메뉴 건너뛰기




Volumn 103, Issue , 2012, Pages 253-262

Sporadic adult-onset ataxia of unknown etiology

Author keywords

[No Author keywords available]

Indexed keywords


EID: 79961146606     PISSN: 00729752     EISSN: None     Source Type: Book Series    
DOI: 10.1016/B978-0-444-51892-7.00015-2     Document Type: Chapter
Times cited : (24)

References (99)
  • 1
    • 0033541126 scopus 로고    scopus 로고
    • Cerebellar ataxia with glutamic acid decarboxylase autoantibodies
    • Abele M., Weller M., Mescheriakov S., et al. Cerebellar ataxia with glutamic acid decarboxylase autoantibodies. Neurology 1999, 52:857-859.
    • (1999) Neurology , vol.52 , pp. 857-859
    • Abele, M.1    Weller, M.2    Mescheriakov, S.3
  • 2
    • 0033965733 scopus 로고    scopus 로고
    • Evoked potentials in multiple system atrophy (MSA)
    • Abele M., Schulz J.B., Bürk K., et al. Evoked potentials in multiple system atrophy (MSA). Acta Neurol. Scand 2000, 101:111-115.
    • (2000) Acta Neurol. Scand , vol.101 , pp. 111-115
    • Abele, M.1    Schulz, J.B.2    Bürk, K.3
  • 3
    • 0036238233 scopus 로고    scopus 로고
    • The aetiology of sporadic adult-onset ataxia
    • Abele M., Bürk K., Schöls L., et al. The aetiology of sporadic adult-onset ataxia. Brain 2002, 125:961-968.
    • (2002) Brain , vol.125 , pp. 961-968
    • Abele, M.1    Bürk, K.2    Schöls, L.3
  • 4
    • 0037512408 scopus 로고    scopus 로고
    • Prevalence of antigliadin antibodies in ataxia patients
    • Abele M., Schöls L., Schwartz S., et al. Prevalence of antigliadin antibodies in ataxia patients. Neurology 2003, 60:1674-1675.
    • (2003) Neurology , vol.60 , pp. 1674-1675
    • Abele, M.1    Schöls, L.2    Schwartz, S.3
  • 5
    • 36148990665 scopus 로고    scopus 로고
    • Sporadic adult onset ataxia of unknown etiology: a clinical, electrophysiological and imaging study
    • Abele M., Minnerop M., Urbach H., et al. Sporadic adult onset ataxia of unknown etiology: a clinical, electrophysiological and imaging study. J Neurol 2007, 254:1384-1389.
    • (2007) J Neurol , vol.254 , pp. 1384-1389
    • Abele, M.1    Minnerop, M.2    Urbach, H.3
  • 6
    • 17644415431 scopus 로고
    • Parenchymatous atrophy of the cerebellum
    • Archambault L.S. Parenchymatous atrophy of the cerebellum. J Nerv Ment Dis 1918, 48:273-312.
    • (1918) J Nerv Ment Dis , vol.48 , pp. 273-312
    • Archambault, L.S.1
  • 7
    • 0022651454 scopus 로고
    • Late cortical cerebellar atrophy. Clinical and oculographic features
    • Baloh R.W., Yee R.D., Honrubia V. Late cortical cerebellar atrophy. Clinical and oculographic features. Brain 1986, 109:159-180.
    • (1986) Brain , vol.109 , pp. 159-180
    • Baloh, R.W.1    Yee, R.D.2    Honrubia, V.3
  • 8
    • 0031029831 scopus 로고    scopus 로고
    • Survival of patients with pathologically proven multiple system atrophy: a meta-analysis
    • Ben Shlomo Y., Wenning G.K., Tison F., et al. Survival of patients with pathologically proven multiple system atrophy: a meta-analysis. Neurology 1997, 48:384-393.
    • (1997) Neurology , vol.48 , pp. 384-393
    • Ben Shlomo, Y.1    Wenning, G.K.2    Tison, F.3
  • 9
    • 0020076144 scopus 로고
    • Olivopontocerebellar atrophy. A review of 117 cases
    • Berciano J. Olivopontocerebellar atrophy. A review of 117 cases. J Neurol Sci 1982, 53:253-272.
    • (1982) J Neurol Sci , vol.53 , pp. 253-272
    • Berciano, J.1
  • 10
    • 0036930653 scopus 로고    scopus 로고
    • Patterns of neuropsychological performance in multiple system atrophy compared to sporadic and hereditary olivopontocerebellar atrophy
    • Berent S., Giordani B., Gilman S., et al. Patterns of neuropsychological performance in multiple system atrophy compared to sporadic and hereditary olivopontocerebellar atrophy. Brain Cogn 2002, 50:194-206.
    • (2002) Brain Cogn , vol.50 , pp. 194-206
    • Berent, S.1    Giordani, B.2    Gilman, S.3
  • 11
    • 19944425949 scopus 로고    scopus 로고
    • FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia
    • Brussino A., Gellera C., Saluto A., et al. FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia. Neurology 2005, 64:145-147.
    • (2005) Neurology , vol.64 , pp. 145-147
    • Brussino, A.1    Gellera, C.2    Saluto, A.3
  • 12
    • 0342527698 scopus 로고    scopus 로고
    • Sporadic cerebellar ataxia associated with gluten sensitivity
    • Bürk K., Bösch S., Müller C.A., et al. Sporadic cerebellar ataxia associated with gluten sensitivity. Brain 2001, 124:1013-1019.
    • (2001) Brain , vol.124 , pp. 1013-1019
    • Bürk, K.1    Bösch, S.2    Müller, C.A.3
  • 13
    • 9144246374 scopus 로고    scopus 로고
    • MRI-based volumetric differentiation of sporadic cerebellar ataxia
    • Bürk K., Globas C., Wahl T., et al. MRI-based volumetric differentiation of sporadic cerebellar ataxia. Brain 2004, 127:175-181.
