Paloma Sanchez-Garay
Las Palmas De Gran Canaria, CN, Spain
Last Updated: 09/26/2026
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Found 9 publications
A Common Variant at the 3'untranslated Region of the CCL7 Gene (rs17735770) Is Associated With Decreased Susceptibility to Coronary Heart Disease.
Journal: Frontiers in cardiovascular medicine
Published: March 30, 2022
Wilson disease: revision of diagnostic criteria in a clinical series with great genetic homogeneity.
Wilson disease: revision of diagnostic criteria in a clinical series with great genetic homogeneity.
Journal: Journal of gastroenterology
Published: May 19, 2020
CYP2C19 or CYP3A5 Genotyping Does Not Predict Clinical Response to Clopidogrel.
Journal: Journal of clinical pharmacology
Published: February 01, 2018
Novel Marfan Syndrome-Associated Mutation in the FBN1 Gene Caused by Parental Mosaicism and Leading to Abnormal Limb Patterning.
Journal: Molecular syndromology
Published: January 27, 2017
CYP2C19 activity and cardiovascular risk factors in patients with an acute coronary syndrome.
Journal: Medicina clinica
Published: November 08, 2016
Paraoxonase 1 (Q192R) gene polymorphism, coronary heart disease and the risk of a new acute coronary event.
Journal: Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis
Published: July 10, 2016
Positive clinical response to clopidogrel is independent of paraoxonase 1 Q192R and CYP2C19 genetic variants.
Journal: Journal of clinical pharmacology
Published: October 16, 2013
Novel Frameshift CHD7 Mutation Related to CHARGE Syndrome.
Journal: Molecular syndromology
Published: August 28, 2013
A novel fibrillin 1 gene mutation leading to marfan syndrome with minimal cardiac features.
Journal: Molecular syndromology
Published: January 10, 2013
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Last Updated: 09/26/2026