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F. Bachmann , F. Duckert (1958)
The Stuart-Prower Assay and Its Clinical SignificanceThrombosis et Diathesis hemorrhagica, 2
F. E. Dische (1958)
Substances with Factor VII ActivityBrit. J. Haemat., 4
A. J. Aballí , V. López Banús, S. Lamerens (1957)
Coagulation Studies in the Newborn Period: Alterations of Thromboplastin Generation and Effects of Vitamin K in Full-Term and Premature InfantsA. M. A. J. Dis. Child., 94
F. Bachmann , F. Duckert, M. Geiger, P. Bear (1957)
Differentiation of Factor VII Complex: Studies on the Stuart-Prower FactorThrombosis et Diathesis hemorrhagica, 1
A. Aballi, V. Banús, S. Lamerens, S. Rozengvaig (1957)
Coagulation studies in the newborn period; alterations of thromboplastin generation and effects of vitamin K in full-term and premature infants.JAMA Pediatrics, 94
R. Biggs , A. A. Sharp, J. Margolis, R. M. Hardesty, J. Stewart (1958)
Defects in the Early Stages of Blood CoagulationBrit. J. Haemat., 4
A. J. Aballí , S. Rozengvaig, V. López Banús, S. Lamerens (1958)
Estudios de la coagulación en el recién Nacido: II. Alteraciones de la Actividad Tromboplástica del SueroRev. cubana pediat., 30
C. Hougie, E. Barrow, J. Graham (1957)
Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency.The Journal of clinical investigation, 36 3
R. Lawson (1941)
Treatment of hypoprothrombinemia (hemorrhagicdisease) of the newborn infantThe Journal of Pediatrics, 18
A. vries, E. Shafrir (1956)
Studies on the clot-promoting activity of glass.The Journal of clinical investigation, 35 11
M. H. Horder (1958)
Der Stuart Factor Während der Cumarin TherapieThrombosis et Diathesis hemorrhagica, 2
Abstract In a previous publication1 and in the preceding paper2 we have presented evidence indicating that the serum of newborns with hypoprothrombinemia has a marked deficit of another thromboplastic substance besides PTC. Moreover, in mixture experiments with the thromboplastin generation test and the Loeliger-Koller technique for determination of proconvertin, newborns with severe hypoprothrombinemia appeared to have the same defect as patients receiving prolonged treatment with coumarin compounds. The various deficits of these newborns were corrected by means of stored normal serum.1,2 The recently described Stuart factor3,4 is a stable substance adsorbed by barium sulfate, which participates in the first and probably in the second stage of blood coagulation. Its deficiency is associated with a low thromboplastic activity of the serum and a very prolonged one-stage prothrombin time. The use of Russell viper venom (Stypven) also gives an abnormal result. The determination of proconvertin with a substrate plasma References 1. Aballí, A. J.; Rozengvaig, S.; López Banús, V.; Lamerens, S., and Arrastía, F.: Estudios de la coagulación en el recién Nacido: II. Alteraciones de la Actividad Tromboplástica del Suero , Rev. cubana pediat. 30:337, 1958. 2. Aballí, A. J.; López Banús, V.; Lamerens, S., and Rozengvaig, S.: Coagulation Studies in the Newborn Period: III. Hemorrhagic Disease of the Newborn, this issue, p. 24. 3. Hougie, C.C.; Barrow, E. M., and Graham, J. B.: The Stuart Factor: A Hitherto Unrecognized Blood Coagulation Factor—Proc. of the Sixth Congress of the International Society of Blood Transfusions, p. 336, 1958. 4. Hougie, C.; Barrow, E. M., and Graham, J. B.: Stuart Clotting Defect: I. Segregation of a Hereditary Hemorrhagic State from the Heterogenous Group Heretofore Called "Stable Factor" (SPCA—Proconvertin, Factor VII) Deficiency , J. Clin. Invest. 36:485, 1957.Crossref 5. Bachmann, F.; Duckert, F.; Geiger, M.; Bear, P., and Koller, F.: Differentiation of Factor VII Complex: Studies on the Stuart-Prower Factor , Thrombosis et Diathesis hemorrhagica 1: 168, 1957. 6. Dische, F. E.: Substances with Factor VII Activity , Brit. J. Haemat. 4:202, 1958.Crossref 7. Bachmann, F.; Duckert, F., and Koller, F.: The Stuart-Prower Assay and Its Clinical Significance , Thrombosis et Diathesis hemorrhagica 2:24, 1958. 8. Horder, M. H.: Der Stuart Factor Während der Cumarin Therapie , Thrombosis et Diathesis hemorrhagica 2:170, 1958. 9. Lawson, R. B.: Treatment of Hypoprothrombinemia (Hemorrhagic Disease) of the Newborn , J. Pediat. 18:224, 1941.Crossref 10. Aballí, A. J.; López Banús, V.; Lamerens, S., and Rozengvaig, S.: Coagulation Studies in the Newborn Period: Alterations of Thromboplastin Generation and Effects of Vitamin K in Full-Term and Premature Infants , A. M. A. J. Dis. Child. 94:589, 1957.Crossref 11. Shafrir, E., and de Vries, A.: Studies on Clot-Promoting Activity of Glass , J. Clin. Invest. 35:1183, 1956.Crossref 12. Biggs, R.; Sharp, A. A.; Margolis, J.; Hardesty, R. M.; Stewart, J., and Davidson, W. M.: Defects in the Early Stages of Blood Coagulation , Brit. J. Haemat. 4:177, 1958.Crossref
A.M.A. Journal of Diseases of Children – American Medical Association
Published: May 1, 1959
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