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Clinical Chemistry
|
February 1, 1990
Unexplained osmolal gap in diabetic ketoacidosis (not due to acetone)
C I Bhagat, P Garcia-Webb, J P Beilby, et al.
Journal of the American College of Cardiology
|
December 12, 2001
Antioxidant vitamins and the risk of carotid atherosclerosis. The Perth Carotid Ultrasound Disease Assessment study (CUDAS)
B M McQuillan, J Hung, J P Beilby, et al.
Circulation
|
May 11, 1999
Hyperhomocysteinemia but not the C677T mutation of methylenetetrahydrofolate reductase is an independent risk determinant of carotid wall thickening. The Perth Carotid Ultrasound Disease Assessment Study (CUDAS)
B M McQuillan, J P Beilby, M Nidorf, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
August 14, 1999
Angiotensin-converting enzyme gene polymorphism and carotid wall thickening in a community population
J Hung, B M McQuillan, M Nidorf, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
June 17, 2006
AluyMICB dimorphism within the class I region of the major histocompatibility complex is associated with asthma and airflow obstruction in the Busselton population
J Hui, L J Palmer, A L James, et al.
Internal Medicine Journal
|
October 17, 2002
Variegate porphyria in Western Australian Aboriginal patients
E Rossi, C Y B Chin, J P Beilby, et al.
Stroke
|
January 11, 2000
Serum ferritin and C282Y mutation of the hemochromatosis gene as predictors of asymptomatic carotid atherosclerosis in a community population
E Rossi, B M McQuillan, J Hung, et al.
European Journal of Endocrinology
|
March 15, 2001
A Pro12Ala polymorphism in the human peroxisome proliferator-activated receptor-gamma 2 is associated with combined hyperlipidaemia in obesity
M M Swarbrick, C M Chapman, B M McQuillan, et al.
Journal of Gastroenterology and Hepatology
|
June 4, 1999
Genotyping as a diagnostic aid in genetic haemochromatosis
E Rossi, S Henderson, C Y Chin, et al.
British Journal of Clinical Pharmacology
|
March 16, 2000
Pharmacokinetics and pharmacodynamics of gliclazide in Caucasians and Australian Aborigines with type 2 diabetes
T M Davis, F Daly, J P Walsh, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
Clinical Chemistry
|
February 1, 1990
Unexplained osmolal gap in diabetic ketoacidosis (not due to acetone)
C I Bhagat, P Garcia-Webb, J P Beilby, et al.
Journal of the American College of Cardiology
|
December 12, 2001
Antioxidant vitamins and the risk of carotid atherosclerosis. The Perth Carotid Ultrasound Disease Assessment study (CUDAS)
B M McQuillan, J Hung, J P Beilby, et al.
Circulation
|
May 11, 1999
Hyperhomocysteinemia but not the C677T mutation of methylenetetrahydrofolate reductase is an independent risk determinant of carotid wall thickening. The Perth Carotid Ultrasound Disease Assessment Study (CUDAS)
B M McQuillan, J P Beilby, M Nidorf, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
August 14, 1999
Angiotensin-converting enzyme gene polymorphism and carotid wall thickening in a community population
J Hung, B M McQuillan, M Nidorf, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
June 17, 2006
AluyMICB dimorphism within the class I region of the major histocompatibility complex is associated with asthma and airflow obstruction in the Busselton population
J Hui, L J Palmer, A L James, et al.
Internal Medicine Journal
|
October 17, 2002
Variegate porphyria in Western Australian Aboriginal patients
E Rossi, C Y B Chin, J P Beilby, et al.
Stroke
|
January 11, 2000
Serum ferritin and C282Y mutation of the hemochromatosis gene as predictors of asymptomatic carotid atherosclerosis in a community population
E Rossi, B M McQuillan, J Hung, et al.
European Journal of Endocrinology
|
March 15, 2001
A Pro12Ala polymorphism in the human peroxisome proliferator-activated receptor-gamma 2 is associated with combined hyperlipidaemia in obesity
M M Swarbrick, C M Chapman, B M McQuillan, et al.
Journal of Gastroenterology and Hepatology
|
June 4, 1999
Genotyping as a diagnostic aid in genetic haemochromatosis
E Rossi, S Henderson, C Y Chin, et al.
British Journal of Clinical Pharmacology
|
March 16, 2000
Pharmacokinetics and pharmacodynamics of gliclazide in Caucasians and Australian Aborigines with type 2 diabetes
T M Davis, F Daly, J P Walsh, et al.
Page
of 4