    • (2004) Brain , vol.127 , pp. 175-181
    • Bürk, K.1    Globas, C.2    Wahl, T.3
  • 14
    • 20844439855 scopus 로고    scopus 로고
    • Clinical and magnetic resonance imaging characteristics of sporadic cerebellar ataxia
    • Bürk K., Buhring U., Schulz J.B., et al. Clinical and magnetic resonance imaging characteristics of sporadic cerebellar ataxia. Arch Neurol 2005, 62:981-985.
    • (2005) Arch Neurol , vol.62 , pp. 981-985
    • Bürk, K.1    Buhring, U.2    Schulz, J.B.3
  • 15
    • 0035073180 scopus 로고    scopus 로고
    • Gluten sensitivity in sporadic and hereditary cerebellar ataxia
    • Bushara K.O., Goebel S.U., Shill H., et al. Gluten sensitivity in sporadic and hereditary cerebellar ataxia. Ann Neurol 2001, 49:540-543.
    • (2001) Ann Neurol , vol.49 , pp. 540-543
    • Bushara, K.O.1    Goebel, S.U.2    Shill, H.3
  • 16
    • 0038082887 scopus 로고    scopus 로고
    • The coeliac iceberg in Italy. A multicentre antigliadin antibodies screening for coeliac disease in school-age subjects
    • Catassi C., Fabiani E., Ratsch I.M., et al. The coeliac iceberg in Italy. A multicentre antigliadin antibodies screening for coeliac disease in school-age subjects. Acta Paediatr Suppl 1996, 412:29-35.
    • (1996) Acta Paediatr Suppl , vol.412 , pp. 29-35
    • Catassi, C.1    Fabiani, E.2    Ratsch, I.M.3
  • 17
    • 0019128551 scopus 로고
    • Computerized tomography in atrophy of the posterior fossa
    • Claus D., Aschoff J.C. Computerized tomography in atrophy of the posterior fossa. Arch Psychiatr Nervenkr 1980, 229:179-187.
    • (1980) Arch Psychiatr Nervenkr , vol.229 , pp. 179-187
    • Claus, D.1    Aschoff, J.C.2
  • 18
    • 0023915446 scopus 로고
    • Central motor conduction in degenerative ataxic disorders: a magnetic stimulation study
    • Claus D., Harding A.E., Hess C.W., et al. Central motor conduction in degenerative ataxic disorders: a magnetic stimulation study. J Neurol Neurosurg Psychiatry 1988, 51:790-795.
    • (1988) J Neurol Neurosurg Psychiatry , vol.51 , pp. 790-795
    • Claus, D.1    Harding, A.E.2    Hess, C.W.3
  • 19
    • 0034720833 scopus 로고    scopus 로고
    • Celiac disease and idiopathic cerebellar ataxia
    • Combarros O., Infante J., Lopez-Hoyos M., et al. Celiac disease and idiopathic cerebellar ataxia. Neurology 2000, 54:2346.
    • (2000) Neurology , vol.54 , pp. 2346
    • Combarros, O.1    Infante, J.2    Lopez-Hoyos, M.3
  • 20
    • 0029130471 scopus 로고
    • Transcranial magnetic stimulation in multiple system and late onset cerebellar atrophies
    • Cruz M.A., Arpa J., Alonso M., et al. Transcranial magnetic stimulation in multiple system and late onset cerebellar atrophies. Acta Neurol Scand 1995, 92:218-224.
    • (1995) Acta Neurol Scand , vol.92 , pp. 218-224
    • Cruz, M.A.1    Arpa, J.2    Alonso, M.3
  • 21
    • 0028120296 scopus 로고
    • Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus
    • De Michele G., Filla A., Cavalcanti F., et al. Late onset Friedreich's disease: clinical features and mapping of mutation to the FRDA locus. J Neurol Neurosurg Psychiatry 1994, 57:977-979.
    • (1994) J Neurol Neurosurg Psychiatry , vol.57 , pp. 977-979
    • De Michele, G.1    Filla, A.2    Cavalcanti, F.3
  • 23
    • 2942567729 scopus 로고    scopus 로고
    • ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias
    • Della Nave R., Foresti S., Tessa C., et al. ADC mapping of neurodegeneration in the brainstem and cerebellum of patients with progressive ataxias. Neuroimage 2004, 22:698-705.
    • (2004) Neuroimage , vol.22 , pp. 698-705
    • Della Nave, R.1    Foresti, S.2    Tessa, C.3
  • 24
    • 0029821176 scopus 로고    scopus 로고
    • Clinical and genetic abnormalities in patients with Friedreich's ataxia
    • Dürr A., Cossee M., Agid Y., et al. Clinical and genetic abnormalities in patients with Friedreich's ataxia. N Engl J Med 1996, 335:1169-1175.
    • (1996) N Engl J Med , vol.335 , pp. 1169-1175
    • Dürr, A.1    Cossee, M.2    Agid, Y.3
  • 25
    • 0028256473 scopus 로고
    • Oculomotor abnormalities and MRI findings in idiopathic cerebellar ataxia
    • Fetter M., Klockgether T., Schulz J.B., et al. Oculomotor abnormalities and MRI findings in idiopathic cerebellar ataxia. J Neurol 1994, 241:234-241.
    • (1994) J Neurol , vol.241 , pp. 234-241
    • Fetter, M.1    Klockgether, T.2    Schulz, J.B.3
  • 26
    • 0347031322 scopus 로고    scopus 로고
    • Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea
    • Fox S.H., Nieves A., Bergeron C., et al. Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea. Mov Disord 2003, 18:1550-1554.
