{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,10]],"date-time":"2025-10-10T13:02:24Z","timestamp":1760101344998},"reference-count":55,"publisher":"Springer Science and Business Media LLC","issue":"1","license":[{"start":{"date-parts":[[1989,12,1]],"date-time":"1989-12-01T00:00:00Z","timestamp":628473600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"},{"start":{"date-parts":[[1989,12,1]],"date-time":"1989-12-01T00:00:00Z","timestamp":628473600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Res. Clin. Lab."],"published-print":{"date-parts":[[1989,12]]},"DOI":"10.1007\/bf02871830","type":"journal-article","created":{"date-parts":[[2021,12,14]],"date-time":"2021-12-14T13:48:44Z","timestamp":1639489724000},"page":"391-402","source":"Crossref","is-referenced-by-count":3,"title":["Screening for inherited thrombotic disorders"],"prefix":"10.1007","volume":"19","author":[{"given":"Jacqueline","family":"Conard","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Marie H\u00e9l\u00e8ne","family":"Horellou","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michel-Meyer","family":"Samama","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"issue":"Suppl. 1","key":"BF02871830_CR1","first-page":"328","volume":"68","author":"H. Al-Mondhiry","year":"1986","unstructured":"Al-Mondhiry H., Galanakis D.: Fibrinogen Hershey, an abnormal fibrinogen associated with thrombosis and lupus anticoagulant \u2014 Blood68 (Suppl. 1), 328, 1986.","journal-title":"Blood"},{"key":"BF02871830_CR2","doi-asserted-by":"publisher","first-page":"243","DOI":"10.1016\/0049-3848(87)90381-1","volume":"47","author":"T. R. Andersson","year":"1987","unstructured":"Andersson T. R., Larsen M. L., Abildgaard U. A.: Low heparin cofactor II associated with abnormal crossed immunoelectrophoresis pattern in two Norwegian families \u2014 Thrombos. Res.47, 243, 1987.","journal-title":"Thrombos. Res."},{"key":"BF02871830_CR3","doi-asserted-by":"publisher","first-page":"871","DOI":"10.1007\/BF00499478","volume":"22","author":"N. Aoki","year":"1984","unstructured":"Aoki N., Tateno K., Sakata Y.: Differences of frequency distributions of plasminogen phenotypes between Japanese and American populations: new method for the detection of plasminogen variants \u2014 Biochem. Genet.22, 871, 1984.","journal-title":"Biochem. Genet."},{"key":"BF02871830_CR4","doi-asserted-by":"crossref","first-page":"1242","DOI":"10.1182\/blood.V62.6.1242.1242","volume":"62","author":"K. A. Bauer","year":"1983","unstructured":"Bauer K. A., Ashenhurst J. B., Chediak J., Rosenberg R. D.: Antithrombin \u2018Chicago\u2019: a functionally abnormal molecule with increased heparin affinity causing familial thrombophilia \u2014 Blood62, 1242, 1983.","journal-title":"Blood"},{"key":"BF02871830_CR5","doi-asserted-by":"crossref","first-page":"196","DOI":"10.1055\/s-0038-1651093","volume":"57","author":"R. M. Bertina","year":"1987","unstructured":"Bertina R. M., van der Linder I. K., Engesser L., Muller H. P., Brommer E. J. P.: Hereditary heparin cofactor II deficiency and the risk of development of thrombosis \u2014 Thrombos. Haemostas.57, 196, 1987.","journal-title":"Thrombos. Haemostas."},{"key":"BF02871830_CR6","doi-asserted-by":"crossref","first-page":"712","DOI":"10.1182\/blood.V73.3.712.712","volume":"73","author":"E. G. Bovill","year":"1989","unstructured":"Bovill E. G., Bauer K. A., Dickerman J. D., Callas P., West B.: The clinical spectrum of heterozygous protein C deficiency in a large New England kindred \u2014 Blood73, 712, 1989.","journal-title":"Blood"},{"key":"BF02871830_CR7","first-page":"203","volume-title":"Protein C and Related Proteins","author":"E. Briet","year":"1988","unstructured":"Briet E., Broekmans A. W., Engesser L.: Hereditary protein S deficiency. In:Bertina R. M. (Ed.): Protein C and Related Proteins. Churchill Livingstone, London, 1988; p. 203."