V. Willebrand's Disease and its Treatment with a Specific Plasma Fraction

Alexander B. Goldstein R. (1953). Dual haemostatic defect in pseudohaemophilia. J. clin. Invest., 32, 551.

Blombäck B. Blombäck M. (1956). Purification of human and bovine fibrinogen. Arkiv. för Kemi., 10, 415.

Blombäck M. (1958). Studies on antihaemophilic globulin. Acta paediat. (Uppsala), 47, Suppl. 114.

Blombäck M. Blombäck B. Nilsson I. M. (1958). Further studies on AHG and related substances. VIIth Congress of the Internal. Society of Haematology, Rome 1958.

Darte J. M. M. (1955). Defect of antihaemophilic globulin in von Willebrand's disease. Amer. J. Dis. Child., 90, 561.

Jürgens R. (1937). Die erblichen Thrombopathien. Ergebn. inn. Med. Kinderheilk., 53, 795.

Jürgens R. Forsius H. (1951). Untersuchungen über die konstitutionelle Thrombopathie (v. Willebrand-Jürgens) in den Ålands-Inseln. Schweiz. med. Wschr., 81, 1248.

Jürgens R. Lehmann W. Wegelius O. Eriksson A. W. Hiepler E. (1957). Mitteilung über den Mangel an antihämophilem Globulin (Faktor VIII) bei der Aaländischen Thrombopathie (v. Willebrand-Jürgens). Thromh. Diath. Haem., 1, 251.

Larrieu M.-J. Soulier J.-P. (1953). Déficit en facteur antihémophilique A, chez une fille associé à un trouble saignement. Rev. Hémat., 8, 361.

Matter M. Comb P. F. New Melly A. Finch C. A. (1956). Vascular hemophilia. The association of a vascular defect with a deficiency of antihemophilic globulin. Amer. J. med. Sci., 232, 421.

Nilsson I. M. (1957). Ein Fall weiblicher Hämophilie und dessen Behandlung mit speziell hergestelltem, menschlichem Antihämophilieglobulin. Intern. Symposion, Malmö, Schweden, Juni 1956, p. 246. Ed. Jürgens R. Waldenström J. , Neben wirk.v. Arzneimitteln auf Blut u. Knochenmark, F. K. Schattauer: Stuttgart 1957.

Nilsson I. M. Blombäck M. V. Fran-Cken I. (1957). On an inherited autosomal haemorrhagic diathesis with antihaemophilic globulin (AHG) deficiency and prolonged bleeding time. Acta med. scand., 159, 35.

Nilsson I. M. Blombäck M. Jorpes E. Blombäck B. Johansson S.-A. (1957). V. Willebrand's disease and its correction with human plasma fraction I–0. Acta med. scand., 159, 179.

Nilsson I. M. Blombäck M. (1958). V. Willebrand's disease, its pathogenesis and treatment. Haemophilia Symposium, 12.9.58. Vllth Congress of the Internal. Society of Haematology, Rome 1958.

Nilsson I. M. Blombäck M. Blombäck B. (1958). On von Willebrand's disease in Sweden, its pathogenesis and treatment. Acta med. scand. (in press).

Schulman I. Smith C. H. Erlandson M. Fort E. (1955). Vascular hemophilia. A familial hemorrhagic disease in males and females characterized by combined antihemophilic deficiency and vascular abnormality. Amer. J. Dis. Child., 90, 526.

Singer K. Ramot B. (1956). Pseudohaemophilia Type B. Hereditary haemorrhagic disease characterized by prolonged bleeding time and decrease in antihaemophilic factor. Arch. intern. Med., 97, 715.

Willebrand E. A. V. (1926). Hereditär pseudohämofili. Finska Läk-Sällsk. Handl., 68, 87.

Willebrand E. A. V. (1931). Uber hereditäre Pseudohämophilie. Acta med.scand., 76, 521.

Willebrand E. A. V. Jürgens R. (1933). Uber ein neues vererbbares Blutungsübel. Die konstitutionelle Thrombophathie. Deutch. Arch. klin. Med., 175, 453.

Willebrand E. A. V. Jürgens R. Dahlberg U. (1934). Konstitutionell trombopati, en ny ärftlig blödarsjukdom. Finska Läk-Sällsk. Handl., 76, 193.