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Shamima Rahman

Showing results (21-30 of 182) with videos related to

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Pediatric Nephrology (Berlin, Germany)|December 13, 2012
Mitochondrial disease--an important cause of end-stage renal failureShamima Rahman, Andrew M Hall
Archives of Disease in Childhood|June 26, 2017
Recognition, investigation and management of mitochondrial diseaseJames E Davison, Shamima Rahman
Neuromuscular Disorders : NMD|April 16, 2013
189th ENMC international workshop complex I deficiency: diagnosis and treatment 20-22 April 2012, Naarden, The NetherlandsShamima Rahman, David R Thorburn
Nature Reviews. Neurology|November 20, 2018
POLG-related disorders and their neurological manifestationsShamima Rahman, William C Copeland
Journal of Inherited Metabolic Disease|June 23, 2022
The doxycycline paradox in primary mitochondrial diseasesTamas Kozicz, Shamima Rahman, Eva Morava
Journal of Inherited Metabolic Disease|January 26, 2019
Disorders of riboflavin metabolismShanti Balasubramaniam, John Christodoulou, Shamima Rahman
Journal of Inherited Metabolic Disease|December 27, 2023
Whole genome sequencing to screen 100 000 newborns for treatable genetic disordersShamima Rahman, David Bick, Richard H Scott
Neuromuscular Disorders : NMD|July 5, 2011
176th ENMC International Workshop: diagnosis and treatment of coenzyme Q₁₀ deficiencyShamima Rahman, Catherine F Clarke, Michio Hirano
Journal of Inherited Metabolic Disease|June 14, 2024
Mitochondrial membrane synthesis, remodelling and cellular traffickingMartina Messina, Frédéric M Vaz, Shamima Rahman
Annals of Neurology|December 16, 2016
Leigh map: A novel computational diagnostic resource for mitochondrial diseaseJoyeeta Rahman, Alberto Noronha, Ines Thiele, et al.
Pageof 19

Showing results (21-30 of 182) with videos related to

Sort By:
Pageof 19
Pediatric Nephrology (Berlin, Germany)|December 13, 2012
Mitochondrial disease--an important cause of end-stage renal failureShamima Rahman, Andrew M Hall
Archives of Disease in Childhood|June 26, 2017
Recognition, investigation and management of mitochondrial diseaseJames E Davison, Shamima Rahman
Neuromuscular Disorders : NMD|April 16, 2013
189th ENMC international workshop complex I deficiency: diagnosis and treatment 20-22 April 2012, Naarden, The NetherlandsShamima Rahman, David R Thorburn
Nature Reviews. Neurology|November 20, 2018
POLG-related disorders and their neurological manifestationsShamima Rahman, William C Copeland
Journal of Inherited Metabolic Disease|June 23, 2022
The doxycycline paradox in primary mitochondrial diseasesTamas Kozicz, Shamima Rahman, Eva Morava
Journal of Inherited Metabolic Disease|January 26, 2019
Disorders of riboflavin metabolismShanti Balasubramaniam, John Christodoulou, Shamima Rahman
Journal of Inherited Metabolic Disease|December 27, 2023
Whole genome sequencing to screen 100 000 newborns for treatable genetic disordersShamima Rahman, David Bick, Richard H Scott
Neuromuscular Disorders : NMD|July 5, 2011
176th ENMC International Workshop: diagnosis and treatment of coenzyme Q₁₀ deficiencyShamima Rahman, Catherine F Clarke, Michio Hirano
Journal of Inherited Metabolic Disease|June 14, 2024
Mitochondrial membrane synthesis, remodelling and cellular traffickingMartina Messina, Frédéric M Vaz, Shamima Rahman
Annals of Neurology|December 16, 2016
Leigh map: A novel computational diagnostic resource for mitochondrial diseaseJoyeeta Rahman, Alberto Noronha, Ines Thiele, et al.
Pageof 19