},{"key":"BF02871830_CR8","first-page":"161","volume-title":"Protein C and Related Proteins","author":"A. W. Broekmans","year":"1988","unstructured":"Broekmans A. W., Conard J.: Hereditary protein C deficiency. In:Bertina R. M. (Ed.): Protein C and Related Proteins. Churchill Livingstone, London, 1988; p. 161."},{"key":"BF02871830_CR9","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1182\/blood.V71.2.335.335","volume":"71","author":"G. J. Broze","year":"1988","unstructured":"Broze G. J., Warren L. A., Novotny W. F., Higuchi D. A., Girard J. J., Miletich J. P.: The lipoprotein-associated coagulation inhibitor that inhibits the factor VII-tissue factor complex also inhibits factor Xa: insight into its possible mechanism of action \u2014 Blood71, 335, 1988.","journal-title":"Blood"},{"key":"BF02871830_CR10","doi-asserted-by":"crossref","first-page":"456","DOI":"10.1161\/01.ATV.7.5.456","volume":"7","author":"B. S. Coller","year":"1987","unstructured":"Coller B. S., Owen J., Jesty J., Horowitz D., Reitman H. J., Spear J., Yeh T., Comp P. C.: Deficiency of plasma protein S, protein C, or antithrombin III and arterial thrombosis \u2014 Arteriosclerosis7, 456, 1987.","journal-title":"Arteriosclerosis"},{"key":"BF02871830_CR11","doi-asserted-by":"publisher","first-page":"2082","DOI":"10.1172\/JCI111632","volume":"74","author":"P. C. Comp","year":"1984","unstructured":"Comp P. C., Nixon R. R., Cooper M. R., Esmon C. T.: Familial protein S deficiency is associated with recurrent thrombosis \u2014 J. clin. Invest.74, 2082, 1984.","journal-title":"J. clin. Invest."},{"issue":"Suppl.","key":"BF02871830_CR12","first-page":"15","volume":"543","author":"J. Conard","year":"1988","unstructured":"Conard J., Horellou M. H., Samama M.: Incidence of thromboembolism in association with congenital disorders in coagulation and fibrinolysis \u2014 Acta chir. scand.543 (Suppl.), 15, 1988.","journal-title":"Acta chir. scand."},{"key":"BF02871830_CR13","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1055\/s-2007-1003540","volume":"12","author":"J. Conard","year":"1986","unstructured":"Conard J., Samama M.: Inhibitors of coagulation atherosclerosis and arterial thrombosis \u2014 Semin. Thrombos. Hemostas.12, 87, 1986.","journal-title":"Semin. Thrombos. Hemostas."},{"key":"BF02871830_CR14","first-page":"205","volume":"24","author":"J. Conard","year":"1982","unstructured":"Conard J., Veuillet-Duval A., Horellou M. H., Samama M.: Etude de la coagulation et de la fibrinolyse dans 131 cas de thromboses veineuses r\u00e9cidivantes \u2014 Nouv. Rev. fran\u00e7. H\u00e9matol.24, 205, 1982.","journal-title":"Nouv. Rev. fran\u00e7. H\u00e9matol."},{"issue":"Suppl. 2","key":"BF02871830_CR15","first-page":"26","volume":"2","author":"G. Dolan","year":"1988","unstructured":"Dolan G., Preston F. E.: Familial plasminogen deficiency and thromboembolism \u2014 Fibrinolysis2 (Suppl. 2), 26, 1988.","journal-title":"Fibrinolysis"},{"key":"BF02871830_CR16","first-page":"516","volume":"13","author":"O. Egeberg","year":"1965","unstructured":"Egeberg O.: Inherited antithrombin III deficiency causing thrombophilia \u2014 Thrombos. Diathes. haemorrh. (Stuttg.)13, 516, 1965.","journal-title":"Thrombos. Diathes. haemorrh. (Stuttg.)"},{"key":"BF02871830_CR17","doi-asserted-by":"crossref","first-page":"677","DOI":"10.7326\/0003-4819-106-5-677","volume":"106","author":"L. Engesser","year":"1987","unstructured":"Engesser L., Broekmans A. W., Briet E., Brommer E. J. P., Bertina R. M.: Hereditary protein S deficiency. Clinical manifestations \u2014 Ann. intern. Med.106, 677, 1987.","journal-title":"Ann. intern. Med."