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K P Vinayan

Showing results (11-20 of 25) with videos related to

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Annals of Indian Academy of Neurology|February 24, 2021
Epilepsy in Ring Chromosome 20 Syndrome Might Have Variable Clinical FeaturesAbhijit Anil Patil, K P Vinayan, Arun Grace Roy
Neurology|December 5, 2020
Teaching NeuroImages: An Imaging Clue in a Boy With Developmental DelayA S Jyotsna, K P Vinayan, Arun Grace Roy
Indian Pediatrics|May 13, 2021
Rare Inherited Hypomagnesemias - An Endocrine Case SeriesS Geethalakshmi, Nisha Bhavani, K P Vinayan, et al.
Indian Journal of Dermatology, Venereology and Leprology|July 9, 2009
Acral dyschromatosis with developmental regression and dystonia in a seven-year-old child: dyschromatosis symmetrica hereditaria variant or a new syndrome?Feroze Kaliyadan, K P Vinayan, Bindiya Fernandes, et al.
Indian Journal of Clinical Biochemistry : IJCB|October 2, 2012
Diagnosis of major organic acidurias in children: two years experience at a tertiary care centreM P Narayanan, Vaidyanathan Kannan, K P Vinayan, et al.
Indian Journal of Pediatrics|May 8, 2000
Jordans' anomalyK Rajeevan, K R Anandan, K P Vinayan, et al.
Indian Journal of Pediatrics|April 19, 2016
Clinical Characteristics and Follow-up of South Indian Children with Autoimmune EncephalopathyYeeshu Singh Sudan, K P Vinayan, Arun Grace Roy, et al.
Clinical Neurology and Neurosurgery|March 14, 2007
Juvenile Behçet's disease: highlighting neuropsychiatric manifestations and putative genetic mechanismsJ N Panicker, K P Vinayan, N V Ahsan Moosa, et al.
BMC Medical Genetics|May 18, 2018
Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: a case reportJoshi Stephen, Sheela Nampoothiri, K P Vinayan, et al.
Indian Pediatrics|March 22, 2024
The Indian Academy of Pediatrics and Directorate General of Health Services, Government of India White Paper on Transition of Care for Youth with Special Health Care NeedsJagdish Chandra, Mamta Manglani, Satinder Aneja, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Annals of Indian Academy of Neurology|February 24, 2021
Epilepsy in Ring Chromosome 20 Syndrome Might Have Variable Clinical FeaturesAbhijit Anil Patil, K P Vinayan, Arun Grace Roy
Neurology|December 5, 2020
Teaching NeuroImages: An Imaging Clue in a Boy With Developmental DelayA S Jyotsna, K P Vinayan, Arun Grace Roy
Indian Pediatrics|May 13, 2021
Rare Inherited Hypomagnesemias - An Endocrine Case SeriesS Geethalakshmi, Nisha Bhavani, K P Vinayan, et al.
Indian Journal of Dermatology, Venereology and Leprology|July 9, 2009
Acral dyschromatosis with developmental regression and dystonia in a seven-year-old child: dyschromatosis symmetrica hereditaria variant or a new syndrome?Feroze Kaliyadan, K P Vinayan, Bindiya Fernandes, et al.
Indian Journal of Clinical Biochemistry : IJCB|October 2, 2012
Diagnosis of major organic acidurias in children: two years experience at a tertiary care centreM P Narayanan, Vaidyanathan Kannan, K P Vinayan, et al.
Indian Journal of Pediatrics|May 8, 2000
Jordans' anomalyK Rajeevan, K R Anandan, K P Vinayan, et al.
Indian Journal of Pediatrics|April 19, 2016
Clinical Characteristics and Follow-up of South Indian Children with Autoimmune EncephalopathyYeeshu Singh Sudan, K P Vinayan, Arun Grace Roy, et al.
Clinical Neurology and Neurosurgery|March 14, 2007
Juvenile Behçet's disease: highlighting neuropsychiatric manifestations and putative genetic mechanismsJ N Panicker, K P Vinayan, N V Ahsan Moosa, et al.
BMC Medical Genetics|May 18, 2018
Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: a case reportJoshi Stephen, Sheela Nampoothiri, K P Vinayan, et al.
Indian Pediatrics|March 22, 2024
The Indian Academy of Pediatrics and Directorate General of Health Services, Government of India White Paper on Transition of Care for Youth with Special Health Care NeedsJagdish Chandra, Mamta Manglani, Satinder Aneja, et al.
Pageof 3