| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| S Sasaki, M Iwat. Characterizations of heterotopic neurons in the spinal cord of amyotrophic lateral sclerosis patients. Acta neuropathologica. vol 95. issue 4. 1998-06-12. PMID:9560014. |
characterizations of heterotopic neurons in the spinal cord of amyotrophic lateral sclerosis patients. |
1998-06-12 |
2023-08-12 |
human |
| K Fujita, M Yamauchi, T Matsui, K Titani, H Takahashi, T Kato, G Isomura, M Ando, Y Nagat. Increase of glial fibrillary acidic protein fragments in the spinal cord of motor neuron degeneration mutant mouse. Brain research. vol 785. issue 1. 1998-05-29. PMID:9526038. |
these processes of degenerative loss of motor neurons and proliferation of reactive astrocytes with increased levels of fragmented gfap in the mnd spinal cord during development seem to be characteristic and preceded the deterioration of motor activities in this animal model of amyotrophic lateral sclerosis. |
1998-05-29 |
2023-08-12 |
mouse |
| R Dawson, E G Marschall, K C Chan, W J Millard, B Eppler, T A Patterso. Neurochemical and neurobehavioral effects of neonatal administration of beta-N-methylamino-L-alanine and 3,3'-iminodipropionitrile. Neurotoxicology and teratology. vol 20. issue 2. 1998-05-14. PMID:9536463. |
amyotrophic lateral sclerosis (als) is a progressive neurodegenerative disease that is characterized by a loss of motor neurons in the spinal cord, brain stem, and cortex. |
1998-05-14 |
2023-08-12 |
rat |
| N Shibata, A Hirano, M Kobayashi, M C Dal Canto, M E Gurney, T Komori, T Umahara, K Asayam. Presence of Cu/Zn superoxide dismutase (SOD) immunoreactivity in neuronal hyaline inclusions in spinal cords from mice carrying a transgene for Gly93Ala mutant human Cu/Zn SOD. Acta neuropathologica. vol 95. issue 2. 1998-04-14. PMID:9498047. |
this investigation deals with the immunocytochemical localization of cu/zn superoxide dismutase (sod) in the spinal cord neurons of transgenic mice that overexpress gly93ala mutant human cu/zn sod and demonstrate clinicopathological features similar to human amyotrophic lateral sclerosis (als) with cu/zn sod mutation. |
1998-04-14 |
2023-08-12 |
mouse |
| M Waraga. MRI and clinical features in amyotrophic lateral sclerosis. Neuroradiology. vol 39. issue 12. 1998-03-13. PMID:9457707. |
mri of the brain and spinal cord was performed in 21 patients with amyotrophic lateral sclerosis (als), 8 normal volunteers and 16 neurological disease controls. |
1998-03-13 |
2023-08-12 |
human |
| N Shahani, A Nalini, M Gourie-Devi, T R Raj. Reactive astrogliosis in neonatal rat spinal cord after exposure to cerebrospinal fluid from patients with amyotrophic lateral sclerosis. Experimental neurology. vol 149. issue 1. 1998-03-06. PMID:9454639. |
reactive astrogliosis in neonatal rat spinal cord after exposure to cerebrospinal fluid from patients with amyotrophic lateral sclerosis. |
1998-03-06 |
2023-08-12 |
rat |
| R Wagey, C Krieger, C A Sha. Abnormal dephosphorylation effect on NMDA receptor regulation in ALS spinal cord. Neurobiology of disease. vol 4. issue 5. 1998-02-24. PMID:9440123. |
previous studies have demonstrated a significant reduction of n-methyl-d-aspartate (nmda) receptor binding in spinal cord sections from patients who died with amyotrophic lateral sclerosis (als) compared to that in control patients. |
1998-02-24 |
2023-08-12 |
human |
| N Makris, A J Worth, A G Sorensen, G M Papadimitriou, O Wu, T G Reese, V J Wedeen, T L Davis, J W Stakes, V S Caviness, E Kaplan, B R Rosen, D N Pandya, D N Kenned. Morphometry of in vivo human white matter association pathways with diffusion-weighted magnetic resonance imaging. Annals of neurology. vol 42. issue 6. 1998-01-02. PMID:9403488. |
in the clinical domain, this method will have a potential impact on the understanding of the diseases that involve white matter such as stroke, multiple sclerosis, amyotrophic lateral sclerosis, head injury, and spinal cord injury. |
1998-01-02 |
2023-08-12 |
human |
| M Jackson, A Al-Chalabi, Z E Enayat, B Chioza, P N Leigh, K E Morriso. Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation. Annals of neurology. vol 42. issue 5. 1997-12-19. PMID:9392581. |
amyotrophic lateral sclerosis (als) is a progressive paralytic disorder resulting from the degeneration of motor neurons in the brain and spinal cord and leading to death within 5 years of symptom onset. |
1997-12-19 |
2023-08-12 |
Not clear |
| E D Hall, J A Oostveen, P K Andrus, D K Anderson, C E Thoma. Immunocytochemical method for investigating in vivo neuronal oxygen radical-induced lipid peroxidation. Journal of neuroscience methods. vol 76. issue 2. 1997-12-09. PMID:9350962. |