    • (2003) Mov Disord , vol.18 , pp. 1550-1554
    • Fox, S.H.1    Nieves, A.2    Bergeron, C.3
  • 27
    • 0031747495 scopus 로고    scopus 로고
    • CAG repeat expansions in patients with sporadic cerebellar ataxia
    • Futamura N., Matsumura R., Fujimoto Y., et al. CAG repeat expansions in patients with sporadic cerebellar ataxia. Acta Neurol Scand 1998, 98:55-59.
    • (1998) Acta Neurol Scand , vol.98 , pp. 55-59
    • Futamura, N.1    Matsumura, R.2    Fujimoto, Y.3
  • 28
    • 0029942905 scopus 로고    scopus 로고
    • The relationship of multiple system atrophy to sporadic olivopontocerebellar atrophy and other forms of idiopathic late-onset cerebellar atrophy
    • Gilman S., Quinn N.P. The relationship of multiple system atrophy to sporadic olivopontocerebellar atrophy and other forms of idiopathic late-onset cerebellar atrophy. Neurology 1996, 46:1197-1199.
    • (1996) Neurology , vol.46 , pp. 1197-1199
    • Gilman, S.1    Quinn, N.P.2
  • 29
    • 0023855143 scopus 로고
    • Cerebellar and brainstem hypometabolism in olivopontocerebellar atrophy detected with positron emission tomography
    • Gilman S., Markel D.S., Koeppe R.A., et al. Cerebellar and brainstem hypometabolism in olivopontocerebellar atrophy detected with positron emission tomography. Ann Neurol 1988, 23:223-230.
    • (1988) Ann Neurol , vol.23 , pp. 223-230
    • Gilman, S.1    Markel, D.S.2    Koeppe, R.A.3
  • 30
    • 0028001433 scopus 로고
    • Patterns of cerebral glucose metabolism detected with positron emission tomography differ in multiple system atrophy and olivopontocerebellar atrophy
    • Gilman S., Koeppe R.A., Junck L., et al. Patterns of cerebral glucose metabolism detected with positron emission tomography differ in multiple system atrophy and olivopontocerebellar atrophy. Ann Neurol 1994, 36:166-175.
    • (1994) Ann Neurol , vol.36 , pp. 166-175
    • Gilman, S.1    Koeppe, R.A.2    Junck, L.3
  • 31
    • 0033081705 scopus 로고    scopus 로고
    • Consensus statement on the diagnosis of multiple system atrophy
    • Gilman S., Low P.A., Quinn N., et al. Consensus statement on the diagnosis of multiple system atrophy. J Neurol Sci 1999, 163:94-98.
    • (1999) J Neurol Sci , vol.163 , pp. 94-98
    • Gilman, S.1    Low, P.A.2    Quinn, N.3
  • 32
    • 0033837087 scopus 로고    scopus 로고
    • Evolution of sporadic olivopontocerebellar atrophy into multiple system atrophy
    • Gilman S., Little R., Johanns J., et al. Evolution of sporadic olivopontocerebellar atrophy into multiple system atrophy. Neurology 2000, 55:527-532.
    • (2000) Neurology , vol.55 , pp. 527-532
    • Gilman, S.1    Little, R.2    Johanns, J.3
  • 33
    • 52449086856 scopus 로고    scopus 로고
    • Second consensus statement on the diagnosis of multiple system atrophy
    • Gilman S., Wenning G.K., Low P.A., et al. Second consensus statement on the diagnosis of multiple system atrophy. Neurology 2008, 71:670-676.
    • (2008) Neurology , vol.71 , pp. 670-676
    • Gilman, S.1    Wenning, G.K.2    Low, P.A.3
  • 34
    • 0014469501 scopus 로고
    • Orthostatic hypotension and nicotine sensitivity in a case of multiple system atrophy
    • Graham J.G., Oppenheimer D.R. Orthostatic hypotension and nicotine sensitivity in a case of multiple system atrophy. J Neurol Neurosurg Psychiatry 1969, 32:28-34.
    • (1969) J Neurol Neurosurg Psychiatry , vol.32 , pp. 28-34
    • Graham, J.G.1    Oppenheimer, D.R.2
  • 35
    • 0030027634 scopus 로고    scopus 로고
    • Does cryptic gluten sensitivity play a part in neurological illness?
    • Hadjivassiliou M., Gibson A., Davies Jones G.A., et al. Does cryptic gluten sensitivity play a part in neurological illness?. Lancet 1996, 347:369-371.
    • (1996) Lancet , vol.347 , pp. 369-371
    • Hadjivassiliou, M.1    Gibson, A.2    Davies Jones, G.A.3
  • 36
    • 0037161239 scopus 로고    scopus 로고
    • The humoral response in the pathogenesis of gluten ataxia
    • Hadjivassiliou M., Boscolo S., Davies-Jones G.A.B., et al. The humoral response in the pathogenesis of gluten ataxia. Neurology 2002, 58:1221-1226.
    • (2002) Neurology , vol.58 , pp. 1221-1226
    • Hadjivassiliou, M.1    Boscolo, S.2    Davies-Jones, G.A.B.3
  • 37
    • 0345505657 scopus 로고    scopus 로고
    • Gluten ataxia in perspective: epidemiology, genetic susceptibility and clinical characteristics
    • Hadjivassiliou M., Grunewald R., Sharrack B., et al. Gluten ataxia in perspective: epidemiology, genetic susceptibility and clinical characteristics. Brain 2003, 126:685-691.
    • (2003) Brain , vol.126 , pp. 685-691
    • Hadjivassiliou, M.1    Grunewald, R.2    Sharrack, B.3
  • 38
    • 2342453253 scopus 로고    scopus 로고
    • Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation
    • Hagerman R.J., Leavitt B.R., Farzin F., et al. Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation. Am J Hum Genet 2004, 74:1051-1056.
