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Anaita Udwadia Hegde

Showing results (1-10 of 21) with videos related to

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Child Neurology Open|May 16, 2017
Temporary Efficacy of Pyrimethamine in Juvenile-Onset Tay-Sachs Disease Caused by 2 Unreported HEXA Mutations in the Indian PopulationAnaita Udwadia-Hegde, Omkar Hajirnis
Movement Disorders Clinical Practice|March 7, 2019
Chronic GM1 Gangliosidosis with Characteristic "Wish Bone Sign" on Brain MRI. Another Type of Neurodegeneration with Brain Iron Accumulation?Omkar Hajirnis, Anaita Udwadia-Hegde
Pediatric Radiology|March 23, 2006
Non-infantile variant of desmoplastic ganglioglioma: a report of 2 casesKarthik Ganesan, Shrinivas Desai, Anaita Udwadia-Hegde
The Neuroradiology Journal|June 20, 2017
Herpes simplex encephalitis with thalamic, brainstem and cerebellar involvementMeenal Garg, Shilpa Kulkarni, Anaita Udwadia Hegde
Movement Disorders Clinical Practice|October 6, 2025
Congenital Mirror Movements in A Family with TUBB2B MutationSuhani Shah, Anaita Udwadia Hegde, Kavya Rajarajan, et al.
Clinical Dysmorphology|June 6, 2021
CK syndrome: a rare cause of developmental delay in a young boyMeenal Garg, Shilpa D Kulkarni, Rafat Sayed, et al.
Journal of Neurosciences in Rural Practice|September 23, 2017
Diabetes Mellitus as the Presenting Feature of Friedreich's AtaxiaMeenal Garg, Shilpa D Kulkarni, Krishnakumar N Shah, et al.
Pediatric Dermatology|February 23, 2019
CEDNIK syndrome in an Indian patient with a novel mutation of the SNAP29 geneShital Poojary, Kapisha S Shah, Krishna B Bhalala, et al.
Neurology India|March 12, 2026
Juvenile Myasthenia Gravis: An Indian PerspectiveMeenal Garg, Shilpa D Kulkarni, Anaita Udwadia Hegde, et al.
Child Neurology Open|March 16, 2019
CLIPPERS Spectrum Disorder: A Rare Pediatric Neuroinflammatory ConditionTarishi Nemani, Anaita Udwadia-Hegde, Purva Keni Karnavat, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Child Neurology Open|May 16, 2017
Temporary Efficacy of Pyrimethamine in Juvenile-Onset Tay-Sachs Disease Caused by 2 Unreported HEXA Mutations in the Indian PopulationAnaita Udwadia-Hegde, Omkar Hajirnis
Movement Disorders Clinical Practice|March 7, 2019
Chronic GM1 Gangliosidosis with Characteristic "Wish Bone Sign" on Brain MRI. Another Type of Neurodegeneration with Brain Iron Accumulation?Omkar Hajirnis, Anaita Udwadia-Hegde
Pediatric Radiology|March 23, 2006
Non-infantile variant of desmoplastic ganglioglioma: a report of 2 casesKarthik Ganesan, Shrinivas Desai, Anaita Udwadia-Hegde
The Neuroradiology Journal|June 20, 2017
Herpes simplex encephalitis with thalamic, brainstem and cerebellar involvementMeenal Garg, Shilpa Kulkarni, Anaita Udwadia Hegde
Movement Disorders Clinical Practice|October 6, 2025
Congenital Mirror Movements in A Family with TUBB2B MutationSuhani Shah, Anaita Udwadia Hegde, Kavya Rajarajan, et al.
Clinical Dysmorphology|June 6, 2021
CK syndrome: a rare cause of developmental delay in a young boyMeenal Garg, Shilpa D Kulkarni, Rafat Sayed, et al.
Journal of Neurosciences in Rural Practice|September 23, 2017
Diabetes Mellitus as the Presenting Feature of Friedreich's AtaxiaMeenal Garg, Shilpa D Kulkarni, Krishnakumar N Shah, et al.
Pediatric Dermatology|February 23, 2019
CEDNIK syndrome in an Indian patient with a novel mutation of the SNAP29 geneShital Poojary, Kapisha S Shah, Krishna B Bhalala, et al.
Neurology India|March 12, 2026
Juvenile Myasthenia Gravis: An Indian PerspectiveMeenal Garg, Shilpa D Kulkarni, Anaita Udwadia Hegde, et al.
Child Neurology Open|March 16, 2019
CLIPPERS Spectrum Disorder: A Rare Pediatric Neuroinflammatory ConditionTarishi Nemani, Anaita Udwadia-Hegde, Purva Keni Karnavat, et al.
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