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Eva Morava

Showing results (11-20 of 355) with videos related to

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Clinical Dysmorphology|June 8, 2011
3-methylglutaconic aciduria type IV: a syndrome with an evolving phenotypeSaskia Brigitte Wortmann, Eva Morava
Journal of Inherited Metabolic Disease|May 1, 2015
Next generation mitochondrial disease: change in diagnostics with eyes on therapyEva Morava, Garry K Brown
Molecular Genetics and Metabolism|July 8, 2025
Dolichol synthesis defects: a cautionary note on the use of statinsMatthew P Wilson, Eva Morava
Journal of Inherited Metabolic Disease|September 21, 2020
Free virtual issue: Novel paradigms for inborn errors with muscular and central neuropathologyEva Morava, Thomas S Jacques
Nutrients|November 8, 2017
Nutritional Therapies in Congenital Disorders of Glycosylation (CDG)Peter Witters, David Cassiman, Eva Morava
Journal of Inherited Metabolic Disease|October 8, 2014
Disease severity and clinical outcome in phosphosglucomutase deficiencyEva Morava, Sunnie Wong, Dirk Lefeber
Pediatric Clinics of North America|March 6, 2018
Complex Phenotypes in Inborn Errors of Metabolism: Overlapping Presentations in Congenital Disorders of Glycosylation and Mitochondrial DisordersThatjana Gardeitchik, Jeroen Wyckmans, Eva Morava
The New England Journal of Medicine|May 23, 2014
Multiple phenotypes in phosphoglucomutase 1 deficiencyThorsten Marquardt, Eva Morava, Stephan Rust
Molecular Genetics and Metabolism|August 3, 2025
Reframing primary mitochondrial disease as a sterile interferonopathyEva Morava, Ibrahim Elsharkawi, Tamas Kozicz
Journal of Inherited Metabolic Disease|June 23, 2022
The doxycycline paradox in primary mitochondrial diseasesTamas Kozicz, Shamima Rahman, Eva Morava
Pageof 36

Showing results (11-20 of 355) with videos related to

Sort By:
Pageof 36
Clinical Dysmorphology|June 8, 2011
3-methylglutaconic aciduria type IV: a syndrome with an evolving phenotypeSaskia Brigitte Wortmann, Eva Morava
Journal of Inherited Metabolic Disease|May 1, 2015
Next generation mitochondrial disease: change in diagnostics with eyes on therapyEva Morava, Garry K Brown
Molecular Genetics and Metabolism|July 8, 2025
Dolichol synthesis defects: a cautionary note on the use of statinsMatthew P Wilson, Eva Morava
Journal of Inherited Metabolic Disease|September 21, 2020
Free virtual issue: Novel paradigms for inborn errors with muscular and central neuropathologyEva Morava, Thomas S Jacques
Nutrients|November 8, 2017
Nutritional Therapies in Congenital Disorders of Glycosylation (CDG)Peter Witters, David Cassiman, Eva Morava
Journal of Inherited Metabolic Disease|October 8, 2014
Disease severity and clinical outcome in phosphosglucomutase deficiencyEva Morava, Sunnie Wong, Dirk Lefeber
Pediatric Clinics of North America|March 6, 2018
Complex Phenotypes in Inborn Errors of Metabolism: Overlapping Presentations in Congenital Disorders of Glycosylation and Mitochondrial DisordersThatjana Gardeitchik, Jeroen Wyckmans, Eva Morava
The New England Journal of Medicine|May 23, 2014
Multiple phenotypes in phosphoglucomutase 1 deficiencyThorsten Marquardt, Eva Morava, Stephan Rust
Molecular Genetics and Metabolism|August 3, 2025
Reframing primary mitochondrial disease as a sterile interferonopathyEva Morava, Ibrahim Elsharkawi, Tamas Kozicz
Journal of Inherited Metabolic Disease|June 23, 2022
The doxycycline paradox in primary mitochondrial diseasesTamas Kozicz, Shamima Rahman, Eva Morava
Pageof 36