Parkinsonism in motor neuron disease: case report and literature review
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James Lowe | Paul G. Ince | Pamela J. Shaw | J. Lowe | P. Ince | P. Shaw | T. Williams | D. Bates | David Bates | Timothy L. Williams | P. Shaw
[1] J. Lowe,et al. Ubiquitin carboxyl‐terminal hydrolase (PGP 9.5) is selectively present in ubiquitinated inclusion bodies characteristic of human neurodegenerative diseases , 1990, The Journal of pathology.
[2] R. Mayer,et al. Ubiquitin in Neurodegenerative Diseases , 1993, Brain pathology.
[3] L. Yealland. Progressive Muscular Atrophy Associated with Paralysis Agitans , 1938, Proceedings of the Royal Society of Medicine.
[4] K. Hasegawa,et al. Extrapyramidal system involvement in motor neuron disease , 1992, Journal of the Neurological Sciences.
[5] J. Lowe. New pathological findings in amyotrophic lateral sclerosis , 1994, Journal of the Neurological Sciences.
[6] M. Šercl,et al. ON THE FAMILIAL INCIDENCE OF AMYOTROPHIC LATERAL SCLEROSIS , 1963, Acta neurologica Scandinavica.
[7] P. Ince,et al. Quantitative neuropathological study of Alzheimer-type pathology in the hippocampus: Comparison of senile dementia of Alzheimer type, senile dementia of Lewy body type, Parkinson's disease and non-demented elderly control patients , 1991, Journal of the Neurological Sciences.
[8] J. Greenfield,et al. THE BRAIN-STEM LESIONS IN PARKINSONISM , 1953, Journal of neurology, neurosurgery, and psychiatry.
[9] M. Swash,et al. Ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis. Morphology, distribution, and specificity. , 1991, Brain : a journal of neurology.
[10] P. Mehraein,et al. Zur Klinik und pathologischen Anatomie des Muskelatrophie-Parkinsonismus-Demenz-Syndroms , 1974, Archiv für Psychiatrie und Nervenkrankheiten.
[11] M. Serdaru,et al. Pallido-luyso-nigral atrophy and amyotrophic lateral sclerosis. , 1981, Acta neuropathologica. Supplementum.
[12] K. Takahashi,et al. Familial amyotrophic lateral sclerosis: Features of multisystem degeneration , 2004, Acta Neuropathologica.
[13] A. Eisen,et al. Amyotrophic Lateral Sclerosis, Parkinson’s Disease and Alzheimer’s Disease: Phylogenetic Disorders of the Human Neocortex Sharing Many Characteristics , 1992, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
[14] M. Bergmann,et al. Motor neuron disease with pallido-luysio-nigral atrophy , 2004, Acta Neuropathologica.
[15] H. Osaka,et al. Two cases of glutaric aciduria type 1: Clinical and neuropathological findings , 1994, Journal of the Neurological Sciences.
[16] P. Blumbergs,et al. Substantia nigra degeneration in motor neurone disease: a quantitative study. , 1992, Australian and New Zealand journal of medicine.
[17] S. Kish,et al. Dementia, parkinsonism, and motor neuron disease: Neurochemical and neuropathological correlates , 1988, Annals of neurology.
[18] M. Alter,et al. Hereditary Amyotrophic Lateral Sclerosis , 1976 .
[19] B. Henderson,et al. A case-control study of amyotrophic lateral sclerosis. , 1986, American journal of epidemiology.
[20] R. Mayer,et al. αB crystallin expression in nonlenticular tissues and selective presence in ubiquitinated inclusion bodies in human disease , 1992, The Journal of pathology.
[21] M. Bergmann. Motor neuron disease/amyotrophic lateral sclerosis--lessons from ubiquitin. , 1993, Pathology, research and practice.
[22] A. Biemond,et al. Tabes of Friedreich with degeneration of the substantia nigra, a special type of hereditary parkinsonism. , 1955, Confinia neurologica.
[23] Shuichi Kato,et al. Total manifestations of amyotrophic lateral sclerosis ALS in the totally locked-in state , 1989, Journal of the Neurological Sciences.
[24] R. Mayer,et al. A filamentous inclusion body within anterior horn neurones in motor neurone disease defined by immunocytochemical localisation of ubiquitin , 1988, Neuroscience Letters.
[25] H. Herzog,et al. Frontal lobe function in amyotrophic lateral sclerosis: a neuropsychologic and positron emission tomography study , 1992, Acta neurologica Scandinavica.
[26] C. Yiannikas,et al. Multimodality evoked potentials in motor neuron disease. , 1990, Archives of neurology.
