| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| S S Jossan, J Ekblom, S M Aquilonius, L Orelan. Monoamine oxidase-B in motor cortex and spinal cord in amyotrophic lateral sclerosis studied by quantitative autoradiography. Journal of neural transmission. Supplementum. vol 41. 1994-11-23. PMID:7931232. |
monoamine oxidase-b in motor cortex and spinal cord in amyotrophic lateral sclerosis studied by quantitative autoradiography. |
1994-11-23 |
2023-08-12 |
Not clear |
| J Ekblom, S S Jossan, L Oreland, E Walum, S M Aquiloniu. Reactive gliosis and monoamine oxidase B. Journal of neural transmission. Supplementum. vol 41. 1994-11-23. PMID:7931234. |
a double-staining method was applied to cryosections of human spinal cord from patients who died with amyotrophic lateral sclerosis (als) and corresponding controls in order to investigate cellular content of monoamine oxidase b (mao-b). |
1994-11-23 |
2023-08-12 |
human |
| D R Rosen, P Sapp, J O'Regan, D McKenna-Yasek, K S Schlumpf, J L Haines, J F Gusella, H R Horvitz, R H Brow. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers. American journal of medical genetics. vol 51. issue 1. 1994-08-08. PMID:7913294. |
amyotrophic lateral sclerosis (als: lou gehrig's disease) is a lethal neurodegenerative disease of upper and lower motorneurons in the brain and spinal cord. |
1994-08-08 |
2023-08-12 |
human |
| H Ito, A Hiran. Comparative study of spinal cord ubiquitin expression in post-poliomyelitis and sporadic amyotrophic lateral sclerosis. Acta neuropathologica. vol 87. issue 4. 1994-07-27. PMID:7517092. |
comparative study of spinal cord ubiquitin expression in post-poliomyelitis and sporadic amyotrophic lateral sclerosis. |
1994-07-27 |
2023-08-12 |
Not clear |
| M Nakamura, S Mita, T Murakami, M Uchino, S Watanabe, M Tokunaga, T Kumamoto, M And. Exonic trinucleotide repeats and expression of androgen receptor gene in spinal cord from X-linked spinal and bulbar muscular atrophy. Journal of the neurological sciences. vol 122. issue 1. 1994-06-24. PMID:7515106. |
forty-nine cag triplet repeats were found in tissues from the spinal cord, cerebrum, cerebellum, cardiac muscle and bladder, while there were 20-24 cag repeats in these tissues from control subjects, consisting of three patients with amyotrophic lateral sclerosis (als) and three patients with lung cancer. |
1994-06-24 |
2023-08-12 |
human |
| F Kimura, R G Smith, O Delbono, O Nyormoi, T Schneider, W Nastainczyk, F Hofmann, E Stefani, S H Appe. Amyotrophic lateral sclerosis patient antibodies label Ca2+ channel alpha 1 subunit. Annals of neurology. vol 35. issue 2. 1994-03-21. PMID:8109897. |
sporadic amyotrophic lateral sclerosis is an idiopathic human degenerative disease of spinal cord and brain motor neurons. |
1994-03-21 |
2023-08-12 |
human |
| K Fujita, Y Nagata, M Hond. [Free amino acid contents in the spinal cord of amyotrophic lateral sclerosis]. Rinsho shinkeigaku = Clinical neurology. vol 33. issue 9. 1994-03-04. PMID:7905368. |
[free amino acid contents in the spinal cord of amyotrophic lateral sclerosis]. |
1994-03-04 |
2023-08-12 |
Not clear |
| K Fujita, Y Nagata, M Hond. [Free amino acid contents in the spinal cord of amyotrophic lateral sclerosis]. Rinsho shinkeigaku = Clinical neurology. vol 33. issue 9. 1994-03-04. PMID:7905368. |
we analysed free amino acid contents in anterior horn, posterior horn, lateral column and posterior column of the spinal cord transections from autopsied cases of amyotrophic lateral sclerosis (als), and compared the results with those from non-als cases. |
1994-03-04 |
2023-08-12 |
Not clear |
| D E Erb, R J Mora, R P Bung. Reinnervation of adult rat gastrocnemius muscle by embryonic motoneurons transplanted into the axotomized tibial nerve. Experimental neurology. vol 124. issue 2. 1994-02-18. PMID:8287933. |
in some cases of spinal cord injury and in certain motoneuron diseases, such as amyotrophic lateral sclerosis and spinal muscular atrophies, lower motoneurons are destroyed and muscle function cannot be restored except by reinnervation from alternate motoneuron sources. |
1994-02-18 |
2023-08-12 |
rat |
| C Confavreux, T Moreau, A Jouvet, M Tommasi, G Aimar. [Association of amyotrophic lateral sclerosis and multiple sclerosis]. Revue neurologique. vol 149. issue 5. 1994-02-03. PMID:8272733. |
the autopsy showed characteristic "old" plaques of multiple sclerosis in the cerebrum with anterior horn cell and pyramidal tracts degeneration, typical of amyotrophic lateral sclerosis, in the spinal cord. |
