91 related articles for article (PubMed ID: 8322279)
1. Spontaneous versus secondary thrombosis in congenital heterozygous plasminogen deficiency.
Girolami A; Sartori MT; Sgarabotto D; Patrassi GM
Thromb Haemost; 1993 May; 69(5):530-1. PubMed ID: 8322279
[No Abstract] [Full Text] [Related]
2. Danazol therapy in hypoplasminogenemia.
Shigekiyo T; Tomonari A; Uno Y; Kishi Y
Thromb Haemost; 1992 Aug; 68(2):233-4. PubMed ID: 1412174
[No Abstract] [Full Text] [Related]
3. No increased risk of thrombosis in heterozygous congenital dysplasminogenemia.
Shigekiyo T; Kanazuka M; Aihara K; Azuma H; Ohshima Y; Horie H; Nakahira H; Takeichi T; Matsumoto T
Int J Hematol; 2000 Aug; 72(2):247-52. PubMed ID: 11039677
[TBL] [Abstract][Full Text] [Related]
4. Isolated familial plasminogen deficiency may not be a risk factor for thrombosis.
Tait RC; Walker ID; Conkie JA; Islam SI; McCall F
Thromb Haemost; 1996 Dec; 76(6):1004-8. PubMed ID: 8972025
[TBL] [Abstract][Full Text] [Related]
5. Type I congenital plasminogen deficiency is not a risk factor for thrombosis.
Shigekiyo T; Uno Y; Tomonari A; Satoh K; Hondo H; Ueda S; Saito S
Thromb Haemost; 1992 Feb; 67(2):189-92. PubMed ID: 1621238
[TBL] [Abstract][Full Text] [Related]
6. Symptomatic versus asymptomatic patients in congenital hypoplasminogenemia: a statistical analysis.
Girolami A; Sartori MT; Saggiorato G; Sgarabotto D; Patrassi GM
Haematologia (Budap); 1994; 26(2):59-65. PubMed ID: 7890263
[TBL] [Abstract][Full Text] [Related]
7. Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis.
Schuster V; Zeitler P; Seregard S; Ozcelik U; Anadol D; Luchtman-Jones L; Meire F; Mingers AM; Schambeck C; Kreth HW
Thromb Haemost; 2001 Jun; 85(6):1004-10. PubMed ID: 11434676
[TBL] [Abstract][Full Text] [Related]
8. [Congenital hypoplasminogenemia and dysplasminogenemia (type I and type II congenital plasminogen deficiency)].
Shigekiyo T; Azuma H
Ryoikibetsu Shokogun Shirizu; 1998; (22 Pt 3):9-10. PubMed ID: 9851072
[No Abstract] [Full Text] [Related]
9. [Congenital plasminogen deficiency in a Japanese family].
Uno Y; Shigekiyo T; Saito S
Rinsho Ketsueki; 1990 Mar; 31(3):341-5. PubMed ID: 2366339
[TBL] [Abstract][Full Text] [Related]
10. [Congenital abnormality of plasminogen].
Aoki N
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):988-91. PubMed ID: 3270918
[No Abstract] [Full Text] [Related]
11. Heterozygous type I plasminogen deficiency is associated with an increased risk for thrombosis: a statistical analysis in 20 kindreds.
Sartori MT; Patrassi GM; Theodoridis P; Perin A; Pietrogrande F; Girolami A
Blood Coagul Fibrinolysis; 1994 Dec; 5(6):889-93. PubMed ID: 7893926
[TBL] [Abstract][Full Text] [Related]
12. Population-based distribution of plasminogen activity and estimated prevalence and relevance to thrombotic diseases of plasminogen deficiency in the Japanese: the Suita Study.
Okamoto A; Sakata T; Mannami T; Baba S; Katayama Y; Matsuo H; Yasaka M; Minematsu K; Tomoike H; Miyata T
J Thromb Haemost; 2003 Nov; 1(11):2397-403. PubMed ID: 14629475
[TBL] [Abstract][Full Text] [Related]
13. Plasminogen deficiency.
Mehta R; Shapiro AD
Haemophilia; 2008 Nov; 14(6):1261-8. PubMed ID: 19141167
[TBL] [Abstract][Full Text] [Related]
14. [Pregnancy and thrombophilia in women with congenital deficit of antithrombin III, protein C, protein S or plasminogen: analysis of 39 cases].
Montagud M; Montserrat I; Oliver A; Adelantado JM; Mateo J; Borrell M; Fontcuberta J
Med Clin (Barc); 1993 Feb; 100(6):201-4. PubMed ID: 8429723
[TBL] [Abstract][Full Text] [Related]
15. Plasminogen deficiency: an additional risk factor for thrombosis in a family with factor V R506Q mutation?
Züger M; Biasiutti FD; Furlan M; Mannhalter C; Lämmle B
Thromb Haemost; 1996 Sep; 76(3):475-6. PubMed ID: 8883289
[No Abstract] [Full Text] [Related]
16. [Abnormal plasminogen and thrombosis].
Sakata Y
Rinsho Byori; 1987 May; 35(5):497-504. PubMed ID: 3112453
[No Abstract] [Full Text] [Related]
17. Congenital heterozygous plasminogen deficiency associated with a severe thrombotic tendency.
Girolami A; Marafioti F; Rubertelli M; Cappellato MG
Acta Haematol; 1986; 75(1):54-7. PubMed ID: 3088889
[TBL] [Abstract][Full Text] [Related]
18. Asymptomatic coinheritance of heterozygous plasminogen deficiency and the factor VLeiden mutation.
McColl MD; Tait RC; Walker ID; McCall F; Conkie JA; Perry DJ
Blood Coagul Fibrinolysis; 1997 Apr; 8(3):195-9. PubMed ID: 9167021
[TBL] [Abstract][Full Text] [Related]
19. Acute sensorineural hearing loss and vertigo in a young adult with congenital plasminogen disorder.
Ishida T; Kitamura K; Tanaka H; Ichimura K; Mimuro J; Madoiwa S; Sakata Y
Auris Nasus Larynx; 2006 Jun; 33(2):187-90. PubMed ID: 16500059
[TBL] [Abstract][Full Text] [Related]
20. [Prevention of thrombosis in orthopedics--what is necessary for patient safety?].
Netz P
Lakartidningen; 1998 Jun; 95(25):2968-70. PubMed ID: 9674371
[No Abstract] [Full Text] [Related]
[Next] [New Search]