Author:
Harden A.,Martinovic Z.,Pampiglione G.
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Neuroscience,Psychiatry and Mental health,Clinical Neurology,Dermatology,General Medicine
Reference19 articles.
1. Adachi, M., Volk, V.W.:Pathology. In:The Gangliosidoses. Ed. B.W. Volk and L. Schneck, pp. 125–158, Plenum Press, London and New York, 1975.
2. Derry, D.M., Fawcett, J.S., Andermann, F., Wolfe, L.S.:Late infantile systemic lipidosis. Neurology (NY), 18: 340–348, 1968.
3. Fricker, H., O'Brien, J.S., Vassella, F., Gugler, E., Muhlethaler, J.P., Spycher, M., Wiesmann, U.N., Herschkowitz, N.:Generalised gangliosidosis: acid β-galactosidase deficiency with early onset, rapid mental deterioration and minimal bone dysplasia. J. Neurol., 213: 273–281, 1976.
4. Gonatas, N.K., Gonatas, J.:Ultrastructural and biochemical observations on a case of systemic late infantile lipidosis and its relationship to TaySachs disease and gargoylism. J. Neuropathol. Exp. Neurol., 24: 318–340, 1965.
5. Hanefeld, F., Pampiglione, G.:EEGs in 18 cases of mucopolysaccharidoses. Electroencephalogr. Clin. Neurophysiol., 33: 447, 1972.
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献