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Medical Care|May 1, 1975
Clinical styles and motivation: a study of laboratory test useD F Hardwick, P Vertinsky, R T Barth, et al.
The Journal of Pediatrics|February 1, 1996
Nonketotic hyperglycinemia: atypical clinical and biochemical manifestationsR D Steiner, D A Sweetser, J R Rohrbaugh, et al.
JAMA|September 25, 1987
Managing bedside glucose testing in the hospitalR Belsey, J I Morrison, K J Whitlow, et al.
Human Mutation|April 29, 1999
Identification of 6 new mutations in the iduronate sulfatase gene. Mutation in brief no. 233. OnlineH D Vallance, L Bernard, M Rashed, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 14, 2004
Home management of haemophiliaJ M Teitel, D Barnard, S Israels, et al.
Journal of Medical Genetics|June 1, 1997
Metachromatic leucodystrophy in three families from Nova Scotia, Canada: a recurring mutation in the arylsulphatase A geneM B Coulter-Mackie, L Gagnier, M J Beis, et al.
Prenatal Diagnosis|July 1, 1986
Prenatal diagnosis of non-ketotic hyperglycinemiaD A Applegarth, H L Levy, V E Shih, et al.
The Journal of Experimental Medicine|March 3, 1997
Granzyme B (GraB) autonomously crosses the cell membrane and perforin initiates apoptosis and GraB nuclear localizationL Shi, S Mai, S Israels, et al.
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