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Shamima Rahman

Showing results (31-40 of 182) with videos related to

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Journal of Inherited Metabolic Disease|March 28, 2019
Cerebral folate deficiency: Analytical tests and differential diagnosisSimon Pope, Rafael Artuch, Simon Heales, et al.
Journal of Inherited Metabolic Disease|January 3, 2024
Gene therapy for mitochondrial disordersNandaki Keshavan, Michal Minczuk, Carlo Viscomi, et al.
Annals of Neurology|September 25, 2024
Interferon Stimulated Gene Expression Is a Biomarker for Primary Mitochondrial DiseaseNandaki Keshavan, Lana Mhaldien, Kimberly Gilmour, et al.
Frontiers in Genetics|February 19, 2019
Systems Biology Approaches Toward Understanding Primary Mitochondrial DiseasesElaina M Maldonado, Fatma Taha, Joyeeta Rahman, et al.
BMC Pediatrics|March 6, 2014
Gentamicin, genetic variation and deafness in preterm childrenMaria Bitner-Glindzicz, Shamima Rahman, Kathy Chant, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|January 3, 2012
Plasma thiol status is altered in children with mitochondrial diseasesHeli Salmi, James V Leonard, Shamima Rahman, et al.
Journal of Inherited Metabolic Disease|December 19, 2020
An international classification of inherited metabolic disorders (ICIMD)Carlos R Ferreira, Shamima Rahman, Markus Keller, et al.
Nature Reviews. Genetics|May 25, 2021
Biparental inheritance of mitochondrial DNA revisitedAlistair T Pagnamenta, Wei Wei, Shamima Rahman, et al.
European Journal of Pediatrics|March 21, 2003
Mitochondrial HMG-CoA synthase deficiency: identification of two further patients carrying two novel mutationsNicole I Wolf, Shamima Rahman, Peter T Clayton, et al.
Journal of Inherited Metabolic Disease|August 27, 2020
Newborn screening: To WES or not to WES, that is the questionEva Morava, Matthias Baumgartner, Marc Patterson, et al.
Pageof 19

Showing results (31-40 of 182) with videos related to

Sort By:
Pageof 19
Journal of Inherited Metabolic Disease|March 28, 2019
Cerebral folate deficiency: Analytical tests and differential diagnosisSimon Pope, Rafael Artuch, Simon Heales, et al.
Journal of Inherited Metabolic Disease|January 3, 2024
Gene therapy for mitochondrial disordersNandaki Keshavan, Michal Minczuk, Carlo Viscomi, et al.
Annals of Neurology|September 25, 2024
Interferon Stimulated Gene Expression Is a Biomarker for Primary Mitochondrial DiseaseNandaki Keshavan, Lana Mhaldien, Kimberly Gilmour, et al.
Frontiers in Genetics|February 19, 2019
Systems Biology Approaches Toward Understanding Primary Mitochondrial DiseasesElaina M Maldonado, Fatma Taha, Joyeeta Rahman, et al.
BMC Pediatrics|March 6, 2014
Gentamicin, genetic variation and deafness in preterm childrenMaria Bitner-Glindzicz, Shamima Rahman, Kathy Chant, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|January 3, 2012
Plasma thiol status is altered in children with mitochondrial diseasesHeli Salmi, James V Leonard, Shamima Rahman, et al.
Journal of Inherited Metabolic Disease|December 19, 2020
An international classification of inherited metabolic disorders (ICIMD)Carlos R Ferreira, Shamima Rahman, Markus Keller, et al.
Nature Reviews. Genetics|May 25, 2021
Biparental inheritance of mitochondrial DNA revisitedAlistair T Pagnamenta, Wei Wei, Shamima Rahman, et al.
European Journal of Pediatrics|March 21, 2003
Mitochondrial HMG-CoA synthase deficiency: identification of two further patients carrying two novel mutationsNicole I Wolf, Shamima Rahman, Peter T Clayton, et al.
Journal of Inherited Metabolic Disease|August 27, 2020
Newborn screening: To WES or not to WES, that is the questionEva Morava, Matthias Baumgartner, Marc Patterson, et al.
Pageof 19