| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| J Doyle, X Ren, G Lennon, L Stubb. Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice. Mammalian genome : official journal of the International Mammalian Genome Society. vol 8. issue 2. 1997-05-22. PMID:9060410. |
mutations in the cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice. |
1997-05-22 |
2023-08-12 |
mouse |
| R Matsumura, T Takayanagi, K Murata, N Futamura, Y Fujimot. Autosomal dominant cerebellar ataxias in the Kinki area of Japan. The Japanese journal of human genetics. vol 41. issue 4. 1997-05-08. PMID:9088110. |
autosomal dominant cerebellar ataxias in the kinki area of japan. |
1997-05-08 |
2023-08-12 |
Not clear |
| R Matsumura, T Takayanagi, K Murata, N Futamura, Y Fujimot. Autosomal dominant cerebellar ataxias in the Kinki area of Japan. The Japanese journal of human genetics. vol 41. issue 4. 1997-05-08. PMID:9088110. |
the autosomal dominant cerebellar ataxias are a heterogeneous group of neurodegenerative disorders characterized by slowly progressive cerebellar ataxia. |
1997-05-08 |
2023-08-12 |
Not clear |
| R Matsumura, T Takayanagi, K Murata, N Futamura, Y Fujimot. Autosomal dominant cerebellar ataxias in the Kinki area of Japan. The Japanese journal of human genetics. vol 41. issue 4. 1997-05-08. PMID:9088110. |
these findings suggest geographic variation in autosomal dominant cerebellar ataxias in japan. |
1997-05-08 |
2023-08-12 |
Not clear |
| D H Geschwind, S Perlman, C P Figueroa, L J Treiman, S M Puls. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia. American journal of human genetics. vol 60. issue 4. 1997-05-08. PMID:9106530. |
the dominant cerebellar ataxias (adcas) represent a clinically and genetically heterogeneous group of disorders linked by progressive deterioration in balance and coordination. |
1997-05-08 |
2023-08-12 |
Not clear |
| D Johnson-Greene, K M Adams, S Gilman, K J Kluin, L Junck, S Martorello, M Heuman. Impaired upper limb coordination in alcoholic cerebellar degeneration. Archives of neurology. vol 54. issue 4. 1997-05-08. PMID:9109745. |
alcoholic cerebellar degeneration (acd) is a disorder resulting from severe chronic alcoholism and malnutrition and is characterized by cognitive disturbances, ataxia of gait, and truncal instability, with generally preserved coordination of the upper extremities. |
1997-05-08 |
2023-08-12 |
Not clear |
| M S Da. Mouse cerebellar adenosinergic modulation of ethanol-induced motor incoordination: possible involvement of cAMP. Brain research. vol 749. issue 2. 1997-05-06. PMID:9138726. |
overall, the data suggested a possible involvement of cerebellar adenylyl cyclase-camp signalling pathway in the adenosinergic modulation of ethanol's ataxia. |
1997-05-06 |
2023-08-12 |
mouse |
| L Forsgren, R Libelius, M Holmberg, U von Döbeln, R Wibom, J Heijbel, O Sandgren, G Holmgre. Muscle morphology and mitochondrial investigations of a family with autosomal dominant cerebellar ataxia and retinal degeneration mapped to chromosome 3p12-p21.1. Journal of the neurological sciences. vol 144. issue 1-2. 1997-04-15. PMID:8994109. |
the autosomal dominant cerebellar ataxias (adca) are a group of neurodegenerative disorders with ataxia and dysarthria as early and dominant signs. |
1997-04-15 |
2023-08-12 |
Not clear |
| H Sasaki, T Fukazawa, A Wakisaka, K Hamada, T Hamada, T Koyama, S Tsuji, K Tashir. Central phenotype and related varieties of spinocerebellar ataxia 2 (SCA2): a clinical and genetic study with a pedigree in the Japanese. Journal of the neurological sciences. vol 144. issue 1-2. 1997-04-15. PMID:8994121. |
additional symptoms were parkinsonism with minor cerebellar deficits, and severe ataxia with choreoathetosis. |
1997-04-15 |
2023-08-12 |
Not clear |
| M H Green, A J Marcovitch, S A Harcourt, J E Lowe, I C Green, C F Arlet. Hypersensitivity of ataxia-telangiectasia fibroblasts to a nitric oxide donor. Free radical biology & medicine. vol 22. issue 1-2. 1997-04-10. PMID:8958160. |
nitric oxide is known to be formed in the cerebellum and we present evidence that a-t fibroblasts are hypersensitive to killing by the nitric oxide donor s-nitrosoglutathione (gsno), as are fibroblasts from a radiosensitive individual without ataxia. |
1997-04-10 |
2023-08-12 |
human |
