1. A disease, probably hereditary, characterized by severe mental deficiency and a constant gross abnormality of aminoacid metabolism;Allan, J.D.; Cusworth, D.C.; Dent, C.E.; Wilson, V.K.;Lancet,1958
2. Argininbernsteinsaure-Krankheit des Neugeborenen mit letalem Verlauf;Baumgartner, R.; Scheidegger, S.; Stalder, G.; Hottinger, A.;Helvetica Paediatrica Acta,1968
3. Comparative biochemistry of urea synthesis. I. Methods for the quantitative assay of urea cycle enzymes in liver;Brown, Jr., G.W.; Cohen, P.P.;J'ournal of Biological Chemistry,1959
4. Argininosuccinic aciduria: neonatal variant with rapid fatal course;Carton, D.; de Schrijver, F.; Kint, J.; van Durme, J.; Hooft, C.;Acta Paediatrica Scandinavica,1969
5. Stimulation of insulin secretion by amino acids;Floyd, Jr., J.C.; Fajans, S.S.; Conn, J.W.; Knopf, R.F.; Rull, J.;journal of Clinical Investigation,1966