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Indian Journal of Palliative Care
|
November 2, 2019
The City of Hope Quality of Life Stoma Questionnaire: Malayalam Translation and Validation
L Mayadevi, B S Geetha Kumary, Mira Wagh Sudam, et al.
Brain Communications
|
December 11, 2023
Early-infantile developmental and epileptic encephalopathy: the aetiologies, phenotypic differences and outcomes-a prospective observational study
Pooja Agarwala, Bhuvandeep Narang, Thenral S Geetha, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 15, 2024
Spectrum of Alport syndrome in an Indian cohort
Menka Yadav, Trishla Jadon, Geetika Singh, et al.
Epilepsy & Behavior Reports
|
November 16, 2020
Infantile spasms: Etiology, lead time and treatment response in a resource limited setting
Priyanka Surana, Joseph D Symonds, Prabhar Srivastava, et al.
Indian Heart Journal
|
July 15, 2024
Results of comprehensive genetic testing in patients presenting to a multidisciplinary inherited heart disease clinic in India
Priya Chockalingam, Thenral S Geetha, Sandhya Nair, et al.
European Journal of Cell Biology
|
November 21, 2007
Nitric oxide/cGMP protects endothelial cells from hypoxia-mediated leakiness
Gopi Krishna Kolluru, K P Tamilarasan, Arun Stephen Rajkumar, 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 sarcoglycanopathy
Shamita Sanga, Sudipta Chakraborty, Mainak Bardhan, et al.
Plos One
|
August 6, 2009
Characterization of conformation-sensitive antibodies to ADAMTS13, the von Willebrand cleavage protease
Zuben E Sauna, Chinyere Okunji, Ryan C Hunt, 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 Review
Kiran Polavarapu, Mainak Bardhan, Ram Murthy Anjanappa, et al.
Annals of Human Genetics
|
April 22, 2022
A novel leaky splice variant in centromere protein J (CENPJ)-associated Seckel syndrome
Navneesh Yadav, Laxmi Kirola, Thenral S Geetha, et al.
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Search research articles
Search
Showing results (91-100 of 117) with videos related to
Sort By:
Page
of 12
Indian Journal of Palliative Care
|
November 2, 2019
The City of Hope Quality of Life Stoma Questionnaire: Malayalam Translation and Validation
L Mayadevi, B S Geetha Kumary, Mira Wagh Sudam, et al.
Brain Communications
|
December 11, 2023
Early-infantile developmental and epileptic encephalopathy: the aetiologies, phenotypic differences and outcomes-a prospective observational study
Pooja Agarwala, Bhuvandeep Narang, Thenral S Geetha, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 15, 2024
Spectrum of Alport syndrome in an Indian cohort
Menka Yadav, Trishla Jadon, Geetika Singh, et al.
Epilepsy & Behavior Reports
|
November 16, 2020
Infantile spasms: Etiology, lead time and treatment response in a resource limited setting
Priyanka Surana, Joseph D Symonds, Prabhar Srivastava, et al.
Indian Heart Journal
|
July 15, 2024
Results of comprehensive genetic testing in patients presenting to a multidisciplinary inherited heart disease clinic in India
Priya Chockalingam, Thenral S Geetha, Sandhya Nair, et al.
European Journal of Cell Biology
|
November 21, 2007
Nitric oxide/cGMP protects endothelial cells from hypoxia-mediated leakiness
Gopi Krishna Kolluru, K P Tamilarasan, Arun Stephen Rajkumar, 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 sarcoglycanopathy
Shamita Sanga, Sudipta Chakraborty, Mainak Bardhan, et al.
Plos One
|
August 6, 2009
Characterization of conformation-sensitive antibodies to ADAMTS13, the von Willebrand cleavage protease
Zuben E Sauna, Chinyere Okunji, Ryan C Hunt, 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 Review
Kiran Polavarapu, Mainak Bardhan, Ram Murthy Anjanappa, et al.
Annals of Human Genetics
|
April 22, 2022
A novel leaky splice variant in centromere protein J (CENPJ)-associated Seckel syndrome
Navneesh Yadav, Laxmi Kirola, Thenral S Geetha, et al.
Page
of 12