Veena Laxmi
Jodhpur, RJ, India
Last Updated: 09/26/2026
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Found 20 publications
Farber Lipogranulomatosis With Spinal Muscular Atrophy With Progressive Myoclonic Epilepsy: Expanding the Phenotypic Spectrum.
Journal: Journal of child neurology
Published: May 23, 2026
Neuroimaging in L-2 Hydroxy Glutaric Aciduria.
Journal: Annals of Indian Academy of Neurology
Published: October 07, 2025
Oculogyric Crisis and Criss-Cross Gait of GLUT1 Deficiency Syndrome.
Journal: Neuropediatrics
Published: May 07, 2025
Neurodevelopmental Disorder with Spasticity, Hypomyelinating Leukodystrophy, and Brain Abnormalities (NEDSPLB) in an Indian Child.
Journal: Indian journal of pediatrics
Published: November 09, 2024
Cogan's Lid Twitch Sign in a Child with Congenital Myasthenia.
Journal: Neuropediatrics
Published: January 16, 2024
Teaching NeuroImage: Neuroimaging Features of Wilson Disease.
Journal: Neurology
Published: January 04, 2024
Skraban-Deardorff Syndrome in an Indian Child - A Very Rare Pathogenic Base Pair Deletion in WDR26 Gene.
Journal: Indian journal of pediatrics
Published: November 17, 2023
Acute Flaccid Paralysis due to Pyruvate Dehydrogenase E1-Alpha Deficiency.
Journal: Indian journal of pediatrics
Published: August 12, 2023
Knobloch Syndrome - Triad of Occipital Encephalocele, Retino-Choroidal Detachment and Epilepsy.
Journal: Indian journal of pediatrics
Published: June 29, 2023
Primary Diffuse Leptomeningeal Melanomatosis in an Indian Child With Review of Literature.
Journal: Pediatric neurology
Published: June 29, 2023
Clinical Profile, Follow-up, and Role of Neuroimaging in Pediatric Guillain-Barré Syndrome in the COVID Era: An Ambispective Study.
Journal: Journal of child neurology
Published: June 27, 2023
Childhood-Onset Neurodegeneration with Brain Atrophy in Association with c.628G>A in UBTF Gene.
Journal: Indian journal of pediatrics
Published: April 01, 2023
Last Updated: 09/26/2026