메뉴 건너뛰기




Volumn 59, Issue 1, 1999, Pages 63-66

Cuban dominant cerebellar ataxia. Perioheral nerve conduction studies in patients and asymptomatic-relatives;Ataxia cerebelosa dominante cubana estudios de conduccion de nervios perifericos en pacientes y familiares asintomaticos

Author keywords

Cuban ataxia; Preclinical electrophysiological alterations; SCA2

Indexed keywords

ARTICLE; CEREBELLAR ATAXIA; COMPARATIVE STUDY; CUBA; ELECTROPHYSIOLOGY; GENETICS; HUMAN; NERVE CONDUCTION; PATHOPHYSIOLOGY; PERIPHERAL NERVE; PHYSIOLOGY;

EID: 0040214978     PISSN: 00257680     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (4)

References (25)
  • 1
    • 0024997225 scopus 로고
    • Autosomal dominant cerebellar ataxia: Clinical analysis of 263 patients from a homogeneous population in Holguin, Cuba
    • Orozco DG, Nodarse FA, Cordovés R, Aurburger G. Autosomal dominant cerebellar ataxia: Clinical analysis of 263 patients from a homogeneous population in Holguin, Cuba. Neurology 1990; 40: 1369-75.
    • (1990) Neurology , vol.40 , pp. 1369-1375
    • Orozco, D.G.1    Nodarse, F.A.2    Cordovés, R.3    Aurburger, G.4
  • 2
    • 0024422743 scopus 로고
    • Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological and biochemical findings
    • Orozco DG, Estrada R, Perry T, Araña J, Fernández R, Gonzalez QA, et al. Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological and biochemical findings. J Neurol Sci 1989; 93: 37-50.
    • (1989) J Neurol Sci , vol.93 , pp. 37-50
    • Orozco, D.G.1    Estrada, R.2    Perry, T.3    Araña, J.4    Fernández, R.5    Gonzalez, Q.A.6
  • 3
    • 0025350263 scopus 로고
    • Autosomal dominant ataxia: Genetic evidence for locus heterogeneity from a Cuban founder effect population
    • Auburger G. Autosomal dominant ataxia: Genetic evidence for locus heterogeneity from a Cuban founder effect population. Am J Hum Genet 1990; 46: 1163-77.
    • (1990) Am J Hum Genet , vol.46 , pp. 1163-1177
    • Auburger, G.1
  • 4
    • 0003437587 scopus 로고
    • Study of 225 patients with autosomal dominant cerebellar ataxia: Presumed founder effect in the province Holguin, Cuba
    • Plaitakis J, ed. Berlin: Springer-Verlag
    • Orozco G, Nodarse A, Cordovés R, Aurburger G, Estrada R. Study of 225 patients with autosomal dominant cerebellar ataxia: Presumed founder effect in the province Holguin, Cuba. In: Plaitakis J, ed. Hereditary Ataxias. Berlin: Springer-Verlag, 1989; p 345-60.
    • (1989) Hereditary Ataxias , pp. 345-360
    • Orozco, G.1    Nodarse, A.2    Cordovés, R.3    Aurburger, G.4    Estrada, R.5
  • 5
    • 0039211646 scopus 로고
    • Clinicalelectrophysiological correlation in patients with hereditary ataxia and asymptomatic relatives
    • Nodarse A, Orozco DG, Gutiérrez S, Coutin P. Clinicalelectrophysiological correlation in patients with hereditary ataxia and asymptomatic relatives. EEG Clin Neurophysiol 1987; 66: 573.
    • (1987) EEG Clin Neurophysiol , vol.66 , pp. 573
    • Nodarse, A.1    Orozco, D.G.2    Gutiérrez, S.3    Coutin, P.4
  • 6
    • 0021828991 scopus 로고
    • Neurophysiologic study of olivopontocerebellar atrophy with or without glutamate dehydrogenase deficiency
    • Chokroverty S, Duvoisin RC, Sachdeo R, Saje J, Lepore F, Nicklas W. Neurophysiologic study of olivopontocerebellar atrophy with or without glutamate dehydrogenase deficiency. Neurology 1985; 35: 652-8.
    • (1985) Neurology , vol.35 , pp. 652-658
    • Chokroverty, S.1    Duvoisin, R.C.2    Sachdeo, R.3    Saje, J.4    Lepore, F.5    Nicklas, W.6
  • 7
    • 0020076144 scopus 로고
    • Olivopontocerebellar atrophies
    • Berciano J. Olivopontocerebellar atrophies. J Neurol Sci 1982; 53: 253-72.
    • (1982) J Neurol Sci , vol.53 , pp. 253-272
    • Berciano, J.1
  • 8
    • 0000051759 scopus 로고
    • Hereditary ataxia. Clinical study trough six generations
    • Schut JW. Hereditary ataxia. Clinical study trough six Generations, Arch Neurol Psychiat 1950; 63: 535-68.
    • (1950) Arch Neurol Psychiat , vol.63 , pp. 535-568
    • Schut, J.W.1
  • 10
    • 0021355782 scopus 로고
    • Large fiber sensory neuronopathy in autosomal dominant spinocerebellar degeneration
    • Bennet RH, Ludvigson P, Deleon G, Berry G. Large fiber sensory neuronopathy in autosomal dominant spinocerebellar degeneration. Arch Neurol 1984; 41: 175-8.
    • (1984) Arch Neurol , vol.41 , pp. 175-178
    • Bennet, R.H.1    Ludvigson, P.2    Deleon, G.3    Berry, G.4
  • 12
    • 0021350013 scopus 로고
    • Electromyography and nerve conduction study in autosomal dominant olivopontocerebellar atrophy
    • Carenini GL, Finocchiaro G, Di Donato S, Visciani A, Negri S. Electromyography and nerve conduction study in autosomal dominant olivopontocerebellar atrophy. J Neurol 1984; 231: 34-7.
