메뉴 건너뛰기




Volumn 65, Issue 2, 2008, Pages 37-41

Posterior column atrophy in autosomal recessive hereditary spastic paraplegia: MRI findings

Author keywords

Hereditary spastic paraplegia; Magnetic resonance imaging; Posterior column degeneration

Indexed keywords


EID: 38949164777     PISSN: 15714675     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejrex.2007.11.009     Document Type: Article
Times cited : (1)

References (23)
  • 1
    • 0023634009 scopus 로고
    • Etiological heterogeneity in X-linked spastic paraplegia
    • Keppen L.D., Leppert M.F., O'Connell P., et al. Etiological heterogeneity in X-linked spastic paraplegia. Am J Hum Genet 41 (1987) 933-943
    • (1987) Am J Hum Genet , vol.41 , pp. 933-943
    • Keppen, L.D.1    Leppert, M.F.2    O'Connell, P.3
  • 2
    • 0024519130 scopus 로고
    • X-linked spastic paraplegia: evidence for homogeneity with a variable phenotype
    • Goldblatt J., Ballo R., Sachs B., et al. X-linked spastic paraplegia: evidence for homogeneity with a variable phenotype. Clin Genet 35 (1989) 116-120
    • (1989) Clin Genet , vol.35 , pp. 116-120
    • Goldblatt, J.1    Ballo, R.2    Sachs, B.3
  • 3
    • 0028037953 scopus 로고
    • The phenotype of "pure" autosomal dominant spastic paraplegia
    • Durr A., Brice A., Serdaru M., et al. The phenotype of "pure" autosomal dominant spastic paraplegia. Neurology 44 (1994) 1274-1277
    • (1994) Neurology , vol.44 , pp. 1274-1277
    • Durr, A.1    Brice, A.2    Serdaru, M.3
  • 4
    • 27644465298 scopus 로고    scopus 로고
    • Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia
    • Hedera P., Eldevik O.P., Maly P., et al. Spinal cord magnetic resonance imaging in autosomal dominant hereditary spastic paraplegia. Neuroradiology 47 (2005) 730-734
    • (2005) Neuroradiology , vol.47 , pp. 730-734
    • Hedera, P.1    Eldevik, O.P.2    Maly, P.3
  • 5
    • 0037465372 scopus 로고    scopus 로고
    • Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families
    • Lesca G., Eymard-Pierre E., Santorelli F.M., et al. Infantile ascending hereditary spastic paralysis (IAHSP): clinical features in 11 families. Neurology 60 (2003) 674-682
    • (2003) Neurology , vol.60 , pp. 674-682
    • Lesca, G.1    Eymard-Pierre, E.2    Santorelli, F.M.3
  • 6
    • 0025147590 scopus 로고
    • Selective involvement of the pyramidal tract on magnetic resonance imaging in primary lateral sclerosis
    • Marti-Fabregas J., and Pujol J. Selective involvement of the pyramidal tract on magnetic resonance imaging in primary lateral sclerosis. Neurology 40 (1990) 1799-1800
    • (1990) Neurology , vol.40 , pp. 1799-1800
    • Marti-Fabregas, J.1    Pujol, J.2
  • 7
    • 0030777273 scopus 로고    scopus 로고
    • MRI of autosomal dominant pure spastic paraplegia
    • Krabbe K., Nielsen J.E., Fallentin E., et al. MRI of autosomal dominant pure spastic paraplegia. Neuroradiology 39 (1997) 724-727
    • (1997) Neuroradiology , vol.39 , pp. 724-727
    • Krabbe, K.1    Nielsen, J.E.2    Fallentin, E.3
  • 8
    • 0029027475 scopus 로고
    • Familial spastic paraplegia with mental impairment and thin corpus callosum
    • Nakamura A., Izumi K., Umehara F., et al. Familial spastic paraplegia with mental impairment and thin corpus callosum. J Neurol Sci 131 (1995) 35-42
    • (1995) J Neurol Sci , vol.131 , pp. 35-42
    • Nakamura, A.1    Izumi, K.2    Umehara, F.3
  • 9
    • 33644821035 scopus 로고    scopus 로고
    • Autopsy case of hereditary spastic paraplegia with thin corpus callosum showing severe gliosis in the cerebral white matter
    • Kuru S., Sakai M., Konagaya M., et al. Autopsy case of hereditary spastic paraplegia with thin corpus callosum showing severe gliosis in the cerebral white matter. Neuropathology 25 (2005) 346-352
    • (2005) Neuropathology , vol.25 , pp. 346-352
    • Kuru, S.1    Sakai, M.2    Konagaya, M.3
  • 10
    • 0023476368 scopus 로고
    • Magnetic resonance imaging in spinocerebellar degenerative diseases (apropos of 8 cases)
    • Nicolau A., Diard F., Fontan D., et al. Magnetic resonance imaging in spinocerebellar degenerative diseases (apropos of 8 cases). Pediatrie 42 (1987) 359-365
