Ana Cuesta-Sanchez
Sevilla, AN, Spain
Last Updated: 09/26/2026
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Found 10 publications
Identification of a new COQ4 spliceogenic variant causing severe primary coenzyme Q deficiency.
Journal: Molecular genetics and metabolism reports
Published: August 05, 2024
New variants expand the neurological phenotype of COQ7 deficiency.
Journal: Journal of inherited metabolic disease
Published: March 30, 2024
COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction.
Journal: European journal of human genetics : EJHG
Published: December 11, 2023
Mutations of GEMIN5 are associated with coenzyme Q10 deficiency: long-term follow-up after treatment.
Journal: European journal of human genetics : EJHG
Published: July 05, 2023
Secondary CoQ10 deficiency, bioenergetics unbalance in disease and aging.
Journal: BioFactors (Oxford, England)
Published: January 18, 2021
High coenzyme Q10 plasma levels improve stress and damage markers in professional soccer players during competition.
Journal: International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition
Published: July 09, 2020
Design of High-Throughput Screening of Natural Extracts to Identify Molecules Bypassing Primary Coenzyme Q Deficiency in Saccharomyces cerevisiae.
Journal: SLAS discovery : advancing life sciences R & D
Published: November 22, 2019
ADCK2 Haploinsufficiency Reduces Mitochondrial Lipid Oxidation and Causes Myopathy Associated with CoQ Deficiency.
Journal: Journal of clinical medicine
Published: August 03, 2019
Bioavailability of coenzyme Q10 supplements depends on carrier lipids and solubilization.
Journal: Nutrition (Burbank, Los Angeles County, Calif.)
Published: January 19, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026