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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f12698d39ab05d299f009a4d596651c4
https://doi.org/10.1002/ajh.2830330108
https://doi.org/10.1002/ajh.2830330108
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::446da0a616478930e5cb7a1d4c366380
https://doi.org/10.1182/blood.v75.1.33.bloodjournal75133
https://doi.org/10.1182/blood.v75.1.33.bloodjournal75133
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a95a1f4e1fea6f334a1540e20a3e7e7
https://doi.org/10.1182/blood.v75.1.33.33
https://doi.org/10.1182/blood.v75.1.33.33
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af35ef3f411dda340183af0b324978c0
https://pubmed.ncbi.nlm.nih.gov/17083510
https://pubmed.ncbi.nlm.nih.gov/17083510
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f59d234243951df2f119c557922921f9
https://pubmed.ncbi.nlm.nih.gov/10651742
https://pubmed.ncbi.nlm.nih.gov/10651742
Publikováno v:
Thrombosis and haemostasis. 82(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5aa0544479336d6dfaae9b616787a457
https://pubmed.ncbi.nlm.nih.gov/10595659
https://pubmed.ncbi.nlm.nih.gov/10595659
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::87565dbfd7000718fc5ea80c170cf70e
https://pubmed.ncbi.nlm.nih.gov/8214362
https://pubmed.ncbi.nlm.nih.gov/8214362
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::853ed5f474cd925fbd5b80b961f255a4
https://pubmed.ncbi.nlm.nih.gov/7886607
https://pubmed.ncbi.nlm.nih.gov/7886607
Autor:
W E, Hathaway
Publikováno v:
Seminars in hematology. 28(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ba016b3cc91f9e7472adca91a159361
https://pubmed.ncbi.nlm.nih.gov/2017687
https://pubmed.ncbi.nlm.nih.gov/2017687
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
