SciELO - Scientific Electronic Library Online

SciELO - Scientific Electronic Library Online

Article References

RADVANY, J. et al. Machado-Joseph disease op azorean ancestry in Brazil: the Catarina kindred neurological, neuroimaging, psychiatric and neuropsychological findings in the largest known family, the «Catarina» kindred. Arq. Neuro-Psiquiatr. [online]. 1993, vol.51, n.1, pp. 21-30. ISSN 0004-282X.  http://dx.doi.org/10.1590/S0004-282X1993000100004.

    1. Asberg M, Montgomery S, Perris C, Schalling D, Sedwall G. A comprehensive psycho-pathological rating scale. Acta Psychiat Scand 1978 (Suppl), 271:5-27. [ Links ]

    2. Barbeau A, Roy M, Cunha L, de Vicente AN, Rosenberg RN, Nyhan WL MacLeod PL, Chazot G, Langston LB, Dawson DM, Coutinho P. The natural history of Machado-Joseph disease: an anylysis of 138 personally examined cases. Can J Neurol Sci 1984, 11:510-525. [ Links ]

    3. Bergstedt J., Johansson M, Muller G. Hereditary spastic ataxia with central retinal degeneration and vestibular impairment: a clinical report on a family. Neurology 1962, 12:124-132. [ Links ]

    4. Carson WJ, Radvany J, Farrer LA, Vincent D, Rosenberg RN, MacLeod PM, Rouleau GA. The Machado-Josep disease locus is different from the spinocerebellar ataxia locus (SCA1). Genomics 1992, 13:852-856. [ Links ]

    5. Coutinho P. Neglected features of Machado-Joseph disease (Abstr) Research Initiatives in Machado-Joseph Disease. Bethesda MD: NINDS, June 3-4, 1991. [ Links ]

    6. 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. [ Links ]

    7. Coutinho P, Calheiros JM, Andrade C. Sobre uma nova doença degenerativa do sistema nervoso central transmitida de modo dominante e afectando famílias originárias dos Açores. (Nota prévia). O Médico 1977, 82:1-3. [ Links ]

    8. Dawson DM, Feudo P, Zubick HH, Rosenberg R, Fowler H. Electrooculographic findings in Machado-Joseph disease. Neurology 1982, 32:1272-1276. [ Links ]

    9. Foster JB, Ingram TTS. Familial cerebro-macular degeneration and ataxia. J Neurol Neurosurg Psychiatry 1962, 25:63-68. [ Links ]

    10. Goto I, Tobimatsu S, Ohta M, Hosokawa S, Shibasaki H, Kuroiwa Y. Dentatorubropallydoluysian degeneration: clinical, neuro-ophtalmologic, biochemical and pathologic studies on autosomal form. Neurology 1982, 32:1395-1399. [ Links ]

    11. Healton EB, Brust JCM, Kerr DR, Resor S, Penn A. Presumably Azorean disease in a presumably non-Azorean family. Neurology 1980, 30:1084-1089. [ Links ]

    12. Iwabuchi K. Clinicopathological study on autosomal dominant forms of spinocerebellar degeneration (SCD) with special reference to Menzel's disease, hereditary ataxia linked to SCA1 and Japanese Machado-Joseph disease in Japan (Abstr). Research Initiatives in Machado-Joseph Disease. Bethesda MD: NINDS, June 3-4, 1991. [ Links ]

    13. Jackson JF, Currier RD, Teriasaki PI, Morton NE. Spinocerebellar ataxia and HLS linkage: risk prediction by HLA typing. N Engl J Med 1977, 296:1138-1141. [ Links ]

    14. Lezak MD: Neuropsychological assesment. New York: Oxford Univ Press, 1983. [ Links ]

    15. Lima L, Coutinho P. Clinical criteria for diagnosis of Machado-Joseph disease: report of a non-Azorean family. Neurology 1980, 30:319-322. [ Links ]

    16. Lisboa MFS, Mariotto GSS. Síndrome de Joseph: observação em uma família (Abstr). Arq Neuro-Psiquiat (São Paulo.) 1984 (Suppl), p 45. [ Links ]

    17. Montgomery S, Asberg M. A new depression scale designed to be sensitive to change. Br J Psychiatry 1979, 134:382-389. [ Links ]

    18. Nákano KK, Dawson DM, Spence A. Machado disease: a hereditary ataxia in Portuguese immigrants to Massachusetts. Neurology 1972, 22:49-55. [ Links ]

    19. Radvany J, Avila JO, Gabbai AA, Bacheschi LA. Doença de Machado-Joseph no Brasil: o relato das primeiras duas famílias (Abstr). Arq Neuro-Psiquiat (São Paulo) 1988 (Supl), 46B. [ Links ]

    20. Romanul FCA, Fowler HL, Radvany J, Feldman RG, Feingold M. Azorean disease of the nervous system. N Engl J Med 1977, 296:1505-1508. [ Links ]

    21. Romanul FCA, Radvany J, Fowler HL, Tarsy D. Azorean disease of the nervous system: report of six additional families (Abstr). Ann Neurol 1978, 4:183. [ Links ]

    22. Rosenberg RN, Nyhan WL, Bay C, Shore P. Autosomal dominant striato-nigral degeneration: a clinical, pathological and biochemical study of a new genetic disorder. Neurology 1976, 26:703-714. [ Links ]

    23. Sakai T, Ohta M, Ishino H. Joseph disease in a non-Portuguese family. Neurology 1983, 33:74-80. [ Links ]

    24. Teive HAG, Arruda WO, Tevisol-Bittencourt PC. Doença de Machado-Joseph. Arq Neuro-Psiquiat (Sao Paulo) 1991, 49:172-179. [ Links ]

    25. Wadia NH, Swami RK. A new form of heredofamilial spinocerebellar degeneration with slow eye movements (nine families). Brain 1971, 94:359-374. [ Links ]

    26. Woods BT, Schaumburg HH. Nigro-spino-dentatal degeneration with nuclear ophtalmoplegia: a unique and partially treatable clinicopathological entity. J Neurol Sci 1972, 17:149-166. [ Links ]

    27. Zoghbi HY, Pollack MS, Lyons LA, Ferrei RE, Daiger SP, Beaudet AL. Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindred. Ann Neurol 1988, 23:580-584. [ Links ]