Zobrazeno 1 - 10
of 208
pro vyhledávání: '"J Stibbe"'
Publikováno v:
European Urology Open Science, Vol 48, Iss , Pp S3- (2023)
Externí odkaz:
https://doaj.org/article/f6c202a56a124aa7bf5248b1d272c9d9
Akademický článek
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Publikováno v:
Transplant International. 5
Publikováno v:
European Journal of Clinical Investigation. 20:72-78
Three patients with congenital, nephrogenic diabetes insipidus (NDI) from two unrelated families were tested for haemostatic and fibrinolytic responses to DDAVP infusion and venous occlusion. None of the three patients showed a response of factor VII
Publikováno v:
Archives of dermatology. 135(12)
Autor:
A. Sturk, J. Stibbe, E. B. Gómez García, M. Kappers, Rogier M. Bertina, S. R. Poort, M. C. L. Schaap
Publikováno v:
British Journal of Haematology. 112:513-518
Congenital factor XIII (FXIII) deficiency is a rare autosomal recessive disorder, usually attributed to a defect in the FXIII A subunit, whose genetic basis has been studied in a number of cases. We describe here the genetic variations found in two u
Publikováno v:
The Netherlands Journal of Medicine. 46:146-152
Heparin-induced thrombocytopenia (HIT) is a severe complication of heparin therapy. Life-threatening thromboembolism (HITT) may occur in a large number of patients with HIT. In this article diagnostic problems and the clinical course of 4 typical pat
Autor:
H H Brackmann, R Egbring, A Ferster, P Fondu, J M Girardel, W Kreuz, R Masure, K Miloszewski, J Stibbe, R Zimmermann, U Krzensk, A Hoos
Publikováno v:
Thrombosis and Haemostasis. 74:622-625
SummaryThe pharmacokinetics and tolerability of factor XIII (FXIII) from plasma were compared with those of FXIII from placenta in a randomised, double-blind, crossover study involving 13 patients with congenital FXIII deficiency. Both FXIII activity
Autor:
R J Porte, J D Blankensteijn, C. M. Bakker, J Stibbe, P Schlejen, M J Gomes, Onno T. Terpstra, H I Lampe
Publikováno v:
HPB Surgery
HPB Surgery, Vol 7, Iss 4, Pp 265-280 (1994)
HPB Surgery, Vol 7, Iss 4, Pp 265-280 (1994)
We compared hemostatic changes during OLT and HLT after various periods of graft storage, to investigate whether the host liver in HLT protects the recipient from hemostatic deterioration induced by severe graft storage damage. In particular, the mec
Autor:
Herold J. Metselaar, J. Stibbe, C. M. Bakker, M J Gomes, Robert J. Porte, S.W. Schalm, Th. N. Groenland, Onno T. Terpstra
Publikováno v:
Thrombosis and Haemostasis. 69:025-028
SummaryIt is still not clear whether disseminated intravascular coagulation (DIC) contributes to the hemostatic disturbances in orthotopic liver transplantation (OLT). Theoretically the lack of hepatic clearance of procoagulant factors during the anh