| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| A H Koeppe. The hereditary ataxias. Journal of neuropathology and experimental neurology. vol 57. issue 6. 1998-06-25. PMID:9630233. |
the autosomal dominant ataxias such as olivopontocerebellar atrophy (opca), familial cortical cerebellar atrophy (fcca), and machado-joseph disease (mjd) have been renamed the spinocerebellar ataxias (sca). |
1998-06-25 |
2023-08-12 |
human |
| B Echenne, F Rivier, M Tardieu, M Brive, A Robert, A M Pages, F Pons, D Morne. Congenital muscular dystrophy and cerebellar atrophy. Neurology. vol 50. issue 5. 1998-06-08. PMID:9596013. |
all had marked ataxia and cerebellar atrophy or hypoplasia. |
1998-06-08 |
2023-08-12 |
Not clear |
| H Watanabe, F Tanaka, M Matsumoto, M Doyu, T Ando, T Mitsuma, G Sobu. Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6. Clinical genetics. vol 53. issue 1. 1998-05-21. PMID:9550356. |
frequency analysis of autosomal dominant cerebellar ataxias in japanese patients and clinical characterization of spinocerebellar ataxia type 6. |
1998-05-21 |
2023-08-12 |
Not clear |
| H Watanabe, F Tanaka, M Matsumoto, M Doyu, T Ando, T Mitsuma, G Sobu. Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6. Clinical genetics. vol 53. issue 1. 1998-05-21. PMID:9550356. |
using a molecular diagnostic approach, we investigated 101 kindreds with autosomal dominant cerebellar ataxias (adcas) from the central honshu island of japan, including spinocerebellar ataxia type 1 (sca1), spinocerebellar ataxia type 2 (sca2), machado-joseph disease (mjd), dentatorubral and pallidoluysian atrophy (drpla) and spinocerebellar ataxia type 6 (sca6). |
1998-05-21 |
2023-08-12 |
Not clear |
| D Shmerling, I Hegyi, M Fischer, T Blättler, S Brandner, J Götz, T Rülicke, E Flechsig, A Cozzio, C von Mering, C Hangartner, A Aguzzi, C Weissman. Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions. Cell. vol 93. issue 2. 1998-05-21. PMID:9568713. |
expression of amino-terminally truncated prp in the mouse leading to ataxia and specific cerebellar lesions. |
1998-05-21 |
2023-08-12 |
mouse |
| D Shmerling, I Hegyi, M Fischer, T Blättler, S Brandner, J Götz, T Rülicke, E Flechsig, A Cozzio, C von Mering, C Hangartner, A Aguzzi, C Weissman. Expression of amino-terminally truncated PrP in the mouse leading to ataxia and specific cerebellar lesions. Cell. vol 93. issue 2. 1998-05-21. PMID:9568713. |
surprisingly, prp lacking residues 32-121 or 32-134, but not with shorter deletions, caused severe ataxia and neuronal death limited to the granular layer of the cerebellum as early as 1-3 months after birth. |
1998-05-21 |
2023-08-12 |
mouse |
| M Steinlin, B Zangger, E Boltshause. Non-progressive congenital ataxia with or without cerebellar hypoplasia: a review of 34 subjects. Developmental medicine and child neurology. vol 40. issue 3. 1998-05-19. PMID:9566649. |
non-progressive congenital ataxia with or without cerebellar hypoplasia: a review of 34 subjects. |
1998-05-19 |
2023-08-12 |
human |
| B L Day, P D Thompson, A E Harding, C D Marsde. Influence of vision on upper limb reaching movements in patients with cerebellar ataxia. Brain : a journal of neurology. vol 121 ( Pt 2). 1998-05-08. PMID:9549511. |
patients with friedreich's ataxia as well as those with intrinsic cerebellar degeneration showed the above abnormalities, although there were some quantitative differences between the two groups. |
1998-05-08 |
2023-08-12 |
human |
| W L Berry, J E Jardine, I W Espi. Pulmonary cryptococcoma and cryptococcal meningoencephalomyelitis in a king cheetah (Acinonyx jubatus). Journal of zoo and wildlife medicine : official publication of the American Association of Zoo Veterinarians. vol 28. issue 4. 1998-05-04. PMID:9523645. |
the ataxia appeared to be spinal in origin, evidenced by apparent conscious proprioceptive deficits in all limbs, and there was no evidence of cerebellar involvement. |
1998-05-04 |
2023-08-12 |
Not clear |
| M A Pujana, V Volpini, M Gratacós, J Corral, I Banchs, A Sánchez, D Genís, C Cervera, X Estivil. Uncloned expanded CAG/CTG repeat sequences in autosomal dominant cerebellar ataxia (ADCA) detected by the repeat expansion detection (RED) method. Journal of medical genetics. vol 35. issue 2. 1998-04-23. PMID:9507387. |
among these neurodegenerative diseases are late onset autosomal dominant cerebellar ataxias (adca). |
1998-04-23 |
