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Studies of fibrinogen fractions isolated from human plasma by precipitation with cold ether. II. Enzymic activities resembling plasma kallikrein and C'l-esterase. British journal of Haematology, 11, 576.","journal-title":"British journal of Haematology"},{"key":"ref_4","series-title":"Proceedings of the 10th Congress of the International Society for Blood Transfusion","first-page":"434","article-title":"Immunhamatologische und klinische Befunde bei einem Transfusionszwischenfall infolge Gm (a)-Antikorperbildung","author":"Fischer, K.","year":"1965","unstructured":"Fischer, K. (1965). Immunhamatologische und klinische Befunde bei einem Transfusionszwischenfall infolge Gm (a)-Antikorperbildung. Proceedings of the 10th Congress of the International Society for Blood Transfusion, Stockholm, 1964, p. 434. Karger, Basle."},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"463","DOI":"10.1101\/SQB.1964.029.01.049","article-title":"Antigenicity of hereditary gamma globulin (Gm) factors-biological and biochemical aspects","volume":"29","author":"Fudenberg, H.H.; Stiehm, E.R.; Franklin, E.C.; Meltzer, M.; Frangione, B.","year":"1964","unstructured":"Fudenberg, H. H., Stiehm, E. R., Franklin, E. C., Meltzer, M., and Frangione, B. (1964). Antigenicity of hereditary gamma globulin (Gm) factors-biological and biochemical aspects. Cold Spring Harbor Symposia on Quantitative Biology, 29, 463.","journal-title":"Cold Spring Harbor Symposia on Quantitative Biology"},{"key":"ref_6","first-page":"327","article-title":"Blood transfusion reaction caused by serum group incompatibility","author":"Jensen, K.G.; Giirtler, H.; Bruusgaard, A.","year":"1968","unstructured":"Jensen, K. G., Giirtler, H., and Bruusgaard, A. (1968). Blood transfusion reaction caused by serum group incompatibility. Proceedings of the 11th Congress of the International Society for Blood Transfusion, Sydney, 1966, Part I. Blood Genetics and Physiology. Haemolytic Disease of the Newborn, p. 327. Karger, Basle.","journal-title":"Proceedings of the 11th Congress of the International Society for Blood Transfusion; Part I. Blood Genetics and Physiology. Haemolytic Disease of the Newborn"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"215","DOI":"10.1111\/j.1365-2141.1963.tb05459.x","article-title":"Further experience with a concentrate containing human antihaemophilic factor","volume":"9","author":"Maycock, W.d'A.; Evans, S.; Vallet, L.; Combridge, B.; Wolf, P.; McGibbon, N.; French, E.E.; Wallett, L.H.; Dacie, J.V.; Biggs, R.; Handley, D.; Macfarlane, R.G.","year":"1963","unstructured":"Maycock, W. d'A., Evans, S., Vallet, L., Combridge, B., Wolf, P., McGibbon, N., French, E. E., Wallett, L. H., Dacie, J. V., Biggs, R., Handley, D., and Macfarlane, R. G. (1963). Further experience with a concentrate containing human antihaemophilic factor. British Journal of Haematology, 9, 215.","journal-title":"British Journal of Haematology"},{"key":"ref_8","doi-asserted-by":"crossref","first-page":"618","DOI":"10.1093\/ajcp\/54.4.618","article-title":"Anaphylactic reactions to IgA: a difficult transfusion problem","volume":"54","author":"Miller, W.V.; Holland, P.V.; Sugarbaker, E.; Strober, W.; Waldmann, T.A.","year":"1970","unstructured":"Miller, W. V., Holland, P. V., Sugarbaker, E., Strober, W., and Waldmann, T. A. (1970). Anaphylactic reactions to IgA: a difficult transfusion problem. American Journal of Clinical Pathology, 54, 618.","journal-title":"American Journal of Clinical Pathology"},{"key":"ref_9","first-page":"542","article-title":"Blood Transfusion in Clinical Medicine","author":"Mollison, P.","year":"1967","unstructured":"Mollison, P. (1967). Blood Transfusion in Clinical Medicine, 4th ed., p. 542. Blackwell Scientific Publications, Oxford and Edinburgh.","edition":"4th ed"},{"key":"ref_10","doi-asserted-by":"crossref","first-page":"305","DOI":"10.1111\/j.1365-2141.1971.tb03442.x","article-title":"Amyloidosis associated with the nephrotic syndrome and transfusion reactions in a haemophiliac","volume":"21","author":"Prentice, C.R.M.; Izatt, M.M.; Adams, J.F.; McNicol, G.P.; Douglas, A.S.","year":"1971","unstructured":"Prentice, C. R. M., Izatt, M. M., Adams, J. F., McNicol, G. P., and