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Sumita Danda

Showing results (11-20 of 155) with videos related to

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Clinical Dysmorphology|April 5, 2016
A novel de-novo frameshift mutation of the ASXL1 gene in a classic case of Bohring-Opitz syndromeGautham Arunachal, Sumita Danda, Sabita Omprakash, et al.
Neuropediatrics|February 22, 2022
Unusual Magnetic Resonance Imaging Findings in 3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase DeficiencyPrateek Malik, Sangeetha Yoganathan, Sumita Danda, et al.
The Journal of the Association of Physicians of India|May 21, 2017
Gaucher Disease Presenting in an Adult with Intracerebral BleedSandeep Nemani, Bhumi Agrawal, Sumita Danda, et al.
Indian Dermatology Online Journal|October 11, 2025
Systematized Linear Porokeratosis, with Underlying Mevalonate Kinase Mutation, Treated with a Combination of Radiosurgery and Oral AcitretinArunima Ray, Susanne A Pulimood, Meera Thomas, et al.
The National Medical Journal of India|July 31, 2014
Juvenile ankylosing spondylitis in Turner syndromeP Sandhya, Debashish Danda, Sumita Danda, et al.
Annals of Indian Academy of Neurology|March 26, 2025
Broadening the Phenotypic Range: KCNJ2 Variant Linked to Isolated Periodic Paralysis with Fixed MyopathyAditya Vijayakrishnan Nair, Ajith Sivadasan, Karthik Muthusamy, et al.
Genetic Testing and Molecular Biomarkers|July 8, 2009
An Indian boy with nephropathic cystinosis: a case report and molecular analysis of CTNS mutationSha Tang, Sumita Danda, Mehrdad Zoleikhaeian, et al.
Clinical Dysmorphology|December 1, 2007
Three siblings with Woodhouse-Sakati syndrome in an Indian familyGeorge Koshy, Sumita Danda, Nihal Thomas, et al.
Indian Journal of Pediatrics|September 1, 2021
An Inherited Cause of Stroke Mimic in a ToddlerSangeetha Yoganathan, Madhan Kumar, Lenka Sushma, et al.
Indian Journal of Pediatrics|August 19, 2022
Novel Mutations in CRLF1: Case Reports with Crisponi SyndromeRekha A, Shanu Chandran, Arpita Roy Ghatak, et al.
Pageof 16

Showing results (11-20 of 155) with videos related to

Sort By:
Pageof 16
Clinical Dysmorphology|April 5, 2016
A novel de-novo frameshift mutation of the ASXL1 gene in a classic case of Bohring-Opitz syndromeGautham Arunachal, Sumita Danda, Sabita Omprakash, et al.
Neuropediatrics|February 22, 2022
Unusual Magnetic Resonance Imaging Findings in 3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase DeficiencyPrateek Malik, Sangeetha Yoganathan, Sumita Danda, et al.
The Journal of the Association of Physicians of India|May 21, 2017
Gaucher Disease Presenting in an Adult with Intracerebral BleedSandeep Nemani, Bhumi Agrawal, Sumita Danda, et al.
Indian Dermatology Online Journal|October 11, 2025
Systematized Linear Porokeratosis, with Underlying Mevalonate Kinase Mutation, Treated with a Combination of Radiosurgery and Oral AcitretinArunima Ray, Susanne A Pulimood, Meera Thomas, et al.
The National Medical Journal of India|July 31, 2014
Juvenile ankylosing spondylitis in Turner syndromeP Sandhya, Debashish Danda, Sumita Danda, et al.
Annals of Indian Academy of Neurology|March 26, 2025
Broadening the Phenotypic Range: KCNJ2 Variant Linked to Isolated Periodic Paralysis with Fixed MyopathyAditya Vijayakrishnan Nair, Ajith Sivadasan, Karthik Muthusamy, et al.
Genetic Testing and Molecular Biomarkers|July 8, 2009
An Indian boy with nephropathic cystinosis: a case report and molecular analysis of CTNS mutationSha Tang, Sumita Danda, Mehrdad Zoleikhaeian, et al.
Clinical Dysmorphology|December 1, 2007
Three siblings with Woodhouse-Sakati syndrome in an Indian familyGeorge Koshy, Sumita Danda, Nihal Thomas, et al.
Indian Journal of Pediatrics|September 1, 2021
An Inherited Cause of Stroke Mimic in a ToddlerSangeetha Yoganathan, Madhan Kumar, Lenka Sushma, et al.
Indian Journal of Pediatrics|August 19, 2022
Novel Mutations in CRLF1: Case Reports with Crisponi SyndromeRekha A, Shanu Chandran, Arpita Roy Ghatak, et al.
Pageof 16