},{"key":"BF02871830_CR18","doi-asserted-by":"publisher","first-page":"355","DOI":"10.1111\/j.1365-2141.1987.tb02357.x","volume":"67","author":"L. Engesser","year":"1987","unstructured":"Engesser L., Kluft C., Briet E., Brommer E. J. P.: Familial elevation of plasma histidine-rich glycoprotein in a family with thrombophilia \u2014 Brit. J. Haematol.67, 355, 1987.","journal-title":"Brit. J. Haematol."},{"key":"BF02871830_CR19","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1055\/s-0038-1647646","volume":"60","author":"L. Engesser","year":"1988","unstructured":"Engesser L., Koopman J., de Munk G., Haverkate F., Novakova I., Verheijen J. H., Briet E., Brommer E. J. P.: Fibrinogen Nijmegen: congenital dysfibrinogenemia associated with impaired t-PA mediated plasminogen activation and decreased binding of t-PA \u2014 Thrombos. Haemostas.60, 113, 1988.","journal-title":"Thrombos. Haemostas."},{"key":"BF02871830_CR20","doi-asserted-by":"crossref","first-page":"1094","DOI":"10.1055\/s-0038-1646063","volume":"58","author":"G. Finazzi","year":"1987","unstructured":"Finazzi G., Caccia R., Barbui T.: Different prevalence of thromboembolism in the subtypes of congenital antithrombin III deficiency: review of 404 cases \u2014 Thrombos. Haemostas.58, 1094, 1987.","journal-title":"Thrombos. Haemostas."},{"key":"BF02871830_CR21","unstructured":"Friedman K. D., Marlar R. A., Houston J. G., Montgomery R. R.: Warfarin-induced skin necrosis in a patient with protein S deficiency \u2014 Blood68, 333a, 1986. (Abstract)."},{"key":"BF02871830_CR22","first-page":"411","volume":"58","author":"S. Gandrille","year":"1987","unstructured":"Gandrille S., Priollet P., Capron L., Roncato M., Fiessinger N., Aiach M.: Association of hereditary dysfibrinogenemia with protein C deficiency in two patients with thrombotic tendency \u2014 Thrombos. Haemostas.58, 411, 1987.","journal-title":"Thrombos. Haemostas."},{"key":"BF02871830_CR23","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1055\/s-0038-1642558","volume":"59","author":"C. L. Gladson","year":"1988","unstructured":"Gladson C. L., Scharrer J., Hach V., Beck K. H., Griffin J. H.: The frequency of type I heterozygous protein S and protein C deficiency in 141 unrelated young patients with venous thrombosis \u2014 Thrombos. Haemostas.59, 18, 1988.","journal-title":"Thrombos. Haemostas."},{"key":"BF02871830_CR24","doi-asserted-by":"crossref","first-page":"248","DOI":"10.1097\/00005792-198307000-00004","volume":"62","author":"L. T. Goodnough","year":"1983","unstructured":"Goodnough L. T., Saito H., Ratnoff O. D.: Thrombosis or myocardial infarction in congenital clotting factor abnormalities and chronic thrombocytopenias: a report of 21 patients and a review of 50 previously reported cases \u2014 Medicine (Baltimore)62, 248, 1983.","journal-title":"Medicine (Baltimore)"},{"key":"BF02871830_CR25","doi-asserted-by":"publisher","first-page":"1370","DOI":"10.1172\/JCI110385","volume":"68","author":"J. H. Griffin","year":"1981","unstructured":"Griffin J. H., Evatt B., Zimmerman T. S., Kleiss A. J., Widemann C.: Deficiency of protein C in congenital thrombotic disease \u2014 J. clin. Invest.68, 1370, 1981.","journal-title":"J. clin. Invest."},{"key":"BF02871830_CR26","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1055\/s-0038-1661463","volume":"55","author":"F. Haverkate","year":"1986","unstructured":"Haverkate F., Koopman J., Kluft C., D\u2019Angelo A., Cattaneo M., Mannucci P. M.: Fibrinogen Milano II: a congenital dysfibrinogenemia associated with juvenile arterial and venous thrombosis \u2014 Thrombos. Haemostas.55, 131, 1986.","journal-title":"Thrombos. Haemostas."},{"key":"BF02871830_CR27","first-page":"440","volume":"62","author":"H. Heijboer","year":"1989","unstructured":"Heijboer H., Brandjes D. P. M., Rutten G. C. F. M., Buller H. R., ten Cate J. W.: Prevalence of hereditary thrombophilia in consecutive outpatients with deep vein thrombosis (DVT) \u2014 Thrombos. Haemostas.62, 440, 1989.","journal-title":"Thrombos. Haemostas."