Shaghayegh Haghjooy-Javanmard
Overview
Explore the profile of Shaghayegh Haghjooy-Javanmard including associated specialties, affiliations and a list of published articles.
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25
Citations
176
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Recent Articles
1.
Heshmat-Ghahdarijani K, Vaseghi G, Hajian S, Taheri M, Haghjooy-Javanmard S, Sarrafzadegan N, et al.
Ann Med Surg (Lond)
. 2024 Nov;
86(11):6502-6506.
PMID: 39525785
Background: Familial hypercholesterolemia (FH), an autosomal dominant disease, is associated with an increased risk of premature cardiovascular disease (CVD). This study aimed to examine the variations in serum levels of...
2.
Vaseghi G, Heshmat-Ghahdarijani K, Taheri M, Ghasempoor G, Hajian S, Haghjooy-Javanmard S, et al.
Biomed Res Int
. 2023 Apr;
2023:9851784.
PMID: 37065721
[This corrects the article DOI: 10.1155/2022/5051434.].
3.
Gharipour M, Sadeghi M, Haghjooy-Javanmard S, Hamledari H, Khosravi E, Dianatkhah M, et al.
ARYA Atheroscler
. 2022 Nov;
17(2):1-7.
PMID: 36338532
Background: The oxidative stress is regarded as one of the main contributors to the health problem. Cyclooxygenase-2 (COX-2) and matrix metallopeptidase-9 (MMP-9) are two of the important genes that are...
4.
Vafaei Z, Najafian J, Shekarchizadeh M, Mostafavi S, Darakhshandeh A, Khosravifarsani M, et al.
ARYA Atheroscler
. 2022 Jun;
17(6):1-10.
PMID: 35685447
Background: Understanding the close interaction between the specialties of cardiology and oncology is necessary for early detection of cardiovascular disease (CVD) events in cancer patients. For the risk assessment of...
5.
Vaseghi G, Heshmat-Ghahdarijani K, Taheri M, Ghasempoor G, Hajian S, Haghjooy-Javanmard S, et al.
Biomed Res Int
. 2022 Jan;
2022:5051434.
PMID: 35083330
Background And Aims: Familial hypercholesterolemia (FH) is an autosomal dominant genetic disorder of lipid metabolism which leads to premature cardiovascular diseases. In patients with FH, blood inflammatory markers may be...
6.
Vaseghi G, Arabi S, Haghjooy-Javanmard S, Sabri M, Sadeghi M, Khosravi A, et al.
ARYA Atheroscler
. 2019 Aug;
15(2):53-58.
PMID: 31440286
Background: Familial hypercholesterolemia (FH) is one of the most common genetic disorders, which leads to premature coronary artery disease (CAD). It has been suggested that heterozygous FH affects around 1:250...
7.
Ghahremani F, Kefayat A, Shahbazi-Gahrouei D, Motaghi H, Mehrgardi M, Haghjooy-Javanmard S
Nanomedicine (Lond)
. 2018 Oct;
13(20):2563-2578.
PMID: 30334677
Aim: Herein, the AS1411 aptamer-targeted ultrasmall gold nanoclusters (GNCs) were assessed at different aspects as a radiosensitizer. Materials & Methods: AS1411 aptamer-conjugated gold nanoclusters (Apt-GNCs) efficacy was evaluated at cancer...
8.
Kheradmand E, Haghjooy-Javanmard S, Dehghani L, Saadatnia M
Iran J Neurol
. 2017 Jul;
16(1):30-33.
PMID: 28717431
Activated protein C (APC) inactivates factor V (FV) by cleavage of its heavy chain at Arg306, Arg506, Arg679, and Lys994. Mutational changes, which abolish APC cleavage sites, may predispose thrombosis...
9.
Vaseghi G, Jafari E, Hassanzadeh F, Haghjooy-Javanmard S, Dana N, Rafieian-Kopaei M
Adv Biomed Res
. 2017 Jul;
6:76.
PMID: 28706884
Background: Quinazolinon as an important class of heterocycles is attractive in medicinal research areas due to their wide range of biological effects. Cytotoxic activities of the quinazolinone derivatives in various...
10.
Haghdoost F, Gharzi M, Faez F, Hosseinzadeh E, Tajaddini M, Ra Ei L, et al.
Iran J Neurol
. 2016 Jun;
15(2):80-4.
PMID: 27326362
Background: Migraine is a common neurovascular disorder with multifactorial and polygenic inheritance. The aim of this study was to investigate the association of a migraine without aura and Ala379Val polymorphism...