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Volumn 103, Issue , 2012, Pages 111-125

Neuropathology of degenerative ataxias

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EID: 79961145156     PISSN: 00729752     EISSN: None     Source Type: Book Series    
DOI: 10.1016/B978-0-444-51892-7.00005-X     Document Type: Chapter
Times cited : (17)

References (48)
  • 1
    • 33750984197 scopus 로고    scopus 로고
    • Olivopontocerebellar atrophy: toward a better nosological definition
    • Berciano J., Boesch S., Perez-Ramos J., et al. Olivopontocerebellar atrophy: toward a better nosological definition. Movement Disorders 2006, 21:1607-1613.
    • (2006) Movement Disorders , vol.21 , pp. 1607-1613
    • Berciano, J.1    Boesch, S.2    Perez-Ramos, J.3
  • 2
    • 0029611008 scopus 로고
    • Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA 2 families
    • Durr A., Smadja D., Cancel G., et al. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA 2 families. Brain 1995, 118:1573-1581.
    • (1995) Brain , vol.118 , pp. 1573-1581
    • Durr, A.1    Smadja, D.2    Cancel, G.3
  • 3
    • 9244225693 scopus 로고    scopus 로고
    • Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular and neuropathological features
    • Durr A., Stevanin G., Cancel G., et al. Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular and neuropathological features. Ann Neurol 1996, 39:490-499.
    • (1996) Ann Neurol , vol.39 , pp. 490-499
    • Durr, A.1    Stevanin, G.2    Cancel, G.3
  • 4
    • 0345391031 scopus 로고    scopus 로고
    • Nuclear inclusions in spinocerebellar ataxia type 1
    • Duyckaerts C., Durr A., Cancel G., et al. Nuclear inclusions in spinocerebellar ataxia type 1. Acta Neuropathol 1999, 97:201-207.
    • (1999) Acta Neuropathol , vol.97 , pp. 201-207
    • Duyckaerts, C.1    Durr, A.2    Cancel, G.3
  • 5
    • 0033046989 scopus 로고    scopus 로고
    • Spinocerebellar ataxia 2 (SCA 2): morphometric analyses of 11 autopsies
    • Estrada R., Galarraga J., Orozco G., et al. Spinocerebellar ataxia 2 (SCA 2): morphometric analyses of 11 autopsies. Acta Neuropathol 1999, 97:306-310.
    • (1999) Acta Neuropathol , vol.97 , pp. 306-310
    • Estrada, R.1    Galarraga, J.2    Orozco, G.3
  • 6
    • 0028819081 scopus 로고
    • Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA 1) kindred: (CAG)n expansion and early premonitory signs and symptoms
    • Genis D., Matilla T., Volpini V., et al. Clinical, neuropathologic, and genetic studies of a large spinocerebellar ataxia type 1 (SCA 1) kindred: (CAG)n expansion and early premonitory signs and symptoms. Neurology 1995, 45:24-30.
    • (1995) Neurology , vol.45 , pp. 24-30
    • Genis, D.1    Matilla, T.2    Volpini, V.3
  • 7
    • 22144453212 scopus 로고    scopus 로고
    • Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA 2)
    • Gierga K., Burk K., Bauer M., et al. Involvement of the cranial nerves and their nuclei in spinocerebellar ataxia type 2 (SCA 2). Acta Neuropathol 2005, 109:617-631.
    • (2005) Acta Neuropathol , vol.109 , pp. 617-631
    • Gierga, K.1    Burk, K.2    Bauer, M.3
  • 8
    • 0030040304 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions
    • Gilman S., Sima A.A.F., Junck L., et al. Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions. Ann Neurol 1996, 39:241-255.
    • (1996) Ann Neurol , vol.39 , pp. 241-255
    • Gilman, S.1    Sima, A.A.F.2    Junck, L.3
  • 9
    • 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
  • 10
    • 0025073902 scopus 로고
    • Immunohistochemical evidence for the selective involvement of dorsal root fibers in Friedreich's ataxia
    • Goto S., Hirano A. Immunohistochemical evidence for the selective involvement of dorsal root fibers in Friedreich's ataxia. Neuropathol Appl Neurobiol 1990, 16:365-370.
