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Gastroenterology
|
June 26, 1999
p53 mutations in british patients with hepatocellular carcinoma: clustering in genetic hemochromatosis
G Vautier, A B Bomford, B C Portmann, et al.
Gut
|
February 1, 1997
Healing with basic fibroblast growth factor is associated with reduced indomethacin induced relapse in a human model of gastric ulceration
M A Hull, A Knifton, B Filipowicz, et al.
The Journal of Pathology
|
January 1, 1997
Interleukin-8 and inducible nitric oxide synthase mRNA levels in inflammatory bowel disease at first presentation
J M McLaughlan, R Seth, G Vautier, et al.
The Medical Journal of Australia
|
October 6, 2001
High prevalence of coeliac disease in a population-based study from Western Australia: a case for screening?
C J Hovell, J A Collett, G Vautier, et al.
Journal of Hepatology
|
February 12, 1998
Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis
C Datz, M R Lalloz, W Vogel, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
Gastroenterology
|
June 26, 1999
p53 mutations in british patients with hepatocellular carcinoma: clustering in genetic hemochromatosis
G Vautier, A B Bomford, B C Portmann, et al.
Gut
|
February 1, 1997
Healing with basic fibroblast growth factor is associated with reduced indomethacin induced relapse in a human model of gastric ulceration
M A Hull, A Knifton, B Filipowicz, et al.
The Journal of Pathology
|
January 1, 1997
Interleukin-8 and inducible nitric oxide synthase mRNA levels in inflammatory bowel disease at first presentation
J M McLaughlan, R Seth, G Vautier, et al.
The Medical Journal of Australia
|
October 6, 2001
High prevalence of coeliac disease in a population-based study from Western Australia: a case for screening?
C J Hovell, J A Collett, G Vautier, et al.
Journal of Hepatology
|
February 12, 1998
Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis
C Datz, M R Lalloz, W Vogel, et al.
Page
of 2