},{"key":"BF02871830_CR28","doi-asserted-by":"publisher","first-page":"1285","DOI":"10.1136\/bmj.289.6454.1285","volume":"289","author":"M. H. Horellou","year":"1984","unstructured":"Horellou M. H., Conard J., Bertina R. M., Samama M.: Congenital protein C deficiency and thrombotic disease in nine French families \u2014 Brit. med. J.289, 1285, 1984.","journal-title":"Brit. med. J."},{"key":"BF02871830_CR29","doi-asserted-by":"crossref","first-page":"477","DOI":"10.1111\/j.0954-6820.1978.tb14911.x","volume":"203","author":"L. Johansson","year":"1978","unstructured":"Johansson L., Hedner U., Nilsson I. M.: A family with thromboembolism disease associated with deficient fibrinolytic activity in vessel wall \u2014 Acta med. scand.203, 477, 1978.","journal-title":"Acta med. scand."},{"key":"BF02871830_CR30","doi-asserted-by":"crossref","first-page":"217","DOI":"10.1111\/j.1600-0609.1982.tb00586.x","volume":"29","author":"M. Jorgensen","year":"1982","unstructured":"Jorgensen M., Mortensen J. Z., Madsen A. G., Thorsen S., Jacobsen B.: A family with reduced plasminogen activator activity in blood associated with recurrent venous thrombosis \u2014 Scand. J. Haematol.29, 217, 1982.","journal-title":"Scand. J. Haematol."},{"key":"BF02871830_CR31","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1055\/s-0038-1651064","volume":"57","author":"I. Juhan-Vague","year":"1987","unstructured":"Juhan-Vague I., Valadier J., Alessi M. C., Aillaud M. F., Ansaldi J., Philip-Joet C., Holvoet P., Serradimigni A., Collen D.: Deficient t-PA release and elevated PA inhibitor levels in patients with spontaneous or recurrent deep venous thrombosis \u2014 Thrombos. Haemostas.57, 67, 1987.","journal-title":"Thrombos. Haemostas."},{"key":"BF02871830_CR32","first-page":"258","volume":"8","author":"M. Kazama","year":"1983","unstructured":"Kazama M., Tahara C., Naito I., Nakamura K., Matsuda J., Abe T.: Incidence of congenital abnormality of plasminogen in healthy adults and in several diseases \u2014 Fibrinolysis8, 258, 1983.","journal-title":"Fibrinolysis"},{"key":"BF02871830_CR33","first-page":"441","volume":"62","author":"B. Lammle","year":"1989","unstructured":"Lammle B., Krauskop F., Zurcher Ch., Huber I., Pflugshaupt R., Furlan M.: Thromboembolism and bleeding tendency in 14 families with factor XII deficiency \u2014 Thrombos. Haemostas.62, 441, 1989.","journal-title":"Thrombos. Haemostas."},{"key":"BF02871830_CR34","doi-asserted-by":"publisher","first-page":"333","DOI":"10.1016\/0049-3848(85)90229-4","volume":"39","author":"S. Manabe","year":"1985","unstructured":"Manabe S., Matsuda M.: Homozygous protein C deficiency combined with heterozygous dysplasminogenemia found in a 21-year-old thrombophilic male \u2014 Thrombos. Res.39, 333, 1985.","journal-title":"Thrombos. Res."},{"key":"BF02871830_CR35","doi-asserted-by":"crossref","first-page":"247","DOI":"10.1055\/s-0038-1651110","volume":"57","author":"P. M. Mannucci","year":"1987","unstructured":"Mannucci P. M., Tripodi A.: Laboratory screening of inherited thrombotic syndromes \u2014 Thrombos. Haemostas.57, 247, 1987.","journal-title":"Thrombos. Haemostas."},{"key":"BF02871830_CR36","first-page":"182","volume-title":"Protein C and Related Proteins","author":"R. A. Marlar","year":"1988","unstructured":"Marlar R. A., Montgomery R. R., Madden R. M.: Homozygous protein C deficiency. In:Bertina R. M. (Ed.): Protein C and Related Proteins. Churchill Livingstone, London, 1988; p. 182."},{"key":"BF02871830_CR37","doi-asserted-by":"crossref","first-page":"991","DOI":"10.1056\/NEJM198710153171604","volume":"317","author":"J. Miletich","year":"1987","unstructured":"Miletich J., Sherman L., Broze G.: Absence of thrombosis in subjects with heterozygous protein C deficiency \u2014 New Engl. J. Med.317, 991, 1987.","journal-title":"New Engl. J. Med."