    • (1990) Neuropathol Appl Neurobiol , vol.16 , pp. 365-370
    • Goto, S.1    Hirano, A.2
  • 13
    • 0031739224 scopus 로고    scopus 로고
    • Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain
    • Hayashi Y., Kakita A., Yamada M., et al. Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain. Acta Neuropathol 1998, 96:547-552.
    • (1998) Acta Neuropathol , vol.96 , pp. 547-552
    • Hayashi, Y.1    Kakita, A.2    Yamada, M.3
  • 14
    • 7144229376 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions
    • Holmberg M., Duyckaerts C., Dürr A., et al. Spinocerebellar ataxia type 7 (SCA7): a neurodegenerative disorder with neuronal intranuclear inclusions. Hum Mol Genet 1998, 7:913-918.
    • (1998) Hum Mol Genet , vol.7 , pp. 913-918
    • Holmberg, M.1    Duyckaerts, C.2    Dürr, A.3
  • 15
    • 0033811788 scopus 로고    scopus 로고
    • Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA 2 pathogenesis in mouse or human
    • Huynh D.P., Figueroa K., Hoang N., et al. Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA 2 pathogenesis in mouse or human. Nat Genet 2000, 26:44-50.
    • (2000) Nat Genet , vol.26 , pp. 44-50
    • Huynh, D.P.1    Figueroa, K.2    Hoang, N.3
  • 16
    • 0035954366 scopus 로고    scopus 로고
    • Cytoplasmic and nuclear polyglutamine aggregates in SCA 6 Purkinje cells
    • Ishikawa K., Owada K., Ishida K., et al. Cytoplasmic and nuclear polyglutamine aggregates in SCA 6 Purkinje cells. Neurology 2001, 56:1753-1756.
    • (2001) Neurology , vol.56 , pp. 1753-1756
    • Ishikawa, K.1    Owada, K.2    Ishida, K.3
  • 17
    • 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
  • 18
    • 0002654217 scopus 로고    scopus 로고
    • Neuropathology of inherited ataxias
    • Cambridge University Press, Cambridge, M.-U. Manto, M. Pandolfo (Eds.)
    • Koeppen A.H. Neuropathology of inherited ataxias. The Cerebellum and its Disorders 2002, Cambridge University Press, Cambridge. M.-U. Manto, M. Pandolfo (Eds.).
    • (2002) The Cerebellum and its Disorders
    • Koeppen, A.H.1
  • 19
    • 34547119562 scopus 로고    scopus 로고
    • The dentate nucleus in Friedreich's ataxia: the role of iron-responsive proteins
    • Koeppen A.H., Michael S.C., Knutson M.D., et al. The dentate nucleus in Friedreich's ataxia: the role of iron-responsive proteins. Acta Neuropathol 2007, 114:163-173.
    • (2007) Acta Neuropathol , vol.114 , pp. 163-173
    • Koeppen, A.H.1    Michael, S.C.2    Knutson, M.D.3
  • 20
    • 71449093193 scopus 로고    scopus 로고
    • The dorsal root ganglion in Friedreich's ataxia
    • Koeppen A.H., Morral J.A., Davis A.N., et al. The dorsal root ganglion in Friedreich's ataxia. Acta Neuropathol 2009, 118:763-776.
    • (2009) Acta Neuropathol , vol.118 , pp. 763-776
    • Koeppen, A.H.1    Morral, J.A.2    Davis, A.N.3
  • 21
    • 0014787658 scopus 로고
    • The olivopontocerebellar atrophies: a review
    • Konigsmark B.W., Weiner L.P. The olivopontocerebellar atrophies: a review. Medicine (Baltimore) 1970, 49:227-241.
    • (1970) Medicine (Baltimore) , vol.49 , pp. 227-241
    • Konigsmark, B.W.1    Weiner, L.P.2
  • 22
    • 0032840052 scopus 로고    scopus 로고
    • Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study
    • Koyano S., Uchihara T., Fujigasaki H., et al. Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study. Neurosci Lett 1999, 273:117-120.
    • (1999) Neurosci Lett , vol.273 , pp. 117-120
    • Koyano, S.1    Uchihara, T.2    Fujigasaki, H.3
  • 23
    • 0033964603 scopus 로고    scopus 로고
    • Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophy and Machado-Joseph disease
    • Kumada S., Hayashi M., Mizuguchi M., et al. Cerebellar degeneration in hereditary dentatorubral-pallidoluysian atrophy and Machado-Joseph disease. Acta Neuropathol 2000, 99:48-54.
