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Sushil Razdan

Showing results (11-20 of 21) with videos related to

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The Journal of the Association of Physicians of India|November 3, 2016
Celiac Neuropathy: A Case Report from Kashmir (India)K K Pandita, Adnan Rafiq, Sushil Razdan, et al.
Case Reports in Pulmonology|January 13, 2015
"Peripheral neuropathy crippling bronchial asthma": two rare case reports of churg-strauss syndromeKamal Kishore Pandita, Khalid Javid Bhat, Sushil Razdan, et al.
Clinical Cases in Mineral and Bone Metabolism : the Official Journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases|October 23, 2012
"Excess gooD can be Dangerous". A case series of iatrogenic symptomatic hypercalcemia due to hypervitaminosis DKamal Kishore Pandita, Sushil Razdan, Rattan Parkash Kudyar, et al.
Epilepsy Research and Treatment|September 8, 2012
Active epilepsy as indicator of neurocysticercosis in rural northwest IndiaSunil Kumar Raina, Sushil Razdan, K K Pandita, et al.
Indian Journal of Human Genetics|July 4, 2012
Inbreeding as a cause for deafness: Dadhkai studySushil Razdan, Sunil Kumar Raina, Kamal K Pandita, et al.
Mitochondrion|June 22, 2018
A case report on a novel MT-ATP6 gene variation in atypical mitochondrial Leigh syndrome associated with bilateral basal ganglia calcificationsArshia Angural, Indu Sharma, Pranav Pandoh, et al.
Scientific Reports|May 15, 2023
Cost-effective Whole Exome Sequencing discovers pathogenic variant causing Neurofibromatosis type 1 in a family from Jammu and Kashmir, IndiaAkshi Spolia, Arshia Angural, Varun Sharma, et al.
Scientific Reports|July 7, 2017
A variation in PANK2 gene is causing Pantothenate kinase-associated Neurodegeneration in a family from Jammu and Kashmir - IndiaArshia Angural, Inderpal Singh, Ankit Mahajan, et al.
Scientific Reports|June 14, 2016
Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-IndiaEkta Rai, Ankit Mahajan, Parvinder Kumar, et al.
Epilepsy & Behavior : E&B|April 5, 2022
Evaluation of one-year effectiveness of clobazam as an add-on therapy to anticonvulsant monotherapy in participants with epilepsy having uncontrolled seizure episodes: An Indian experienceParthasarathy Satishchandra, Chaturbhuj Rathore, Anirudha Apte, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
The Journal of the Association of Physicians of India|November 3, 2016
Celiac Neuropathy: A Case Report from Kashmir (India)K K Pandita, Adnan Rafiq, Sushil Razdan, et al.
Case Reports in Pulmonology|January 13, 2015
"Peripheral neuropathy crippling bronchial asthma": two rare case reports of churg-strauss syndromeKamal Kishore Pandita, Khalid Javid Bhat, Sushil Razdan, et al.
Clinical Cases in Mineral and Bone Metabolism : the Official Journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases|October 23, 2012
"Excess gooD can be Dangerous". A case series of iatrogenic symptomatic hypercalcemia due to hypervitaminosis DKamal Kishore Pandita, Sushil Razdan, Rattan Parkash Kudyar, et al.
Epilepsy Research and Treatment|September 8, 2012
Active epilepsy as indicator of neurocysticercosis in rural northwest IndiaSunil Kumar Raina, Sushil Razdan, K K Pandita, et al.
Indian Journal of Human Genetics|July 4, 2012
Inbreeding as a cause for deafness: Dadhkai studySushil Razdan, Sunil Kumar Raina, Kamal K Pandita, et al.
Mitochondrion|June 22, 2018
A case report on a novel MT-ATP6 gene variation in atypical mitochondrial Leigh syndrome associated with bilateral basal ganglia calcificationsArshia Angural, Indu Sharma, Pranav Pandoh, et al.
Scientific Reports|May 15, 2023
Cost-effective Whole Exome Sequencing discovers pathogenic variant causing Neurofibromatosis type 1 in a family from Jammu and Kashmir, IndiaAkshi Spolia, Arshia Angural, Varun Sharma, et al.
Scientific Reports|July 7, 2017
A variation in PANK2 gene is causing Pantothenate kinase-associated Neurodegeneration in a family from Jammu and Kashmir - IndiaArshia Angural, Inderpal Singh, Ankit Mahajan, et al.
Scientific Reports|June 14, 2016
Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-IndiaEkta Rai, Ankit Mahajan, Parvinder Kumar, et al.
Epilepsy & Behavior : E&B|April 5, 2022
Evaluation of one-year effectiveness of clobazam as an add-on therapy to anticonvulsant monotherapy in participants with epilepsy having uncontrolled seizure episodes: An Indian experienceParthasarathy Satishchandra, Chaturbhuj Rathore, Anirudha Apte, et al.
Pageof 3