},{"key":"BF02871830_CR38","doi-asserted-by":"publisher","first-page":"6132","DOI":"10.1073\/pnas.79.20.6132","volume":"79","author":"T. Miyata","year":"1982","unstructured":"Miyata T., Iwanaga S., Skata Y., Aoki N.: Plasminogen Tochigi: inactive plasmin resulting from replacement of alanine-600 by threonine in the active site \u2014 Proc. nat. Acad. Sci. (Wash.)79, 6132, 1982.","journal-title":"Proc. nat. Acad. Sci. (Wash.)"},{"key":"BF02871830_CR39","doi-asserted-by":"crossref","first-page":"601","DOI":"10.1182\/blood.V72.2.601.601","volume":"72","author":"G. Nguyen","year":"1988","unstructured":"Nguyen G., Horellou M. H., Kruithof E. K. O., Conard J., Samama M.: Residual plasminogen activator inhibitor after venous stasis as a criterion for hypofibrinolysis study in 83 patients with confirmed deep vein thrombosis \u2014 Blood72, 601, 1988.","journal-title":"Blood"},{"key":"BF02871830_CR40","first-page":"7","volume":"127","author":"O. R. Odegard","year":"1977","unstructured":"Odegard O. R., Abildgaard U. A.: Antithrombin III: critical review of assay methods. Significance of variations in health and disease \u2014 Haemostasis127, 7, 1977.","journal-title":"Haemostasis"},{"key":"BF02871830_CR41","doi-asserted-by":"crossref","first-page":"393","DOI":"10.1111\/j.1365-2141.1989.tb04297.x","volume":"71","author":"J. Petaja","year":"1989","unstructured":"Petaja J., Rasi V., Myllyla G., Vahtera E., Hallman H.: Familial hypofibrinolysis and venous thrombosis \u2014 Brit. J. Haematol.71, 393, 1989.","journal-title":"Brit. J. Haematol."},{"key":"BF02871830_CR42","first-page":"281","volume-title":"Fibrinogen 2. Biochemistry, Physiology and Clinical Relevance","author":"G. Phillips","year":"1987","unstructured":"Phillips G., Kaufman R. E., Pizzo S. V.: Tissue plasminogen activator deficiency: a molecular analysis. In:Lowe G. D. O., Douglas J. T., Forbes C. D., Henschen A. (Eds): Fibrinogen 2. Biochemistry, Physiology and Clinical Relevance. Excerpta Medica, Amsterdam, 1987; p. 281."},{"key":"BF02871830_CR43","doi-asserted-by":"crossref","first-page":"479","DOI":"10.1182\/blood.V73.2.479.479","volume":"73","author":"H. K. Ploos van Amstel","year":"1989","unstructured":"Ploos van Amstel H. K., Huisman M. V., Reitsma P. H., ten Cate J. W., Bertina R. M.: Partial protein S gene deletion in a family with hereditary thrombophilia \u2014 Blood73, 479, 1989.","journal-title":"Blood"},{"key":"BF02871830_CR44","doi-asserted-by":"crossref","first-page":"645","DOI":"10.1182\/blood.V69.2.645.645","volume":"69","author":"L. V. M. Rao","year":"1987","unstructured":"Rao L. V. M., Rapaport S. I.: Studies of a mechanism inhibiting the initiation of the extrinsic pathway of coagulation \u2014 Blood69, 645, 1987.","journal-title":"Blood"},{"issue":"Suppl. 2","key":"BF02871830_CR45","first-page":"18","volume":"2","author":"M. Samama","year":"1988","unstructured":"Samama M., Conard J., Soria J.: Congenital dysfibrinogenemia and thrombosis \u2014 Fibrinolysis2 (Suppl. 2), 18, 1988.","journal-title":"Fibrinolysis"},{"key":"BF02871830_CR46","doi-asserted-by":"publisher","first-page":"389","DOI":"10.1016\/0049-3848(87)90454-3","volume":"47","author":"P. M. Sandset","year":"1987","unstructured":"Sandset P. M., Abildgaard U. A., Pettersen M.: A sensitive assay of extrinsic coagulation pathway inhibitor (EPI) in plasma and plasma fractions \u2014 Thrombos. Res.47, 389, 1987.","journal-title":"Thrombos. Res."