Detalhe da pesquisa
1.
Silent myocardial infarction fatty scars detected by coronary calcium score CT scan in diabetic patients without history of coronary heart disease.
Eur Radiol
; 34(1): 214-225, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37530810
2.
Maternal Inheritance of Familial Hypercholesterolemia Gene Mutation Predisposes to Coronary Atherosclerosis as Assessed by Calcium Score in Adulthood.
Arterioscler Thromb Vasc Biol
; 43(2): e94-e103, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36579650
3.
Additive Effect of APOE Rare Variants on the Phenotype of Familial Hypercholesterolemia.
Arterioscler Thromb Vasc Biol
; 43(7): e270-e278, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37128917
4.
Assessment of three equations to calculate plasma LDL cholesterol concentration in fasting and non-fasting hypertriglyceridemic patients.
Clin Chem Lab Med
; 62(2): 270-279, 2024 Jan 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37678263
5.
Identification of a Gain-of-Function LIPC Variant as a Novel Cause of Familial Combined Hypocholesterolemia.
Circulation
; 146(10): 724-739, 2022 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35899625
6.
Factors Predicting Statin Initiation During Childhood in Familial Hypercholesterolemia: Importance of Genetic Diagnosis.
J Pediatr
; 253: 18-24.e2, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36049522
7.
Variants in the GPR146 Gene Are Associated With a Favorable Cardiometabolic Risk Profile.
Arterioscler Thromb Vasc Biol
; 42(10): 1262-1271, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36047410
8.
X-Ray Tomography Crystal Characterization: Automatic 3D Segmentation.
Microsc Microanal
; 29(3): 983-993, 2023 Jun 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37749669
9.
SGLT2 inhibitors in type 2 diabetes: a systematic review and meta-analysis of cardiovascular outcome trials balancing their risks and benefits.
Diabetologia
; 65(12): 2000-2010, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35925319
10.
Phenotypic Differences Between Polygenic and Monogenic Hypobetalipoproteinemia.
Arterioscler Thromb Vasc Biol
; 41(1): e63-e71, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33207932
11.
Triglyceride-rich lipoproteins and their remnants: metabolic insights, role in atherosclerotic cardiovascular disease, and emerging therapeutic strategies-a consensus statement from the European Atherosclerosis Society.
Eur Heart J
; 42(47): 4791-4806, 2021 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-34472586
12.
APOB CRISPR-Cas9 Engineering in Hypobetalipoproteinemia: A Promising Tool for Functional Studies of Novel Variants.
Int J Mol Sci
; 23(8)2022 Apr 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35457099
13.
Predictors of hospital discharge and mortality in patients with diabetes and COVID-19: updated results from the nationwide CORONADO study.
Diabetologia
; 64(4): 778-794, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33599800
14.
Use of dipeptidyl peptidase-4 inhibitors and prognosis of COVID-19 in hospitalized patients with type 2 diabetes: A propensity score analysis from the CORONADO study.
Diabetes Obes Metab
; 23(5): 1162-1172, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33528920
15.
CKD Increases Carbonylation of HDL and Is Associated with Impaired Antiaggregant Properties.
J Am Soc Nephrol
; 31(7): 1462-1477, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32518085
16.
Milk polar lipids reduce lipid cardiovascular risk factors in overweight postmenopausal women: towards a gut sphingomyelin-cholesterol interplay.
Gut
; 69(3): 487-501, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31189655
17.
Autoantibodies against GPIHBP1 as a Cause of Hypertriglyceridemia.
N Engl J Med
; 376(17): 1647-1658, 2017 04 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-28402248
18.
Development of a new expanded next-generation sequencing panel for genetic diseases involved in dyslipidemia.
Clin Genet
; 98(6): 589-594, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33111339
19.
Combination of heterozygous APOB gene mutation with PNPLA3 and TM6SF2 variants promotes steatotic liver disease, cirrhosis and HCC development.
Liver Int
; 44(6): 1474-1477, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38421084
20.
Diagnostic challenge between a frequent polygenic hypocholesterolemia and an unusual Smith Lemli Opitz syndrome related to bi-allelic DHCR7 mutations.
Clin Chem Lab Med
; 2024 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38581293