F M. De Coo
Rotterdam, ZH, Netherlands
Last Updated: 09/26/2026
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Found 14 publications
Blood biomarkers for assessment of mitochondrial dysfunction: An expert review.
Journal: Mitochondrion
Published: April 13, 2021
Renal Phenotype in Mitochondrial Diseases: A Multicenter Study.
Journal: Kidney diseases (Basel, Switzerland)
Published: February 13, 2021
Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases.
Journal: Journal of inherited metabolic disease
Published: August 14, 2019
A clinical diagnostic algorithm for early onset cerebellar ataxia.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: January 22, 2019
NDUFA9 point mutations cause a variable mitochondrial complex I assembly defect.
Journal: Clinical genetics
Published: June 06, 2017
Novel pathogenic SLC25A46 splice-site mutation causes an optic atrophy spectrum disorder.
Journal: Clinical genetics
Published: November 26, 2015
How do changes in the mtDNA and mitochondrial dysfunction influence cancer and cancer therapy? Challenges, opportunities and models.
Journal: Mutation research. Reviews in mutation research
Published: August 28, 2014
Forty-Five Years of Duchenne Muscular Dystrophy in The Netherlands.
Journal: Journal of neuromuscular diseases
Published: January 01, 2014
Decreased excitability of the distal motor nerve of young patients with type 1 diabetes mellitus.
Journal: Pediatric diabetes
Published: November 14, 2012
Physical activity is the key determinant of skeletal muscle mitochondrial function in type 2 diabetes.
Journal: The Journal of clinical endocrinology and metabolism
Published: July 18, 2012
Last Updated: 09/26/2026