    • (2004) Am J Hum Genet , vol.74 , pp. 1051-1056
    • Hagerman, R.J.1    Leavitt, B.R.2    Farzin, F.3
  • 39
    • 0019484086 scopus 로고
    • "Idiopathic" late onset cerebellar ataxia. A clinical and genetic study of 36 cases
    • Harding A.E. "Idiopathic" late onset cerebellar ataxia. A clinical and genetic study of 36 cases. J Neurol Sci 1981, 51:259-271.
    • (1981) J Neurol Sci , vol.51 , pp. 259-271
    • Harding, A.E.1
  • 40
    • 0025916523 scopus 로고
    • Discordance for late-onset degenerative ataxia in monozygous triplets
    • Harding A.E., Sura T., Tippett P., et al. Discordance for late-onset degenerative ataxia in monozygous triplets. J Neurol 1991, 238:242-243.
    • (1991) J Neurol , vol.238 , pp. 242-243
    • Harding, A.E.1    Sura, T.2    Tippett, P.3
  • 41
    • 0032842276 scopus 로고    scopus 로고
    • Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxia
    • Hassin B.S., Bar S.A., Gilad S., et al. Absence of mutations in ATM, the gene responsible for ataxia telangiectasia in patients with cerebellar ataxia. J Neurol 1999, 246:716-719.
    • (1999) J Neurol , vol.246 , pp. 716-719
    • Hassin, B.S.1    Bar, S.A.2    Gilad, S.3
  • 42
    • 0033769620 scopus 로고    scopus 로고
    • An open trial of amantadine and buspirone for cerebellar ataxia: a disappointment
    • Hassin-Baer S., Korczyn A.D., Giladi N. An open trial of amantadine and buspirone for cerebellar ataxia: a disappointment. J Neural Transm 2000, 107:1187-1189.
    • (2000) J Neural Transm , vol.107 , pp. 1187-1189
    • Hassin-Baer, S.1    Korczyn, A.D.2    Giladi, N.3
  • 43
    • 0035112661 scopus 로고    scopus 로고
    • Cerebellar ataxia with anti-glutamic acid decarboxylase antibodies - study of 14 patients
    • Honnorat J., Saiz A., Giometto B., et al. Cerebellar ataxia with anti-glutamic acid decarboxylase antibodies - study of 14 patients. Arch Neurol 2001, 58:225-230.
    • (2001) Arch Neurol , vol.58 , pp. 225-230
    • Honnorat, J.1    Saiz, A.2    Giometto, B.3
  • 44
    • 0032961945 scopus 로고    scopus 로고
    • High prevalence of asymptomatic coeliac disease in Norway: a study of blood donors
    • Hovdenak N., Hovlid E., Aksnes L., et al. High prevalence of asymptomatic coeliac disease in Norway: a study of blood donors. Eur J Gastroenterol Hepatol 1999, 11:185-187.
    • (1999) Eur J Gastroenterol Hepatol , vol.11 , pp. 185-187
    • Hovdenak, N.1    Hovlid, E.2    Aksnes, L.3
  • 45
    • 0032864720 scopus 로고    scopus 로고
    • Selective suppression of cerebellar GABAergic transmission by an autoantibody to glutamic acid decarboxylase
    • Ishida K., Mitoma H., Song S.Y., et al. Selective suppression of cerebellar GABAergic transmission by an autoantibody to glutamic acid decarboxylase. Ann Neurol 1999, 46:263-267.
    • (1999) Ann Neurol , vol.46 , pp. 263-267
    • Ishida, K.1    Mitoma, H.2    Song, S.Y.3
  • 46
    • 0025611496 scopus 로고
    • An autopsied case of idiopathic late cortical cerebellar atrophy - comparison with other cortical cerebellar atrophy
    • Iwabuchi K., Yagishita S. An autopsied case of idiopathic late cortical cerebellar atrophy - comparison with other cortical cerebellar atrophy. Rinsho Shinkeigaku 1990, 30:1190-1196.
    • (1990) Rinsho Shinkeigaku , vol.30 , pp. 1190-1196
    • Iwabuchi, K.1    Yagishita, S.2
  • 47
    • 0037384643 scopus 로고    scopus 로고
    • Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates
    • Jacquemont S., Hagerman R.J., Leehey M., et al. Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. Am J Hum Genet 2003, 72:869-878.
    • (2003) Am J Hum Genet , vol.72 , pp. 869-878
    • Jacquemont, S.1    Hagerman, R.J.2    Leehey, M.3
  • 48
    • 17644380702 scopus 로고
    • Eine Systemerkrankung im Kleinhirn
    • Jelgersma G. Eine Systemerkrankung im Kleinhirn. J Psychol Neurol 1919, 25:42-46.
    • (1919) J Psychol Neurol , vol.25 , pp. 42-46
    • Jelgersma, G.1
  • 49
    • 27644473572 scopus 로고    scopus 로고
    • Late-onset pure cerebellar ataxia: differentiating those with and without identifiable mutations
    • Kerber K.A., Jen J.C., Perlman S., et al. Late-onset pure cerebellar ataxia: differentiating those with and without identifiable mutations. J Neurol Sci 2005, 238:41-45.
    • (2005) J Neurol Sci , vol.238 , pp. 41-45
    • Kerber, K.A.1    Jen, J.C.2    Perlman, S.3
  • 50
    • 0025275242 scopus 로고
    • Idiopathic cerebellar ataxia of late onset: natural history and MRI morphology
    • Klockgether T., Schroth G., Diener H.C., et al. Idiopathic cerebellar ataxia of late onset: natural history and MRI morphology. J Neurol Neurosurg Psychiatry 1990, 53:297-305.