    • (2000) Acta Neuropathol , vol.99 , pp. 48-54
    • Kumada, S.1    Hayashi, M.2    Mizuguchi, M.3
  • 24
    • 0036050825 scopus 로고    scopus 로고
    • Peripheral neuropathy of Machado-Joseph disease in Taiwan: a morphometric and genetic study
    • Lin K.P., Soong B.W. Peripheral neuropathy of Machado-Joseph disease in Taiwan: a morphometric and genetic study. Eur Neurol 2002, 48:210-217.
    • (2002) Eur Neurol , vol.48 , pp. 210-217
    • Lin, K.P.1    Soong, B.W.2
  • 25
    • 0028067442 scopus 로고
    • On an autosomal dominant form of retino-cerebellar degeneration: an autopsy study of 5 patients in one family
    • Martin J.-J., Van Regemorter N., Kros L., et al. On an autosomal dominant form of retino-cerebellar degeneration: an autopsy study of 5 patients in one family. Acta Neuropathol 1994, 88:277-286.
    • (1994) Acta Neuropathol , vol.88 , pp. 277-286
    • Martin, J.-J.1    Van Regemorter, N.2    Kros, L.3
  • 26
    • 0032751030 scopus 로고    scopus 로고
    • Dentatorubropallidoluysian atrophy in a Spanish family: a clinical, radiological, pathological and genetic study
    • Munoz E., Mila M., Sanchez A., et al. Dentatorubropallidoluysian atrophy in a Spanish family: a clinical, radiological, pathological and genetic study. J Neurol Neurosurg Psychiatry 1999, 67:811-814.
    • (1999) J Neurol Neurosurg Psychiatry , vol.67 , pp. 811-814
    • Munoz, E.1    Mila, M.2    Sanchez, A.3
  • 27
    • 0034950232 scopus 로고    scopus 로고
    • Small fibers involvement in Friedreich's ataxia
    • Nolano M., Provitera V., Crisci C., et al. Small fibers involvement in Friedreich's ataxia. Ann Neurol 2001, 50:17-25.
    • (2001) Ann Neurol , vol.50 , pp. 17-25
    • Nolano, M.1    Provitera, V.2    Crisci, C.3
  • 28
    • 0018392248 scopus 로고
    • Brain lesions in Friedreich's ataxia
    • Oppenheimer D.R. Brain lesions in Friedreich's ataxia. Can J Neurol Sci 1979, 6:173-176.
    • (1979) Can J Neurol Sci , vol.6 , pp. 173-176
    • Oppenheimer, D.R.1
  • 29
    • 0024422743 scopus 로고
    • Dominantly inherited olivopontocerebellar atrophy from Eastern Cuba. Clinical, neuropathological, and biochemical findings
    • Orozco G., Estrada R., Perry T., 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, G.1    Estrada, R.2    Perry, T.3
  • 30
    • 0033772916 scopus 로고    scopus 로고
    • Hereditary dentatorubral-pallidoluysian atrophy
    • Oyanagi S. Hereditary dentatorubral-pallidoluysian atrophy. Neuropathology 2000, 20:S42-S46.
    • (2000) Neuropathology , vol.20
    • Oyanagi, S.1
  • 31
    • 0036185711 scopus 로고    scopus 로고
    • Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases
    • Pang J.T., Giunti P., Chamberlain S., et al. Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases. Brain 2002, 125:656-663.
    • (2002) Brain , vol.125 , pp. 656-663
    • Pang, J.T.1    Giunti, P.2    Chamberlain, S.3
  • 32
    • 0030847065 scopus 로고    scopus 로고
    • The neuropathology of CAG repeat diseases: review and update of genetic and molecular features
    • Robitaille Y., Lopes-Cendes I., Becher M., et al. The neuropathology of CAG repeat diseases: review and update of genetic and molecular features. Brain Pathol 1997, 7:901-926.