| G Stevanin, Y Trottier, G Cancel, A Dürr, G David, O Didierjean, K Bürk, G Imbert, F Saudou, M Abada-Bendib, I Gourfinkel-An, A Benomar, N Abbas, T Klockgether, D Grid, Y Agid, J L Mandel, A Bric. Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias. Human molecular genetics. vol 5. issue 12. 1997-03-14. PMID:8968739. |
screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias. |
1997-03-14 |
2023-08-12 |
Not clear |
| G Stevanin, Y Trottier, G Cancel, A Dürr, G David, O Didierjean, K Bürk, G Imbert, F Saudou, M Abada-Bendib, I Gourfinkel-An, A Benomar, N Abbas, T Klockgether, D Grid, Y Agid, J L Mandel, A Bric. Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxias. Human molecular genetics. vol 5. issue 12. 1997-03-14. PMID:8968739. |
expansion of trinucleotide cag repeats coding for polyglutamine has been implicated in five neurodegenerative disorders, including spinocerebellar ataxia (sca) 1 and sca3 or machado-joseph disease (sca3/mjd), two forms of type i autosomal dominant cerebellar ataxias (adca). |
1997-03-14 |
2023-08-12 |
Not clear |
| R W Baloh, Q Yue, J M Furman, S F Nelso. Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p. Annals of neurology. vol 41. issue 1. 1997-02-25. PMID:9005860. |
episodes varied from pure ataxia to combinations of symptoms suggesting involvement of the cerebellum, brainstem, and cortex. |
1997-02-25 |
2023-08-12 |
Not clear |
| M S Da. Mouse cerebellar GABAB participation in the expression of acute ethanol-induced ataxia and in its modulation by the cerebellar adenosinergic A1 system. Brain research bulletin. vol 41. issue 1. 1997-01-24. PMID:8883916. |
mouse cerebellar gabab participation in the expression of acute ethanol-induced ataxia and in its modulation by the cerebellar adenosinergic a1 system. |
1997-01-24 |
2023-08-12 |
mouse |
| L Bettendorff, F Mastrogiacomo, J LaMarche, S Dozić, S J Kis. Brain levels of thiamine and its phosphate esters in Friedreich's ataxia and spinocerebellar ataxia type 1. Movement disorders : official journal of the Movement Disorder Society. vol 11. issue 4. 1996-12-26. PMID:8813226. |
to determine whether a thiamine deficiency is present in the brain, we measured levels of thiamine and its phosphate esters thiamine monophosphate (tmp) and thiamine diphosphate (tdp), in postmortem cerebellar and cerebral cortices of patients with friedreich's ataxia (fa) and spinocerebellar ataxia type 1 (sca1). |
1996-12-26 |
2023-08-12 |
Not clear |
| U Muller, M B Graebe. Neurogenetic diseases: molecular diagnosis and therapeutic approaches. Journal of molecular medicine (Berlin, Germany). vol 74. issue 2. 1996-12-16. PMID:8820402. |
huntington disease, spinobulbar muscular atrophy, and the autosomal dominant cerebellar ataxias are examples of autosomal dominant disorders caused by the expansion of trinucleotides (cag) within disease genes. |
1996-12-16 |
2023-08-12 |
Not clear |
| Y Washimi, K Saito. [Movement-related cortical potentials (MRCPs) and voluntary movement--clinical usefulness of MRCPs]. Rinsho shinkeigaku = Clinical neurology. vol 35. issue 12. 1996-12-04. PMID:8752452. |
we recorded the mrcps of thirty nine patients with cerebellar ataxias and sixteen patients with parkinson disease (pd). |
1996-12-04 |
2023-08-12 |
human |
| M Urushitani, H Inoue, K Kawamura, T Kageyama, M Fujisawa, K Nishinaka, F Udaka, M Kameyam. [Disappearance of essential neck tremor after pontine base infarction]. No to shinkei = Brain and nerve. vol 48. issue 8. 1996-12-04. PMID:8797210. |
neurological examination showed right hemiparesis including the ipsilateral face, scanning speech, and cerebellar limb ataxia on the same side. |
1996-12-04 |
2023-08-12 |
Not clear |
| L KILHAM, G MARGOLI. CEREBELLAR ATAXIA IN HAMSTERS INOCULATED WITH RAT VIRUS. Science (New York, N.Y.). vol 143. issue 3610. 1996-12-01. PMID:14107432. |
chronic ataxia associated with hypoplasia of the cerebellum was induced by intracerebral inoculation of newborn hamsters with various strains of rat virus. |
1996-12-01 |
2023-08-12 |
rat |
| L KILHAM, G MARGOLI. CEREBELLAR DISEASE IN CATS INDUCED BY INOCULATION OF RAT VIRUS. Science (New York, N.Y.). vol 148. issue 3667. 1996-12-01. PMID:14259767. |
these effects suggest that the spontaneous ataxia of cats which is accompanied by cerebellar hypoplasia, may be of viral origin. |
1996-12-01 |
2023-08-12 |
rat |