QUINOLINIC ACID AND KYNURENINE PATHWAY METABOLISM IN INFLAMMATORY AND NON-INFLAMMATORY NEUROLOGICAL DISEASE von HEYES, M. P., SAITO, K., CROWLEY, J. S., DAVIS, L. E., DEMITRACK, M. A., DER, M., DILLING, L. A., ELIA, J., KRUESI, M. J. P., LACKNER, A., LARSEN, S. A., LEE, K., LEONARD, H. L., MARKEY, S. P., MARTIN, A., MILSTEIN, S., MOURADIAN, M. M., PRANZATELLI, M. R., QUEARRY, B. J., SALAZAR, A., SMITH, M., STRAUSS, S. E., SUNDERLAND, T., SWEDO, S. W., TOURTELLOTTE, W. W.

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Outcome of the First 3-Years of a DNA-Based Neonatal Screening Program for Glutaric Acidemia Type 1 in Manitoba and Northwestern Ontario, Canada von Greenberg, C.R., Prasad, A.N., Dilling, L.A., Thompson, J.R.G., Haworth, J.C., Martin, B., Wood-Steiman, P., Seargeant, L.E., Seifert, B., Booth, F.A., Prasad, C.

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Hepatic Carnitine Palmitoyl Transferase 1 (CPT1 A) Deficiency in North American Hutterites (Canadian and American): Evidence for a Founder Effect and Results of a Pilot Study on a... von Prasad, C., Johnson, J.P., Bonnefont, J.P., Dilling, L.A., Innes, A.M., Haworth, J.C., Beischel, L., Thuillier, L., Prip-Buus, C., Singal, R., Thompson, J.R.G., Prasad, A.N., Buist, N., Greenberg, C.R.

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Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome von Hsu, Betty Y.L., Kelly, Andrea, Thornton, Paul S., Greenberg, Cheryl R., Dilling, Louise A., Stanley, Charles A.

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A simple screening test for fatty acid oxidation defects using whole‐blood palmitate oxidation von Seargeant, L. E., Balachandra, K., Mallory, C., Dilling, L. A., Greenberg, C. R.

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Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindreds von Haworth, J.C., Booth, F.A., Chudley, A.E., deGroot, G.W., Dilling, L.A., Goodman, S.I., Greenberg, C.R., Mallory, C.J., McClarty, B.M., Seargeant, L.E.

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A G-to-T transversion at the +5 position of intron 1 in the glutaryl CoA dehydrogenase gene is associated with the island Lake variant of glutaric acidemia type I von Greenberg, Cheryl R., Reimer, David, Singal, Rupinder, Triggs-Raine, Barbara, Chudley, Albert E., Dilling, Louise A., Philipps, Sylvia, Haworth, James C., Seargeant, Lorne E., Goodman, Stephen I.

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Primary oxaluria type 2 ( l-glyceric aciduria): A rare cause of nephrolithiasis in children von Seargeant, L.E., deGroot, G.W., Dilling, L.A., Mallory, C.J., Haworth, J.C.

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Vitamin D Deficiency in a Manitoba Community von Lebrun, John B., Moffatt, Michael E.K., Mundy, Ronald J.T., Sangster, Robert K., Postl, Brian D., Dooley, Joseph P., Dilling, Louise A., Godel, John C., Haworth, James C.

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Vitamin-D-deficient rickets in Manitoba, 1972-84 von Haworth, J. C, Dilling, L. A

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Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite family von Haworth, James C., Demaugre, France, Booth, Frances A., Dilling, Louise A., Moroz, Stanley P., Seshia, Shashikant S., Seargeant, Lorne E., Coates, Paul M.

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Increased prevalence of hereditary metabolic diseases among native Indians in Manitoba and northwestern Ontario von Haworth, J C, Dilling, L A, Seargeant, L E

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Aspartylglycosaminuria presenting with hepatosplenomegaly in early infancy von Haworth, J. C., Seargeant, L. E., Dilling, L. A.

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Carrier detection in glutaric aciduria type I using interleukin‐2‐dependent cultured lymphocytes von Seargeant, L. E., Chudley, A. E., Dilling, L. A., Mallory, C. J., Haworth, J. C.

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Mitochondrial encephalomyopathy with associated aminoacidopathy in a male sibship von Booth, F.A., Haworth, J.C., Dilling, L.A., Perry, T.L., Greenberg, C.R., Seargeant, L.E., Penn, A.M., Rhead, W.J.

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An unusual aminoacidopathy associated with mitochondrial encephalomyopathy von Perry, T. L., Hansen, S., Booth, F. A., Penn, A. M. W., Jones, K., Dilling, L. A.

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Breast-feeding protects against infection in Indian infants von Ellestad-Sayed, J, Coodin, F. J, Dilling, L. A, Haworth, J. C

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Newborn screening for galactosemia: a new method used in Manitoba von Greenberg, C R, Dilling, L A, Thompson, R, Ford, J D, Seargeant, L E, Haworth, J C

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Fetal growth retardation in cigarette-smoking mothers is not due to decreased maternal food intake von Haworth, J.C., Ellestad-Sayed, J.J., King, Jean, Dilling, Louise A.

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Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothers von Haworth, J. C., Dilling, L. A., Surtees, R. A. H., Seargeant, L. E., Lue-Shing, H., Cooper, B. A., Rosenblatt, D. S.

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