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Veena Laxmi

Showing results (1-10 of 20) with videos related to

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Indian Journal of Pediatrics|February 2, 2023
Use of Ketogenic Diet in Two Indian Children with a Rare Early-Onset Epileptic EncephalopathyPradeep Kumar Gunasekaran, Veena Laxmi, Asha Bilamge, et al.
Annals of Indian Academy of Neurology|March 12, 2026
Neuroimaging in L-2 Hydroxy Glutaric AciduriaLokesh Saini, Pradeep Kumar Gunasekaran, Veena Laxmi, et al.
Indian Journal of Pediatrics|August 27, 2020
SARS-COV-2 Infection in a Term Neonate Presenting with Respiratory Failure on Day 3 of LifeKanya Mukhopadhyay, Ashish Agarwal, Veena Laxmi, et al.
Neuropediatrics|January 16, 2024
Cogan's Lid Twitch Sign in a Child with Congenital MyastheniaSujatha Manjunathan, Pradeep Kumar Gunasekaran, Veena Laxmi, et al.
Neurology|January 4, 2024
Teaching NeuroImage: Neuroimaging Features of Wilson DiseasePradeep Kumar Gunasekaran, Sarbesh Tiwari, Ashna Kumar, et al.
Neuropediatrics|May 7, 2025
Oculogyric Crisis and Criss-Cross Gait of GLUT1 Deficiency SyndromeAshna Kumar, Pradeep Kumar Gunasekaran, Veena Laxmi, et al.
Indian Journal of Pediatrics|October 3, 2023
Acute Flaccid Paralysis due to Pyruvate Dehydrogenase E1-Alpha DeficiencyVeena Laxmi, Pradeep Kumar Gunasekaran, Ashna Kumar, et al.
Journal of Neurosciences in Rural Practice|March 9, 2023
A rare case of intermediate phenotype Niemann-Pick disease with a rare pathogenic variant of 1624C>T in SMPD1 geneDeepthi Krishna, Pradeep Kumar Gunasekaran, Janki Kumari, et al.
Journal of Neurosciences in Rural Practice|September 11, 2023
Associated movement disorder as a clue for the diagnosis of paroxysmal kinesigenic dyskinesia in a child with focal epilepsyVeena Laxmi, Pradeep Kumar Gunasekaran, Sujatha Manjunathan, et al.
Indian Journal of Pediatrics|May 10, 2023
Childhood-Onset Neurodegeneration with Brain Atrophy in Association with c.628G>A in UBTF GenePradeep Kumar Gunasekaran, Veena Laxmi, Sujatha Manjunathan, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Indian Journal of Pediatrics|February 2, 2023
Use of Ketogenic Diet in Two Indian Children with a Rare Early-Onset Epileptic EncephalopathyPradeep Kumar Gunasekaran, Veena Laxmi, Asha Bilamge, et al.
Annals of Indian Academy of Neurology|March 12, 2026
Neuroimaging in L-2 Hydroxy Glutaric AciduriaLokesh Saini, Pradeep Kumar Gunasekaran, Veena Laxmi, et al.
Indian Journal of Pediatrics|August 27, 2020
SARS-COV-2 Infection in a Term Neonate Presenting with Respiratory Failure on Day 3 of LifeKanya Mukhopadhyay, Ashish Agarwal, Veena Laxmi, et al.
Neuropediatrics|January 16, 2024
Cogan's Lid Twitch Sign in a Child with Congenital MyastheniaSujatha Manjunathan, Pradeep Kumar Gunasekaran, Veena Laxmi, et al.
Neurology|January 4, 2024
Teaching NeuroImage: Neuroimaging Features of Wilson DiseasePradeep Kumar Gunasekaran, Sarbesh Tiwari, Ashna Kumar, et al.
Neuropediatrics|May 7, 2025
Oculogyric Crisis and Criss-Cross Gait of GLUT1 Deficiency SyndromeAshna Kumar, Pradeep Kumar Gunasekaran, Veena Laxmi, et al.
Indian Journal of Pediatrics|October 3, 2023
Acute Flaccid Paralysis due to Pyruvate Dehydrogenase E1-Alpha DeficiencyVeena Laxmi, Pradeep Kumar Gunasekaran, Ashna Kumar, et al.
Journal of Neurosciences in Rural Practice|March 9, 2023
A rare case of intermediate phenotype Niemann-Pick disease with a rare pathogenic variant of 1624C>T in SMPD1 geneDeepthi Krishna, Pradeep Kumar Gunasekaran, Janki Kumari, et al.
Journal of Neurosciences in Rural Practice|September 11, 2023
Associated movement disorder as a clue for the diagnosis of paroxysmal kinesigenic dyskinesia in a child with focal epilepsyVeena Laxmi, Pradeep Kumar Gunasekaran, Sujatha Manjunathan, et al.
Indian Journal of Pediatrics|May 10, 2023
Childhood-Onset Neurodegeneration with Brain Atrophy in Association with c.628G>A in UBTF GenePradeep Kumar Gunasekaran, Veena Laxmi, Sujatha Manjunathan, et al.
Pageof 2