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Clinical Chemistry|April 1, 1991
Comparison of four methods for free thyroxinD Deam, M Goodwin, S RatnaikeAnnals of Clinical Biochemistry|June 8, 2001
Multiple sclerosis: use of light-chain typing to assist diagnosisM A Jenkins, L Cheng, S RatnaikeThe Medical Journal of Australia|October 15, 1983
Effect of oral intake of thyroxine on results of thyroid function tests in patients receiving thyroid replacement therapyD R Deam, D G Campbell, S RatnaikeBritish Journal of Haematology|May 1, 1997
A novel form of hereditary sideroblastic anaemia with macrocytosisA Tuckfield, S Ratnaike, S Hussein, et al.The Medical Journal of Australia|September 6, 1993
Albuminuria in aborigines and Europids of south-eastern AustraliaC S Guest, S Ratnaike, R G LarkinsClinical 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.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.Pageof 42