Spontaneous Versus Secondary Thrombosis in Congenital Heterozygous Plasminogen Deficiency

Antonio Girolami; Maria Teresa Sartori; Dino Sgarabotto; Giovanni Maurizio Patrassi

doi:10.1055/s-0038-1651651

Thrombosis and Haemostasis, Inhaltsverzeichnis

Thromb Haemost 1993; 69(05): 530-531
DOI: 10.1055/s-0038-1651651

Letter to the Editor

Schattauer GmbH Stuttgart

Spontaneous Versus Secondary Thrombosis in Congenital Heterozygous Plasminogen Deficiency

Autoren

Antonio Girolami

University of Padua Medical School, Institute of Medical Semiotics, IV Chair of Internal Medicine, Padua, Italy
Maria Teresa Sartori

University of Padua Medical School, Institute of Medical Semiotics, IV Chair of Internal Medicine, Padua, Italy
Dino Sgarabotto

University of Padua Medical School, Institute of Medical Semiotics, IV Chair of Internal Medicine, Padua, Italy
Giovanni Maurizio Patrassi

University of Padua Medical School, Institute of Medical Semiotics, IV Chair of Internal Medicine, Padua, Italy

Abstract

als PDF herunterladen

PDF (370 kb)

Referenzen

References
1 Shigekiyo T, Tomonari A, Uno Y, Kishi Y. Danazol therapy in hypoplasminogenemia. Thromb Haemostas 1992; 68: 233-234
2 Shigekiyo T, Uno Y, Tomonari A, Satoh K, Hondo U, Ueda S, Saito S. Type I congenital plasminogen deficiency is not a risk factor for thrombosis. Thromb Haemostas 1992; 67: 189-192
3 Hasegawa DK, Tyler BJ, Edson Jr. Thrombotic disease in three families with inherited plasminogen deficiency. Blood 1982; 60 (Suppl. 01) 213a
4 Ten Cate JW, Peters M, Büller H. Isolated plasminogen deficiency in a patient with recurrent thromboembolic complication. Thromb Haemostas 1983; 50: 59
5 Lottemberg R, Dolly FR, Kitchens CS. Recurring thromboembolic disease and pulmonary hypertension associated with severe hypoplasminogenemia. Am J Hematol 1985; 181: 93
6 Girolami A, Marafioti F, Rubertelli M, Cappellato MG. Congenital heterozygous plasminogen deficiency associated with a severe thrombotic tendency. Acta Haematol 1986; 75: 54-57
7 Priollet P, Roncato M, Vayssairat M, Aiach M, Fiessinger JN, Mexme M, Leclerc M, Housset E. Von Recklinghausen neurofibromatosis and hereditary plasminogen deficiency. Dermatologica 1986; 172: 62-63
8 Mannucci PM, Kluft C, Traas DW, Seveso P, D’Angelo A. Congenital plasminogen deficiency associated with venous thromboembolism: therapeutic trial with stanazolol. Br J Haematol 1986; 63: 753-759
9 Tengborn L, Johannessen M, Hender U. Family with hypoplas-minogenemia. Thromb Haemostas 1987; 58: 93
10 Dolan G, Greaves M, Cooper P, Preston EE. Thrombovascular disease and familial plasminogen deficiency: a report of three kindreds. Br J Haematol 1988; 70: 417-421
11 Hach-Wunderle V, Scharrer I, Lottemberg R. Congenital deficiency of plasminogen and its relationship to venous thrombosis. Thromb Haemostas 1988; 59: 277-280
12 Skoda U, Goldmann SF, Händler C, Hummel K, Lechler E, Lübcke I, Mauff A, Meyer-Börnecke D, Pesch S, Pulverer G. Plasminogen hemizygosity. Vox Sang 1988; 54: 210-214
13 Mayer K, Hartmann H, Immel A, Seitz R, Egbring R. Congenital heterozygote hypoplasminogenemia as a risk factor for thrombosis. Fibrinolysis 1988; 2 (Suppl. 02) 37-38
14 Tabernero MD, Gonzalez SarmientoR, Tomas JF, Alberca I. Plasminogen deficiency in a Spanish family. Fibrinolysis 1988; 2 (Suppl. 02) 40-42
15 Conard J, Horellou MH, Samama M. Incidence of thromboembolism in association with congenital disorders in coagulation and fibrinolysis. Acta Chir Scand 1988; 543 (Suppl) 15-25
16 Leebeck FWG, Knot EAR, Ten Cate JW, Traas DW. Severe thrombotic tendency associated with a type I plasminogen deficiency. Am J Hematol 1989; 30: 32-35
17 Okamura T, Tsuda Y, Murakawa M, Suehiro K, Matsubara F, Kamura T, Shibuya T, Harada M, Niho Y. Congenital plasminogen deficiency associated with a primary pulmonary hypertension. Thromb Haemostas 1991; 65 (06) 1336