1. A disease, probably hereditary, characterised 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. Auerbach, V. H., Di George, A. M., Baldridge, R. C., Tourtellotte, C. D. and Brigham, M. P. (1962). Histidinemia. J. Pediat., 60, 487.
3. Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant ranal amino-aciduria, and other bizarre biochemical features;Baron, D.N.; Dent, C.E.; Harris, H.; Hart, E.W.; Jepso[L, J.B.;Lancet,1956
4. On the colorimetric determination of creatinine by the Jaffe reaction;Bonsnes, R.W.; Taussky, H.H.;J. biol. Chem,1945
5. Cystinuria. The excretion of a cystine complex which decomposes in the urine with the liberation of free cystine;Brand, E.; Harris, M.M.; Biloon, S.;ibid,1930