Chen F, Peng D, Xia Y, Sun H, Shen H, Xia M
Lipids Health Dis. 2024; 23(1):330.
PMID: 39385249
PMC: 11462670.
DOI: 10.1186/s12944-024-02315-6.
Abdelsamei E, Hakeem G, El Amin N, Yousef M, Ghalioub H, Mohamed Z
Ann Hematol. 2024; 103(11):4749-4757.
PMID: 39349608
DOI: 10.1007/s00277-024-06002-5.
Kobayashi T, Sugiura K, Ojima T, Serizawa M, Hirai K, Morishita E
Thromb J. 2024; 22(1):18.
PMID: 38331787
PMC: 10854103.
DOI: 10.1186/s12959-024-00581-z.
Al-Awadhi A, Marouf R, Jadaon M, Al-Awadhy M
Clin Appl Thromb Hemost. 2024; 30:10760296231223195.
PMID: 38225166
PMC: 10793187.
DOI: 10.1177/10760296231223195.
Xu F, Zhou X, Jin Y, Yang L, Pan J, Wang M
Ann Hematol. 2024; 103(2):653-662.
PMID: 38175252
DOI: 10.1007/s00277-023-05607-6.
Case Report: PROS1 (p.Leu584Arg) pathogenic mutation causes portal and superior mesenteric venous thromboembolism.
Ding P, Zhou Y, Zhang K, Li S, Long K, Chen J
Front Cardiovasc Med. 2023; 10:1277676.
PMID: 38034377
PMC: 10682651.
DOI: 10.3389/fcvm.2023.1277676.
Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency.
Xu F, Zhang K, Xu Q, Ye L, Zeng M, Jin Y
Ann Hematol. 2023; 103(2):645-652.
PMID: 37950050
DOI: 10.1007/s00277-023-05487-w.
Case report: Blotchy skin in a puffy neonate: is there a new association?.
Joseph C, Lodha A, Thomas S, Awad E, Wright N, Constantinescu C
Front Pediatr. 2023; 11:1247343.
PMID: 37808560
PMC: 10552855.
DOI: 10.3389/fped.2023.1247343.
Whole-Exome Sequencing in a Family with an Unexplained Tendency for Venous Thromboembolism: Multicomponent Prediction of Low-Frequency Variant Deleteriousness and of Individual Protein Interaction.
Lunghi B, Ziliotto N, Balestra D, Rossi L, Della Valle P, Pignatelli P
Int J Mol Sci. 2023; 24(18).
PMID: 37762110
PMC: 10530467.
DOI: 10.3390/ijms241813809.
A review of venous thromboembolism in India.
Tabassum H, Chakraborty R, Chatterjee N
Indian J Med Res. 2023; 157(4):281-292.
PMID: 37282391
PMC: 10438400.
DOI: 10.4103/ijmr.ijmr_1538_22.
Testing for Factor V Leiden (FVL) and Prothrombin G20210A Genetic Variants.
Pajic T
Methods Mol Biol. 2023; 2663:233-251.
PMID: 37204714
DOI: 10.1007/978-1-0716-3175-1_14.
Laboratory Evaluation of Thrombophilia.
Marlar R
Methods Mol Biol. 2023; 2663:177-201.
PMID: 37204710
DOI: 10.1007/978-1-0716-3175-1_10.
Thromboembolic Disease in Haemophilic Patients Undergoing Major Orthopaedic Surgery: Is Thromboprophylaxis Mandatory?.
Badulescu O, Bararu Bojan I, Badescu M, Filip N, Chelsau A, Ciocoiu M
Diagnostics (Basel). 2023; 13(1).
PMID: 36611305
PMC: 9818461.
DOI: 10.3390/diagnostics13010013.
Risk Factors of Venous Thromboembolism in Sudanese Pregnant Women.
Abdalhabib E, Alfeel A, Ali E, Ibrahim I, Mobarki A, Dobie G
Balkan J Med Genet. 2022; 24(2):49-54.
PMID: 36249520
PMC: 9524171.
DOI: 10.2478/bjmg-2021-0018.
Evaluation of outcome from endovascular therapy for Budd-Chiari syndrome: a systematic review and meta-analysis.
Mukhiya G, Zhou X, Han X, Jiao D, Pokhrel G, Li Y
Sci Rep. 2022; 12(1):16166.
PMID: 36171454
PMC: 9519873.
DOI: 10.1038/s41598-022-20399-x.
Protein S Deficiency and the Risk of Venous Thromboembolism in the Han Chinese Population.
Wu Y, Liu J, Zeng W, Hu B, Hu Y, Tang L
Front Cardiovasc Med. 2022; 8:796755.
PMID: 35815065
PMC: 9260107.
DOI: 10.3389/fcvm.2021.796755.
Establishment of normal reference range for thromboelastography based on 17,708 cases in Beijing, China.
Wei C, Zhao J, Wang S, Sun H, Guan N
Ann Transl Med. 2022; 10(10):550.
PMID: 35722362
PMC: 9201150.
DOI: 10.21037/atm-22-1731.
Venous thoracic outlet syndrome.
Habibollahi P, Zhang D, Kolber M, Pillai A
Cardiovasc Diagn Ther. 2021; 11(5):1150-1158.
PMID: 34815966
PMC: 8569271.
DOI: 10.21037/cdt-20-168.
Vaccine-induced immune thrombotic thrombocytopenia after vaccination against Covid-19: A clinical dilemma for clinicians and patients.
Mohseni Afshar Z, Babazadeh A, Janbakhsh A, Afsharian M, Saleki K, Barary M
Rev Med Virol. 2021; 32(2):e2273.
PMID: 34197678
PMC: 8420499.
DOI: 10.1002/rmv.2273.
Sport and Venous Thromboembolism—Site, Accompanying Features, Symptoms, and Diagnosis.
Hilberg T, Ransmann P, Hagedorn T
Dtsch Arztebl Int. 2021; 118(11):181-187.
PMID: 34024313
PMC: 8245860.
DOI: 10.3238/arztebl.m2021.0021.
