Familial Cirrhosis

Achar S. T. Raju V. B. Sriramachari S. (1960). Indian childhood cirrhosis. Journal of Pediatrics, 57, 744.

Beam A. G. (1961). Genetic considerations in Wilson's disease. In Wilson's Disease, Some Current Concepts, p.118, edited by Walshe J. M. Cumings J. N. . Oxford: Blackwell Scientific Publications.

Blackwood W. Buxton P. H. Cumings J. N. Robertson D. J. Tucker S. M. (1963). Diffuse cerebral degeneration in infancy (Alpers' disease). Archives of Diseases of Childhood, 38, 193.

British Medical Journal (1973). Leading Article. Alpha₁ antitrypsin deficiency and liver disease in childhood. British Medical Journal, i, 758.

Cavell B. Leonhardt T. (1965). Hereditary hypergammaglobulinemia and lupoid hepatitis. Acta medica Scandinavica, 177, 751.

Chohan M. R. (1973). Primary biliary cirrhosis in twin sisters. Gut, 14, 213.

Elling P. Ranlov P. Bildoe P. (1966). A genetic approach to the pathogenesis of hepatic cirrhosis. Acta medica Scandinavica, 179, 527.

Feizi T. Naccarato R. Sherlock S. Doniach D. (1972). Mitochondrial and other tissue antibodies in relatives of patients with primary biliary cirrhosis. Clinical and experimental Immunology, 10, 609.

Fell G. S. Smith H. Howie R. A. (1968). Neutron activation analysis for copper in biological material applied to Wilson's disease. Journal of Clinical Pathology, 21, 8.

Fisher M. M. Spear S. Samols E. Sherlock S. (1964). Erythrocytic galactose-1-phosphate uridyl transferase levels in hepatic cirrhosis. Gut, 5, 170.

Gans H. Sharp H. L. Tan B. H. (1969). Antipro-tease deficiency and familial infantile liver cirrhosis. Surgery, Gynecology and Obstetrics, 129, 289.

Hsia D. Y. Walker F. A. (1961). Variability in the clinical manifestations of galactosemia. Journal of Pediatrics, 59, 872.

Iber F. L. Maddrey W. C. (1965). Familial hepatic disease with portal hypertension with or without cirrhosis. In Progress in Liver Diseases, Vol. II, p. 290, edited by Popper H. Schaffner F. . New York and London: Grune and Stratton.

Isselbacher K. J. (1959). Galactose metabolism and galactosemia. American Journal of Medicine, 26, 715.

Joske R. A. Laurence B. H. (1970). Familial cirrhosis with autoimmune features and raised immunoglobulin levels. Gastroenterology, 59, 546.

MacSween R. N. M. Ross Sheila K. Williamson J. Watkinson G. (1973). Primary biliary cirrhosis: Clinical and immunological associations. (In preparation).

MacSween R. N. M. Scott A. R. (1973). Hepatic cirrhosis: A clinico-pathological review of 520 cases over the period 1900–1969. Journal of Clinical Pathology (In press).

Maclachlan M. J. Rodnan G. P. Cooper W. M. Fennell R. H. (1965). Chronic active (‘lupoid’) hepatitis. Annals of Internal Medicine, 62, 425.

Maddrey W. C. Iber F. L. (1964). Familial cirrhosis-A clinical and pathological study. Annals of Internal Medicine, 61, 667.

Nelson W. E. Vaughan V. C. III McKay R. J. (Editors) (1969). Textbook of Pediatrics, 9th edition p. 842. London: W. B. Saunders.

Ohbayashi A. Mayumi M. Okochi K. (1971). Australia antigen in familial cirrhosis. Lancet, 1, 244.

Popper H. Schaffner F. (1961). The hepatic lesion in Wilson's disease. In Wilson's Disease, Some Current Concepts, p. 192, edited by Walshe J. M. Cumings J. N. . Oxford: Blackwell Scientific Publications.

Sharp H. L. Freier E. F. Bridges R. (1968). Alpha-1-globulin deficiency in a familial infantile liver disease. Pediatrics Research, 2, 298.

Sharp H. L. Bridges R. A. Krivit W. Freier E. F. (1969). Cirrhosis associated with alpha-1-antitrypsin deficiency: A previously unrecognised inherited disorder. Journal of Laboratory and Clinical Medicine, 73, 934.

Smallwood R. A. Williams H. A. Rosenoer V. M. Sherlock S. (1968). Liver-copper levels in liver disease. Studies using neutron activation analysis. Lancet, 2, 1310.

Smetana H. F. Hadley G. C. Sirsat S. M. (1961). Infantile cirrhosis. Pediatrics, 28, 107.

Smetana H. F. Olen E. , (1962). Hereditary galactose disease. Journal of Clinical Pathology 38, 3.

Stanbury J. B. Wyngaarden J. B. Fredrikson D. S. (Editors) (1966). The Metabolic Basis of Inherited Disease, 2nd edition. New York: McGraw Hill Book Company, Inc..

Sternlieb I. (1972). Evolution of the hepatic lesion in Wilson's disease (hepatolenticular degeneration). In Progress in Liver Disease, Vol. IV p. 511. New York and London: Grune and Stratton.

Walker J. G. Bates D. Doniach D. Ball P. A. J. Sherlock S. (1972). Chronic liver disease and mitochondrial antibodies: A family study. British Medical Journal, 1, 146.

Wefring K. W. Lamvik J. O. (1967). Familial progressive poliodystrophy with cirrhosis of the liver. Acta paediatricia Scandinavica, 56, 295.