sters: SCA21 Due to <i>TMEM240</i> Variation Presenting as Myoclonus Dystonia SyndromeAjith Cherian, Divya K P, Asish Vijayaraghavan, et al.
Pageof 5