| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| G Campanella, A Filla, G De Michel. Classifications of hereditary ataxias. A critical overview. Acta neurologica. vol 14. issue 4-6. 1993-04-08. PMID:1293984. |
however, we suggest the inclusion of late onset recessive cerebellar ataxias in harding's classification. |
1993-04-08 |
2023-08-11 |
Not clear |
| U Wüllner, T Klockgether, D Petersen, T Naegele, J Dichgan. Magnetic resonance imaging in hereditary and idiopathic ataxia. Neurology. vol 43. issue 2. 1993-03-23. PMID:8437696. |
five patients with friedreich's ataxia (n = 7) and all with late-onset friedreich's ataxia (n = 3) had sa without major involvement of the brainstem or cerebellum. |
1993-03-23 |
2023-08-12 |
Not clear |
| N Yuki, S Sato, S Tsuji, T Ohsawa, T Miyatak. Frequent presence of anti-GQ1b antibody in Fisher's syndrome. Neurology. vol 43. issue 2. 1993-03-23. PMID:8437711. |
moreover, anti-gq1b antibody-positive patients had more severe ataxia of cerebellar type than the antibody-negative patients. |
1993-03-23 |
2023-08-12 |
Not clear |
| R M Alvarado-Mallart, C Sotel. Cerebellar grafting in murine heredodegenerative ataxia. Current limitations for a therapeutic approach. Advances in neurology. vol 61. 1993-02-18. PMID:8421968. |
cerebellar grafting in murine heredodegenerative ataxia. |
1993-02-18 |
2023-08-12 |
Not clear |
| S N Illarioshkin, P A Fedin, I A Ivanova-smolenskaia, O I Solov'e. [Brain stem auditory evoked potentials in spinocerebellar degeneration]. Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952). vol 92. issue 4. 1993-01-07. PMID:1333700. |
27 patients with olivopontocerebellar degeneration (opcd), 13 patients suffering from friedreich's disease (fd), 10 patients with pierre marie's familial ataxia (pmfa), 6 patients with late onset cerebellar atrophy (loca), and 10 patients with other forms of scd were examined. |
1993-01-07 |
2023-08-11 |
Not clear |
| R M Feddersen, R Ehlenfeldt, W S Yunis, H B Clark, H T Or. Disrupted cerebellar cortical development and progressive degeneration of Purkinje cells in SV40 T antigen transgenic mice. Neuron. vol 9. issue 5. 1992-12-17. PMID:1419002. |
the sv5 line (containing > 30 transgene copies), exhibited embryonic transgene expression that caused selective death of immature purkinje cells and a subsequent block in cerebellar development and ataxia at 2 weeks. |
1992-12-17 |
2023-08-11 |
mouse |
| T Revesz, S Fletcher, L I al-Gazali, P DeBus. Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome? Journal of medical genetics. vol 29. issue 9. 1992-11-13. PMID:1404302. |
additional features of this seemingly new syndrome were intrauterine growth retardation, fine sparse hair, fine reticulate skin pigmentation, ataxia because of cerebellar hypoplasia, cerebral calcifications, extensor hypertonia, and progressive psychomotor retardation. |
1992-11-13 |
2023-08-11 |
Not clear |
| P J Vig, S H Subramony, R D Currier, D Desaia. Inositol 1,4,5-trisphosphate metabolism in the cerebella of Lurcher mutant mice and patients with olivopontocerebellar atrophy. Journal of the neurological sciences. vol 110. issue 1-2. 1992-09-23. PMID:1506853. |
we have investigated inositol 1,4,5-trisphosphate (insp3) metabolism in cerebellar membranes of normal humans and patients with dominant ataxia ('c' kindred), and also in cerebellar microsomes of lurcher mutant mouse (a suggested model for cerebellar ataxia). |
1992-09-23 |
2023-08-11 |
mouse |
| R D Verschoyle, A W Brown, C Nolan, D E Ray, T Liste. A comparison of the acute toxicity, neuropathology, and electrophysiology of N,N-diethyl-m-toluamide and N,N-dimethyl-2,2-diphenylacetamide in rats. Fundamental and applied toxicology : official journal of the Society of Toxicology. vol 18. issue 1. 1992-07-15. PMID:1601213. |
the insect repellent deet and the structurally related herbicide diphenamid both cause ataxia associated with a spongiform myelinopathy largely confined to the cerebellar roof nuclei. |
1992-07-15 |
2023-08-11 |
human |
| M Poloni, P Mazzarello, U Laforenza, C Caramella, C Patrin. Thiamin contents of cerebrospinal fluid, plasma and erythrocytes in cerebellar ataxias. European neurology. vol 32. issue 3. 1992-07-01. PMID:1592072. |
thiamin contents of cerebrospinal fluid, plasma and erythrocytes in cerebellar ataxias. |
1992-07-01 |
