Author:
Milovanović D. D.,Milovanović L.,Stanković B.,Radulović D.
Reference12 articles.
1. Baron, D.N., Dent, C.E., Harris, H., Hart, E.W., and Jepson, J.B., 1956, Hereditary pellegra-like skin rash with temporary cerebellar ataxia, constant renal aminoaciduria, and other bizarre biochemical feature, Lancet, 2: 421–428.
2. Jepson, J.B., 1955, Paper chromatography of urinary indoles, Lancet, 2: 1009–1011.
3. Komrower, G.M., Wilson, V., Clamp, J.R., and Westall, R.G., 1964, Hydroxykyn-ureninuria, Arch. Dis. Childh., 39: 250–256.
4. Lato, M., Rufini, S., Ghebergzabher, M., Cuiffini, G., and Mezzetti, T., 1974, A sensitive Chromatographie technique for screening of amino acid metabolic defects in the newborn, Clin. Chim. Acta, 53: 273–280.
5. Milne, M.D., Crawford, M.A., Girao, C.B., and Loughridge, L.M., 1960, The metabolic disorder in Hartnup disease, Quart. J. Med., 29: 407–421.
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