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Biswaroop Chakrabarty

Showing results (81-90 of 153) with videos related to

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Neurology India|January 4, 2024
Novel <i>SLC16A2</i> Gene Mutation: A Rare Case of Delayed Myelination with Dysthyroidism,v Allan-Herndon-Dudley SyndromeAakash Mahesan, Gautam Kamila, Puneet Choudhary, et al.
Neurology India|August 28, 2023
Teaching Neuroimage: Juvenile Krabbe - A MRI Pattern Recognition in LeukodystrophyAakash Mahesan, Gautam Kamila, Puneet Choudhary, et al.
Indian Journal of Pediatrics|October 8, 2023
Spinal Muscular Atrophy with Predominant Lower Extremity (SMA-LED) with Intellectual Disability and DysmorphismArvinder Wander, Ankit Kumar Meena, Pawan Kumar Ghanghoriya, et al.
Journal of Child Neurology|April 9, 2013
Dystrophinopathy diagnosis made easy: skin biopsy, an emerging novel toolBiswaroop Chakrabarty, M C Sharma, Sheffali Gulati, et al.
Journal of Pediatric Neurosciences|June 4, 2014
Menkes disease - An important cause of early onset refractory seizuresPuneet Jain, Lakshminarayanan Kannan, Biswaroop Chakrabarty, et al.
Neurology India|July 23, 2024
MELAS Syndrome: Rare Early Presentation of a Known Stroke MimicAakash Mahesan, Gautam Kamila, Mohana Sundaram, 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.
Pageof 16

Showing results (81-90 of 153) with videos related to

Sort By:
Pageof 16
Neurology India|January 4, 2024
Novel <i>SLC16A2</i> Gene Mutation: A Rare Case of Delayed Myelination with Dysthyroidism,v Allan-Herndon-Dudley SyndromeAakash Mahesan, Gautam Kamila, Puneet Choudhary, et al.
Neurology India|August 28, 2023
Teaching Neuroimage: Juvenile Krabbe - A MRI Pattern Recognition in LeukodystrophyAakash Mahesan, Gautam Kamila, Puneet Choudhary, et al.
Indian Journal of Pediatrics|October 8, 2023
Spinal Muscular Atrophy with Predominant Lower Extremity (SMA-LED) with Intellectual Disability and DysmorphismArvinder Wander, Ankit Kumar Meena, Pawan Kumar Ghanghoriya, et al.
Journal of Child Neurology|April 9, 2013
Dystrophinopathy diagnosis made easy: skin biopsy, an emerging novel toolBiswaroop Chakrabarty, M C Sharma, Sheffali Gulati, et al.
Journal of Pediatric Neurosciences|June 4, 2014
Menkes disease - An important cause of early onset refractory seizuresPuneet Jain, Lakshminarayanan Kannan, Biswaroop Chakrabarty, et al.
Neurology India|July 23, 2024
MELAS Syndrome: Rare Early Presentation of a Known Stroke MimicAakash Mahesan, Gautam Kamila, Mohana Sundaram, 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.
Pageof 16