These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
170 related articles for article (PubMed ID: 16181984)
1. Inherited bleeding disorder due to familial type 2 platelet cyclo-oxygenase deficiency. Dargaud Y; Bordet JC; Trzeciak MC; Mazet M; Dechavanne M; Negrier C Thromb Res; 2005; 116(6):483-9. PubMed ID: 16181984 [TBL] [Abstract][Full Text] [Related]
2. Familial and constitutional bleeding disorder due to platelet cyclo-oxygenase deficiency. Horellou MH; Lecompte T; Lecrubier C; Fouque F; Chignard M; Conard J; Vargaftig BB; Dray F; Samama M Am J Hematol; 1983 Feb; 14(1):1-9. PubMed ID: 6404162 [TBL] [Abstract][Full Text] [Related]
3. Spectrum of Von Willebrand disease and inherited platelet function disorders amongst Indian bleeders. Gupta PK; Charan VD; Saxena R Ann Hematol; 2007 Jun; 86(6):403-7. PubMed ID: 17375300 [TBL] [Abstract][Full Text] [Related]
4. Clinical and laboratory phenotypes associated with the aspirin-like defect: a study in 17 unrelated families. Rolf N; Knoefler R; Bugert P; Gehrisch S; Siegert G; Kuhlisch E; Suttorp M Br J Haematol; 2009 Feb; 144(3):416-24. PubMed ID: 19036102 [TBL] [Abstract][Full Text] [Related]
5. Radioimmune assay of human platelet prostaglandin synthetase. Roth GJ; Machuga ET J Lab Clin Med; 1982 Feb; 99(2):187-96. PubMed ID: 6801166 [TBL] [Abstract][Full Text] [Related]
6. Bleeding disorders in childhood II: Inherited platelet dysfunctions. Han P J Singapore Paediatr Soc; 1985; 27(1-2):100-11. PubMed ID: 3928968 [No Abstract] [Full Text] [Related]
7. [Anesthetic management of a patient with platelet cyclo-oxygenase deficiency]. Kitahara T; Fukuda M; Matsuki M; Shimoji K; Takeshige S Masui; 1987 Feb; 36(2):261-5. PubMed ID: 3108556 [No Abstract] [Full Text] [Related]
8. [Thrombocytopathy caused by congenital cyclo-oxygenase deficiency]. Boda Z; Tamás E; Neuwirth G; Altorjay I; Rák K Orv Hetil; 1981 May; 122(19):1121-4. PubMed ID: 6791088 [No Abstract] [Full Text] [Related]
10. [Epistaxis caused by an acquired thrombocytopathy]. Veldhuizen JA; de Wolf JT; Buiter CT; Cats H Ned Tijdschr Geneeskd; 1989 Mar; 133(12):622-4. PubMed ID: 2716879 [TBL] [Abstract][Full Text] [Related]
11. The value of proteomics for the diagnosis of a platelet-related bleeding disorder. Maurer-Spurej E; Kahr WH; Carter CJ; Pittendreigh C; Cameron M; Cyr TD Platelets; 2008 Aug; 19(5):342-51. PubMed ID: 18791940 [TBL] [Abstract][Full Text] [Related]
12. [Antiplatelet therapy can unmask an inherited bleeding disorder. Aspirin-like defect of platelets does not protect against atherosclerosis]. Elikowski W; Hanszke E; Biczysko W; Rzeźniczak J; Kruk-Zagajewska A; Zawilska K Kardiol Pol; 2007 Aug; 65(8):985-91; discussion 992-3. PubMed ID: 17853322 [TBL] [Abstract][Full Text] [Related]
18. Diagnosis of Scott syndrome in patient with bleeding disorder of unknown cause. Flores-Nascimento MC; Orsi FL; Yokoyama AP; Pereira FG; Lorand-Metze I; De Paula EV; Castro V; Annichino-Bizzacchi JM Blood Coagul Fibrinolysis; 2012 Jan; 23(1):75-7. PubMed ID: 22027759 [TBL] [Abstract][Full Text] [Related]
19. Inherited platelet function disorders versus other inherited bleeding disorders: an Indian overview. Ahmad F; Kannan M; Ranjan R; Bajaj J; Choudhary VP; Saxena R Thromb Res; 2008; 121(6):835-41. PubMed ID: 17850851 [TBL] [Abstract][Full Text] [Related]
20. [Clinical and laboratory aspects of the Aspirin-like defect as hereditary thrombocytopathy]. Rolf N; Bugert P; Gehrisch S; Siegert G; Suttorp M; Knöfler R Hamostaseologie; 2009 May; 29(2):177-83. PubMed ID: 19404514 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]