Author:
Federico A.,Ciacci G.,d'Amore I.,Pallini R.,Palmeri S.,Rossi A.,Rizzuto N.,Guazzi G. C.
Subject
Genetics(clinical),Genetics
Reference8 articles.
1. Argov, Z. and Navon, R. Clinical and genetic variations in the syndrome of adult GM2 gangliosidosis resulting from hexosaminidase A deficiency.Ann. Neurol. 16 (1984) 14–20
2. Barbeau, A., Plasse, L., Cloutier, T., Paris, S. and Roy, M. Lysosomal enzymes in ataxia: discovery of two cases of late-onset hexosaminidase A and B deficiency (adult Sandoff disease) in French Canadians.Canad. J. Neurol. Sci. 11 (1984) 601–606
3. Conzelman, E. and Sandhoff, K. Partial enzyme deficiencies: residual activities and the development of neurologic disorders.Dev. Neurosci. 6 (1984) 58–71
4. Federico, A. GM2 gangliosidosis with motor neuron disease phenotype: clinical heterogeneity of hexosaminidase deficiency disease. In Kato, A., Cosi V., Parlette W., Pinelli, P. and Poloni, M. (eds.)Therapeutic, Psychologic and Research Aspects of ALS, Plenum Press, London, in press
5. Guazzi, G. C., Rizzuto, N., Ciacci, G., D'Amore, I. and Rossi, A. Polyneuritiform spinocerebellar ataxia with dominant autosomic transmission.Neuropath. Acta Neurol. 5 (1983) 303–304
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