Thrombosis and Haemostasis, Inhaltsverzeichnis Thromb Haemost 1960; 4(03): 331-335DOI: 10.1055/s-0038-1654514 Originalarbeiten — Original Articles — Travaux Originaux Schattauer GmbH The Relative Frequency of Haemophilia A and B Ernst G. Jung 1 Coagulation Laboratory (Prof. F. Koller) of the Department of Medicine (Prof. P. H. Rossier) University of Zurich, Switzerland › Institutsangaben Artikel empfehlen Abstract Artikel einzeln kaufen Summary Two tables show the haemophilia cases observed in Zurich and the relative frequency of haemophilia A and haemophilia B in Switzerland and some other countries. Volltext Referenzen References (1) Aggeler P. M, White S. G, Gelndening M. B, Page E. D, Leake T. B, Bates G. Plasma thromboplastin component (PTC) deficiency: a new disease resembling haemophilia. Proc. Soc. exp. Biol. (N. Y.) 79: 692 1952; (2) Bachmann F, Duckert F, Flückiger P, Hitzig W, Koller F. Über einen neuartigen kongenitalen Gerinnungsdefekt (Mangel an Stuartfaktor). Thromb. Diath. haem. 1: 87 1957; (3) Biggs R, Douglas A. S, Macfarlane R. G, Dacie J. V, Pitney W. R, Merskey C, O’Brien J. F. Christmas disease, a condition previously mistaken for haemophilia. Brit. med. J. 27: 1378 1952; (4) Biggs R, Douglas A. S. The thromboplastin generation test. J. clin. Pathol. 6: 23 1953; (5) Biggs R, Macfarlane R. G. Human blood coagulation. 2nd Ed.. Blackwell; Oxford: 1957 (6) Biggs R, Macfarlane R. G. Haemophilia and related conditions: a survey of 187 cases. Brit. J. Haemat. 4: 1 1958; (7) Bounameaux Y. Dosage du facteur VIII en un temps. Acta haemat. 17: 355 1957; (8) Brinkhous K. M, Langdell R. D, Penick G. D, Graham J. B, Wagner R. H. Newer approches to the study of haemophilia and haemophiloid states. J. Amer. med. Ass. 154: 481 1954; (9) Brinkhous K. M. Haemophilia. Bull. N. Y. Acad. Med. 3: 325 1954; (10) Cramer R, Matter M, Loeliger A. Die Hämophilie B. Zwei familiäre Fälle der Bluterkrankheit bedingt durch einen Mangel eines neuen Gerinnungsfaktors (Christmas disease). Helv. paediat. Acta 8: 185 1953; (11) Cramer R, Flückiger P, Gasser C, Koller F, Loeliger A, Matter M. Hämophilie B. Acta haemat. 10: 65 1953; (12) van Crefeld S. Haemophilia and allied diseases. Rocky Mount. med. J.. march 1958 (13) Deutsch E. Verschiedene Formen der Hämophilie. Thromb. Diath. haem. 1: 93 1957; (14) Duckert F, Flückiger P, Isenschmid H, Matter M, Vogel-Meng Koller F. A modification of the thromboplastin generation test. Acta haemat. 12: 197 1954; (15) Duckert F. Le diagnostic des coagulopathies. 8 Coll. Biol. clin.. Bruxelles: presse acad. europ.; 635 1958 (16) Fantl P, Sawers R. J. A syndrome under review. Austr. Ann. Med. 3: 245 1954; (17) Fisch U, Duckert F. Some aspects of kinetics of the first stages of blood thromboplastin formation. Thromb. Diath. haem. 3: 98 1958; (18) Frick P. G. The relative incidence of antihaemophilic globulin (AHG), PTC and PTA deficiency. J. Lab. clin. Med. 43: 860 1954; (19) Geiger M, Duckert F, Koller F. Quantitative Bestimmung von Faktor VIII und IX bei Blutersippen. Kongr. europ. Ges. Haemat.. 413 Springer; Heidelberg: 1956 (20) Graham J. B, MacLendon W. W, Brinkhous K. M. Mild haemophilia, an allelic form of the disease. Brit. med. J. 2: 97 1953; (21) Hougie C, Graham J. B. The blood clotting role and mode of inheritance of the Stuart factor. 6th Congr. int. Soc. Bl. Transf.. 