Detalhe da pesquisa
1.
PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.
PLoS Genet
; 12(10): e1006367, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27792790
2.
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.
Nat Commun
; 12(1): 6031, 2021 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34654805
3.
Genetic association study between T-786C NOS3 polymorphism and essential hypertension in an Algerian population of the Oran city.
Diabetes Metab Syndr
; 13(2): 1317-1320, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31336484
4.
Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.
Nat Commun
; 13(1): 2251, 2022 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-35443759
5.
The relationship between MTHFR C677T gene polymorphism and essential hypertension in a sample of an Algerian population of Oran city.
Int J Cardiol
; 225: 408-411, 2016 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27780089
6.
The MITF, p.E318K Variant, as a Risk Factor for Pheochromocytoma and Paraganglioma.
J Clin Endocrinol Metab
; 101(12): 4764-4768, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27680874
7.
Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences.
J Clin Endocrinol Metab
; 101(5): 2185-95, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26963950
8.
Investigation of the Matrix Metalloproteinase-2 Gene in Patients with Non-Syndromic Mitral Valve Prolapse.
J Cardiovasc Dev Dis
; 2(3): 176-189, 2015 Jul 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29371517
9.
Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia.
J Hypertens
; 33(9): 1802-10; discussion 1810, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26147384