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Nandaki Keshavan

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Journal of Inherited Metabolic Disease|November 7, 2020
Comment on "A severe linezolid-induced rhabdomyolysis and lactic acidosis in Leigh syndrome"Laurence A Bindoff, David A Brown, Gráinne S Gorman, et al.
Journal of Inherited Metabolic Disease|February 8, 2020
Safety of drug use in patients with a primary mitochondrial disease: An international Delphi-based consensusMaaike C De Vries, David A Brown, Mitchell E Allen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 30, 2019
The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiencyNandaki Keshavan, Jose Abdenur, Glenn Anderson, et al.
Annals of Clinical and Translational Neurology|October 18, 2021
Expanding the phenotypic spectrum of BCS1L-related mitochondrial diseaseOmar Hikmat, Pirjo Isohanni, Nandaki Keshavan, et al.
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Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Journal of Inherited Metabolic Disease|November 7, 2020
Comment on "A severe linezolid-induced rhabdomyolysis and lactic acidosis in Leigh syndrome"Laurence A Bindoff, David A Brown, Gráinne S Gorman, et al.
Journal of Inherited Metabolic Disease|February 8, 2020
Safety of drug use in patients with a primary mitochondrial disease: An international Delphi-based consensusMaaike C De Vries, David A Brown, Mitchell E Allen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 30, 2019
The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiencyNandaki Keshavan, Jose Abdenur, Glenn Anderson, et al.
Annals of Clinical and Translational Neurology|October 18, 2021
Expanding the phenotypic spectrum of BCS1L-related mitochondrial diseaseOmar Hikmat, Pirjo Isohanni, Nandaki Keshavan, et al.
Pageof 2