References
Akiyama K, Tsutsumi Y, Onoda N, Ogawa K, Saito H, Yoshii H, Shinohara Y (1987) An autopsy case of amyotrophic lateral sclerosis associated with sensory disturbance and eye movement disorder: pathological consideration on development of multisystem degeneration of the nervous system in a patient with prolonged survival (in Japanese with English abstract). Byori To Rinsho 5: 921–028
Hayashi H, Kato S (1989) Total manifestations of amyotrophic lateral sclerosis: ALS in the totally locked-in state. J Neurol Sci 93: 19–35
Hayashi H, Kato S, Kawada A (1991) Amyotrophic lateral sclerosis patients living beyond respiratory failure. J Neurol Sci 105:73–78
Kato S, Hayashi H, Yagishita A (1993) Involvement of the frontotemporal lobe and limbic system in amyotrophic lateral sclerosis as assessed by serial computed tomography and magnetic resonance imaging. J Neurol Sci 116: 52–58
Komachi H, Okeda R, Ishii N, Yanagisawa K, Yamada M, Miyatake T (1994) Motor neuron disease with dementia and ophthalmoplegia: a clinical and pathological study. J Neurol 241: 592–596
Kuroda Y, Sugihara H (1991) Autopsy report of HTLV-I-associated myelopathy presenting with ALS-like manifestations. J Neurol Sci 106: 199–205
Marti-Fabregas J, Roig C (1993) Oculomotor abnormalities in motor neuron disease. J Neurol 240:475–478
Mizutani T, Aki N, Shiozawa R, Unakami M, Nozawa T, Yajima K, Tanabe H, Hara M (1990) Development of ophthalmoplegia in amyotrophic lateral sclerosis during long-term use of respirators. J Neurol Sci 99:311–319
Mizutani T, Sakamaki S, Tsuchiya N, Kamei S, Kohzu H, Horiuchi R, Ida M, Shiozawa R, Takasu T (1992) Amytrophic lateral sclerosis with ophthalmoplegia and multisystem degeneration in patients on long-term use of respirators. Acta Neuropathol 84:372–377
Okamoto K, Hirai S, Amari M, Iizuka T, Watanabe M, Murakami N, Takatama M (1993) Oculomotor nuclear pathology in Amyotrophic lateral sclerosis. Acta Neuropathol (Berl) 85:458–462
Onufrowicz B (1900) On the arrangement and function of the cell groups of sacral region of the spinal cord in man. Arch Neurol Psychopathol 3:387–412
Rowland LP (1991) Ten central themes in a decade of ALS Research. Adv Neurol 56:3–23
Takasu T, Mizutani T, Sakamaki S, Tsuchiya N, Kamei S, Kohzu H (1985) An autopsy case of sporadic amyotrophic lateral sclerosis with degenerations of the spinocerebellar tracts and the posterior column (in Japanese with English abstract). Annual Report of the Neurodegenerative Disease Research Committee of Japan, Tokyo, pp 94–100
Toyokura A (1979) Negative features in ALS. In: Japanese Medical Research Foundation (ed) Amyotrophic lateral sclerosis. University of Tokyo Press, Tokyo, pp 53–58
Yoshida M, Murakami N, Hashizume Y, Itoh E, Takahashi A (1992) A clinicopathological study of two respirator-aided long-survial cases of amyotrophic lateral sclerosis (in Japanese with English abstract). Clin Neurol (Tokyo) 32:259–265
Younger DS, Rowland LP, Latov N, Sherman W, Pesce M, Lange DJ, Trojaborg W, Miller JR, Loveralse RE, Hays AP, Kim TS (1990) Motor neuron disease and amyotrophic lateral sclerosis: relation of high CSF protein content to paraproteinemia and clinical syndromes. Neurology 40:595–599
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Yuki, N., Yamada, M., Yuasa, T. et al. Atypical motor neuron disease with severe ophthalmoloplegia: a report of two cases. J Neurol 242, 541–546 (1995). https://doi.org/10.1007/BF00867427
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DOI: https://doi.org/10.1007/BF00867427