[27] Hitoshi Takahashi,et al. Widespread multiple system degeneration in a patient with familial amyotrophic lateral sclerosis , 1993, Journal of the Neurological Sciences.
[28] R. Escourolle,et al. Évolution simultanée d'une sclérose latérale amyotrophique, d'un syndrome parkinsonnien et d'une démence progressive: A propos de deux observations anatomo-cliniques Essai d'interprétation , 1968 .
[29] P. Lantos,et al. Cortical Lewy body dementia: clinical features and classification. , 1989, Journal of neurology, neurosurgery, and psychiatry.
[30] D. Irving,et al. Lewy body prevalence in the aging brain: relationship to neuropsychiatric disorders, Alzheimer-type pathology and catecholaminergic nuclei , 1990, Journal of the Neurological Sciences.
[31] E. Hirsch,et al. Motor neuron disease, parkinsonism and dementia , 2004, Acta Neuropathologica.
[32] C. Vital,et al. [Familial syndrome of amyotrophic lateral sclerosis with dementia]. , 1971, L'Encephale.
[33] L. V. Bogaert,et al. XXII. Scléroses latérales amyotrophiques typiques et paralysies agitantes héréditaires, dans une même famille, avec une forme de passage possible entre les deux affections , 1954 .
[34] S. Fahn,et al. Sporadic and familial parkinsonism and motor neuron disease , 1973, Neurology.
[35] G. Serratrice,et al. Chronic spinal muscular atrophy and pallidonigral degeneration , 1983, Neurology.
[36] W. Emser,et al. Familial occurrence of amyotrophic lateral sclerosis, parkinsonism, and dementia , 1984, Annals of neurology.
[37] B. Crain,et al. Degeneration of the substantia nigra in familial amyotrophic lateral sclerosis. , 1991, Clinical neuropathology.
[38] Y. Tsutsumi,et al. Sporadic amyotrophic lateral sclerosis with extensive neurological involvement , 2004, Acta Neuropathologica.
[39] J. Warter,et al. Familial motor neuron disease with Lewy body-like inclusions in the substantia nigra, the subthalamic nucleus, and the globus pallidus , 1992, Journal of the Neurological Sciences.
[40] A. Hirano,et al. Alzheimer's neurofibrillary changes. A topographic study. , 1962, Archives of neurology.
[41] A. Stracciari,et al. Cognitive impairment in motor neuron disease , 1985, Acta neurologica Scandinavica.
[42] T. Takasu,et al. Amyotrophic lateral sclerosis with ophthalmoplegia and multisystem degeneration in patients on long-term use of respirators , 2004, Acta Neuropathologica.
[43] M. Oda,et al. Diminution of dopaminergic neurons in the substantia nigra of sporadic amyotrophic lateral sclerosis , 1993, Neuropathology and applied neurobiology.
[44] J. Kepes,et al. Late onset ataxia, rigidity, and peripheral neuropathy. A familial syndrome with variable therapeutic response to levodopa. , 1972, Archives of neurology.
[45] P N Leigh,et al. The relationship between abnormalities of cognitive function and cerebral activation in amyotrophic lateral sclerosis. A neuropsychological and positron emission tomography study. , 1993, Brain : a journal of neurology.
[46] B. Snow,et al. Evidence for a dopaminergic deficit in sporadic amyotrophic lateral sclerosis on positron emission scanning , 1993, The Lancet.
[47] A. Biemond,et al. neural muscle atrophy with degeneration of the substantia nigra. , 1955, Confinia neurologica.
[48] J. Degos,et al. Luyso-pallido-nigral atrophy and amyotrophic lateral sclerosis , 2004, Acta Neuropathologica.
[49] P N Leigh,et al. Cortical function in amyotrophic lateral sclerosis. A positron emission tomography study. , 1993, Brain : a journal of neurology.
[50] S. Yagishita,et al. Atypical senile dementia with widespread Lewy type inclusion in the cerebral cortex , 2004, Acta Neuropathologica.
[51] B. Brownell,et al. The central nervous system in motor neurone disease , 1970, Journal of neurology, neurosurgery, and psychiatry.
[52] K. Ikeda,et al. Cognitive impairment in amyotrophic lateral sclerosis and its relation to motor disabilities , 1990, Acta neurologica Scandinavica.
[53] W. Matthews,et al. POST-ENCEPHALITIC PARKINSONISM WITH AMYOTROPHY , 1954, Journal of neurology, neurosurgery, and psychiatry.
[54] C. Davison,et al. AMYOTROPHIC LATERAL SCLEROSIS WITH MENTAL SYMPTOMS , 1932 .