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Eva Morava

Showing results (21-30 of 355) with videos related to

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Molecular Genetics and Metabolism|September 29, 2018
Central nervous involvement is common in PGM1-CDGSilvia Radenkovic, Peter Witters, Eva Morava
JAMA Psychiatry|March 16, 2018
Mitochondrial Etiology of Psychiatric Disorders: Is This the Full Story?Tamas Kozicz, Aart Schene, Eva Morava
The European Journal of Neuroscience|April 16, 2021
Powering the brain in health and diseaseTamas Kozicz, Eva Morava, Tal Yardeni
American Journal of Medical Genetics|October 31, 2002
Provisional new syndrome of MR/MCA with evolving phenotypeYves Lacassie, Eva Morava, Ivan LaMotta
Journal of Inherited Metabolic Disease|July 9, 2011
How to find and diagnose a CDG due to defective N-glycosylationDirk J Lefeber, Eva Morava, Jaak Jaeken
Trends in Molecular Medicine|May 13, 2022
Nutrition interventions in congenital disorders of glycosylationSuzanne W Boyer, Christin Johnsen, Eva Morava
Journal of Inherited Metabolic Disease|February 12, 2019
The phenotype modifier: is the mitochondrial DNA background responsible for individual differences in disease severityEva Morava, Tamas Kozicz, Douglas C Wallace
Expert Review of Molecular Diagnostics|February 15, 2014
Defining the phenotype and diagnostic considerations in adults with congenital disorders of N-linked glycosylationDavid F G J Wolthuis, Miriam C Janssen, David Cassiman, et al.
Epilepsia|February 12, 2021
Is X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy a congenital disorder of glycosylation?Gerard T Berry, Hudson H Freeze, Eva Morava
Orvosi Hetilap|February 14, 2003
[Maternal toxoplasma infection and mosaic trisomy 8 syndrome]Eva Morava, Levente Varga, Márta Czakó, et al.
Pageof 36

Showing results (21-30 of 355) with videos related to

Sort By:
Pageof 36
Molecular Genetics and Metabolism|September 29, 2018
Central nervous involvement is common in PGM1-CDGSilvia Radenkovic, Peter Witters, Eva Morava
JAMA Psychiatry|March 16, 2018
Mitochondrial Etiology of Psychiatric Disorders: Is This the Full Story?Tamas Kozicz, Aart Schene, Eva Morava
The European Journal of Neuroscience|April 16, 2021
Powering the brain in health and diseaseTamas Kozicz, Eva Morava, Tal Yardeni
American Journal of Medical Genetics|October 31, 2002
Provisional new syndrome of MR/MCA with evolving phenotypeYves Lacassie, Eva Morava, Ivan LaMotta
Journal of Inherited Metabolic Disease|July 9, 2011
How to find and diagnose a CDG due to defective N-glycosylationDirk J Lefeber, Eva Morava, Jaak Jaeken
Trends in Molecular Medicine|May 13, 2022
Nutrition interventions in congenital disorders of glycosylationSuzanne W Boyer, Christin Johnsen, Eva Morava
Journal of Inherited Metabolic Disease|February 12, 2019
The phenotype modifier: is the mitochondrial DNA background responsible for individual differences in disease severityEva Morava, Tamas Kozicz, Douglas C Wallace
Expert Review of Molecular Diagnostics|February 15, 2014
Defining the phenotype and diagnostic considerations in adults with congenital disorders of N-linked glycosylationDavid F G J Wolthuis, Miriam C Janssen, David Cassiman, et al.
Epilepsia|February 12, 2021
Is X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy a congenital disorder of glycosylation?Gerard T Berry, Hudson H Freeze, Eva Morava
Orvosi Hetilap|February 14, 2003
[Maternal toxoplasma infection and mosaic trisomy 8 syndrome]Eva Morava, Levente Varga, Márta Czakó, et al.
Pageof 36