using the anti-mda-rsa, we herein illustrate increased mda-derived immunostaining: (1) in the spinal cord of transgenic familial amyotrophic lateral sclerosis (als) mice; and (2) in the selectively vulnerable gerbil hippocampal ca1 region after a 5 min episode of forebrain ischemia and its relationship to the time course of neuronal degeneration. |
1997-12-09 |
2023-08-12 |
mouse |
| M Yasui, M Yoshida, T Tamaki, Y Taniguchi, K Ot. [Similarities in calcium and magnesium metabolism between amyotrophic lateral sclerosis and calcification of the spinal cord in the Kii Peninsula ALS focus]. No to shinkei = Brain and nerve. vol 49. issue 8. 1997-10-17. PMID:9282369. |
[similarities in calcium and magnesium metabolism between amyotrophic lateral sclerosis and calcification of the spinal cord in the kii peninsula als focus]. |
1997-10-17 |
2023-08-12 |
rat |
| M L Messi, M Renganathan, E Grigorenko, O Delbon. Activation of alpha7 nicotinic acetylcholine receptor promotes survival of spinal cord motoneurons. FEBS letters. vol 411. issue 1. 1997-09-11. PMID:9247137. |
spinal cord motoneurons (mns) undergo a process of cell death during embryonic development and are the target of lethal acquired or inherited disorders, such as the amyotrophic lateral sclerosis. |
1997-09-11 |
2023-08-12 |
chicken |
| X Mu, J E Springer, R Bowse. FAC1 expression and localization in motor neurons of developing, adult, and amyotrophic lateral sclerosis spinal cord. Experimental neurology. vol 146. issue 1. 1997-08-07. PMID:9225734. |
fac1 expression and localization in motor neurons of developing, adult, and amyotrophic lateral sclerosis spinal cord. |
1997-08-07 |
2023-08-12 |
Not clear |
| X Mu, J E Springer, R Bowse. FAC1 expression and localization in motor neurons of developing, adult, and amyotrophic lateral sclerosis spinal cord. Experimental neurology. vol 146. issue 1. 1997-08-07. PMID:9225734. |
in this study we report the localization and expression of fac1 protein in developing, normal adult and amyotrophic lateral sclerosis (als) lumbar spinal cord. |
1997-08-07 |
2023-08-12 |
Not clear |
| M C González Deniselle, S González, G Piroli, M Ferrini, A E Lima, A F De Nicol. Glucocorticoid receptors and actions in the spinal cord of the Wobbler mouse, a model for neurodegenerative diseases. The Journal of steroid biochemistry and molecular biology. vol 60. issue 3-4. 1997-07-10. PMID:9191978. |
we have studied glucocorticoid receptors (gr) and actions in the spinal cord of the wobbler mouse, a model for amyotrophic lateral sclerosis and infantile spinal muscular atrophy. |
1997-07-10 |
2023-08-12 |
mouse |
| A Kishino, Y Ishige, T Tatsuno, C Nakayama, H Noguch. BDNF prevents and reverses adult rat motor neuron degeneration and induces axonal outgrowth. Experimental neurology. vol 144. issue 2. 1997-06-19. PMID:9168829. |
these results provide a rationale for bdnf treatment in motor neuron diseases such as spinal cord injury and amyotrophic lateral sclerosis. |
1997-06-19 |
2023-08-12 |
rat |
| R M Duberley, I P Johnson, P Anand, P N Leigh, N J Cairn. Neurotrophin-3-like immunoreactivity and Trk C expression in human spinal motoneurones in amyotrophic lateral sclerosis. Journal of the neurological sciences. vol 148. issue 1. 1997-06-16. PMID:9125388. |
we have demonstrated neurotrophin-3 (nt-3)-like immunoreactivity and tyrosine kinase c (trk c) receptor expression in motoneurones in postmortem amyotrophic lateral sclerosis (als) and control human spinal cord sections. |
1997-06-16 |
2023-08-12 |
human |
| S Pradhan, R K Gupt. Magnetic resonance imaging in juvenile asymmetric segmental spinal muscular atrophy. Journal of the neurological sciences. vol 146. issue 2. 1997-06-09. PMID:9077509. |
the study included 5 normal individuals and 5 disease-negative controls who had spinal cord atrophy due to amyotrophic lateral sclerosis. |
1997-06-09 |
2023-08-12 |
Not clear |
| P H Tu, M E Gurney, J P Julien, V M Lee, J Q Trojanowsk. Oxidative stress, mutant SOD1, and neurofilament pathology in transgenic mouse models of human motor neuron disease. Laboratory investigation; a journal of technical methods and pathology. vol 76. issue 4. 1997-05-09. PMID:9111507. |
amyotrophic lateral sclerosis (als) is a neurodegenerative disease that primarily affects motor neurons in the spinal cord and brain stem. |
1997-05-09 |
2023-08-12 |
mouse |
| F F Cruz-Sánchez, A Moral, M L Rossi, L Quintó, C Castejón, E Tolosa, J de Belleroch. Synaptophysin in spinal anterior horn in aging and ALS: an immunohistological study. Journal of neural transmission (Vienna, Austria : 1996). vol 103. issue 11. 1997-04-17. PMID:9013418. |
aged-related spinal cord changes such as neuronal loss have been related to the degree of clinical severity of amyotrophic lateral sclerosis (als); morphological data on synapses are, however, wanting. |
1997-04-17 |
2023-08-12 |
mouse |