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Journal of Clinical Medicine
|
June 12, 2020
Sperm Antioxidant Biomarkers and Their Correlation with Clinical Condition and Lifestyle with Regard to Male Reproductive Potential
Wirginia Krzyściak, Monika Papież, Ewelina Bąk, et al.
Molecular Genetics and Metabolism
|
February 9, 2025
Causes of mortality in the congenital disorders of glycosylation
Hana 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 glycosylation
Karen 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 myopathy
Judith 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 groups
Suzan Wopereis, Eva Morava, Stephanie Grünewald, et al.
American Journal of Medical Genetics. Part A
|
February 16, 2006
Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndrome
Eva 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-glycans
Ziad 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 nomenclature
Saskia 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 worse
Tim 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 cases
Ruqaiah Altassan, Michael M Allers, Diederik De Graef, et al.
Page
of 36
Search research articles
Search
Showing results (141-150 of 355) with videos related to
Sort By:
Page
of 36
Journal of Clinical Medicine
|
June 12, 2020
Sperm Antioxidant Biomarkers and Their Correlation with Clinical Condition and Lifestyle with Regard to Male Reproductive Potential
Wirginia Krzyściak, Monika Papież, Ewelina Bąk, et al.
Molecular Genetics and Metabolism
|
February 9, 2025
Causes of mortality in the congenital disorders of glycosylation
Hana 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 glycosylation
Karen 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 myopathy
Judith 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 groups
Suzan Wopereis, Eva Morava, Stephanie Grünewald, et al.
American Journal of Medical Genetics. Part A
|
February 16, 2006
Mitochondrial dysfunction in Brooks-Wisniewski-Brown syndrome
Eva 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-glycans
Ziad 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 nomenclature
Saskia 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 worse
Tim 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 cases
Ruqaiah Altassan, Michael M Allers, Diederik De Graef, et al.
Page
of 36