| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| G Stevanin, A Dürr, G David, O Didierjean, G Cancel, S Rivaud, A Tourbah, J M Warter, Y Agid, A Bric. Clinical and molecular features of spinocerebellar ataxia type 6. Neurology. vol 49. issue 5. 1997-12-08. PMID:9371901. |
we looked for this mutation in 91 families with autosomal-dominant cerebellar ataxias and found that sca6 is a minor locus in our series (2%) and is rare in france (1%). |
1997-12-08 |
2023-08-12 |
Not clear |
| E N Ponomareva, A V Astapenko, S A Likhachev, G I Ovsiankina, G V Pashko, A I Antonenk. [The cerebellar cortical atrophy syndrome]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova. vol 97. issue 9. 1997-12-01. PMID:9410595. |
the study allowed to reveal both the cause of the disease and to refer etiologically late cerebellar cortical ataxia to alcohol factor. |
1997-12-01 |
2023-08-12 |
Not clear |
| Y Ugawa, Y Terao, R Hanajima, K Sakai, T Furubayashi, K Machii, I Kanazaw. Magnetic stimulation over the cerebellum in patients with ataxia. Electroencephalography and clinical neurophysiology. vol 104. issue 5. 1997-11-13. PMID:9344082. |
magnetic stimulation over the cerebellum in patients with ataxia. |
1997-11-13 |
2023-08-12 |
human |
| Y Ugawa, Y Terao, R Hanajima, K Sakai, T Furubayashi, K Machii, I Kanazaw. Magnetic stimulation over the cerebellum in patients with ataxia. Electroencephalography and clinical neurophysiology. vol 104. issue 5. 1997-11-13. PMID:9344082. |
we studied 20 patients with ataxia caused by various disorders using magnetic stimulation over the cerebellum. |
1997-11-13 |
2023-08-12 |
human |
| Y Ugawa, Y Terao, R Hanajima, K Sakai, T Furubayashi, K Machii, I Kanazaw. Magnetic stimulation over the cerebellum in patients with ataxia. Electroencephalography and clinical neurophysiology. vol 104. issue 5. 1997-11-13. PMID:9344082. |
two other clinical uses of this technique were that it revealed clinically undetectable cerebellar dysfunction in patients whose extrapyramidal signs masked cerebellar signs, and that the slow progression of ataxia could be followed quantitatively in patients with degenerative late-onset ataxia. |
1997-11-13 |
2023-08-12 |
human |
| T Botez-Marquard, M I Bote. Olivopontocerebellar atrophy and Friedreich's ataxia: neuropsychological consequences of bilateral versus unilateral cerebellar lesions. International review of neurobiology. vol 41. 1997-11-07. PMID:9378599. |
olivopontocerebellar atrophy and friedreich's ataxia: neuropsychological consequences of bilateral versus unilateral cerebellar lesions. |
1997-11-07 |
2023-08-12 |
Not clear |
| T Botez-Marquard, M I Bote. Olivopontocerebellar atrophy and Friedreich's ataxia: neuropsychological consequences of bilateral versus unilateral cerebellar lesions. International review of neurobiology. vol 41. 1997-11-07. PMID:9378599. |
this chapter deals with neuropsychological disturbances in patients with bilateral cerebellar damage (bcd), i.e., epileptic patients chronically receiving phenytoin, patients with olivopontocerebellar atrophy (opca), and friedreich's ataxia (fa) versus those with unilateral cerebellar damage (ucd), i.e., patients with cerebellar strokes. |
1997-11-07 |
2023-08-12 |
Not clear |
| T W Clarkso. The toxicology of mercury. Critical reviews in clinical laboratory sciences. vol 34. issue 4. 1997-10-22. PMID:9288445. |
in adults, brain damage is focal affecting the function of such areas as the cerebellum (ataxia) and the visual cortex (constricted visual fields). |
1997-10-22 |
2023-08-12 |
human |
| B Kores, M H Lade. Irreversible lithium neurotoxicity: an overview. Clinical neuropharmacology. vol 20. issue 4. 1997-09-29. PMID:9260727. |
the irreversible neurologic sequelae are generally cerebellar signs, especially ataxia and dysarthria. |
1997-09-29 |
2023-08-12 |
Not clear |
| M Augustin, P Heimann, S Rathke, H Jockusc. Spinal muscular atrophy gene wobbler of the mouse: evidence from chimeric spinal cord and testis for cell-autonomous function. Developmental dynamics : an official publication of the American Association of Anatomists. vol 209. issue 3. 1997-09-12. PMID:9215643. |
human hereditary neurodegenerative diseases are genetically and mechanistically very heterogeneous and so are spinal muscular atrophies and cerebellar ataxias in the mouse, despite the common phenomenon of neuronal death. |
1997-09-12 |
2023-08-12 |
mouse |
