Zobrazeno 1 - 10
of 16
pro vyhledávání: '"A. F. H. Britten"'
Publikováno v:
Thrombosis and Haemostasis. 24:256-264
SummaryA radioisotope method has been used for measuring factor XIII activity. The incorporation of 14C putrescine into casein is used as a model, substituting for the physiologic transamidation fibrin-fibrin bond.The reaction takes place in two phas
Publikováno v:
British Journal of Haematology. 18:399-410
Summary. The urea and acetic acid solubility tests to detect deficiency of factor XIII were compared. The urea test is more specific, but the acetic acid test is more sensitive, quicker, and therefore more convenient. A radioisotope assay method for
Publikováno v:
New England Journal of Medicine. 273:633-637
THERE is increasing evidence of an association between the ABO blood groups and certain diseases of the upper gastrointestinal tract.1 , 2 This association has been noted with gastric carcinoma and with the gastric atrophy of pernicious anemia, both
Publikováno v:
Transfusion. 24:513-515
Providing neutrophil transfusions to septic neonatal patients with depleted neutrophil reserves can be troublesome and require unscheduled blood donations. Buffy coats from stored whole blood are a potential source of neutrophils provided they remain
Autor:
D. G. Geurtze, A. F. H. Britten
Publikováno v:
Transfusion. 19(6)
A system of weekly turnover of blood inventory has been shown capable of reducing outdating in small hospitals. One problem is ensuring the return of unused blood at the end of the first week. Outdating becomes intolerable if the blood is returned to
Autor:
Anthony F. H. Britten
Publikováno v:
XIIth Congress of The World Federation of Hemophilia.
Some surprisingly simple artificial factors influence the availability of factor VIII for hemophilia treatment. Demand is affected by choice of product, and choice of treatment style (episodic vs. prophylactic), and also by availability funds.Autobio
Autor:
P. Jones, A. F. H. Britten
Publikováno v:
Supportive therapy in haematology ISBN: 9781461296171
Twenty years ago, the child with severe haemophilia was not expected to survive beyond the fourth decade [1]. If he did he was likely to have marked haemophilic arthropathy, affecting hips and shoulders, knees, ankles and elbows. His arthritis would
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8237867eca104f5441ad8d42b9616b7f
https://doi.org/10.1007/978-1-4613-2577-2_35
https://doi.org/10.1007/978-1-4613-2577-2_35
Autor:
Anthony F. H. Britten
Publikováno v:
JAMA. 187
To the Editor:— Dr. J. B. Miale is to be congratulated on his excellent study ( JAMA 185 :752 [Sept 7] 1963) of the value of the partial thromboplastin time (PTT) as a screening test. His introduction of the strikingly reliable micro technique will
Publikováno v:
American journal of clinical pathology. 59(2)
Acetylsalicylic acid (aspirin) alters platelet function, causing impairment of small vessel hemostasis and prolongation of the bleeding time. This effect may exacerbate hemorrhage and also suggests a role for this drug as an antithrombotic agent. Nor