    • (1984) J Neurol , vol.231 , pp. 34-37
    • Carenini, G.L.1    Finocchiaro, G.2    Di Donato, S.3    Visciani, A.4    Negri, S.5
  • 13
    • 0039211644 scopus 로고
    • Peripheral nerve involvement in late-onset familial ataxias
    • Subramony SH, Currier RD. Peripheral nerve involvement in late-onset familial ataxias. Muscle & Nerve 1983; 6: 537-8.
    • (1983) Muscle & Nerve , vol.6 , pp. 537-538
    • Subramony, S.H.1    Currier, R.D.2
  • 14
    • 0040396119 scopus 로고
    • A family with autosomal dominant spinocerebellar degenerations
    • Frey MJ. A family with autosomal dominant spinocerebellar degenerations. Muscle & Nerve 1981; 4: 51-61.
    • (1981) Muscle & Nerve , vol.4 , pp. 51-61
    • Frey, M.J.1
  • 15
    • 0019484086 scopus 로고
    • Idiopatic late onset cerebellar ataxia. A clinical and genetic study of 36 cases
    • Harding AE. Idiopatic late onset cerebellar ataxia. A clinical and genetic study of 36 cases. J Neurol Sci 1981; 51: 259-71.
    • (1981) J Neurol Sci , vol.51 , pp. 259-271
    • Harding, A.E.1
  • 17
    • 0019377696 scopus 로고
    • Peripheral neuropathy in Spinocerebellar degenerations
    • Me Leod JG, Evans WA. Peripheral neuropathy in Spinocerebellar degenerations. Mucle & Nerve 1981; 4: 51-61.
    • (1981) Mucle & Nerve , vol.4 , pp. 51-61
    • Me Leod, J.G.1    Evans, W.A.2
  • 18
    • 0039803708 scopus 로고
    • Evidence of peripheral neuropathy in a variety of heredo-familial olivoponto-cerebellar degeneration frequently seen in India
    • Sobue I (ed) Japan: University of Tokyo Press
    • Wadia N, Irani P, Mehta L, Purohit B. Evidence of peripheral neuropathy in a variety of heredo-familial olivoponto-cerebellar degeneration frequently seen in India In: Sobue I (ed) Spinocerebellar degenerations. Japan: University of Tokyo Press, 1980, p 239-50.
    • (1980) Spinocerebellar Degenerations , pp. 239-250
    • Wadia, N.1    Irani, P.2    Mehta, L.3    Purohit, B.4
  • 19
    • 0019954153 scopus 로고
    • Ultraestructural observation on spinal ganglion biopsy in Friedreich's ataxia: A preliminary report
    • Lamarche J. Ultraestructural observation on spinal ganglion biopsy in Friedreich's ataxia: a preliminary report. J Can Sci Neurol 1982; 9: 137-9.
    • (1982) J Can Sci Neurol , vol.9 , pp. 137-139
    • Lamarche, J.1
  • 20
    • 0019979781 scopus 로고
    • Friedreich's ataxia. Early detection and progression of peripheral nerve abnormalities
    • Oubier RA. Friedreich's ataxia. Early detection and progression of peripheral nerve abnormalities. J Neurol Sci 1982; 55: 137-45.
    • (1982) J Neurol Sci , vol.55 , pp. 137-145
    • Oubier, R.A.1
  • 21
    • 0016606476 scopus 로고
    • Motor conduction velocity in patients with Friedreich ataxia
    • Salisachs P. Motor conduction velocity in patients with Friedreich ataxia. J Neurol Sci 1975; 24: 331-7.
    • (1975) J Neurol Sci , vol.24 , pp. 331-337
    • Salisachs, P.1
  • 22
    • 0020696198 scopus 로고
    • Friedreich's ataxia: Electrophysiological and histological findings
    • Caruso G. Friedreich's ataxia: electrophysiological and histological findings. Acta Neurol Scand 1983; 67: 26-40.
    • (1983) Acta Neurol Scand , vol.67 , pp. 26-40
    • Caruso, G.1
  • 23
    • 0021618123 scopus 로고
    • Electrophysiological findings in relatives of patients with Friedreich's ataxia
    • Caruso G, Santoro L, Peretti A, Campanella G, Rosato R, Crisci C, et al. Electrophysiological findings in relatives of patients with Friedreich's ataxia. Ital J Neurol Sci 1984; (Suppl)4: 98-105.
    • (1984) Ital J Neurol Sci , vol.4 , Issue.SUPPL. , pp. 98-105
    • Caruso, G.1    Santoro, L.2    Peretti, A.3    Campanella, G.4    Rosato, R.5    Crisci, C.6
  • 24
    • 0019902437 scopus 로고
    • The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendents of the drew family of walworth
    • Harding AE. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendents of the drew family of walworth. Brain 1982; 105: 1-28.
    • (1982) Brain , vol.105 , pp. 1-28
    • Harding, A.E.1
  • 25
    • 0018766158 scopus 로고
    • Electromyography and nerve conduction studies in Friedreich's ataxia and autosomal recessive spastic ataxia of Charlevoix-Saguenay
    • Bouchard JP, Barbeau A, Bouchard R, Bouchard RW. Electromyography and nerve conduction studies in Friedreich's ataxia and autosomal recessive spastic ataxia of Charlevoix-Saguenay. J Can Des Sci Neurol 1979; 6: 185-9.
    • (1979) J Can Des Sci Neurol , vol.6 , pp. 185-189
    • Bouchard, J.P.1    Barbeau, A.2    Bouchard, R.3    Bouchard, R.W.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.