Menkes, J.H. , Hurst, P.L. and Craig, J.M.: A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance. Pediatrics14: 462, 1954.
2.
Smith, B.A. and Waisman, H.A.: Leucine exchange system in managing branched chain ketoaciduria. J. Amer. Diet. Assoc.59: 342, 1971.
3.
Westall, R.G. : Dietary treatment of maple syrup urine disease . Amer. J. Dis. Child.113: 58, 1967.
4.
Gaull, G.E.: Pathogenesis of maple-syrup urine disease: observations during dietary management and treatment of coma by peritoneal dialysis. Biochem. Med.3: 130, 1969.
5.
Rey, F., Rey, J., Cloup, M., Féron, J.-F., Doré, F., Labrune, B. and Frezal, J.: Traitement d'urgence d'une forme aigue de leucinose par dialyse peritoneale . Arch. Franç. Péd.26: 133, 1969.
6.
Fischer, M. and Gerritsen, T.: Biochemical studies on a variant of branched chain ketoaciduria in a 19-year-old female. Pediatrics48: 795, 1971.
7.
Innominate.Words from the laboratory. Vol. 1 (6), Jan., 1971. Distributed to staff of the University of Wisconsin Medical Center, Madison, Wisconsin , U. S. A.
8.
Nelson, W.E. : Textbook of Pediatrics. Seventh edition. Philadelphia, W. B. Saunders Co., 1959, p.174.
9.
Kiil, R. and Rokkones, T.: Late manifesting variant of branched-chain ketoaciduria. Acta Pediatrica53: 356, 1964.