    • (1997) Brain Pathol , vol.7 , pp. 901-926
    • Robitaille, Y.1    Lopes-Cendes, I.2    Becher, M.3
  • 33
    • 0037327486 scopus 로고    scopus 로고
    • Guidelines for the pathoanatomical examination of the lower brain stem in ingestive and swallowing disorders and its application to a dysphagic spinocerebellar ataxia type 3 patient
    • Rüb U., Brunt E.R., Del Turco D., et al. Guidelines for the pathoanatomical examination of the lower brain stem in ingestive and swallowing disorders and its application to a dysphagic spinocerebellar ataxia type 3 patient. Neuropathol Appl Neurobiol 2003, 29:1-13.
    • (2003) Neuropathol Appl Neurobiol , vol.29 , pp. 1-13
    • Rüb, U.1    Brunt, E.R.2    Del Turco, D.3
  • 34
    • 4344644922 scopus 로고    scopus 로고
    • Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significance
    • Rüb U.E., Brunt E.R., de Vos R.A.I. Degeneration of the central vestibular system in spinocerebellar ataxia type 3 (SCA3) patients and its possible clinical significance. Neuropathol Appl Neurobiol 2004, 30:402-414.
    • (2004) Neuropathol Appl Neurobiol , vol.30 , pp. 402-414
    • Rüb, U.E.1    Brunt, E.R.2    de Vos, R.A.I.3
  • 35
    • 27144467422 scopus 로고    scopus 로고
    • Spinocerebellar ataxias types 2 and 3:degeneration of the precerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum
    • Rüb U., Gierga K., Brunt E.R., et al. Spinocerebellar ataxias types 2 and 3:degeneration of the precerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum. J Neural Transm 2005, 112:1523-1545.
    • (2005) J Neural Transm , vol.112 , pp. 1523-1545
    • Rüb, U.1    Gierga, K.2    Brunt, E.R.3
  • 36
    • 27944503345 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeat
    • Rüb U., Brunt E.R., Gierga K., et al. Spinocerebellar ataxia type 7 (SCA7): first report of a systematic neuropathological study of the brain of a patient with a very short expanded CAG-repeat. Brain Pathol 2005, 15:287-295.
    • (2005) Brain Pathol , vol.15 , pp. 287-295
    • Rüb, U.1    Brunt, E.R.2    Gierga, K.3
  • 37
    • 33746859957 scopus 로고    scopus 로고
    • Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7
    • Rüb U., Brunt E.R., Petrasch-Parwez E., et al. Degeneration of ingestion-related brainstem nuclei in spinocerebellar ataxia type 2, 3, 6 and 7. Neuropathol Appl Neurobiol 2006, 32:635-649.
    • (2006) Neuropathol Appl Neurobiol , vol.32 , pp. 635-649
    • Rüb, U.1    Brunt, E.R.2    Petrasch-Parwez, E.3
  • 38
    • 33846635034 scopus 로고    scopus 로고
    • Consistent affection of the central somatosensory system in spinocerebellar ataxia type 2 and type 3 and its significance for clinical symptoms and rehabilitative therapy
    • Rüb U., Seidela K., Özerden I., et al. Consistent affection of the central somatosensory system in spinocerebellar ataxia type 2 and type 3 and its significance for clinical symptoms and rehabilitative therapy. Brain Res Rev 2007, 53:235-249.
    • (2007) Brain Res Rev , vol.53 , pp. 235-249
    • Rüb, U.1    Seidela, K.2    Özerden, I.3
  • 39
    • 42649118505 scopus 로고    scopus 로고
    • New insights into the pathoanatomy of spinocerebellar ataxia type 3 (Machado-Joseph disease)
    • Rüb U., Brunt E.R., Deller T. New insights into the pathoanatomy of spinocerebellar ataxia type 3 (Machado-Joseph disease). Curr Opin Neurol 2008, 21:111-116.
    • (2008) Curr Opin Neurol , vol.21 , pp. 111-116
    • Rüb, U.1    Brunt, E.R.2    Deller, T.3
  • 40
    • 0031883338 scopus 로고    scopus 로고
    • Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA 6)
    • Sasaki H., Kojima H., Yabe I., et al. Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA 6). Acta Neuropathol 1998, 95:199-204.
    • (1998) Acta Neuropathol , vol.95 , pp. 199-204
    • Sasaki, H.1    Kojima, H.2    Yabe, I.3
  • 41
    • 0027356605 scopus 로고
    • Epidemiology and clinical aspects of Machado-Joseph disease
    • Raven Press, New York
    • Sequeiros J., Coutinho P. Epidemiology and clinical aspects of Machado-Joseph disease. Advances in Neurology 1993, Vol. 61. Raven Press, New York.
