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Vedam Ramprasad

Showing results (1-10 of 12) with videos related to

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Future Oncology (London, England)|January 17, 2015
Evolution of targeted therapies in cancer: opportunities and challenges in the clinicSam Santhosh, Prasanna Kumar, Vedam Ramprasad, et al.
Familial Cancer|December 20, 2024
Haplotype analysis detects MLH1 founder variant in Indian Lynch syndrome patient cohortHarsh Sheth, Jyoti Sadhwani, Abhinav Jain, et al.
Metabolic Brain Disease|August 5, 2017
Asparagine Synthetase deficiency-report of a novel mutation and review of literatureNeerja Gupta, Vishal Vishnu Tewari, Manoj Kumar, et al.
Scientific Reports|September 12, 2023
Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathyShamita Sanga, Sudipta Chakraborty, Mainak Bardhan, et al.
Journal of Clinical Neurology (Seoul, Korea)|June 29, 2021
Nemaline Rod/Cap Myopathy Due to Novel Homozygous <i>MYPN</i> Mutations: The First Report from South Asia and Comprehensive Literature ReviewKiran Polavarapu, Mainak Bardhan, Ram Murthy Anjanappa, et al.
American Journal of Medical Genetics. Part A|October 15, 2024
KBG Syndrome in 16 Indian IndividualsShruti Bajaj, Sheela Nampoothiri, Roshni Chugh, et al.
Neurogenetics|April 13, 2022
Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A > CMainak Bardhan, Ram Murthy Anjanappa, Kiran Polavarapu, et al.
Journal of Medical Genetics|March 9, 2023
Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysisGaurav Joshi, Nancy Beryl Janet Arthur, Thenral S Geetha, et al.
Human Molecular Genetics|November 21, 2007
SLC4A11 mutations in Fuchs endothelial corneal dystrophyEranga N Vithana, Patricio E Morgan, Vedam Ramprasad, et al.
Neurogenetics|December 29, 2022
Genotype-phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from IndiaSaraswati Nashi, Kiran Polavarapu, Mainak Bardhan, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Future Oncology (London, England)|January 17, 2015
Evolution of targeted therapies in cancer: opportunities and challenges in the clinicSam Santhosh, Prasanna Kumar, Vedam Ramprasad, et al.
Familial Cancer|December 20, 2024
Haplotype analysis detects MLH1 founder variant in Indian Lynch syndrome patient cohortHarsh Sheth, Jyoti Sadhwani, Abhinav Jain, et al.
Metabolic Brain Disease|August 5, 2017
Asparagine Synthetase deficiency-report of a novel mutation and review of literatureNeerja Gupta, Vishal Vishnu Tewari, Manoj Kumar, et al.
Scientific Reports|September 12, 2023
Identification of a shared, common haplotype segregating with an SGCB c.544 T > G mutation in Indian patients affected with sarcoglycanopathyShamita Sanga, Sudipta Chakraborty, Mainak Bardhan, et al.
Journal of Clinical Neurology (Seoul, Korea)|June 29, 2021
Nemaline Rod/Cap Myopathy Due to Novel Homozygous <i>MYPN</i> Mutations: The First Report from South Asia and Comprehensive Literature ReviewKiran Polavarapu, Mainak Bardhan, Ram Murthy Anjanappa, et al.
American Journal of Medical Genetics. Part A|October 15, 2024
KBG Syndrome in 16 Indian IndividualsShruti Bajaj, Sheela Nampoothiri, Roshni Chugh, et al.
Neurogenetics|April 13, 2022
Clinical, genetic profile and disease progression of sarcoglycanopathies in a large cohort from India: high prevalence of SGCB c.544A > CMainak Bardhan, Ram Murthy Anjanappa, Kiran Polavarapu, et al.
Journal of Medical Genetics|March 9, 2023
Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysisGaurav Joshi, Nancy Beryl Janet Arthur, Thenral S Geetha, et al.
Human Molecular Genetics|November 21, 2007
SLC4A11 mutations in Fuchs endothelial corneal dystrophyEranga N Vithana, Patricio E Morgan, Vedam Ramprasad, et al.
Neurogenetics|December 29, 2022
Genotype-phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from IndiaSaraswati Nashi, Kiran Polavarapu, Mainak Bardhan, et al.
Pageof 2