    • (1990) J Neurol Neurosurg Psychiatry , vol.53 , pp. 297-305
    • Klockgether, T.1    Schroth, G.2    Diener, H.C.3
  • 51
    • 0027250194 scopus 로고
    • Late-onset Friedreich's ataxia. Molecular genetics, clinical neurophysiology, and magnetic resonance imaging
    • Klockgether T., Chamberlain S., Wüllner U., et al. Late-onset Friedreich's ataxia. Molecular genetics, clinical neurophysiology, and magnetic resonance imaging. Arch Neurol 1993, 50:803-806.
    • (1993) Arch Neurol , vol.50 , pp. 803-806
    • Klockgether, T.1    Chamberlain, S.2    Wüllner, U.3
  • 53
    • 0344542052 scopus 로고    scopus 로고
    • Risk factors for idiopathic cerebellar ataxia of late onset
    • Klockgether T., Bürk K., Wüllner U., et al. Risk factors for idiopathic cerebellar ataxia of late onset. J Neurol Sci 1998, 160:171-174.
    • (1998) J Neurol Sci , vol.160 , pp. 171-174
    • Klockgether, T.1    Bürk, K.2    Wüllner, U.3
  • 54
    • 6844236985 scopus 로고    scopus 로고
    • The natural history of degenerative ataxia: a retrospective study in 466 patients
    • Klockgether T., Lüdtke R., Kramer B., et al. The natural history of degenerative ataxia: a retrospective study in 466 patients. Brain 1998, 121:589-600.
    • (1998) Brain , vol.121 , pp. 589-600
    • Klockgether, T.1    Lüdtke, R.2    Kramer, B.3
  • 55
    • 0028087201 scopus 로고
    • Cellular pathology of multiple system atrophy: a review
    • Lantos P.L., Papp M.I. Cellular pathology of multiple system atrophy: a review. J Neurol Neurosurg Psychiatry 1994, 57:129-133.
    • (1994) J Neurol Neurosurg Psychiatry , vol.57 , pp. 129-133
    • Lantos, P.L.1    Papp, M.I.2
  • 56
    • 0028965481 scopus 로고
    • Hereditary ataxias and paraplegias in Valle d'Aosta, Italy: a study of prevalence and disability
    • Leone M., Bottacchi E., D'Alessandro G., et al. Hereditary ataxias and paraplegias in Valle d'Aosta, Italy: a study of prevalence and disability. Acta Neurol Scand 1995, 91:183-187.
    • (1995) Acta Neurol Scand , vol.91 , pp. 183-187
    • Leone, M.1    Bottacchi, E.2    D'Alessandro, G.3
  • 57
    • 17644422502 scopus 로고
    • L'astasie-abasie cérébelleuse par atrophie vermienne chez le vieillard
    • Lhermitte J. L'astasie-abasie cérébelleuse par atrophie vermienne chez le vieillard. Rev Neurol 1922, 29:313-316.
    • (1922) Rev Neurol , vol.29 , pp. 313-316
    • Lhermitte, J.1
  • 58
    • 0030841071 scopus 로고    scopus 로고
    • What is the accuracy of the clinical diagnosis of multiple system atrophy? A clinicopathologic study
    • Litvan I., Goetz C.G., Jankovic J., et al. What is the accuracy of the clinical diagnosis of multiple system atrophy? A clinicopathologic study. Arch Neurol 1997, 54:937-944.
    • (1997) Arch Neurol , vol.54 , pp. 937-944
    • Litvan, I.1    Goetz, C.G.2    Jankovic, J.3
  • 59
    • 7144227939 scopus 로고    scopus 로고
    • Retrospective application of a set of clinical diagnostic criteria for the diagnosis of multiple system atrophy
    • Litvan I., Booth V., Wenning G.K., et al. Retrospective application of a set of clinical diagnostic criteria for the diagnosis of multiple system atrophy. J Neural Transm 1998, 105:217-227.
    • (1998) J Neural Transm , vol.105 , pp. 217-227
    • Litvan, I.1    Booth, V.2    Wenning, G.K.3
  • 60
    • 0029122451 scopus 로고
    • Use of buspirone for treatment of cerebellar ataxia - an open-label study
    • Lou J.S., Goldfarb L., McShane L., et al. Use of buspirone for treatment of cerebellar ataxia - an open-label study. Arch Neurol 1995, 52:982-988.
    • (1995) Arch Neurol , vol.52 , pp. 982-988
    • Lou, J.S.1    Goldfarb, L.2    McShane, L.3
  • 61
    • 0038281167 scopus 로고    scopus 로고
    • Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia
    • Macpherson J., Waghorn A., Hammans S., et al. Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia. Hum Genet 2003, 112:619-620.
    • (2003) Hum Genet , vol.112 , pp. 619-620
    • Macpherson, J.1    Waghorn, A.2    Hammans, S.3
  • 62
    • 0001614829 scopus 로고
    • De l'atrophie cérébelleuse tardive a prédominance corticale
    • Marie P., Foix C., Alajouanine T. De l'atrophie cérébelleuse tardive a prédominance corticale. Rev Neurol 1922, 38:849-885.
    • (1922) Rev Neurol , vol.38 , pp. 849-885
    • Marie, P.1    Foix, C.2    Alajouanine, T.3
  • 63
    • 0026645103 scopus 로고
    • Nerve conduction study, electromyography and somatosensory evoked potentials in non-Friedreich early onset cerebellar ataxia. A comparative study with Friedreich's ataxia and late onset cerebellar ataxia
    • Mondelli M., Decchi B., Parlanti S., et al. Nerve conduction study, electromyography and somatosensory evoked potentials in non-Friedreich early onset cerebellar ataxia. A comparative study with Friedreich's ataxia and late onset cerebellar ataxia. Electromyogr Clin Neurophysiol 1992, 32:207-214.