Douglas, A. S. (1971). Amyloidosis associated with the nephrotic syndrome and transfusion reactions in a haemophiliac. British Journal of Haematology, 21, 305.","journal-title":"British Journal of Haematology"},{"key":"ref_11","first-page":"343","article-title":"Haemophilia today","volume":"6","author":"Rizza, C.R.; Biggs, R.","year":"1971","unstructured":"Rizza, C. R., and Biggs, R. (1971). Haemophilia today. British Journal of Hospital Medicine, 6, 343.","journal-title":"British Journal of Hospital Medicine"},{"key":"ref_12","doi-asserted-by":"crossref","first-page":"451","DOI":"10.1136\/adc.47.253.451","article-title":"Management of the haemophilic child","volume":"47","author":"Rizza, C.R.; Matthews, J.M.","year":"1972","unstructured":"Rizza, C. R., and Matthews, J. M. (1972). Management of the haemophilic child. Archives of Disease in Childhood, 47, 451.","journal-title":"Archives of Disease in Childhood"},{"key":"ref_13","doi-asserted-by":"crossref","first-page":"188","DOI":"10.1056\/NEJM196901232800404","article-title":"Anaphylactic transfusion reactions associated with anti-IgA antibody","volume":"280","author":"Schmidt, A.P.; Taswell, H.F.; Gleich, G.J.","year":"1969","unstructured":"Schmidt, A. P., Taswell, H. F., and Gleich, G. J. (1969). Anaphylactic transfusion reactions associated with anti-IgA antibody. New England Journal of Medicine, 280, 188.","journal-title":"New England Journal of Medicine"},{"key":"ref_14","first-page":"312","article-title":"Anaphylactoid transfusion reactions associated with anti-IgA","volume":"2","author":"Vyas, G.N.; Perkins, H.A.; Fudenberg, H.H.","year":"1968","unstructured":"Vyas, G. N., Perkins, H. A., and Fudenberg, H. H. (1968). Anaphylactoid transfusion reactions associated with anti-IgA. Lancet, 2, 312.","journal-title":"Lancet"},{"key":"ref_15","article-title":"tPresent address: City Hospital, Nottingham. *Present address: Queen Elizabeth Hospital for Children, London E.2","author":"al., 1967, Cannon","year":"1966","unstructured":"tPresent address: City Hospital, Nottingham. *Present address: Queen Elizabeth Hospital for Children, London E.2. (Beilin et al., 1967; Cannon et al., 1968; Greenberg et al., 1966). Those with the severe type have symptoms of lethargy, poor appetite, dehydration, seizures, failure to thrive from the early months of life, and usually succumb before 1 year of age (Sutherland et al., 1970; Walker, 1971). This report describes the apparent life-saving effects of magnesium supplementation in an infant with the severe form of Bartter's syndrome.","journal-title":"et al; Those with the severe type have symptoms of lethargy, poor appetite, dehydration, seizures, failure to thrive from the early months of life, and usually succumb before 1 year of age (Sutherland"},{"issue":"777","key":"ref_16","article-title":"Severe allergic pulmonary oedema after plasma transfusion","volume":"23","author":"Kernoff, P.B.A.; Durrant, I.J.; Rizza, C.R.; Wright, F.W.","year":"1972","unstructured":"Kernoff, P. B. A., Durrant, I. J., Rizza, C. R., and Wright, F. W. (1972). Severe allergic pulmonary oedema after plasma transfusion. British Journal of Haematology, 23.777 a.","journal-title":"British Journal of Haematology"},{"key":"ref_17","article-title":"Magnesium supplementation in Bartter's syndrome Bartter's syndrome (hypokalaemic, hypochloraemic alkalosis, normotension, growth failure, and juxtaglomerular hyperplasia) is a rare disorder with less than 25 reported cases (Sutherland","year":"1970","unstructured":"Magnesium supplementation in Bartter's syndrome Bartter's syndrome (hypokalaemic, hypochloraemic alkalosis, normotension, growth failure, and juxtaglomerular hyperplasia) is a rare disorder with less than 25 reported cases (Sutherland et al., 1970). There appear to be two forms of this syndrome. The mild form usually has its onset after the first year of life, presenting with electrolyte imbalance, growth failure, and weakness, and markedly improves with electrolyte correction","journal-title":"et al; There appear to be two forms of this syndrome. 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