| Y Ikeda, T Terashim. Corticospinal tract neurons are radially malpositioned in the sensory-motor cortex of the Shaking rat Kawasaki. The Journal of comparative neurology. vol 383. issue 3. 1997-08-26. PMID:9205047. |
shaking rat kawasaki (srk) is an autosomal recessive mutant rat that exhibits tremor, dystonia, and ataxia and that is characterized by abnormal lamination of the cerebral and cerebellar cortices and the hippocampus. |
1997-08-26 |
2023-08-12 |
mouse |
| K Stasi, A Mitsacos, L C Triarhou, E D Kouvela. Cerebellar grafts partially reverse amino acid receptor changes observed in the cerebellum of mice with hereditary ataxia: quantitative autoradiographic studies. Cell transplantation. vol 6. issue 3. 1997-07-21. PMID:9171167. |
cerebellar grafts partially reverse amino acid receptor changes observed in the cerebellum of mice with hereditary ataxia: quantitative autoradiographic studies. |
1997-07-21 |
2023-08-12 |
mouse |
| K Suzuki, K Meguro, J Nakayama, T Aoki, H Tsurushim. MRI of an infant with Fisher syndrome. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. vol 13. issue 2. 1997-07-17. PMID:9105745. |
the ataxia of fisher syndrome is not compatible with polyneuritis, but can be explained by a cerebellar lesion, as seen in this case. |
1997-07-17 |
2023-08-12 |
Not clear |
| L Calandriello, L Veneziano, A Francia, G Sabbadini, C Colonnese, E Mantuano, C Jodice, F Trettel, P Viviani, M Manfredi, M Frontal. Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13. Brain : a journal of neurology. vol 120 ( Pt 5). 1997-07-10. PMID:9183251. |
a large italian kindred affected with acetazolamide-responsive episodic ataxia is reported, with onset in adulthood, a strong vestibular component during attacks and a high frequency of cerebellar vermis degeneration. |
1997-07-10 |
2023-08-12 |
Not clear |
| T M Gunn, D M Juriloff, M J Harri. Exencephaly and cleft cerebellum in SELH/Bc mouse embryos are alternative developmental consequences of the same underlying genetic defect. Teratology. vol 54. issue 5. 1997-07-08. PMID:9035344. |
the results of this genetic approach have supported the hypothesis, based on observation of embryos, that one basic multifactorial genetic defect in selh mice leads to an abnormal cranial neural tube closure mechanism, to exencephaly to cleft cerebellum, and to ataxia. |
1997-07-08 |
2023-08-12 |
mouse |
| A J Bastia. Mechanisms of ataxia. Physical therapy. vol 77. issue 6. 1997-06-26. PMID:9184691. |
common causes of ataxia include damage of the cerebellum and damage of sensory structures. |
1997-06-26 |
2023-08-12 |
Not clear |
| W Classen, P Gretener, M Rauch, E Weber, G J Krink. Susceptibility of various areas of the nervous system of hens to TOCP-induced delayed neuropathy. Neurotoxicology. vol 17. issue 3-4. 1997-06-23. PMID:9086480. |
ataxia and body weight loss occurred in high-dose animals only, while dose-related neuropathy was seen in the distal tibial nerve, medulla oblongata and cerebellum. |
1997-06-23 |
2023-08-12 |
chicken |
| W Classen, P Gretener, M Rauch, E Weber, G J Krink. Susceptibility of various areas of the nervous system of hens to TOCP-induced delayed neuropathy. Neurotoxicology. vol 17. issue 3-4. 1997-06-23. PMID:9086480. |
ataxia was correlated best with neuropathy in peripheral nerves while degeneration of nerve fibers in the cerebellum, seen best in mid-longitudinal sections, was the most sensitive histological indicator of tocp-induced delayed neuropathy. |
1997-06-23 |
2023-08-12 |
chicken |
| D Liaw, D J Marsh, J Li, P L Dahia, S I Wang, Z Zheng, S Bose, K M Call, H C Tsou, M Peacocke, C Eng, R Parson. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nature genetics. vol 16. issue 1. 1997-06-16. PMID:9140396. |
lhermitte-duclos disease (ldd) cosegregates with a subset of cd families and is associated with macrocephaly, ataxia and dysplastic cerebellar gangliocytomatosis. |
1997-06-16 |
2023-08-12 |
Not clear |
| P Trouillas, T Takayanagi, M Hallett, R D Currier, S H Subramony, K Wessel, A Bryer, H C Diener, S Massaquoi, C M Gomez, P Coutinho, M Ben Hamida, G Campanella, A Filla, L Schut, D Timann, J Honnorat, N Nighoghossian, B Manya. International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome. The Ataxia Neuropharmacology Committee of the World Federation of Neurology. Journal of the neurological sciences. vol 145. issue 2. 1997-06-13. PMID:9094050. |
international cooperative ataxia rating scale for pharmacological assessment of the cerebellar syndrome. |
1997-06-13 |
2023-08-12 |
Not clear |