    • (1992) Electromyogr Clin Neurophysiol , vol.32 , pp. 207-214
    • Mondelli, M.1    Decchi, B.2    Parlanti, S.3
  • 64
    • 0031647246 scopus 로고    scopus 로고
    • Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families
    • Moseley M.L., Benzow K.A., Schut L.J., et al. Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families. Neurology 1998, 51:1666-1671.
    • (1998) Neurology , vol.51 , pp. 1666-1671
    • Moseley, M.L.1    Benzow, K.A.2    Schut, L.J.3
  • 65
    • 79961136497 scopus 로고
    • Degenerazione cerebellare de intossicazione enterogeny
    • Murri A. Degenerazione cerebellare de intossicazione enterogeny. Riv Crit Clin Med 1900, 1:593-608.
    • (1900) Riv Crit Clin Med , vol.1 , pp. 593-608
    • Murri, A.1
  • 66
    • 3442875652 scopus 로고    scopus 로고
    • Population based study of late onset cerebellar ataxia in south east Wales
    • Muzaimi M.B., Thomas J., Palmer-Smith S., et al. Population based study of late onset cerebellar ataxia in south east Wales. J Neurol Neurosurg Psychiatry 2004, 75:1129-1134.
    • (2004) J Neurol Neurosurg Psychiatry , vol.75 , pp. 1129-1134
    • Muzaimi, M.B.1    Thomas, J.2    Palmer-Smith, S.3
  • 67
    • 0023836562 scopus 로고
    • Spinocerebellar degeneration: qualitative and quantitative MR analysis of atrophy
    • Nabatame H., Fukuyama H., Akiguchi I., et al. Spinocerebellar degeneration: qualitative and quantitative MR analysis of atrophy. J Comput Assist Tomogr 1988, 12:298-303.
    • (1988) J Comput Assist Tomogr , vol.12 , pp. 298-303
    • Nabatame, H.1    Fukuyama, H.2    Akiguchi, I.3
  • 68
    • 2942731275 scopus 로고    scopus 로고
    • Pharmacological treatments of cerebellar ataxia
    • Ogawa M. Pharmacological treatments of cerebellar ataxia. Cerebellum 2004, 3:107-111.
    • (2004) Cerebellum , vol.3 , pp. 107-111
    • Ogawa, M.1
  • 69
    • 0028339722 scopus 로고
    • The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology
    • Papp M.I., Lantos P.L. The distribution of oligodendroglial inclusions in multiple system atrophy and its relevance to clinical symptomatology. Brain 1994, 117:235-243.
    • (1994) Brain , vol.117 , pp. 235-243
    • Papp, M.I.1    Lantos, P.L.2
  • 70
    • 0024843373 scopus 로고
    • Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome
    • Papp M.I., Kahn J.E., Lantos P.L. Glial cytoplasmic inclusions in the CNS of patients with multiple system atrophy (striatonigral degeneration, olivopontocerebellar atrophy and Shy-Drager syndrome. J Neurol Sci 1989, 94:79-100.
    • (1989) J Neurol Sci , vol.94 , pp. 79-100
    • Papp, M.I.1    Kahn, J.E.2    Lantos, P.L.3
  • 71
    • 0032992333 scopus 로고    scopus 로고
    • Idiopathic cerebellar ataxia associated with celiac disease: lack of distinctive neurological features
    • Pellecchia M.T., Scala R., Filla A., et al. Idiopathic cerebellar ataxia associated with celiac disease: lack of distinctive neurological features. J Neurol Neurosurg Psychiatry 1999, 66:32-35.
    • (1999) J Neurol Neurosurg Psychiatry , vol.66 , pp. 32-35
    • Pellecchia, M.T.1    Scala, R.2    Filla, A.3
  • 72
    • 0029004076 scopus 로고
    • Multiple systems atrophy and nonfamilial olivopontocerebellar atrophy are the same disease
    • Penney J.B. Multiple systems atrophy and nonfamilial olivopontocerebellar atrophy are the same disease. Ann Neurol 1995, 37:553-554.
    • (1995) Ann Neurol , vol.37 , pp. 553-554
    • Penney, J.B.1
  • 73
    • 0025876335 scopus 로고
    • Hereditary ataxias and paraplegias in Cantabria. Spain. An epidemiological and clinical study
    • Polo J.M., Calleja J., Combarros O., et al. Hereditary ataxias and paraplegias in Cantabria. Spain. An epidemiological and clinical study. Brain 1991, 114:855-866.
    • (1991) Brain , vol.114 , pp. 855-866
    • Polo, J.M.1    Calleja, J.2    Combarros, O.3
  • 74
    • 0032777834 scopus 로고    scopus 로고
    • Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group
    • Pujana M.A., Corral J., Gratacos M., et al. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group. Hum Genet 1999, 104:516-522.
    • (1999) Hum Genet , vol.104 , pp. 516-522
    • Pujana, M.A.1    Corral, J.2    Gratacos, M.3
  • 75
    • 0024474837 scopus 로고
    • Multiple system atrophy - the nature of the beast
    • Quinn N. Multiple system atrophy - the nature of the beast. J Neurol Neurosurg Psychiatry 1989, 78-89.
    • (1989) J Neurol Neurosurg Psychiatry , pp. 78-89
    • Quinn, N.1
  • 76
    • 0023374166 scopus 로고
    • CT findings in spinocerebellar degeneration
    • Ramos A., Quintana F., Diez C., et al. CT findings in spinocerebellar degeneration. Am J Neuroradiol 1987, 8:635-640.
