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The Veterinary Clinics of North America. Small Animal Practice|April 1, 2015
Micturition disordersJulie K ByronHuman 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.Pathology|October 1, 1991
Four cases of IgD multiple myelomaD R Deam, I A Busmanis, S Hussein, 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.Thyroid : Official Journal of the American Thyroid Association|April 1, 1996
A prospective study of the effect of nonionic contrast media on thyroid functionJ J Conn, M J Sebastian, D Deam, 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.Annals of Clinical Biochemistry|July 21, 2000
Measurement of iohexol by capillary electrophoresis: minimizing practical problems encounteredM A Jenkins, C Houlihan, S Ratnaike, et al.The Journal of Physiology|June 1, 1995
Vasopressin stimulation of Ca2+ mobilization, two bivalent cation entry pathways and Ca2+ efflux in A7r5 rat smooth muscle cellsK Byron, C W TaylorPageof 8