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Clinical Chemistry|October 1, 1994
Complex pattern of alternative splicing in the normal uroporphyrinogen decarboxylase gene: implications for diagnosis of familial porphyria cutanea tardaJ F McManus, C G Begley, S RatnaikeThe Medical Journal of Australia|September 21, 1987
Assessment of the Albuscreen microalbuminuria kit in diabetic outpatientsP J Leedman, A Nankervis, M Goodwin, et al.The American Journal of Physiology|June 1, 1995
Behavior of sheep drinking ethanol solutionJ R Blair-West, D R Deam, D A Denton, et al.Blood|November 1, 1996
Five new mutations in the uroporphyrinogen decarboxylase gene identified in families with cutaneous porphyriaJ F McManus, C G Begley, S Sassa, et al.Human Mutation|May 25, 1999
Three new mutations in the uroporphyrinogen decarboxylase gene in familial porphyria cutanea tarda. Mutation in brief no. 237. OnlineJ F McManus, C G Begley, S Sassa, et al.The Medical Journal of Australia|November 15, 1993
The investigation of chest pain: audit and interventionS Ratnaike, D Hunt, L J Eilermann, et al.Annals of Clinical Biochemistry|December 10, 1999
An unusual alkaline phosphatase isoenzyme associated with gastric carcinomaM A Jenkins, C B Steer, L W Cheng, et al.Journal of Gastroenterology and Hepatology|March 29, 2000
Effect of hepatobiliary disease, chronic hepatitis C and hepatitis B virus infections and interferon-alpha on porphyrin profiles in plasma, urine and faecesP R Gibson, J Grant, V Cronin, et al.Diabetes Research and Clinical Practice|February 1, 1995
The 75 g oral glucose tolerance in pregnancyF I Martin, S Ratnaike, A Wootton, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 13, 1999
Lambda light chain induced nephropathy: a rare cause of the Fanconi syndrome and severe osteomalaciaK L Bate, D Clouston, D Packham, et al.Pageof 57