    • (1987) Am J Neuroradiol , vol.8 , pp. 635-640
    • Ramos, A.1    Quintana, F.2    Diez, C.3
  • 77
    • 84857106460 scopus 로고
    • Atrophie primitive du cervelet à localisation corticale
    • Rossi I. Atrophie primitive du cervelet à localisation corticale. Nouv Icon Salp 1907, 20:66-87.
    • (1907) Nouv Icon Salp , vol.20 , pp. 66-87
    • Rossi, I.1
  • 78
    • 0034538962 scopus 로고    scopus 로고
    • Relative sparing of the parietal cortex in cerebellar ataxia documented by positron emission tomography
    • Rudolf J., Grond M., Hilker R., et al. Relative sparing of the parietal cortex in cerebellar ataxia documented by positron emission tomography. Clin Neurol Neurosurg 2000, 102:210-214.
    • (2000) Clin Neurol Neurosurg , vol.102 , pp. 210-214
    • Rudolf, J.1    Grond, M.2    Hilker, R.3
  • 79
    • 0030725680 scopus 로고    scopus 로고
    • Autoantibodies to glutamic acid decarboxylase in three patients with cerebellar ataxia, late-onset insulin-dependent diabetes mellitus, and polyendocrine autoimmunity
    • Saiz A., Arpa J., Sagasta A., et al. Autoantibodies to glutamic acid decarboxylase in three patients with cerebellar ataxia, late-onset insulin-dependent diabetes mellitus, and polyendocrine autoimmunity. Neurology 1997, 49:1026-1030.
    • (1997) Neurology , vol.49 , pp. 1026-1030
    • Saiz, A.1    Arpa, J.2    Sagasta, A.3
  • 80
    • 0033811949 scopus 로고    scopus 로고
    • Genetic background of apparently idiopathic sporadic cerebellar ataxia
    • Schöls L., Szymanski S., Peters S., et al. Genetic background of apparently idiopathic sporadic cerebellar ataxia. Hum Genet 2000, 107:132-137.
    • (2000) Hum Genet , vol.107 , pp. 132-137
    • Schöls, L.1    Szymanski, S.2    Peters, S.3
  • 81
    • 0028659025 scopus 로고
    • Multiple system atrophy: natural history, MRI morphology, and dopamine receptor imaging with 123IBZM-SPECT
    • Schulz J.B., Klockgether T., Petersen D., et al. Multiple system atrophy: natural history, MRI morphology, and dopamine receptor imaging with 123IBZM-SPECT. J Neurol Neurosurg Psychiatry 1994, 57:1047-1056.
    • (1994) J Neurol Neurosurg Psychiatry , vol.57 , pp. 1047-1056
    • Schulz, J.B.1    Klockgether, T.2    Petersen, D.3
  • 82
    • 0033043572 scopus 로고    scopus 로고
    • Regional differences in coeliac disease prevalence in Scandinavia?
    • Sjoberg K., Eriksson S. Regional differences in coeliac disease prevalence in Scandinavia?. Scand J Gastroenterol 1999, 34:41-45.
    • (1999) Scand J Gastroenterol , vol.34 , pp. 41-45
    • Sjoberg, K.1    Eriksson, S.2
  • 83
    • 0141993606 scopus 로고    scopus 로고
    • In vivo voxel-based morphometry in multiple system atrophy of the cerebellar type
    • Specht K., Minnerop M., Abele M., et al. In vivo voxel-based morphometry in multiple system atrophy of the cerebellar type. Arch Neurol 2003, 60:1431-1435.
    • (2003) Arch Neurol , vol.60 , pp. 1431-1435
    • Specht, K.1    Minnerop, M.2    Abele, M.3
  • 84
    • 2542554327 scopus 로고    scopus 로고
    • Adult-onset ataxia telangiectasia due to ATM 5762ins137 mutation homozygosity
    • Sutton I.J., Last J.I., Ritchie S.J., et al. Adult-onset ataxia telangiectasia due to ATM 5762ins137 mutation homozygosity. Ann Neurol 2004, 55:891-895.
    • (2004) Ann Neurol , vol.55 , pp. 891-895
    • Sutton, I.J.1    Last, J.I.2    Ritchie, S.J.3
  • 85
    • 3242774429 scopus 로고    scopus 로고
    • Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort
    • Tan E.K., Zhao Y., Puong K.Y., et al. Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort. Neurology 2004, 63:362-363.
    • (2004) Neurology , vol.63 , pp. 362-363
    • Tan, E.K.1    Zhao, Y.2    Puong, K.Y.3
  • 86
    • 0141937909 scopus 로고
    • Atrophie lamellaire des cellules de Purkinje
    • Thomas A. Atrophie lamellaire des cellules de Purkinje. Rev Neurol 1905, 13:917-924.
    • (1905) Rev Neurol , vol.13 , pp. 917-924
    • Thomas, A.1
  • 87
    • 0023757433 scopus 로고
    • Improvement of cerebellar ataxia with levorotatory form of 5-hydroxytryptophan. A double-blind study with quantified data processing
    • Trouillas P., Brudon F., Adeleine P. Improvement of cerebellar ataxia with levorotatory form of 5-hydroxytryptophan. A double-blind study with quantified data processing. Arch Neurol 1988, 45:1217-1222.
    • (1988) Arch Neurol , vol.45 , pp. 1217-1222
    • Trouillas, P.1    Brudon, F.2    Adeleine, P.3
  • 88
    • 0030610808 scopus 로고    scopus 로고
    • Buspirone, a 5-hydroxytryptamine1A agonist, is active in cerebellar ataxia - results of a double-blind drug placebo study in patients with cerebellar cortical atrophy
    • Trouillas P., Xie J., Adeleine P., et al. Buspirone, a 5-hydroxytryptamine1A agonist, is active in cerebellar ataxia - results of a double-blind drug placebo study in patients with cerebellar cortical atrophy. Arch Neurol 1997, 54:749-752.
