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CONGENITAL FACTOR XIII DEFICIENCY: TYPE I AND TYPE II DISEASE

1985; Wiley; Volume: 60; Issue: 2 Linguagem: Inglês

10.1111/j.1365-2141.1985.tb07423.x

1365-2141

Antonio Girolami, M Cappellato, M. Vicarioto,

Lysosomal Storage Disorders Research

British Journal of HaematologyVolume 60, Issue 2 p. 375-376 Free Access CONGENITAL FACTOR XIII DEFICIENCY: TYPE I AND TYPE II DISEASE Antonio Girolami, Antonio Girolami University of Padua Medical School, Institute of Medical Semiotics and Second Chair of Medicine, Padua, ItalySearch for more papers by this authorMaria Giovanna Cappellato, Maria Giovanna Cappellato University of Padua Medical School, Institute of Medical Semiotics and Second Chair of Medicine, Padua, ItalySearch for more papers by this authorMaria Angela Vicarioto, Maria Angela Vicarioto University of Padua Medical School, Institute of Medical Semiotics and Second Chair of Medicine, Padua, ItalySearch for more papers by this author Antonio Girolami, Antonio Girolami University of Padua Medical School, Institute of Medical Semiotics and Second Chair of Medicine, Padua, ItalySearch for more papers by this authorMaria Giovanna Cappellato, Maria Giovanna Cappellato University of Padua Medical School, Institute of Medical Semiotics and Second Chair of Medicine, Padua, ItalySearch for more papers by this authorMaria Angela Vicarioto, Maria Angela Vicarioto University of Padua Medical School, Institute of Medical Semiotics and Second Chair of Medicine, Padua, ItalySearch for more papers by this author First published: June 1985 https://doi.org/10.1111/j.1365-2141.1985.tb07423.xCitations: 9AboutPDF 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 No abstract is available for this article. REFERENCES Barbui, T., Rodeghiero, F., Dini, E., Mariani, G., Papa, M.L., de Biasi, R, Murillo, R.C. & Umana, C.M. (1978) Subunits A and S inheritance in four families with congenital factor XIII deficiency. British Journal of Haematology, 38, 267–271. Berliner, S.H., Lusky, A., Zivelin, A., Modan, M. & Seligsohn, U. (1984) Hereditary factor XIII deficiency: report of four families and definition of the carrier state. British Journal of Haemato-logy, 56, 495–505. Fear, J.D., Miloszewski, J.A. & Losowsky, M.S. (1983) Factor XIII levels in five families of patients with inherited factor XIII deficiency: support for an autosomal recessive inheritance. Thrombosis and Haemostasis, 50, 588–590. Francis, J.L. & Todd, P.J. (1979) Factor XIII deficiency. A family study by measurement of factor XIII Subunit A and S. Acta Haematologica, 62, 162–172. Girolami, A., Burul, A. & Cappellato, M.G. (1977) A tentative classification of factor XIII deficiency in two groups. Acta Haematologica, 58, 318–320. Girolami, A., Burul, A., Fabris, F., Cappellato, G. & Betterle, C. (1978) Studies on factor XIII antigen in congenital factor XIII deficiency. A tentative classification of the disease in two groups. Folia Haematologica, 105, 131–141. Girolami, A., Cappellato, G., Falezza, G., Gabrielli, G.B. & Vianello, C. (1981) Demonstration of a double hereditary pattern for congenital afibrinogenemia. Blut, 43, 249–256. Israels, E.D., Paraskevas, F. & Israels, G.L. (1973) Immunological studies of coagulation factor XIII. Journal of Clinical Investigation, 52, 2398–2403. Citing Literature Volume60, Issue2June 1985Pages 375-376 ReferencesRelatedInformation