},{"key":"BF02871830_CR47","doi-asserted-by":"crossref","first-page":"1297","DOI":"10.1182\/blood.V64.6.1297.1297","volume":"64","author":"H. P. Schwarz","year":"1984","unstructured":"Schwarz H. P., Fischer M., Hopmeier P., Batard M. A., Griffin J. D.: Plasma protein S deficiency in familial thrombotic disease \u2014 Blood64, 1297, 1984.","journal-title":"Blood"},{"key":"BF02871830_CR48","doi-asserted-by":"publisher","first-page":"414","DOI":"10.1016\/S0140-6736(85)92737-0","volume":"ii","author":"P. Sie","year":"1985","unstructured":"Sie P., Dupouy D., Pichon J., Boneu B.: Constitutional heparin cofactor II deficiency associated with recurrent thrombosis \u2014 Lancetii, 414, 1985.","journal-title":"Lancet"},{"key":"BF02871830_CR49","doi-asserted-by":"publisher","first-page":"575","DOI":"10.1111\/j.1365-2141.1983.tb07309.x","volume":"53","author":"J. Soria","year":"1983","unstructured":"Soria J., Soria C., Caen J.-P.: A new type of dysfibrinogenemia with defective fibrinolysis: Dusard syndrome. Possible relation with thrombosis \u2014 Brit. J. Haematol.53, 575, 1983.","journal-title":"Brit. J. Haematol."},{"key":"BF02871830_CR50","doi-asserted-by":"publisher","first-page":"33","DOI":"10.1016\/0002-9343(83)91115-4","volume":"74","author":"N. W. Stead","year":"1983","unstructured":"Stead N. W., Bauer K. A., Kinney T. R., Lewis J. G., Campbell E. E., Shifman M. A., Rosenberg R. D., Pizzo S. V.: Venous thrombosis in a family with defective release of vascular plasminogen activator and elevated plasma factor VIII\/von Willebrand factor \u2014 Amer. J. Med.74, 33, 1983.","journal-title":"Amer. J. Med."},{"key":"BF02871830_CR51","first-page":"369","volume-title":"Clinics in Haematology","author":"E. Thaler","year":"1981","unstructured":"Thaler E., Lechner K.: Antithrombin III deficiency and thromboembolism. In:Prentice C. R. M. (Ed.): Clinics in Haematology. W. B. Saunders, London, 1981; p. 369."},{"key":"BF02871830_CR52","first-page":"480","volume":"62","author":"D. Thommen","year":"1989","unstructured":"Thommen D., Buhrfeind E., Felix R., Sulzer I., Furlan M., Lammle B.: Hemostasis parameters in 55 patients with venous and\/or arterial thromboembolism \u2014 Thrombos. Haemostas.62, 480, 1989.","journal-title":"Thrombos. Haemostas."},{"key":"BF02871830_CR53","doi-asserted-by":"publisher","first-page":"413","DOI":"10.1016\/S0140-6736(85)92736-9","volume":"ii","author":"T. H. Tran","year":"1985","unstructured":"Tran T. H., Marbet G. A., Duckert F.: Association of hereditary heparin cofactor II deficiency with thrombosis \u2014 Lancetii, 413, 1985.","journal-title":"Lancet"},{"key":"BF02871830_CR54","first-page":"121","volume":"62","author":"A. von Felten","year":"1989","unstructured":"von Felten A., Schaefer H. P.: Protein S deficiency in young patients with cerebral arterial thrombosis \u2014 Thrombos. Haemostas.62, 121, 1989.","journal-title":"Thrombos. Haemostas."},{"issue":"Suppl. 1","key":"BF02871830_CR55","first-page":"215","volume":"57","author":"N. Yoshida","year":"1987","unstructured":"Yoshida N., Terukina S., Matsuda M., Moroi M., Okuma M., Aoki N.: Fibrinogens Kyoto and Tochigi, each with an apparent abnormal mol. wt. \u03b3Asn-308 by Lys and \u03b3Arg-275 by Cys, respectively \u2014 Thrombos. Haemostas.57 (Suppl. 1), 215, 1987.","journal-title":"Thrombos. Haemostas."}],"container-title":["La Ricerca in Clinica e in Laboratorio"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02871830.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/article\/10.1007\/BF02871830\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02871830.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,12,14]],"date-time":"2021-12-14T13:49:18Z","timestamp":1639489758000},"score":1,"resource":{"primary":{"URL":"https:\/\/link.springer.com\/10.1007\/BF02871830"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1989,12]]},"references-count":55,"journal-issue":{"issue":"1","published-print":{"date-parts":[[1989,12]]}},"alternative-id":["BF02871830"],"URL":"https:\/\/doi.org\/10.1007\/bf02871830","relation":{},"ISSN":["0390-5748"],"issn-type":[{"value":"0390-5748","type":"print"}],"subject":[],"published":{"date-parts":[[1989,12]]}}}