Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Eva Morava

Showing results (141-150 of 355) with videos related to

Pageof 36
Sort By:
Journal of Clinical Medicine|June 12, 2020
Sperm Antioxidant Biomarkers and Their Correlation with Clinical Condition and Lifestyle with Regard to Male Reproductive PotentialWirginia Krzyściak, Monika Papież, Ewelina Bąk, et al.
Molecular Genetics and Metabolism|February 9, 2025
Causes of mortality in the congenital disorders of glycosylationHana Alharbi, Seishu Horikoshi, Sabrina Malone Jenkins, et al.
Molecular Genetics and Metabolism|January 22, 2026
Multi-omics analysis reveals ER stress as a main feature in two endothelial cell models of N-linked congenital disorders of glycosylationKaren Driesen, Veronika Holubová, Pedro Magalhães, et al.
Nature Genetics|December 26, 2006
The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathyJudith Fischer, Caroline Lefèvre, Eva Morava, et al.
Glycobiology|July 23, 2005
Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groupsSuzan Wopereis, Eva Morava, Stephanie Grünewald, et al.
American Journal of Medical Genetics. Part A|February 16, 2006
Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndromeEva Morava, Richard Rodenburg, Frans Hol, et al.
European Journal of Pediatrics|January 18, 2006
CDG: a new case of a combined defect in the biosynthesis of N- and O-glycansZiad Albahri, Eliska Marklová, Petr Dedek, et al.
Journal of Inherited Metabolic Disease|January 9, 2013
Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclatureSaskia B Wortmann, Marinus Duran, Yair Anikster, et al.
Neuroscience and Biobehavioral Reviews|May 17, 2021
Effect of neuropsychiatric medications on mitochondrial function: For better or for worseTim L Emmerzaal, Gerben Nijkamp, Marin Veldic, et al.
Molecular Genetics and Metabolism|August 30, 2023
Defining the phenotype of PGAP3-congenital disorder of glycosylation; a review of 65 casesRuqaiah Altassan, Michael M Allers, Diederik De Graef, et al.
Pageof 36

Showing results (141-150 of 355) with videos related to

Sort By:
Pageof 36
Journal of Clinical Medicine|June 12, 2020
Sperm Antioxidant Biomarkers and Their Correlation with Clinical Condition and Lifestyle with Regard to Male Reproductive PotentialWirginia Krzyściak, Monika Papież, Ewelina Bąk, et al.
Molecular Genetics and Metabolism|February 9, 2025
Causes of mortality in the congenital disorders of glycosylationHana Alharbi, Seishu Horikoshi, Sabrina Malone Jenkins, et al.
Molecular Genetics and Metabolism|January 22, 2026
Multi-omics analysis reveals ER stress as a main feature in two endothelial cell models of N-linked congenital disorders of glycosylationKaren Driesen, Veronika Holubová, Pedro Magalhães, et al.
Nature Genetics|December 26, 2006
The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathyJudith Fischer, Caroline Lefèvre, Eva Morava, et al.
Glycobiology|July 23, 2005
Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groupsSuzan Wopereis, Eva Morava, Stephanie Grünewald, et al.
American Journal of Medical Genetics. Part A|February 16, 2006
Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndromeEva Morava, Richard Rodenburg, Frans Hol, et al.
European Journal of Pediatrics|January 18, 2006
CDG: a new case of a combined defect in the biosynthesis of N- and O-glycansZiad Albahri, Eliska Marklová, Petr Dedek, et al.
Journal of Inherited Metabolic Disease|January 9, 2013
Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclatureSaskia B Wortmann, Marinus Duran, Yair Anikster, et al.
Neuroscience and Biobehavioral Reviews|May 17, 2021
Effect of neuropsychiatric medications on mitochondrial function: For better or for worseTim L Emmerzaal, Gerben Nijkamp, Marin Veldic, et al.
Molecular Genetics and Metabolism|August 30, 2023
Defining the phenotype of PGAP3-congenital disorder of glycosylation; a review of 65 casesRuqaiah Altassan, Michael M Allers, Diederik De Graef, et al.
Pageof 36