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Saskia Koene

Showing results (1-10 of 57) with videos related to

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Journal of Inherited Metabolic Disease|February 15, 2017
Erratum to: International Paediatric Mitochondrial Disease ScaleSaskia Koene
Journal of Inherited Metabolic Disease|March 3, 2011
Mitochondrial medicineSaskia Koene, Jan Smeitink
Journal of Inherited Metabolic Disease|July 30, 2010
Metabolic manipulators: a well founded strategy to combat mitochondrial dysfunctionSaskia Koene, Jan Smeitink
JIMD Reports|June 27, 2019
Mitochondrial Migraine: Disentangling the angiopathy paradigm in m.3243A>G patientsJan Smeitink, Saskia Koene, Julien Beyrath, et al.
Mitochondrion|May 29, 2020
Mitochondrial migraine; a prevalence, impact and treatment efficacy cohort studyLaurie H Tiehuis, Saskia Koene, Christiaan G J Saris, et al.
Clinical Dysmorphology|June 11, 2008
Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay, ectodermal abnormalities, neonatal progeroid appearance, and developmental delaySaskia Koene, Leo A J Kluijtmans, Ron Wevers, et al.
Orphanet Journal of Rare Diseases|May 17, 2017
Quantification of gait in mitochondrial m.3243A > G patients: a validation studyRob Ramakers, Saskia Koene, Jan T Groothuis, et al.
Orphanet Journal of Rare Diseases|October 29, 2017
Erratum to: Quantification of gait in mitochondrial m.3243A > G patients: a validation studyRob Ramakers, Saskia Koene, Jan T Groothuis, et al.
Journal of Medical Genetics|May 23, 2020
Six-year prospective follow-up study in 151 carriers of the mitochondrial DNA 3243 A>G variantPaul de Laat, Richard R Rodenburg, Nel Roeleveld, et al.
Orphanet Journal of Rare Diseases|November 15, 2018
Fear of disease progression in carriers of the m.3243A > G mutationJosé A E Custers, Paul de Laat, Saskia Koene, et al.
Pageof 6

Showing results (1-10 of 57) with videos related to

Sort By:
Pageof 6
Journal of Inherited Metabolic Disease|February 15, 2017
Erratum to: International Paediatric Mitochondrial Disease ScaleSaskia Koene
Journal of Inherited Metabolic Disease|March 3, 2011
Mitochondrial medicineSaskia Koene, Jan Smeitink
Journal of Inherited Metabolic Disease|July 30, 2010
Metabolic manipulators: a well founded strategy to combat mitochondrial dysfunctionSaskia Koene, Jan Smeitink
JIMD Reports|June 27, 2019
Mitochondrial Migraine: Disentangling the angiopathy paradigm in m.3243A>G patientsJan Smeitink, Saskia Koene, Julien Beyrath, et al.
Mitochondrion|May 29, 2020
Mitochondrial migraine; a prevalence, impact and treatment efficacy cohort studyLaurie H Tiehuis, Saskia Koene, Christiaan G J Saris, et al.
Clinical Dysmorphology|June 11, 2008
Biotin-sensitive 3-methylcrotonylglycinuria in a patient with severe growth delay, ectodermal abnormalities, neonatal progeroid appearance, and developmental delaySaskia Koene, Leo A J Kluijtmans, Ron Wevers, et al.
Orphanet Journal of Rare Diseases|May 17, 2017
Quantification of gait in mitochondrial m.3243A > G patients: a validation studyRob Ramakers, Saskia Koene, Jan T Groothuis, et al.
Orphanet Journal of Rare Diseases|October 29, 2017
Erratum to: Quantification of gait in mitochondrial m.3243A > G patients: a validation studyRob Ramakers, Saskia Koene, Jan T Groothuis, et al.
Journal of Medical Genetics|May 23, 2020
Six-year prospective follow-up study in 151 carriers of the mitochondrial DNA 3243 A>G variantPaul de Laat, Richard R Rodenburg, Nel Roeleveld, et al.
Orphanet Journal of Rare Diseases|November 15, 2018
Fear of disease progression in carriers of the m.3243A > G mutationJosé A E Custers, Paul de Laat, Saskia Koene, et al.
Pageof 6