Literature DB >> 1086116

Von Willebrand's disease.

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Year:  1976        PMID: 1086116      PMCID: PMC1688784     

Source DB:  PubMed          Journal:  Br Med J        ISSN: 0007-1447


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  16 in total

1.  Failure of AHF concentration to control bleeding in von Willebrand's disease.

Authors:  D Green; E V Potter
Journal:  Am J Med       Date:  1976-03       Impact factor: 4.965

2.  Diagnosis of von Willebrand's disease. A comparative study of diagnostic tests on nine families with von Willebrand's disease and its differential diagnosis from hemophilia and thrombocytopathy.

Authors:  E C Lian; D Deykin
Journal:  Am J Med       Date:  1976-03       Impact factor: 4.965

3.  Factor 8 on the vascular intima: possible importance in haemostasis and thrombosis.

Authors:  A L Bloom; J C Giddings; C J Wilks
Journal:  Nat New Biol       Date:  1973-02-14

4.  Detection of heterozygotes for recessive von Willebrand's disease by the assay of antihemophilic-factor-like antigen.

Authors:  J J Veltkamp; N H van Tilburg
Journal:  N Engl J Med       Date:  1973-10-25       Impact factor: 91.245

5.  Inherited variants of factor-VIII-related protein in von Willebrand's disease.

Authors:  I R Peake; A L Bloom; J C Giddings
Journal:  N Engl J Med       Date:  1974-07-18       Impact factor: 91.245

6.  Nature of von Willebrand factor: a new assay and a specific inhibitor.

Authors:  K E Sarji; R D Stratton; R H Wagner; K M Brinkhous
Journal:  Proc Natl Acad Sci U S A       Date:  1974-08       Impact factor: 11.205

7.  Antigen-biological-activity ratio for factor VIII.

Authors:  C Hougie; R Sargeant
Journal:  Lancet       Date:  1973-03-17       Impact factor: 79.321

8.  Ristocetin--a new tool in the investigation of platelet aggregation.

Authors:  M A Howard; B G Firkin
Journal:  Thromb Diath Haemorrh       Date:  1971-10-31

9.  Genetic variants of von Willebrand's disease.

Authors:  L Holmberg; I M Nilsson
Journal:  Br Med J       Date:  1972-08-05

10.  Immunologic differentiation of classic hemophilia (factor 8 deficiency) and von Willebrand's dissase, with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V) and on an acquired circulating anticoagulant against antihemophilic factor.

Authors:  T S Zimmerman; O D Ratnoff; A E Powell
Journal:  J Clin Invest       Date:  1971-01       Impact factor: 14.808

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