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Essays in Biochemistry
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July 8, 2018
Natural history of mitochondrial disorders: a systematic review
Nandaki Keshavan, Shamima Rahman
Molecular Genetics and Metabolism
|
July 30, 2024
Natural history of deoxyguanosine kinase deficiency
Nandaki Keshavan, Shamima Rahman
Journal of Inherited Metabolic Disease
|
January 15, 2024
Mission possible: Gene therapy for inherited metabolic diseases
Julien Baruteau, Nandaki Keshavan, Charles P Venditti
Journal of Inherited Metabolic Disease
|
January 3, 2024
Gene therapy for mitochondrial disorders
Nandaki Keshavan, Michal Minczuk, Carlo Viscomi, et al.
Annals of Neurology
|
September 25, 2024
Interferon Stimulated Gene Expression Is a Biomarker for Primary Mitochondrial Disease
Nandaki Keshavan, Lana Mhaldien, Kimberly Gilmour, et al.
Journal of Inherited Metabolic Disease
|
July 4, 2020
Moving towards clinical trials for mitochondrial diseases
Robert D S Pitceathly, Nandaki Keshavan, Joyeeta Rahman, et al.
Development (Cambridge, England)
|
January 23, 2014
A nutrient-sensitive restriction point is active during retinal progenitor cell differentiation
Nicola K Love, Nandaki Keshavan, Rebecca Lewis, et al.
JIMD Reports
|
March 14, 2022
Clinical status, biochemical profile and management of a single cohort of patients with arginase deficiency
Nandaki Keshavan, Michelle Wood, Lucy M Alderson, et al.
Molecular Therapy. Methods & Clinical Development
|
February 3, 2025
Gene therapy prevents hepatic mitochondrial dysfunction in murine deoxyguanosine kinase deficiency
Nandaki Keshavan, Miriam Greenwood, Helen Prunty, et al.
Journal of Medical Genetics
|
November 28, 2019
Cardiac valve involvement in <i>ADAR</i>-related type I interferonopathy
Yanick Crow, Nandaki Keshavan, Jacques Patrick Barbet, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Essays in Biochemistry
|
July 8, 2018
Natural history of mitochondrial disorders: a systematic review
Nandaki Keshavan, Shamima Rahman
Molecular Genetics and Metabolism
|
July 30, 2024
Natural history of deoxyguanosine kinase deficiency
Nandaki Keshavan, Shamima Rahman
Journal of Inherited Metabolic Disease
|
January 15, 2024
Mission possible: Gene therapy for inherited metabolic diseases
Julien Baruteau, Nandaki Keshavan, Charles P Venditti
Journal of Inherited Metabolic Disease
|
January 3, 2024
Gene therapy for mitochondrial disorders
Nandaki Keshavan, Michal Minczuk, Carlo Viscomi, et al.
Annals of Neurology
|
September 25, 2024
Interferon Stimulated Gene Expression Is a Biomarker for Primary Mitochondrial Disease
Nandaki Keshavan, Lana Mhaldien, Kimberly Gilmour, et al.
Journal of Inherited Metabolic Disease
|
July 4, 2020
Moving towards clinical trials for mitochondrial diseases
Robert D S Pitceathly, Nandaki Keshavan, Joyeeta Rahman, et al.
Development (Cambridge, England)
|
January 23, 2014
A nutrient-sensitive restriction point is active during retinal progenitor cell differentiation
Nicola K Love, Nandaki Keshavan, Rebecca Lewis, et al.
JIMD Reports
|
March 14, 2022
Clinical status, biochemical profile and management of a single cohort of patients with arginase deficiency
Nandaki Keshavan, Michelle Wood, Lucy M Alderson, et al.
Molecular Therapy. Methods & Clinical Development
|
February 3, 2025
Gene therapy prevents hepatic mitochondrial dysfunction in murine deoxyguanosine kinase deficiency
Nandaki Keshavan, Miriam Greenwood, Helen Prunty, et al.
Journal of Medical Genetics
|
November 28, 2019
Cardiac valve involvement in <i>ADAR</i>-related type I interferonopathy
Yanick Crow, Nandaki Keshavan, Jacques Patrick Barbet, et al.
Page
of 2