    • (1993) Advances in Neurology , vol.61
    • Sequeiros, J.1    Coutinho, P.2
  • 42
    • 0029882009 scopus 로고    scopus 로고
    • Dominant cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia 1, Machado-Joseph disease or dentato-rubro-pallido-luysian atrophy locus
    • Subramony S.H., Manyam B.N., Currier R.D., et al. Dominant cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia 1, Machado-Joseph disease or dentato-rubro-pallido-luysian atrophy locus. Mov Disord 1996, 11:174-180.
    • (1996) Mov Disord , vol.11 , pp. 174-180
    • Subramony, S.H.1    Manyam, B.N.2    Currier, R.D.3
  • 43
    • 0031934596 scopus 로고    scopus 로고
    • Autosomal dominant cerebellar ataxia (SCA 6): clinical, genetic and neuropathological study in a family
    • Takahashi H., Ikeuchi T., Houma Y., et al. Autosomal dominant cerebellar ataxia (SCA 6): clinical, genetic and neuropathological study in a family. Acta Neuropathol 1998, 95:333-337.
    • (1998) Acta Neuropathol , vol.95 , pp. 333-337
    • Takahashi, H.1    Ikeuchi, T.2    Houma, Y.3
  • 44
    • 0028141691 scopus 로고
    • A clinical and pathologic study of a large Japanese family with Machado-Joseph disease tightly linked to the DNA markers on chromosome 14q
    • Takiyama Y., Oynagi S., Kawashima S., et al. A clinical and pathologic study of a large Japanese family with Machado-Joseph disease tightly linked to the DNA markers on chromosome 14q. Neurology 1994, 44:1302-1308.
    • (1994) Neurology , vol.44 , pp. 1302-1308
    • Takiyama, Y.1    Oynagi, S.2    Kawashima, S.3
  • 45
    • 0030056030 scopus 로고    scopus 로고
    • Decreased parvalbumin immunoreactivity in surviving Purkinje cells of patients with spinocerebellar ataxia-1
    • Vig P.J.S., Fratkin J.D., Desaiah D., et al. Decreased parvalbumin immunoreactivity in surviving Purkinje cells of patients with spinocerebellar ataxia-1. Neurology 1996, 47:249-253.
    • (1996) Neurology , vol.47 , pp. 249-253
    • Vig, P.J.S.1    Fratkin, J.D.2    Desaiah, D.3
  • 46
    • 0039803708 scopus 로고
    • Evidence of peripheral neuropathy in a variety of heredo-familial olivo-ponto-cerebellar degenerations frequently seen in India
    • University of Tokyo Press, Tokyo, I. Sobue (Ed.)
    • Wadia N., Irani P., Mehta L., et al. Evidence of peripheral neuropathy in a variety of heredo-familial olivo-ponto-cerebellar degenerations frequently seen in India. Spinocerebellar Degenerations 1980, University of Tokyo Press, Tokyo. I. Sobue (Ed.).
    • (1980) Spinocerebellar Degenerations
    • Wadia, N.1    Irani, P.2    Mehta, L.3
  • 47
    • 33746117919 scopus 로고    scopus 로고
    • Polyglutamine disease: recent advances in the neuropathology of dentatorubral-pallidoluysian atrophy
    • Yamada M., Shimohata M., Sato T., et al. Polyglutamine disease: recent advances in the neuropathology of dentatorubral-pallidoluysian atrophy. Neuropathology 2006, 26:346-351.
    • (2006) Neuropathology , vol.26 , pp. 346-351
    • Yamada, M.1    Shimohata, M.2    Sato, T.3
  • 48
    • 36949022900 scopus 로고    scopus 로고
    • CAG repeat disorder models and human neuropathology: similarities and differences
    • Yamada M., Sato T., Tsuji S., et al. CAG repeat disorder models and human neuropathology: similarities and differences. Acta Neuropathol 2008, 115:71-86.
    • (2008) Acta Neuropathol , vol.115 , pp. 71-86
    • Yamada, M.1    Sato, T.2    Tsuji, S.3


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