2023-08-11 |
human |
| M C La Regina, K Yates-Siilata, L Woods, D Tolber. Preliminary characterization of hereditary cerebellar ataxia in rats. Laboratory animal science. vol 42. issue 1. 1992-06-15. PMID:1316503. |
the preliminary findings are discussed in relationship to human cerebellar ataxias and mouse models of purkinje cell degeneration. |
1992-06-15 |
2023-08-11 |
mouse |
| K Leyshon, A J Morga. An integrated study of the morphological and gross-elemental consequences of methyl mercury intoxication in rats, with particular attention on the cerebellum. Scanning microscopy. vol 5. issue 3. 1992-05-18. PMID:1808720. |
methylmercury accumulates in the kidney and liver of rats, but fairly selectively damages the cerebellum, resulting in the clinical symptoms of neurological ataxia after prolonged exposures. |
1992-05-18 |
2023-08-11 |
rat |
| C Kleingoor, M Ewert, G von Blankenfeld, P H Seeburg, H Kettenman. Inverse but not full benzodiazepine agonists modulate recombinant alpha 6 beta 2 gamma 2 GABAA receptors in transfected human embryonic kidney cells. Neuroscience letters. vol 130. issue 2. 1992-04-08. PMID:1665550. |
(nature, 346 (1990) 648-651) have previously demonstrated that the alpha 6 subunit is part of a cerebellar receptor subtype which selectively binds ro15-4513, an antagonist of alcohol-induced motor ataxia. |
1992-04-08 |
2023-08-11 |
human |
| O L Pedraza, M I Bote. Thiamine status in inherited degenerative ataxias. Journal of neurology, neurosurgery, and psychiatry. vol 55. issue 2. 1992-03-31. PMID:1538220. |
these results, discussed in terms of the high degree of cerebellar atrophy on ct scans in opca v friedreich's ataxia patients, seem to correlate with cerebellar thiamine turnover and content. |
1992-03-31 |
2023-08-11 |
human |
| M Ben Hamida, N Attia-Romdhane, C H Triki, S Oueslati, F Hentat. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias]. Revue neurologique. vol 147. issue 12. 1992-03-10. PMID:1780608. |
two main clinical groups were identified: 227 cases of friedreich ataxia and 74 cases of cerebellar hereditary ataxia of p. marie type. |
1992-03-10 |
2023-08-11 |
Not clear |
| M Ben Hamida, N Attia-Romdhane, C H Triki, S Oueslati, F Hentat. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias]. Revue neurologique. vol 147. issue 12. 1992-03-10. PMID:1780608. |
the association in the same patient of peroneal atrophy of charcot marie type with friedreich ataxia (17 cases) or p. marie cerebellar hereditary ataxia (13 definite cases and 13 probable) was the most striking finding. |
1992-03-10 |
2023-08-11 |
Not clear |
| M I Botez, J Léveillé, R Lambert, T Bote. Single photon emission computed tomography (SPECT) in cerebellar disease: cerebello-cerebral diaschisis. European neurology. vol 31. issue 6. 1992-02-06. PMID:1756768. |
single photon emission computed tomography assessments were conducted in normal controls (n = 25), patients with unilateral cerebellar infarctions (n = 4), patients with olivopontocerebellar atrophy (opca; n = 15) and patients with friedreich's ataxia (fa; n = 6). |
1992-02-06 |
2023-08-11 |
human |
| C Sotelo, R M Alvarado-Mallar. The reconstruction of cerebellar circuits. Trends in neurosciences. vol 14. issue 8. 1992-01-28. PMID:1721740. |
grafting experiments carried out on the cerebellum of the adult pcd (purkinje-cell-degeneration) mutant mouse (an animal model of hereditary degenerative ataxia) reveal that embryonic purkinje cells, by some unknown sorting mechanism, selectively invade the deprived cerebellar cortex. |
1992-01-28 |
2023-08-11 |
mouse |
| K R Thomas, T S Musci, P E Neumann, M R Capecch. Swaying is a mutant allele of the proto-oncogene Wnt-1. Cell. vol 67. issue 5. 1992-01-07. PMID:1835670. |
mice homozygous for the recessive mutation swaying (sw) are characterized by ataxia and hypertonia, attributed to the malformation of anterior regions of the cerebellum. |
1992-01-07 |
2023-08-11 |
mouse |
| Y Watanabe, A Shikano, M Ohba, M Ohkubo, T Niw. [A case of acute cerebellar encephalitis due to Cryptococcus neoformans]. Rinsho shinkeigaku = Clinical neurology. vol 31. issue 6. 1991-12-26. PMID:1934783. |
on admission, cerebellar signs (disturbance of finger-to-nose test and of heel-to-knee test, intention tremor, and truncal ataxia) were neurologically noted. |
1991-12-26 |
2023-08-11 |
Not clear |