Items where Author is "Mehrjardi, M. Y. V."

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Number of items: 3.

Article

(2024) ELFN1 deficiency is associated with an autosomal recessive neurodevelopmental disorder with epilepsy. European Journal of Human Genetics. pp. 1510-1511. ISSN 1018-4813

(2023) Joint effects of paraoxonase 1 rs662 polymorphism and vitamins C/E intake on coronary artery disease severity (Gensini and SYNTAX scores) and lipid profile in patients undergoing coronary angiography. Frontiers in Nutrition. p. 11. ISSN 2296-861X

(2023) The association of the paraoxonase 1 Q192R polymorphism with coronary artery disease (CAD) and cardiometabolic risk factors in Iranian patients suspected of CAD. Frontiers in Cardiovascular Medicine. p. 10. ISSN 2297-055X

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