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• W2014598161 abstract "British Journal of HaematologyVolume 2, Issue 3 p. 265-275 Congenital Familial Deficiency of Factor V (Parahaemophilia) Combined with Deficiency of Antihaemophilic Globulin TORBEN IVERSEN, TORBEN IVERSEN Department of Medicine, Aarhus Amtssygehus, University ofAarhus, DenmarkSearch for more papers by this authorPOUL BASTRUP-MADSEN, POUL BASTRUP-MADSEN Department of Medicine, Aarhus Amtssygehus, University ofAarhus, Denmark In receipt of a grant from the King Christian the Tenth Foundation.Search for more papers by this author TORBEN IVERSEN, TORBEN IVERSEN Department of Medicine, Aarhus Amtssygehus, University ofAarhus, DenmarkSearch for more papers by this authorPOUL BASTRUP-MADSEN, POUL BASTRUP-MADSEN Department of Medicine, Aarhus Amtssygehus, University ofAarhus, Denmark In receipt of a grant from the King Christian the Tenth Foundation.Search for more papers by this author First published: July 1956 https://doi.org/10.1111/j.1365-2141.1956.tb06698.xCitations: 21 AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat References Alexander, B. and Goldstein, R. (1952). ‘Parahemo-philia in three siblings (Owren's disease). With studies on certain plasma components affecting prothrombin conversion. Amer. J. Med., 13, 255. Bergsagel, D. E., Setna, S. S., Cartwright, G. E. and Wintrobe, M. M. (1954) ‘Mild PTC (plasma thrombo-plastin component) deficiency occurring in two brothers. Blood, 9, 866. Biggs, R. and Douglas, A. S. (1953). ‘The thromboplastin generation test. J. din. Path., 6, 23. Biggs, R., Douglas, A. S. and Macfarlane, R. G. (1953). ‘The initial stages of blood coagulation. J. Physiol., 122, 538. Brennan, M. J., Monto, R. W. and Shafer, H. C. (1952). ‘Haemorrhagic diathesis due to Ac-globulin deficiency. Amer. J. din. Path., 22, 150. Brink, A. J. and Kingsley, C. S. (1952). ‘A familial disorder of blood coagulation due to deficiency of the labile factor. Quart.J. Med., 21, 19. Frank, E., Bilhan, N. and Ekren, H. (1950).Parahamophilie (Owren), eine neue Form der hamor- rhagischen Diathese. Acta haemat., 3, 70. Hauser, F. (1950). ‘Idiopathische Hypoprothrombinamie versus Mangel an Faktor V. Ann. paediat., 174, 19. Heni, F. and Krauss, I. (1954). ‘Angeborener Faktor V-Mangel (Owrensche Krankheit). Klin. Wschr., 32, 633. Hjort, P., Rapaport, S. I. and Owren, P. A. (1955). ‘Evidence that platelet accelerator (platelet factor 1) is adsorbed plasma proaccelerin. Blood, 10, 1139. Kingsley, C. S. (1954). ‘Familial factor V deficiency; the pattern of heredity. Quart. J. Med., 23, 323. Roller, F. (1955). ‘ Klinik und Therapie der plasmatisch bedingten hamorrhagischen Diathesen’ R. Jurgens and E. Deutsch (ed.) Hamorrhagische Diathesen, p. 89. Springer-Verlag, Vienna . Lewis, J. H. and Ferguson, J. H. (1955). ‘Hypoproac- celerinemia. Blood, 10, 351. Marx, R. (1950). ‘Konstitutionelle Pseudohypopro- thrombinaemien. Arztl. Forsch., 4, 567. Oeri, J., Matter, M., Isenschmid, H., Hauser, F. and Roller, F. (1954). ‘ Angeborener Mangel an Faktor V (Parahaemophilie) verbunden mit echter Haemophilie A bei zwei Briidern. Bibl, paediat., No.58, 575. Owen, C. A., Jr. and Cooper, T. (1955). ‘Parahemophilia. Arch, intern. Med., 95, 194. Owren, P. (1944). ‘ Nye underskelser over blodets koagulasjon. Arb. norske VidenskAkad., 21. Owren, P. A. (1947). ‘ The coagulation of blood; investi-gations on a new clotting factor. Acta med. scand., Suppl. 194. Owren, P. A. (1949). ‘A quantitative one-stage method for the assay of prothrombin. Scand.]. din. Lab. Invest., I, 81. Owren, P. A. (1953). ‘Prothrombin and accessory factors. Clinical significance. Amer. J. Med., 14, 201. Owren, P. A. (1955). Discussion on ‘Factor X and Haemo-philia’ in Thrombose und Embolie, Basle, Schwabe, p. 1207. Owren, P. A. and Aas, K. (1951).‘The control of dicu-marol therapy and the quantitative determination of prothrombin and proconvertin. Scand. J. din. Lab. Invest., 3, 201. Quick, A. J. (1935). ‘Prothrombin in hemophilia and in obstructive jaundice. J. biol. Chem., 109, lxxiii. Redner, B., Scalettar, H. and Weiner, M. (1953). ‘Parahemophilia (Owren's disease). Pediatrics, 12, 5. Sacks, M. S. and Raccuglia, G. (1955). ‘Hereditary deficiency of proaccelerin (parahemophilia): a family study. J. Lab. din. Med., 46, 98. Stohlman, F. Jr., Harrington, W.J. and Moloney, W. C. (1951). ‘Parahemophilia (Owren's disease); report of a case in a woman with studies on other members of her family. J. Lab. din. Med., 38, 842. Wolf, P. (1953). ‘A modification for routine laboratory use of Stefanini's method of estimating factor V activity in human oxalated plasma. J. din. Path., 6, 34. De Vries, A., Matoth, Y. and Shamir, Z. (1951). ‘Familial congenital labile factor deficiency with syndactylism. Investigation on the mode of action of the labile factor. Acta haemat., 5, 129. Citing Literature Volume2, Issue3July 1956Pages 265-275 ReferencesRelatedInformation" @default.
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• W2014598161 title "Congenital Familial Deficiency of Factor V (Parahaemophilia) Combined with Deficiency of Antihaemophilic Globulin" @default.
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