Hemophilia, von Willebrand's disease, and related conditions: a spectrum of laboratory and clinical disorders.

[1]  R. Biggs,et al.  Two Types of Haemophilia (A+ and A−): A Study of 48 Cases , 1969, British journal of haematology.

[2]  Y. Sultan,et al.  Congenital bleeding disorders with long bleeding time and normal platelet count. II. Von Willebrand's disease (report of thirty-seven patients). , 1968, The American journal of medicine.

[3]  N. Shulman,et al.  Relationships between Spleen, Platelets and Factor VIII Levels , 1968 .

[4]  P. Mannucci,et al.  An investigation of three patients with Christmas disease due to an abnormal type of factor ix , 1968, Journal of clinical pathology.

[5]  J. White,et al.  The enigma of severe factor XI deficiency without hemmorrhagic symptoms. Distinction from Hageman factor and "Fletcher factor" deficiency; family study; and problems of diagnosis. , 1967, Thrombosis et diathesis haemorrhagica.

[6]  H. Perkins Brief Report: Correction of the Hemostatic Defects in Von Willebrand’s Disease , 1967 .

[7]  P. Didisheim,et al.  The Spectrum of von Willebrand’s Disease , 1967, Thrombosis and Haemostasis.

[8]  C. Hougie,et al.  Haemophilia Bm: a new type of factor-IX deficiency. , 1967, Lancet.

[9]  L. Gaston,et al.  Factor IX deficiency and prolonged bleeding time. , 1966, The New England journal of medicine.

[10]  J. Caen,et al.  Congenital bleeding disorders with long bleeding time and normal platelet count: I. Glanzmann's thrombasthenia (report of fifteen patients) , 1966 .

[11]  A. Hensen,et al.  Haemophilia A with apparently autosomal dominant inheritance. Evidence for a second autosomal locus involved in factor 8 production. , 1965, Thrombosis et diathesis haemorrhagica.

[12]  C. Abildgaard,et al.  Blood coagulation in thyroid dysfunction. , 1965, The New England journal of medicine.

[13]  H. Strauss,et al.  VON WILLEBRAND'S DISEASE: USE OF A PLATELET-ADHESIVENESS TEST IN DIAGNOSIS AND FAMILY INVESTIGATION. , 1965 .

[14]  T. Spaet,et al.  Studies on Platelet Factor‐3 Availability , 1965, British journal of haematology.

[15]  H. Bang A SIMPLE METHOD FOR DETERMINATION OF LIPASE (ESTERASE) IN PANCREATIC JUICE. , 1965, Scandinavian journal of clinical and laboratory investigation.

[16]  O. Egeberg An inherited hemorrhagic trait with characteristics resembling both mild hemophilia of type A and Von Willebrand's disease. , 1965, Scandinavian journal of clinical and laboratory investigation.

[17]  J. Robertson,et al.  COMBINED HEMOPHILIA AND CHRISTMAS DISEASE. , 1964, Blood.

[18]  A. Barr,et al.  The Plasma Concentration of Factor VIII in the Normal Population , 1964, British journal of haematology.

[19]  E. Salzman MEASUREMENT OF PLATELET ADHESIVENESS. A SIMPLE IN VITRO TECHNIQUE DEMONSTRATING AN ABNORMALITY IN VON WILLEBRAND'S DISEASE. , 1963, The Journal of laboratory and clinical medicine.

[20]  J. Caen,et al.  Transfusion Studies in von Willebrand's Disease: Effect on Bleeding Time and Factor VIII , 1963, British journal of haematology.

[21]  J. A. Spittell,et al.  Hypercoagulability associated with malignant disease and with the postoperative state. Evidence for elevated levels of antihemophilic globulin. , 1963, Annals of internal medicine.

[22]  P. Owren,et al.  Oral Contraception and Blood Coagulability , 1963, British medical journal.

[23]  O. Egererg CHANGES IN THE ACTIVITY OF ANTIHEMOPHILIC A FACTOR (F. VIII) AND IN THE BLEEDING TIME ASSOCIATED WITH MUSCULAR EXERCISE AND ADRENALIN INFUSION. , 1963 .

[24]  H. Strauss,et al.  Effects of Corticosteroids on Coagulation of the Blood , 1962, Nature.

[25]  E. Blackburn,et al.  Antihaemophilic factor deficiency, capillary defect of von Willebrand type, and idiopathic thrombocytopenia occurring in one family , 1961, Journal of clinical pathology.

[26]  G. Ingram Increase in antihaemophilic globulin activity following infusion of adrenaline , 1961, The Journal of physiology.

[27]  K. Sjølin Classical haemophilia (AHF deficiency) and Christmas factor (PTC) deficiency as simultaneous defects. , 2009, Acta medica Scandinavica.

[28]  G. Ingram Observations in a Case of Multiple Haemostatic Defect , 1956, British journal of haematology.