    • (1997) Arch Neurol , vol.54 , pp. 749-752
    • Trouillas, P.1    Xie, J.2    Adeleine, P.3
  • 89
    • 0031713491 scopus 로고    scopus 로고
    • Glial cytoplasmic inclusions in white matter oligodendrocytes of multiple system atrophy brains contain insoluble alpha-synuclein
    • Tu P.H., Galvin J.E., Baba M., et al. Glial cytoplasmic inclusions in white matter oligodendrocytes of multiple system atrophy brains contain insoluble alpha-synuclein. Ann Neurol 1998, 44:415-422.
    • (1998) Ann Neurol , vol.44 , pp. 415-422
    • Tu, P.H.1    Galvin, J.E.2    Baba, M.3
  • 90
    • 19944434329 scopus 로고    scopus 로고
    • Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxia
    • Van Esch H., Dom R., Bex D., et al. Screening for FMR-1 premutations in 122 older Flemish males presenting with ataxia. Eur J Hum Genet 2005, 13:121-123.
    • (2005) Eur J Hum Genet , vol.13 , pp. 121-123
    • Van Esch, H.1    Dom, R.2    Bex, D.3
  • 91
    • 0035024530 scopus 로고    scopus 로고
    • Neuroimaging study with morphometric analysis of hereditary and idiopathic ataxia
    • Villanueva-Haba V., Garces-Sanchez M., Bataller L., et al. Neuroimaging study with morphometric analysis of hereditary and idiopathic ataxia. Neurologia 2001, 16:105-111.
    • (2001) Neurologia , vol.16 , pp. 105-111
    • Villanueva-Haba, V.1    Garces-Sanchez, M.2    Bataller, L.3
  • 92
    • 0036241996 scopus 로고    scopus 로고
    • Progression and prognosis in multiple system atrophy - an analysis of 230 Japanese patients
    • Watanabe H., Saito Y., Terao S., et al. Progression and prognosis in multiple system atrophy - an analysis of 230 Japanese patients. Brain 2002, 125:1070-1083.
    • (2002) Brain , vol.125 , pp. 1070-1083
    • Watanabe, H.1    Saito, Y.2    Terao, S.3
  • 93
    • 0027930620 scopus 로고
    • Clinical features and natural history of multiple system atrophy. An analysis of 100 cases
    • Wenning G.K., Ben Shlomo Y., Magalhaes M., et al. Clinical features and natural history of multiple system atrophy. An analysis of 100 cases. Brain 1994, 117:835-845.
    • (1994) Brain , vol.117 , pp. 835-845
    • Wenning, G.K.1    Ben Shlomo, Y.2    Magalhaes, M.3
  • 94
    • 0030986997 scopus 로고    scopus 로고
    • Multiple system atrophy: a review of 203 pathologically proven cases
    • Wenning G.K., Tison F., Ben Shlomo Y., et al. Multiple system atrophy: a review of 203 pathologically proven cases. Mov Disord 1997, 12:133-147.
    • (1997) Mov Disord , vol.12 , pp. 133-147
    • Wenning, G.K.1    Tison, F.2    Ben Shlomo, Y.3
  • 95
    • 0034066538 scopus 로고    scopus 로고
    • What clinical features are most useful to distinguish definite multiple system atrophy from Parkinson's disease?
    • Wenning G.K., Ben Shlomo Y., Hughes A., et al. What clinical features are most useful to distinguish definite multiple system atrophy from Parkinson's disease?. J Neurol Neurosurg Psychiatry 2000, 68:434-440.
    • (2000) J Neurol Neurosurg Psychiatry , vol.68 , pp. 434-440
    • Wenning, G.K.1    Ben Shlomo, Y.2    Hughes, A.3
  • 96
    • 0027469873 scopus 로고
    • Follow-up of neurophysiological tests and CT in late-onset cerebellar ataxia and multiple system atrophy
    • Wessel K., Huss G.P., Bruckmann H., et al. Follow-up of neurophysiological tests and CT in late-onset cerebellar ataxia and multiple system atrophy. J Neurol 1993, 240:168-176.
    • (1993) J Neurol , vol.240 , pp. 168-176
    • Wessel, K.1    Huss, G.P.2    Bruckmann, H.3
  • 97
    • 0028908390 scopus 로고
    • Double-blind crossover study with levorotatory form of hydroxytryptophan in patients with degenerative cerebellar diseases
    • Wessel K., Hermsdörfer J., Deger K., et al. Double-blind crossover study with levorotatory form of hydroxytryptophan in patients with degenerative cerebellar diseases. Arch Neurol 1995, 52:451-455.
    • (1995) Arch Neurol , vol.52 , pp. 451-455
    • Wessel, K.1    Hermsdörfer, J.2    Deger, K.3
  • 98
    • 79961141395 scopus 로고    scopus 로고
    • Cerebellar ataxia associated with gluten sensitivity: no evidence for humoral immune reactivity to cerebellar neurons
    • Wiendl H., Mehling M., Dichgans J., et al. Cerebellar ataxia associated with gluten sensitivity: no evidence for humoral immune reactivity to cerebellar neurons. Neurology 2002, 60:1397.
    • (2002) Neurology , vol.60 , pp. 1397
    • Wiendl, H.1    Mehling, M.2    Dichgans, J.3
  • 99
    • 0027405101 scopus 로고
    • Magnetic resonance imaging in hereditary and idiopathic ataxia
    • Wüllner U., Klockgether T., Petersen D., et al. Magnetic resonance imaging in hereditary and idiopathic ataxia. Neurology 1993, 43:318-325.
    • (1993) Neurology , vol.43 , pp. 318-325
    • Wüllner, U.1    Klockgether, T.2    Petersen, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.