References
- Araki S., Kurihara T., Tawara S., Kuribayashi T. Familial amyloidotic polyneuropathy in Japanese. Amyloid and Amyloidosis, G. G. Glenner, P. P. Costa, A. F. Freitas. Exerpta Medica, Amsterdam 1980; 67–77
- Brown J. W., Coleman R. F. Hereditary spastic paraplegia with ocular and extra-pyramidal signs. Bull. Los Angeles Neurol. Soc 1966; 32: 21–34
- Coutinho P., Andrade C. Autosomal dominant system degeneration in Portuguese families of the Azores Islands: a new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions. Neurology 1978; 28: 703–709
- Coutinho P., Sequeiros J. Aspects cliniques genetiques et pathologiques de la maladie de Machado-Joseph. J. Genet. Hum. 1981; 29: 203–209
- Ferguson F., Critchley M. A clinical study of heredofamilial disease resembling disseminated sclerosis. Brain 1929; 52: 203–225
- Gray R. C., Oliver C. P. Marie's hereditary cerebellar ataxia (olivopontocerebellar atrophy). Minn. Med. 1941; 24: 327–335
- Healton E. B., Brust J. CM., Kerr D. L., et al. Familial cerebellar ataxia, dystonia and abnormal eye movements in a non-Portuguese family. Neurology 1979; 29: 559–560
- Klippel M., Durante G. Affections nerveuses familiales et héréditaires. Rev. Med. (Paris) 1892; 12: 745–785
- Landau W. M., Gitt J. J. Hereditary spastic paraplegia and hereditary ataxia: a family demonstrating a variety of phenotypic manifestations. Arch. Neurol. Psychiatr. 1951; 66: 346–354
- Lima L., Coutinho P. Clinical criteria for diagnosis of Machado-Joseph disease: report of a non-Azorean Portuguese family. Neurology 1980; 30: 319–322
- Nakano K. K., Dawson D. M., Spence A. Machado disease: a hereditary ataxia in Portuguese emigrants to Massachusetts. Neurology 1972; 22: 49–55
- Romanul F. C. A., Fowler H. L., Radvany J., et al. Azorean disease of the nervous system. N. Engl. J. Med. 1977; 296: 1505–1508
- Rosenberg R. N., Nyhan W. L., Bay C., et al. Autosomal dominant striatonigral degeneration: a clinical, pathological and biochemical study of a new genetic disorder. Neurology 1976; 26: 703–714
- Sakai T., Ohta M., Ishino H. Joseph disease in a non-Portuguese family. Neurology 1983; 33: 74–80
- Schut J. W. Hereditary ataxia: clinical study through six generations. Arch. Neurol. Psychiatry 1950; 63: 535–568
- Sequeiros J., Coutinho P. Genetic aspects of Machado-Joseph disease. Broteria-Genetica 1981; II: 137–147
- Woods B. T., Shaumburg H. H. Nigrospinodentatal degeneration with nuclear ophthalmoplegia – a unique and partially treatable clinicopathological entity. J. Neurol. Set 1972; 17: 149–166