Cystathionine β-synthase deficiency in Georgia (USA): Correlation of clinical and biochemical phenotype with genotype von Kruger, W.D., Wang, L., Jhee, K.H., Singh, R.H., Elsas II, L.J.

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Molecular and biochemical characterization of human galactokinase and its small molecule inhibitors von Tang, M., Wierenga, K., Elsas, L.J., Lai, K.

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GALT deficiency causes UDP-hexose deficit in human galactosemic cells von Lai, K., Langley, S.D., Khwaja, F.W., Schmitt, E.W., Elsas, L.J.

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ARHI: A new target of galactose toxicity in Classic Galactosemia von Lai, K, Tang, M, Yin, X, Klapper, H, Wierenga, K, Elsas, Lj

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Cystathionine?-synthase deficiency in Georgia (USA): Correlation of clinical and biochemical phenotype with genotype von Kruger, W.D., Wang, L., Jhee, K.H., Singh, R.H., Elsas, L.J.

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A prevalent mutation for galactosemia among black Americans von Lai, Kent, Langley, S.D., Singh, R.H., Dembure, P.P., Hjelm, L.N., Elsas, L.J.

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Cystathionine ²-synthase deficiency in Georgia (USA): Correlation of clinical and biochemical phenotype with genotype von Kruger, W D, Wang, L, Jhee, K H, Singh, R H, L.J. Elsas II

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A common mutation associated with the duarte galactosemia allele von ELSAS, L. J, DEMBURE, P. P, LANGLEY, S, PAULK, E. M, HJELM, L. N, FRIDOVICH-KEIL, J

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Activation of insulin receptor signaling by a single amino acid substitution in the transmembrane domain von LONGO, N, SHUSTER, RC, GRIFFIN, LD, LANGLEY, SD, ELSAS, LJ

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Cystathionine-β-synthase deficiency: Detection of heterozygotes by the ratios of homocystein to cysteine and folate von Boddie, A.M., Steen, M.T., Sullivan, K.M., Pasquali, M., Dembure, P.P., Coates, R.J., Elsas, L.J.

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Biochemical discrimination of heterozygotes for cystathionine β-synthase (CβS) deficiency von Steen, M.T., Boddie, A.M., Langley, S., Cotsonis, G., MacMahon, W., Saxe, D., Dembure, P.P., Kim, C., Kruger, W.D., Elsas, L.J.

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The role of thiamin in Maple syrup urine disease von Elsas II, Louis J., Danner, Dean J.

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Prenatal diagnosis in metropolitan Atlanta and the impact on autosomal trisomies von Priest, J.H., Fernhoff, P.M., Elsas, L.J., Huether, C.A.

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Aspartame and headache von Lipton, R.B, Newman, L.C, Solomon, S, Steinmetzer, R.V, Kunkel, R.S, Elsas, L.J. II, Schiffman, S.S, Buckley, C.E, Sampson, H.A, Massey, E.W

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Clofibric acid and phenylpyruvic acid as biochemical probes for studying soluble bovine liver branched chain ketoacid dehydrogenase von DANNER, D. J, SEWELL, E. T, ELSAS, L. J

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Amino acid transport by aggregates of cultured chicken heart cells: Effect of insulin von Elsas, L.J, Wheeler, F.B, Danner, D.J, DeHaan, R.L

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Pretreatment Serum Phenylalanine Levels As a Predictor of the Severity of the Mutation in the Phenylalanine Hydroxylase Gene and Phenylalanine Tolerance in Patients with Phenylketo... von Singh, R.H., Dembure, P., Eisensmith, R.C., Guerrero, N.V., Sullivan, K., Elsas, L.J.

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Characterization and regulation of insulin binding by embryonic chick heart cells von Serravezza, June C., Wheeler, Frances B., DeHaan, Robert L., Elsas, Louis J.

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In Vivo Oxidation of [13C]Galactose in Patients with Galactose-1-Phosphate Uridyltransferase Deficiency von Berry, G.T., Nissim, I., Mazur, A.T., Elsas, L.J., Singh, R.H., Klein, P.D., Gibson, J.B., Lin, Z.P., Segal, S.

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Thiamin-Responsive Maple Syrup Urine Disease in a Patient Antigenically Missing Dihydrolipoamide Acyltransferase von Ellerine, N.P., Herring, W.J., Elsas, L.J., Mckean, M.C., Klein, P.D., Danner, D.J.

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