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2022 1
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Page 1
Population-Scale Studies of Protein S Abnormalities and Thrombosis.
Chaudhry SA, Haj AK, Ryu J, Jurgens SJ, Rodriguez Espada A, Wang X, Choi SH, Sanna-Cherchi S, Grover SP, Bauer KA, Ellinor PT, Bendapudi PK. Chaudhry SA, et al. JAMA. 2025 Apr 22;333(16):1423-1432. doi: 10.1001/jama.2025.0155. JAMA. 2025. PMID: 40029645 Free PMC article.
Population-scale multiomic datasets offer an unprecedented opportunity to answer questions regarding the epidemiology and clinical impacts of protein S deficiency. OBJECTIVE: To evaluate the risk associated with protein S deficiency acros …
Population-scale multiomic datasets offer an unprecedented opportunity to answer questions regarding the epidemiology and clinical impacts o …
Diagnosing protein S deficiency - Navigating challenges.
Hansen RS, Nissen PH, Larsen JB, Bor MV. Hansen RS, et al. Clin Biochem. 2025 Aug;138:110950. doi: 10.1016/j.clinbiochem.2025.110950. Epub 2025 May 24. Clin Biochem. 2025. PMID: 40419135 Free article.
OBJECTIVE: Describe challenges in diagnosing protein S deficiency. METHODS: A women in her late 20 s and pregnant in third trimester (G1P0) suffered non-hemorrhagic adrenal infarction. ...
OBJECTIVE: Describe challenges in diagnosing protein S deficiency. METHODS: A women in her late 20 s and pregnant in th …
Proteome and Metabolome Profiling of Anticoagulant Disorders Induced by Familial Protein S Deficiency.
Zhang C, Zhang Y, Liu B, Chen Y, Xie Y, Huang H, Liu Z, He Z. Zhang C, et al. J Proteome Res. 2024 Oct 4;23(10):4538-4552. doi: 10.1021/acs.jproteome.4c00399. Epub 2024 Sep 12. J Proteome Res. 2024. PMID: 39265992 Free PMC article.
Protein S deficiency (PSD) is an autosomal dominant disorder characterized by congenital thrombophilia. ...
Protein S deficiency (PSD) is an autosomal dominant disorder characterized by congenital thrombophilia. ...
A Rare Case with Pulmonary Embolism and Literature Review.
Liao J, Wu Z. Liao J, et al. Clin Lab. 2023 Dec 1;69(12). doi: 10.7754/Clin.Lab.2023.230629. Clin Lab. 2023. PMID: 38084685 Review.
For children with pulmonary embolism without clear inducement, hereditary thrombophilia should be considered. Genetic protein S deficiency (PSD) is a kind of thrombophilia, which is caused by the mutation of PROS 1 gene, resulting in an increased tendency to …
For children with pulmonary embolism without clear inducement, hereditary thrombophilia should be considered. Genetic protein S …
Spinal Cord Infarction in an Adolescent with Protein S Deficiency: A Case Report and Literature Review.
Kubota T, Hosaka T, Ando D, Ikeda K, Izumi R, Misu T, Warita H, Aoki M. Kubota T, et al. Intern Med. 2023 Aug 15;62(16):2415-2418. doi: 10.2169/internalmedicine.0153-22. Epub 2023 Jan 12. Intern Med. 2023. PMID: 36631088 Free PMC article. Review.
Protein S deficiency causes spinal cord infarction in rare cases. We herein report the first case of severe cervicothoracic cord infarction in an adolescent with protein S deficiency. ...Protein S deficiency should be …
Protein S deficiency causes spinal cord infarction in rare cases. We herein report the first case of severe cervicothor …
PROS1 variant c.1574C>T p.Ala525Val causes portal vein thrombosis with protein S deficiency.
Ye X, Mi X, Sun J, ShenTu Y, Fei Y, Tang D, Ye X, Ma X, Shi J, Chen G, Gong L. Ye X, et al. Clin Res Hepatol Gastroenterol. 2023 May;47(6):102141. doi: 10.1016/j.clinre.2023.102141. Epub 2023 May 18. Clin Res Hepatol Gastroenterol. 2023. PMID: 37207893
CASE REPORT AND RESULTS: Our case described a 60-year-old male patient presented portal vein thrombosis with protein S deficiency. Imaging findings of the patient revealed extensive thrombosis involving the portal vein and superior mesenteric vein. ...
CASE REPORT AND RESULTS: Our case described a 60-year-old male patient presented portal vein thrombosis with protein S defi …
Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiency.
Xu F, Zhou X, Jin Y, Yang L, Pan J, Wang M, Chen X. Xu F, et al. Ann Hematol. 2024 Feb;103(2):653-662. doi: 10.1007/s00277-023-05607-6. Epub 2024 Jan 4. Ann Hematol. 2024. PMID: 38175252
We report three heterozygous PROS1 mutations that caused type I protein S deficiency in three unrelated Chinese families. We measured protein S activity and antigen levels for all participants, screened them for mutations in the PROS1 gene. ...
We report three heterozygous PROS1 mutations that caused type I protein S deficiency in three unrelated Chinese familie …
Isolated gastric varices associated with antiphospholipid syndrome and protein S deficiency: a case report and review of the literature.
Li X, Wu J, Fang F, Liu Y, Jiang W, Li G, Song J. Li X, et al. J Int Med Res. 2024 Apr;52(4):3000605241240579. doi: 10.1177/03000605241240579. J Int Med Res. 2024. PMID: 38603605 Free PMC article. Review.
Although IGVs commonly form in the setting of splenic vein occlusion, the combination of antiphospholipid syndrome and protein S deficiency leading to splenic vein occlusion is rare. We herein present a case of a 28-year-old woman with intermittent epigastric …
Although IGVs commonly form in the setting of splenic vein occlusion, the combination of antiphospholipid syndrome and protein S …
22 results