Soto R. Kiando
Paris, 75001, France
Last Updated: 09/26/2026
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Found 9 publications
Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.
Journal: Nature communications
Published: April 21, 2022
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.
Journal: Nature communications
Published: November 10, 2020
Genetic association study between T-786C NOS3 polymorphism and essential hypertension in an Algerian population of the Oran city.
Journal: Diabetes & metabolic syndrome
Published: January 30, 2019
The MITF, p.E318K Variant, as a Risk Factor for Pheochromocytoma and Paraganglioma.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 30, 2016
The relationship between MTHFR C677T gene polymorphism and essential hypertension in a sample of an Algerian population of Oran city.
Journal: International journal of cardiology
Published: August 08, 2016
Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences.
Journal: The Journal of clinical endocrinology and metabolism
Published: March 11, 2016
Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia.
Journal: Journal of hypertension
Published: July 07, 2015
Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse.
Journal: Journal of cardiovascular development and disease
Published: June 03, 2015
Showing 1-9 of 9
Last Updated: 09/26/2026