References
- Lowe JS, Leigh N. Motor neuron disease. Graham DI, Lantos P. Greenfields's Neuropathology, 7th New York: Oxford University Press; 2002. 372–83.
- Arai T, Hasegawa M, Akiyama H, Ikeda K, Nonaka T, Mori H, . TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun. 2006;351:602–11.
- Neumann M, Sampathu DM, Kwong LK, Truax AC, Micsenyi MC, Chou TT, . Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science. 2006;314:130–3.
- Kushner PD, Stephenson DT, Wright S. Reactive astrogliosis is widespread in the subcortical white matter of amyotrophic lateral sclerosis brain. J Neuropathol Exp Neurol. 1991;50:263–77.
- Rafalowska J, Dziewulska D. White matter injury in amyotrophic lateral sclerosis (ALS). Folia Neuropathol. 1996; 34:87–91.
- Senda J, Ito M, Watanabe H, Atsuta N, Kawai Y, Katsuno M, . Correlation between pyramidal tract degeneration and widespread white matter involvement in amyotrophic lateral sclerosis: a study with tractography and diffusion-tensor imaging. Amyotroph Lateral Scler. 2009;10:1–8.
- Braak H, Braak E. Neuropathological stageing of Alzheimer's-related changes. Acta Neuropathol. 1991;82:239–59.
- Fischer LR, Culver DG, Tennant P, Davis AA, Wang M, Castellano-Sanchez A, . Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man. Exp Neurol. 2004;185:232–40.
- Hiji M, Takahashi T, Fukuba H, Yamashita H, Kohriyama T, Matsumoto M. White matter lesions in the brain with frontotemporal lobar degeneration with motor neuron disease: TDP-43-immunopositive inclusions colocalize with p62, but not ubiquitin. Acta Neuropathol. 2008;116:183–91.
- Arai T, Mackenzie IR, Hasegawa M, Nonoka T, Niizato K, Tsuchiya K, . Phosphorylated TDP-43 in Alzheimer's disease and dementia with Lewy bodies. Acta Neuropathol. 2009;117:125–36.
- Amador-Ortiz C, Ahmed Z, Zehr C, Dickson DW. Hippocampal sclerosis dementia differs from hippocampal sclerosis in frontal lobe degeneration. Acta Neuropathol. 2007;113: 245–52.
- Davidson Y, Amin H, Kelley T, Shi J, Tian J, Kumaran R, . TDP-43 in ubiquitinated inclusions in the inferior olives in frontotemporal lobar degeneration and in other neurodegenerative diseases: a degenerative process distinct from normal ageing. Acta Neuropathol. 2009;118:359–69.
- Fujishiro H, Uchikado H, Arai T, Hasegawa M, Akiyama H, Yokota O, . Accumulation of phosphorylated TDP-43 in brains of patients with argyrophilic grain disease. Acta Neuropathol. 2009;117:151–8.
- Leveille A, Kiernan J, Goodwin JA, Antel J. Eye movements in amyotrophic lateral sclerosis. Arch Neurol. 1982;39:684–6.
- Toyokura Y. Amyotrophic lateral sclerosis. A clinical and pathological study on the ‘negative features’ of the disease (author's transl)]. Nihon Naika Gakkai zasshi. 1977;66: 751–62.
- Esteban A, de Andres C, Gimenez-Roldan S. Abnormalities of Bell's phenomenon in amyotrophic lateral sclerosis: a clinical and electrophysiological evaluation. J Neurol Neurosurg Psychiatry. 1978;41:690–8.
- Harvey DG, Torack RM, Rosenbaum HE. Amyotrophic lateral sclerosis with ophthalmoplegia. A clinicopathologic study. Arch Neurol. 1979;36:615–7.
- Yoshii F. Oculomotor abnormalities in amyotrophic lateral sclerosis. Rinsho Shinkeigaku. 1988;28:983–91.
- Eisen A. Amyotrophic lateral sclerosis: a 40-year personal perspective. J Clin Neurosci. 2009;16:505–12.
- Hayashi H, Kato S. Total manifestations of amyotrophic lateral sclerosis. ALS in the totally locked-in state. J Neurol Sci. 1989;93:19–35.
- Mizutani T, Sakamaki S, Tsuchiya N, Kamei S, Kohzu H, Horiuchi R, . Amyotrophic lateral sclerosis with ophthalmoplegia and multisystem degeneration in patients on long-term use of respirators. Acta Neuropathol. 1992;84:372–7.
- Kobayashi M, Ikeda K, Kinoshita M, Iwasaki Y. Amyotrophic lateral sclerosis with supranuclear ophthalmoplegia and rigidity. Neurol Res. 1999;21:661–4.
- Komachi H, Okeda R, Ishii N, Yanagisawa K, Yamada M, Miyatake T. Motor neuron disease with dementia and ophthalmoplegia: a clinical and pathological study. J Neurol. 1994;241:592–6.
- Takahashi T, Yagishita S, Amano N, Yamaoka K, Kamei T. Amyotrophic lateral sclerosis with numerous axonal spheroids in the corticospinal tract and massive degeneration of the cortex. Acta Neuropathol. 1997;94:294–9.
- Alajouanine T, Thurel R. La Diplégie faciale cérébrale. Forme corticale de la paralysie pseudobulbaire. (Contribution à l’étude de la dissociation des activités volontaires et réflexes). Rev Neurol. 1933;2:441–58.
- Bruyn GW, Gathier JC. The operculum syndrome. Vinken PJ, Bruyn GW. Handbook of Clinical Neurology. Amsterdam: North-Holland Publishing Company; 1969. 776–83.
- Leichnetz GR, Spencer RF, Smith DJ. Cortical projections to nuclei adjacent to the oculomotor complex in the medial dien-mesencephalic tegmentum in the monkey. J Comp Neurol. 1984;228:359–87.
- Oba H, Araki T, Ohtomo K, Monzawa S, Uchiyama G, Koizumi K, . Amyotrophic lateral sclerosis: T2 shortening in motor cortex at MR imaging. Radiology. 1993;189:843–6.
- Hecht MJ, Fellner F, Fellner C, Hilz MJ, Neundorfer B, Heuss D. Hyperintense and hypointense MRI signals of the precentral gyrus and corticospinal tract in ALS: a follow-up examination including FLAIR images. J Neurol Sci. 2002; 199:59–65.
- Rosen AD. Amyotrophic lateral sclerosis: clinical features and prognosis. Arch Neurol. 1978;35:638–42.
- Alcaz S, Jarebinski M, Pekmezovic T, Stevic-Marinkovic Z, Pavlovic S, Apostolski S. Epidemiological and clinical characteristics of ALS in Belgrade, Yugoslavia. Acta Neurol Scand. 1996;94:264–8.
- Nalini A, Thennarasu K, Gourie-Devi M, Shenoy S, Kulshreshtha D. Clinical characteristics and survival pattern of 1153 patients with amyotrophic lateral sclerosis: experience over 30 years from India. J Neurol Sci. 2008;272:60–70.