    • (1987) Pediatrie , vol.42 , pp. 359-365
    • Nicolau, A.1    Diard, F.2    Fontan, D.3
  • 11
    • 0033924732 scopus 로고    scopus 로고
    • Hereditary spastic paraparesis: a review of new developments
    • McDermott C., White K., Bushby K., et al. Hereditary spastic paraparesis: a review of new developments. J Neurol Neurosurg Psychiatry 69 (2000) 150-160
    • (2000) J Neurol Neurosurg Psychiatry , vol.69 , pp. 150-160
    • McDermott, C.1    White, K.2    Bushby, K.3
  • 12
    • 0032858597 scopus 로고    scopus 로고
    • Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 families
    • Coutinho P., Barros J., Zemmouri R., et al. Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 families. Arch Neurol 56 (1999) 943-949
    • (1999) Arch Neurol , vol.56 , pp. 943-949
    • Coutinho, P.1    Barros, J.2    Zemmouri, R.3
  • 13
    • 20544476698 scopus 로고    scopus 로고
    • MR-pathologic comparison of the upper spinal cord in different motor neuron diseases
    • Sperfeld A.D., Bretschneider V., Flaith L., et al. MR-pathologic comparison of the upper spinal cord in different motor neuron diseases. Eur Neurol 53 (2005) 74-77
    • (2005) Eur Neurol , vol.53 , pp. 74-77
    • Sperfeld, A.D.1    Bretschneider, V.2    Flaith, L.3
  • 14
    • 0031971694 scopus 로고    scopus 로고
    • Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study
    • Nielsen J.E., Krabbe K., Jennum P., et al. Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study. J Neurol Neurosurg Psychiatry 64 (1998) 61-66
    • (1998) J Neurol Neurosurg Psychiatry , vol.64 , pp. 61-66
    • Nielsen, J.E.1    Krabbe, K.2    Jennum, P.3
  • 17
    • 4644268519 scopus 로고    scopus 로고
    • Troyer syndrome revisited. A clinical and radiological study of a complicated hereditary spastic paraplegia
    • Proukakis C., Cross H., Patel H., et al. Troyer syndrome revisited. A clinical and radiological study of a complicated hereditary spastic paraplegia. J Neurol 251 (2004) 1105-1110
    • (2004) J Neurol , vol.251 , pp. 1105-1110
    • Proukakis, C.1    Cross, H.2    Patel, H.3
  • 18
    • 0029001756 scopus 로고
    • X-linked pure familial spastic paraparesis. Characterization of a large kindred with magnetic resonance imaging studies
    • Cambi F., Tartaglino L., Lublin F., et al. X-linked pure familial spastic paraparesis. Characterization of a large kindred with magnetic resonance imaging studies. Arch Neurol 52 (1995) 665-669
    • (1995) Arch Neurol , vol.52 , pp. 665-669
    • Cambi, F.1    Tartaglino, L.2    Lublin, F.3
  • 19
    • 0033930099 scopus 로고    scopus 로고
    • Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15
    • Shibasaki Y., Tanaka H., Iwabuchi K., et al. Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15. Ann Neurol 48 (2000) 108-112
    • (2000) Ann Neurol , vol.48 , pp. 108-112
    • Shibasaki, Y.1    Tanaka, H.2    Iwabuchi, K.3
  • 20
    • 0033845095 scopus 로고    scopus 로고
    • Neurological and neuroradiological progression in hereditary spastic paraplegia with a thin corpus callosum
    • Okubo S., Ueda M., Kamiya T., et al. Neurological and neuroradiological progression in hereditary spastic paraplegia with a thin corpus callosum. Acta Neurol Scand 102 (2000) 196-199
    • (2000) Acta Neurol Scand , vol.102 , pp. 196-199
    • Okubo, S.1    Ueda, M.2    Kamiya, T.3
  • 21
    • 0029003729 scopus 로고
    • Hereditary spastic paraparesis with dementia, amyotrophy and peripheral neuropathy. A neuropathological study
    • Ferrer I., Olive M., Rivera R., et al. Hereditary spastic paraparesis with dementia, amyotrophy and peripheral neuropathy. A neuropathological study. Neuropathol Appl Neurobiol 21 (1995) 255-261
    • (1995) Neuropathol Appl Neurobiol , vol.21 , pp. 255-261
    • Ferrer, I.1    Olive, M.2    Rivera, R.3
  • 23
    • 0347949644 scopus 로고    scopus 로고
    • Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11)
    • Winner B., Uyanik G., Gross C., et al. Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11). Arch Neurol 61 (2004) 117-121
    • (2004) Arch Neurol , vol.61 , pp. 117-121
    • Winner, B.1    Uyanik, G.2    Gross, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.