Zobrazeno 1 - 10
of 84
pro vyhledávání: '"W E, Hathaway"'
Autor:
W E Hathaway, Donna M. Dimichele
Publikováno v:
American Journal of Hematology. 33:39-45
Twenty-one patients with prolonged bleeding times secondary to inherited disorders of platelet function and eight patients with prolonged bleeding times secondary to acquired platelet dysfunction were given 0.3 micrograms per kilogram of DDAVP, 1-dea
Autor:
D Menache, M. B. Hultin, J. P. Ómalley, C. Williams, W. E. Hathaway, J. O. Ballard, B. Wagner, B. M. Alving, J. B. Schorr, S. H. Goodnight
Publikováno v:
Blood. 75:33-39
Antithrombin III (Human) (AT III) was administered to 18 patients with documented hereditary AT III deficiency. In eight patients with no ongoing clinical symptoms of thrombosis, the percent increase per unit AT III infused per kilogram of body weigh
Autor:
J. A. Penner, B. Wagner, C. S. Kitchens, S. H. Goodnight, J. O. Ballard, J. P. Ómalley, J. E. Sanders, Marilyn J. Manco-Johnson, J. B. Schorr, M. B. Hultin, W. G. Mcgehee, B. M. Alving, W. E. Hathaway, H. E. Lessner, D Menache, C. Williams, A. Z. Makary
Publikováno v:
Blood. 75:33-39
Antithrombin III (Human) (AT III) was administered to 18 patients with documented hereditary AT III deficiency. In eight patients with no ongoing clinical symptoms of thrombosis, the percent increase per unit AT III infused per kilogram of body weigh
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 12(6)
Summary. The objectives of the present study were to evaluate the analytical sensitivity of the recently developed Clot Formation and Lysis (CloFAL) global assay for factor VIII (FVIII) deficiency, both in vitro and ex vivo, to determine whether this
Autor:
J B, Lefkowitz, T, Haver, S, Clarke, L, Jacobson, A, Weller, R, Nuss, M, Manco-Johnson, W E, Hathaway
Publikováno v:
British journal of haematology. 108(1)
Dysprothrombinaemia is a rare, congenital cause of bleeding. Fewer than 25 families who express a functional prothrombin (factor II) defect have been reported. The original patient with prothrombin Denver had a severe haemophilia-like bleeding disord
Publikováno v:
Thrombosis and haemostasis. 82(5)
Publikováno v:
The American journal of pediatric hematology/oncology. 15(4)
A prospective study of coagulation in 15 children who received L-asparaginase, vincristine, or prednisone plus or minus an anthracycline as part of a treatment program for leukemia or leukemia-lymphoma syndrome was conducted.One patient developed a c
Autor:
W E, Hathaway
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 24
Vitamin K (phylloquinone, K1; menaquinone, K2) functions as an essential cofactor for the synthesis of the coagulation protein factors II, VII, IX, X and protein C and S by promoting a unique post-translational modification of specific glutamic acid
Autor:
W E, Hathaway
Publikováno v:
Seminars in hematology. 28(1)
Autor:
W. E. Hathaway
Publikováno v:
Perinatal Thrombosis and Hemostasis ISBN: 9784431658733
The causes of intracranial hemorrhage in the newborn infant include congenital bleeding disorders (hemophilia), thrombocytopenia, disseminated intravascular coagulation (DIC), asphyxia, infection, trauma, hemorrhagic disease of the newborn (vitamin K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29859fc085d39d381d561fd2aa2ad693
https://doi.org/10.1007/978-4-431-65871-9_25
https://doi.org/10.1007/978-4-431-65871-9_25