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Prashant Jauhari

Showing results (61-70 of 98) with videos related to

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Neurology|January 25, 2024
Child Neurology: Allgrove Syndrome: An Intriguing Etiology of Motor Neuron Disease in ChildrenJuhi Gupta, Sayoni Roy Chowdhury, Prashant Jauhari, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 30, 2022
STAMBP gene mutation causing microcephaly-capillary malformation syndrome: a recognizable developmental and epileptic encephalopathyVaishakh Anand, Bhawana Aggarwal, Prashant Jauhari, et al.
Developmental Medicine and Child Neurology|November 20, 2010
Aetiology of intellectual disability in paediatric outpatients in Northern IndiaPrashant Jauhari, Raju Boggula, Anupama Bhave, et al.
Archives of Virology|September 15, 2012
Molecular identification of enteroviruses associated with aseptic meningitis in children from IndiaArvind Kumar, Deepti Shukla, Rashmi Kumar, et al.
Neurology India|November 6, 2023
Teaching Neuroimage - Aicardi Syndrome: A Triad of Epileptic Spasms, Agenesis of Corpus Callosum, and Chorio-Retinal LacunaeAakash Mahesan, Gautam Kamila, Prabhav Puri, et al.
Brain & Development|August 29, 2020
A rare infective cause of stroke in an immunocompetent childJuhi Gupta, Biswaroop Chakrabarty, Gagandeep Singh, et al.
Epilepsy & Behavior : E&B|May 1, 2024
Efficacy of verbal suggestion, verbal suggestion with a tuning fork, and verbal suggestion with a cotton swab for inducing the paroxysmal event during video-EEG recording in children with suspected psychogenic nonepileptic seizuresPrateek Kumar Panda, Sachendra Badal, Vivek Sirolia, et al.
Neurology India|April 3, 2025
POLR3-Related Leukodystrophy: A Case Series from the Indian ScenarioAnkit Kumar Meena, Arvinder Wander, Aakash Mahesan, et al.
Seizure|August 20, 2024
'Remote inhibition' of motor cortex in Epileptic encephalopathy with spike-wave activation in sleep (EE-SWAS): A TMS based cortical excitability studyGautam Kamila, Prashant Jauhari, Sheffali Gulati, et al.
Neurology India|March 5, 2024
Congenital Myasthenia Syndrome Due to a Novel DPAGT1 Gene Mutation - An Error of Glycosylation Masquerading as a Congenital MyopathyAakash Mahesan, Gautam Kamila, Richa Tiwari, et al.
Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:
Pageof 10
Neurology|January 25, 2024
Child Neurology: Allgrove Syndrome: An Intriguing Etiology of Motor Neuron Disease in ChildrenJuhi Gupta, Sayoni Roy Chowdhury, Prashant Jauhari, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 30, 2022
STAMBP gene mutation causing microcephaly-capillary malformation syndrome: a recognizable developmental and epileptic encephalopathyVaishakh Anand, Bhawana Aggarwal, Prashant Jauhari, et al.
Developmental Medicine and Child Neurology|November 20, 2010
Aetiology of intellectual disability in paediatric outpatients in Northern IndiaPrashant Jauhari, Raju Boggula, Anupama Bhave, et al.
Archives of Virology|September 15, 2012
Molecular identification of enteroviruses associated with aseptic meningitis in children from IndiaArvind Kumar, Deepti Shukla, Rashmi Kumar, et al.
Neurology India|November 6, 2023
Teaching Neuroimage - Aicardi Syndrome: A Triad of Epileptic Spasms, Agenesis of Corpus Callosum, and Chorio-Retinal LacunaeAakash Mahesan, Gautam Kamila, Prabhav Puri, et al.
Brain & Development|August 29, 2020
A rare infective cause of stroke in an immunocompetent childJuhi Gupta, Biswaroop Chakrabarty, Gagandeep Singh, et al.
Epilepsy & Behavior : E&B|May 1, 2024
Efficacy of verbal suggestion, verbal suggestion with a tuning fork, and verbal suggestion with a cotton swab for inducing the paroxysmal event during video-EEG recording in children with suspected psychogenic nonepileptic seizuresPrateek Kumar Panda, Sachendra Badal, Vivek Sirolia, et al.
Neurology India|April 3, 2025
POLR3-Related Leukodystrophy: A Case Series from the Indian ScenarioAnkit Kumar Meena, Arvinder Wander, Aakash Mahesan, et al.
Seizure|August 20, 2024
'Remote inhibition' of motor cortex in Epileptic encephalopathy with spike-wave activation in sleep (EE-SWAS): A TMS based cortical excitability studyGautam Kamila, Prashant Jauhari, Sheffali Gulati, et al.
Neurology India|March 5, 2024
Congenital Myasthenia Syndrome Due to a Novel DPAGT1 Gene Mutation - An Error of Glycosylation Masquerading as a Congenital MyopathyAakash Mahesan, Gautam Kamila, Richa Tiwari, et al.
Pageof 10