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Maaike C de Vries

Showing results (11-20 of 52) with videos related to

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Orphanet Journal of Rare Diseases|October 1, 2022
Cognitive functioning and mental health in children with a primary mitochondrial diseaseKim F E van de Loo, José A E Custers, Lonneke de Boer, et al.
Molecular Genetics and Metabolism|January 12, 2020
Does the 48-hour BH4 loading test miss responsive PKU patients?Annemiek M J van Wegberg, Roeland A F Evers, Esther van Dam, et al.
International Journal of Systematic and Evolutionary Microbiology|July 15, 2005
The first true obligately syntrophic propionate-oxidizing bacterium, Pelotomaculum schinkii sp. nov., co-cultured with Methanospirillum hungatei, and emended description of the genus PelotomaculumFrank A M de Bok, Hermie J M Harmsen, Caroline M Plugge, et al.
Pediatric Research|December 20, 2008
Mitochondrial energy production correlates with the age-related BMISaskia B Wortmann, Heidi Zweers-van Essen, Richard J T Rodenburg, et al.
Microorganisms|April 28, 2023
Identification of <i>Francisella tularensis</i> Subspecies in a Clinical Setting Using MALDI-TOF MS: An In-House <i>Francisella</i> Library and BiomarkersMaaike C de Vries, B J A Hoeve-Bakker, Maaike J C van den Beld, et al.
Molecular Genetics and Metabolism|November 17, 2020
Gray and white matter are both affected in classical galactosemia: An explorative study on the association between neuroimaging and clinical outcomeMendy M Welsink-Karssies, Anouk Schrantee, Matthan W A Caan, et al.
Standards in Genomic Sciences|February 7, 2014
Draft genome sequence of Francisella tularensis subsp. holarctica BD11-00177Jordy P M Coolen, Andreas Sjödin, Boulos Maraha, et al.
Emerging Infectious Diseases|June 22, 2023
Epidemiology of Pathogens Listed as Potential Bioterrorism Agents, the Netherlands, 2009‒2019Jorrit Broertjes, Eelco Franz, Ingrid H M Friesema, et al.
Journal of the Neurological Sciences|January 25, 2013
A novel mutation in COQ2 leading to fatal infantile multisystem diseaseBernadette S Jakobs, Lambert P van den Heuvel, Roel J P Smeets, et al.
Brain : a Journal of Neurology|April 20, 2013
A complex V ATP5A1 defect causes fatal neonatal mitochondrial encephalopathyAn I Jonckheere, G Herma Renkema, Maaike Bras, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Orphanet Journal of Rare Diseases|October 1, 2022
Cognitive functioning and mental health in children with a primary mitochondrial diseaseKim F E van de Loo, José A E Custers, Lonneke de Boer, et al.
Molecular Genetics and Metabolism|January 12, 2020
Does the 48-hour BH4 loading test miss responsive PKU patients?Annemiek M J van Wegberg, Roeland A F Evers, Esther van Dam, et al.
International Journal of Systematic and Evolutionary Microbiology|July 15, 2005
The first true obligately syntrophic propionate-oxidizing bacterium, Pelotomaculum schinkii sp. nov., co-cultured with Methanospirillum hungatei, and emended description of the genus PelotomaculumFrank A M de Bok, Hermie J M Harmsen, Caroline M Plugge, et al.
Pediatric Research|December 20, 2008
Mitochondrial energy production correlates with the age-related BMISaskia B Wortmann, Heidi Zweers-van Essen, Richard J T Rodenburg, et al.
Microorganisms|April 28, 2023
Identification of <i>Francisella tularensis</i> Subspecies in a Clinical Setting Using MALDI-TOF MS: An In-House <i>Francisella</i> Library and BiomarkersMaaike C de Vries, B J A Hoeve-Bakker, Maaike J C van den Beld, et al.
Molecular Genetics and Metabolism|November 17, 2020
Gray and white matter are both affected in classical galactosemia: An explorative study on the association between neuroimaging and clinical outcomeMendy M Welsink-Karssies, Anouk Schrantee, Matthan W A Caan, et al.
Standards in Genomic Sciences|February 7, 2014
Draft genome sequence of Francisella tularensis subsp. holarctica BD11-00177Jordy P M Coolen, Andreas Sjödin, Boulos Maraha, et al.
Emerging Infectious Diseases|June 22, 2023
Epidemiology of Pathogens Listed as Potential Bioterrorism Agents, the Netherlands, 2009‒2019Jorrit Broertjes, Eelco Franz, Ingrid H M Friesema, et al.
Journal of the Neurological Sciences|January 25, 2013
A novel mutation in COQ2 leading to fatal infantile multisystem diseaseBernadette S Jakobs, Lambert P van den Heuvel, Roel J P Smeets, et al.
Brain : a Journal of Neurology|April 20, 2013
A complex V ATP5A1 defect causes fatal neonatal mitochondrial encephalopathyAn I Jonckheere, G Herma Renkema, Maaike Bras, et al.
Pageof 6