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Sheffali Gulati

Showing results (201-210 of 368) with videos related to

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Neurology India|July 23, 2024
MELAS Syndrome: Rare Early Presentation of a Known Stroke MimicAakash Mahesan, Gautam Kamila, Mohana Sundaram, et al.
Brain & Development|February 9, 2011
Novel non-identical MECP2 mutations in Rett syndrome family: a rare presentationRajni Khajuria, Neerja Gupta, Savita Sapra, et al.
Journal of Child Neurology|February 3, 2011
A novel MECP2 change in an indian boy with variant rett phenotype and congenital blindness: implications for genetic counseling and prenatal diagnosisRajni Khajuria, Neerja Gupta, Savita Sapra, et al.
Journal of Tropical Pediatrics|July 3, 2015
A Combination of Moyamoya Pattern and Cerebral Venous Sinus Thrombosis: A Case of Tubercular VasculopathyRanjith M Kumar, Lokesh Saini, Jaya Shankar Kaushik, et al.
Annals of Indian Academy of Neurology|October 8, 2024
Uncommon Pediatric Immune-Mediated Epilepsy: Disease Course, Diagnosis, and Outcome - A Series of Three CasesAakash Mahesan, Aradhana Rohil, Prashant Jauhari, et al.
Journal of Child Neurology|May 18, 2013
Skin biopsy: a new tool to diagnose sarcoglycanopathyBiswaroop Chakrabarty, M C Sharma, Sheffali Gulati, et al.
Indian Journal of Pediatrics|December 11, 2023
ASAH1 Variants Causing Spinal Muscular Atrophy PhenotypeArvinder Wander, Ankit Kumar Meena, Pawan Kumar Ghangoriya, et al.
Annals of Indian Academy of Neurology|December 17, 2013
Autoimmune encephalitis: A potentially reversible cause of status epilepticus, epilepsy, and cognitive declineAwadh Kishor Pandit, Kavish Ihtisham, Ajay Garg, et al.
Annals of Indian Academy of Neurology|April 29, 2021
Bilateral Facial Palsy in Lymphomatous MeningitisPriyanka Madaan, Prashant Jauhari, Biswaroop Chakrabarty, et al.
Indian Journal of Pediatrics|January 12, 2011
Hyperekplexia masquerading as epilepsyJitendra Kumar Sahu, Anita Choudhary, Indranil Ghosh, et al.
Pageof 37

Showing results (201-210 of 368) with videos related to

Sort By:
Pageof 37
Neurology India|July 23, 2024
MELAS Syndrome: Rare Early Presentation of a Known Stroke MimicAakash Mahesan, Gautam Kamila, Mohana Sundaram, et al.
Brain & Development|February 9, 2011
Novel non-identical MECP2 mutations in Rett syndrome family: a rare presentationRajni Khajuria, Neerja Gupta, Savita Sapra, et al.
Journal of Child Neurology|February 3, 2011
A novel MECP2 change in an indian boy with variant rett phenotype and congenital blindness: implications for genetic counseling and prenatal diagnosisRajni Khajuria, Neerja Gupta, Savita Sapra, et al.
Journal of Tropical Pediatrics|July 3, 2015
A Combination of Moyamoya Pattern and Cerebral Venous Sinus Thrombosis: A Case of Tubercular VasculopathyRanjith M Kumar, Lokesh Saini, Jaya Shankar Kaushik, et al.
Annals of Indian Academy of Neurology|October 8, 2024
Uncommon Pediatric Immune-Mediated Epilepsy: Disease Course, Diagnosis, and Outcome - A Series of Three CasesAakash Mahesan, Aradhana Rohil, Prashant Jauhari, et al.
Journal of Child Neurology|May 18, 2013
Skin biopsy: a new tool to diagnose sarcoglycanopathyBiswaroop Chakrabarty, M C Sharma, Sheffali Gulati, et al.
Indian Journal of Pediatrics|December 11, 2023
ASAH1 Variants Causing Spinal Muscular Atrophy PhenotypeArvinder Wander, Ankit Kumar Meena, Pawan Kumar Ghangoriya, et al.
Annals of Indian Academy of Neurology|December 17, 2013
Autoimmune encephalitis: A potentially reversible cause of status epilepticus, epilepsy, and cognitive declineAwadh Kishor Pandit, Kavish Ihtisham, Ajay Garg, et al.
Annals of Indian Academy of Neurology|April 29, 2021
Bilateral Facial Palsy in Lymphomatous MeningitisPriyanka Madaan, Prashant Jauhari, Biswaroop Chakrabarty, et al.
Indian Journal of Pediatrics|January 12, 2011
Hyperekplexia masquerading as epilepsyJitendra Kumar Sahu, Anita Choudhary, Indranil Ghosh, et al.
Pageof 37