Subunit molecular mass assignment of 14,654 Da to the soluble beta-galactoside-binding lectin from bovine heart muscle and demonstration of intramolecular disulfide bonding associa... von TRACEY, BM, FEIZI, T, ABBOTT, WM, CARRUTHERS, RA, GREEN, BN, LAWSON, AM

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Novel management of ureteral stent migration with mini-PCNL von Mansbridge, Margaret M, Tsing, Vaite LM, Latif, Edward R, Tracey, Christopher BM

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Mutation and DNA modification in Salmonella exposed to N-nitrosodimethylamine under UVA- and sunlight-irradiation von Arimoto-Kobayashi, Sakae, Tracey, Beryl M, Asao, Mieko, Hayatsu, Hikoya, Farmer, Peter B

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CONTRIBUTION OF GUT BACTERIAL METABOLISM TO HUMAN METABOLIC DISEASE von Bain, M.D., Borriello, S.P., Tracey, B.M., Jones, M., Reed, P.J., Chalmers, R.A., Stacey, T.E.

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Hypovitaminosis D is Associated with Greater Body Mass Index and Disease Activity in Pediatric Systemic Lupus Erythematosus von Wright, Tracey B., MD, Shults, Justine, PhD, Leonard, Mary B., MD, MSCE, Zemel, Babette S., PhD, Burnham, Jon M., MD, MSCE

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Enzymologic studies on patients with methylmalonic aciduria : basis for a clinical trial of deoxyadenosylcobalamin in a hydroxocobalamin-unresponsive patient von CHALMERS, R. A, BAIN, M. D, MISTRY, J, TRACEY, B. M, WEAVER, C

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Metabolic response to carnitine in methylmalonic aciduria. An effective strategy for elimination of propionyl groups von Roe, C R, Hoppel, C L, Stacey, T E, Chalmers, R A, Tracey, B M, Millington, D S

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The response to L-carnitine and glycine therapy in isovaleric acidaemia von DE SOUSA, C, CHALMERS, R. A, STACEY, T. E, TRACEY, B. M, WEAVER, C. M, BRADLEY, D

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Urinary C6-C12 dicarboxylic acylcarnitines in Reye's syndrome von TRACEY, B. M, CHENG, K. N, ROSANKIEWICZ, J, STACEY, T. E, CHALMERS, R. A

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Characterization of Azo Coupling Adducts of Benzenediazonium Ions with Aromatic Amino Acids in Peptides and Proteins von Tracey, Beryl M, Shuker, David E. G

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Prenatal diagnosis of 3‐Hydroxy‐3‐methylglutaric aciduria by GC‐MS and enzymology on cultured amniocytes and chorionic villi von Chalmers, R. A., Tracey, B. M., Mistry, J., Stacey, T. E., McFadyen, I. R.

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Dizygotic twins with 3-hydroxy-3-methylglutaric aciduria; unusual presentation, family studies and dietary management von STACEY, T. E, DE SOUSA, C, TRACEY, B. M, WHITELAW, A, MISTRY, J, TIMBRELL, J, CHALMERS, R. A

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L-Carnitine insufficiency in disorders of organic acid metabolism: response to L-carnitine by patients with methylmalonic aciduria and 3-hydroxy-3-methylglutaric aciduria von CHALMERS, R. A, STACEY, T. E, TRACEY, B. M, DE SOUSA, C, ROE, C. R, MILLINGTON, D. S, HOPPEL, C. L

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L-Glyceric aciduria (primary hyperoxaluria type 2) in siblings in two unrelated families von CHALMERS, R. A, TRACEY, B. M, MISTRY, J, GRIFFITHS, K. D, GREEN, A, WINTERBORN, M. H

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The prenatal diagnosis of glutaric aciduria type II, using quantitative GC‐MS von Chalmers, R. A., Tracey, B. M., King, G. S., Pettit, B., Rocchiccioli, F., Saudubray, J. ‐M., Gray, R. G. F., Boué, J., Keeling, J. W., Lindenbaum, R. H.

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Regulation of Casein Kinase-2 (CK2) Activity by Inositol Phosphates von Solyakov, Lev, Cain, Kelvin, Tracey, Beryl M, Jukes, Rebekah, Riley, Andrew M, Potter, Barry V L, Tobin, Andrew B

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L‐carnitine and glycine therapy in isovaleric acidaemia von Chalmers, R. A., Sousa, C., Tracey, B. M., Stacey, T. E., Weaver, C., Bradley, D.

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Experience with prenatal diagnosis of propionic acidaemia and methylmalonic aciduria von FENSOM, A. H, BENSON, P. F, CHALMERS, R. A, TRACEY, B. M, WATSON, D, KING, G. S, PETTIT, B. R, RODECK, C. H

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Characterization of acylcarnitines as their isobutyl ester derivatives using fast atom bombardment mass spectrometry and constant neutral loss scan von Cheng, K. N., Rosankiewicz, J., Tracey, B. M., Chalmers, R. A.

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Visual Field Changes after Transient Elevation of Intraocular Pressure in Eyes with and without Glaucoma von Chan, Kenneth C.Y., MB ChB, Poostchi, Ali, BSc, MB ChB, Wong, Tracey, MB ChB, Insull, Elizabeth A., BSc, Sachdev, Nisha, MB ChB, PhD, Wells, Anthony P., MB ChB, FRANZCO

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