2023-08-12 |
human |
| K Matsunaga, T Sakai, S Tsuj. [The diagnosis and follow-up evaluation of acute cerebellar ataxia supported by a cerebellar stimulation study]. Rinsho shinkeigaku = Clinical neurology. vol 37. issue 10. 1998-04-21. PMID:9490907. |
we examined cerebellar stimulation in order to determine whether the ataxia was due to dysfunction of the cerebellum or peripheral nervous system. |
1998-04-21 |
2023-08-12 |
Not clear |
| S Rivaud-Pechoux, A Dürr, B Gaymard, G Cancel, C J Ploner, Y Agid, A Brice, C Pierrot-Deseillign. Eye movement abnormalities correlate with genotype in autosomal dominant cerebellar ataxia type I. Annals of neurology. vol 43. issue 3. 1998-04-10. PMID:9506545. |
we compared horizontal eye movements (visually guided saccades, antisaccades, and smooth pursuit) in control subjects (n = 14) and patients with three forms of autosomal dominant cerebellar ataxias type i: spinocerebellar ataxias 1 and 2 (sca1, n = 11; sca2, n = 10) and sca3/machado-joseph disease (mjd) (n = 16). |
1998-04-10 |
2023-08-12 |
human |
| J E Jan, S Kearney, M Groenveld, M A Sargent, K J Poskit. Speech, cognition, and imaging studies in congenital ocular motor apraxia. Developmental medicine and child neurology. vol 40. issue 2. 1998-03-24. PMID:9489497. |
the neurological examination showed clinical evidence of cerebellar vermis abnormality (hypotonia and truncal ataxia) in all cases. |
1998-03-24 |
2023-08-12 |
human |
| M N Abdulla, T E Sokrab, Z A Zaidan, H E Siddig, M E Al. Post-malarial cerebellar ataxia in adult Sudanese patients. East African medical journal. vol 74. issue 9. 1998-03-12. PMID:9487432. |
it was also found that in patients who demonstrated cerebellar infarction or atrophy on computerised tomography the duration of ataxia was significantly long. |
1998-03-12 |
2023-08-12 |
Not clear |
| St Probst-Cousi. [Olivopontocerebellar atrophy--a heterogenous morphologic syndrome]. Fortschritte der Neurologie-Psychiatrie. vol 65. issue 12. 1998-03-05. PMID:9451569. |
clinical and genetic classification systems include opca in sporadic cerebellar ataxias such as multiple system atrophy as well as in different autosomal recessive, autosomal dominant and x-chromosomal recessive cerebellar ataxias. |
1998-03-05 |
2023-08-12 |
Not clear |
| T Brandt, M Strup. Episodic ataxia type 1 and 2 (familial periodic ataxia/vertigo). Audiology & neuro-otology. vol 2. issue 6. 1998-02-19. PMID:9390841. |
as effective as acetazolamide is in preventing attacks, prospective studies still have to prove whether it can prevent progressive ataxia in ea-2 or even improve chronic cerebellar deficits. |
1998-02-19 |
2023-08-12 |
Not clear |
| P E Mecenas, S E Tsirka, F Sallés, S Stricklan. Removal of tissue plasminogen activator does not protect against neuronal degeneration in the cerebellum of the weaver mouse. Brain research. vol 772. issue 1-2. 1998-02-19. PMID:9406977. |
weaver mice suffer extensive degeneration of cerebellar granular neurons during development, leading to severe malformation of the cerebellum as well as abnormal behavior (ataxia). |
1998-02-19 |
2023-08-12 |
mouse |
| J P Hubble, K L Busenbark, R Pahwa, K Lyons, W C Kolle. Clinical expression of essential tremor: effects of gender and age. Movement disorders : official journal of the Movement Disorder Society. vol 12. issue 6. 1998-02-10. PMID:9399222. |
ataxia (tandem gait difficulty) is common in et and may be an accentuation of cerebellar dysfunction due to aging. |
1998-02-10 |
2023-08-12 |
Not clear |
| M Watanabe, H Miyasaka, N Iwata, S Maeda, S Kishida, H Hayash. [A case of superficial siderosis of the central nervous system with bilateral vestibular dysfunction]. No to shinkei = Brain and nerve. vol 49. issue 10. 1998-01-09. PMID:9368892. |
her disturbance of gait and station was apparently similar to cerebellar ataxic gait, however, she did not have limb ataxia. |
1998-01-09 |
2023-08-12 |
Not clear |
| S N Illarioshkin, I A Ivanova-Smolenskaia, E D Markova, N N Nikol'skaia, S Tsudz. [A new form of hereditary ataxia: X-linked congenital cerebellar hypoplasia (a clinical and molecular genetic analysis)]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. vol 97. issue 10. 1998-01-05. PMID:9424342. |
[a new form of hereditary ataxia: x-linked congenital cerebellar hypoplasia (a clinical and molecular genetic analysis)]. |
1998-01-05 |
2023-08-12 |
Not clear |