1994-02-03 |
2023-08-12 |
Not clear |
| J M Godoy, M A de Oliveira, J B de Moraes Neto, S L Balassiano, N Montagna, J R Pinto, M Skace. [Sporadic amyotrophic lateral sclerosis. Diagnostic criteria]. Arquivos de neuro-psiquiatria. vol 51. issue 2. 1994-02-01. PMID:8274087. |
the authors report two cases of amyotrophic lateral sclerosis (als) misdiagnosis (a craniocervical junction disorder, and a cervical spinal cord ependymoma). |
1994-02-01 |
2023-08-12 |
Not clear |
| C Krieger, R Wagey, C Sha. Amyotrophic lateral sclerosis: quantitative autoradiography of [3H]MK-801/NMDA binding sites in spinal cord. Neuroscience letters. vol 159. issue 1-2. 1994-01-25. PMID:8264965. |
amyotrophic lateral sclerosis: quantitative autoradiography of [3h]mk-801/nmda binding sites in spinal cord. |
1994-01-25 |
2023-08-12 |
human |
| M E Westarp, D Fuchs, P Bartmann, R Hoff-Jörgensen, J Clausen, H Wachter, H H Kornhube. Amyotrophic lateral sclerosis an enigmatic disease with B-cellular and anti-retroviral immune responses. The European journal of medicine. vol 2. issue 6. 1994-01-11. PMID:8252177. |
the most frequent sporadic adult motor neuron disease, amyotrophic lateral sclerosis, affects more men, follows no epidemiologic pattern, and was long considered a pure spinal cord disorder. |
1994-01-11 |
2023-08-12 |
Not clear |
| S Sasaki, S Maruyam. A fine structural study of Onuf's nucleus in sporadic amyotrophic lateral sclerosis. Journal of the neurological sciences. vol 119. issue 1. 1994-01-05. PMID:8246008. |
onuf's nucleus of the second sacral spinal cord level was examined in twelve patients with sporadic amyotrophic lateral sclerosis (als). |
1994-01-05 |
2023-08-12 |
Not clear |
| J L Seeburger, S Tarras, H Natter, J E Springe. Spinal cord motoneurons express p75NGFR and p145trkB mRNA in amyotrophic lateral sclerosis. Brain research. vol 621. issue 1. 1993-12-09. PMID:8221061. |
spinal cord motoneurons express p75ngfr and p145trkb mrna in amyotrophic lateral sclerosis. |
1993-12-09 |
2023-08-12 |
Not clear |
| J L Seeburger, S Tarras, H Natter, J E Springe. Spinal cord motoneurons express p75NGFR and p145trkB mRNA in amyotrophic lateral sclerosis. Brain research. vol 621. issue 1. 1993-12-09. PMID:8221061. |
in the present study, in situ hybridization was used to examine the expression of nerve growth factor (ngf) receptor (p75ngfr), trk (p140trk) and trkb (p145trkb) mrna in spinal cord sections from patients with amyotrophic lateral sclerosis (als). |
1993-12-09 |
2023-08-12 |
Not clear |
| J Ekblom, S M Aquilonius, S S Jossa. Differential increases in catecholamine metabolizing enzymes in amyotrophic lateral sclerosis. Experimental neurology. vol 123. issue 2. 1993-11-22. PMID:8405291. |
the enzyme activities were determined in postmortem spinal cord tissue from controls and cases with amyotrophic lateral sclerosis (als). |
1993-11-22 |
2023-08-12 |
human |
| J Ekblom, S M Aquilonius, S S Jossa. Differential increases in catecholamine metabolizing enzymes in amyotrophic lateral sclerosis. Experimental neurology. vol 123. issue 2. 1993-11-22. PMID:8405291. |
these results suggest that the two enzyme proteins are regulated by more complex mechanisms in the spinal cord in amyotrophic lateral sclerosis than simple general increases caused by elevated astroglial cell numbers. |
1993-11-22 |
2023-08-12 |
human |
| J A Kiernan, A J Hudso. Anti-neurone antibodies are not characteristic of amyotrophic lateral sclerosis. Neuroreport. vol 4. issue 4. 1993-07-01. PMID:8499603. |
autoantibodies, a suggested cause of motor neurone degeneration in amyotrophic lateral sclerosis (als), were sought immunohistochemically after applying diluted sera to sections of normal human spinal cord. |
1993-07-01 |
2023-08-12 |
human |
| Z Mourelatos, A Yachnis, L Rorke, J Mikol, N K Gonata. The Golgi apparatus of motor neurons in amyotrophic lateral sclerosis. Annals of neurology. vol 33. issue 6. 1993-06-24. PMID:8498841. |
using an organelle-specific antiserum we have examined by immunocytochemistry the golgi apparatus of motor neurons in the spinal cord in 4 patients with amyotrophic lateral sclerosis and 1 patient with werdnig hoffmann's disease, 1 with infantile neuronal degeneration, 1 with adult-type familial bulbospinal atrophy, 1 with mitochondrial myopathy with cytochrome c oxidase deficiency, 1 with centronuclear myopathy, and 1 with duchenne's muscular dystrophy, and in 9 age-matched control subjects. |
1993-06-24 |
2023-08-12 |
human |