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W Halliday

Showing results (211-220 of 231) with videos related to

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Journal of the National Cancer Institute|July 1, 1985
Cohort study of internal malignancy in genetic hemochromatosis and other chronic nonalcoholic liver diseasesR A Bradbear, C Bain, V Siskind, et al.
The New England Journal of Medicine|February 5, 1976
Normal serum ferritin concentrations in precirrhotic hemochromatosisJ R Wands, J A Rowe, S E Mezey, et al.
American Journal of Human Genetics|August 1, 1995
Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the geneD H Crawford, L W Powell, B A Leggett, et al.
Journal of Medical Genetics|August 1, 1992
Congenital hydrocephalus secondary to Walker-Warburg syndrome identified on the Manitoba Neonatal Screening Programme for Duchenne muscular dystrophyC R Greenberg, H K Jacobs, T E Nylen, et al.
American Journal of Medical Genetics|October 23, 1997
Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD lociT Weiler, C R Greenberg, E Nylen, et al.
American Journal of Human Genetics|February 1, 1995
Haplotype analysis in Australian hemochromatosis patients: evidence for a predominant ancestral haplotype exclusively associated with hemochromatosisE C Jazwinska, W R Pyper, M J Burt, 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.
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.
Hepatology (Baltimore, Md.)|May 1, 1986
The prognosis of chronic active hepatitis without cirrhosis in relation to bridging necrosisW G Cooksley, R A Bradbear, W Robinson, et al.
Gastroenterology|March 13, 1998
Distribution of transferrin saturation in an Australian population: relevance to the early diagnosis of hemochromatosisC E McLaren, G J McLachlan, J W Halliday, et al.
Pageof 24

Showing results (211-220 of 231) with videos related to

Sort By:
Pageof 24
Journal of the National Cancer Institute|July 1, 1985
Cohort study of internal malignancy in genetic hemochromatosis and other chronic nonalcoholic liver diseasesR A Bradbear, C Bain, V Siskind, et al.
The New England Journal of Medicine|February 5, 1976
Normal serum ferritin concentrations in precirrhotic hemochromatosisJ R Wands, J A Rowe, S E Mezey, et al.
American Journal of Human Genetics|August 1, 1995
Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the geneD H Crawford, L W Powell, B A Leggett, et al.
Journal of Medical Genetics|August 1, 1992
Congenital hydrocephalus secondary to Walker-Warburg syndrome identified on the Manitoba Neonatal Screening Programme for Duchenne muscular dystrophyC R Greenberg, H K Jacobs, T E Nylen, et al.
American Journal of Medical Genetics|October 23, 1997
Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD lociT Weiler, C R Greenberg, E Nylen, et al.
American Journal of Human Genetics|February 1, 1995
Haplotype analysis in Australian hemochromatosis patients: evidence for a predominant ancestral haplotype exclusively associated with hemochromatosisE C Jazwinska, W R Pyper, M J Burt, 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.
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.
Hepatology (Baltimore, Md.)|May 1, 1986
The prognosis of chronic active hepatitis without cirrhosis in relation to bridging necrosisW G Cooksley, R A Bradbear, W Robinson, et al.
Gastroenterology|March 13, 1998
Distribution of transferrin saturation in an Australian population: relevance to the early diagnosis of hemochromatosisC E McLaren, G J McLachlan, J W Halliday, et al.
Pageof 24