80 Boston: 1956 (22) Hougie C. Studies on the fate of coagulation factors during clotting of normal and pathological blood. Thromb. Diath. haem. 3: 578 1959; (23) Koller F, Krüsi G, Luchsinger P. Über eine hämophilieartige hereditäre hämorrhagische Diathese mit Störung der ersten Gerinnungsphase. Arch. Jul. Klaus-Stiftg. 25: 16 1950; (24) Koller F, Krüsi G, Luchsinger P. Über eine besondere Form der hämorraghischen Diathese. Schweiz. med. Wschr. 80: 1101 1950; (25) Koller F, Loeliger A, Duckert F. Experiments on a new clotting factor (factor VII). Acta haemat. 6: 1 1951; (26) Koller F. Zur Differenzierung der Hämophilie. Arch. Jul. Klaus-Stiftg. 28: 254 1953; (27) Koller F. Das Verhalten der Gerinnungsfaktoren in vitro und in vivo. Proc. 7th Congr. int. Soc. Bl. Transf.. 731 Rome: 1958 (28) Langdell R. D, Wagner R. H, Brinkhous K. M. Effect of antihaemophilic factor on one-stage clotting tests. A presumptive test for haemophilia and a simple one-stage antihaemophilic assay procedure. J. Lab. clin. Med. 41: 637 1953; (29) Lewis J. H, Ferguson J. H, Fresh J. W, Zucker M. B. Primary haemorrhagic diseases. J. Lab. clin. Med. 49: 211 1957; (30) Loeliger A, Koller F. Behaviour of factor VII and prothrombin in late pregnancy and in the newborn. Acta haemat. 7: 157 1952; (31) Marx R. Über Hämophilie und Pseudohämophilie. Münch. med. Wschr. 101 (881) 924 1959; (32) Moor-Jankowski J. K, Huser H. J, Rosin S, Truog G, Schneeberger M, Geiger M. Hämophilie B. Genetische, klinische und gerinnungsphysiologische Aspekte. S. Karger; Basel: 1958 (33) den Ottolander G. H, Hoorweg P. G. De frequentie van haemophilie A en B. Ned. T. Geneesk. 99: 2037 1955; (34) Owren P. The coagulation of blood. Investigation on a new clotting factor. Acta med. scand.. 194. Suppl. 1947 (35) Pavlovsky A. Haemophilia: Comparative study of the varieties A and B. 6th Congr. int. Soc. Haemat.. 415 Boston: 1956 (36) Pitney W. R, Arnold B. J. Plasma antihaemophilic factor (AHF) concentrations in families of patients with haemorrhagic states. Brit. J. Haemat. 5: 184 1959; (37) Pool J. G, Robinson J. Observation on Plasma banking and transfusion procedures for haemophilie patients using a quantitative assay for AHG. Brit. J. Haemat. 5: 24 1959; (38) Quick A. J. The prothrombin in haemophilia and in obstructive jaundice. J. biol. Chem. 109: 523 1935; (39) Rappaport S. I. Survey of large haemophilie population. Congr. int. Soc. Haemat.. Boston: 1956 (40) Ratnoff O. D, Margolis A. On the epidemiology of haemophilia and Christmas disease. New Engl. J. Med. 256: 845 1957; (41) Remde W. Thrombozytenfunktionsstörungen bei Hämophiliekranken. Transact. 6th Congr. europ. Soc. Haemat.. 579 Kopenhagen: 1957 (42) Rosenthal R. L, Dreskin O. H, Rosenthal N. New haemophilia-like disease caused by deficiency of a third plasma thromboplastin factor. Proc. Soc. exp. Biol. (N.Y.) 82: 171 1953; (43) Rosenthal R. L. Haemophilia and haemophilia-like diseases caused by deficiencies in plasma thromboplastin factors. Amer. J. Med. 17: 57 1954; (44) Soulier J. B, Larrieu M. M. Nouvelle méthode du diagnostic de l’hémophilie. Dosage des facteurs antihémophiliques A et B. Sang 24: 205 1953; (45) Soulier J. P. Formes cliniques de l’hémophilie. Rev. Prat. (Paris) 6: 2295 1956; (46) Verstraete M, Vanderbrouke J. Deficient thromboplastin formation in man. Amer. J. Med. 22: 624 1957; (47) Waaler B. A. A simple one-stage method for the assay of antihemophilic factor A. Scand. J. clin. Lab. Invest. 11: 194 1959; (48) Wolf P. Studies of temperature and pH stability of human antihaemophilic factor (AHF) in plasma and in a concentrate. Brit. J. Haemat. 5: 169 1959;
