1. Uber das Verhalten der Ganglioside im Gehirn bei 2 Fallen von spaitinfantiler amaurotischer Idiotie. Wienerklinische together with the confirmation of the enzyme defect. Though the proportion of total ganglio-;Bernheimer, H.; Seitelberger, F.,1968
2. Cumings, J. N. (1968). (1968). Genetically determined neurological diseases of children. In Biochemical Aspects of sides present as GM2 is greatly raised above the Neurological Disorders, 3rd series, p. 268. Edited by J. N.
3. Inborn errors of metabolism in as that found in cases of Tay-Sachs disease neurology (Wilson's disease, Refsum's disease, and (Wherrett and Cumings, 1963) and is comparable with that reported by Suzuki;Cumings, J.N.;et al,1971
4. who found a figure of 37-6%. Their patient showed the first signs of the disease when aged 6 years (as compared with ours of 5 years) and lipidoses);Proceedings of the Royal Society of Medicine
5. An infantile case of subacute sclerosing panencephalitis with an abnormal ganglioside pattern in the brain;Dayan, A.D.; Cumings, J.N.;Archives of Diseases in Childhood,1969