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Gut|July 11, 1998
Evidence for altered hepatic matrix degradation in genetic haemochromatosisD K George, G A Ramm, L W Powell, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 21, 1998
The spinal muscular atrophy gene region at 5q13.1 has a paralogous chromosomal region at 6p21.3J L Banyer, S Goldwurm, L Cullen, et al.Journal of Hepatology|April 29, 1998
The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patientsK A Stuart, F Busfield, E C Jazwinska, et al.Journal of Hepatology|April 1, 1997
Evidence that "myofibroblast-like" cells are the cellular source of capsular collagen in hepatocellular carcinomaL P Ooi, D H Crawford, D C Gotley, et al.Gastroenterology|February 7, 1998
Increased hepatic iron concentration in nonalcoholic steatohepatitis is associated with increased fibrosisD K George, S Goldwurm, G A MacDonald, et al.Journal of Gastroenterology and Hepatology|March 1, 1995
Carbohydrate-deficient transferrin in alcoholics with liver diseaseS H Caldwell, J W Halliday, L M Fletcher, et al.Annals of Internal Medicine|December 29, 1998
Management of hemochromatosis. Hemochromatosis Management Working GroupJ C Barton, S M McDonnell, P C Adams, et al.American Journal of Human Genetics|March 31, 2000
Effects of HFE C282Y and H63D polymorphisms and polygenic background on iron stores in a large community sample of twinsJ B Whitfield, L M Cullen, E C Jazwinska, et al.Hepatology (Baltimore, Md.)|July 1, 1994
Establishment of a cell line from a hepatocellular carcinoma from a patient with hemochromatosisG K Sing, R Pace, S Prior, et al.Gut|July 17, 2003
A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patientK E Arden, D F Wallace, J L Dixon, et al.Pageof 20