| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| D Sappey-Marinier, A Vighetto, R Peyron, E Broussolle, A Bonmarti. Phosphorus and proton magnetic resonance spectroscopy in episodic ataxia type 2. Annals of neurology. vol 46. issue 2. 1999-08-31. PMID:10443893. |
localized phosphorus (31p) and proton (1h) magnetic resonance spectroscopy was performed in the cerebellum and the occipital lobe of 6 patients with episodic ataxia type 2. |
1999-08-31 |
2023-08-12 |
Not clear |
| K Bürk, T Klockgether, J Dichgan. [New insights in the molecular genetics and pathophysiology of hereditary ataxias]. Der Nervenarzt. vol 70. issue 6. 1999-08-30. PMID:10412692. |
the hereditary ataxias are a heterogeneous group of inherited neurodegenerative disorders characterised by progressive ataxia that results from degeneration of the cerebellum and its afferent and efferent connections. |
1999-08-30 |
2023-08-12 |
Not clear |
| W F Kaemmerer, W C Lo. Cerebellar allografts survive and transiently alleviate ataxia in a transgenic model of spinocerebellar ataxia type-1. Experimental neurology. vol 158. issue 2. 1999-08-24. PMID:10415138. |
cerebellar allografts survive and transiently alleviate ataxia in a transgenic model of spinocerebellar ataxia type-1. |
1999-08-24 |
2023-08-12 |
mouse |
| A H Koeppen, A C Dickson, J B Lamarche, Y Robitaill. Synapses in the hereditary ataxias. Journal of neuropathology and experimental neurology. vol 58. issue 7. 1999-07-27. PMID:10411345. |
the neuropathological phenotype included 18 cases of olivopontocerebellar atrophy (opca), 14 cases of familial cortical cerebellar atrophy (fcca), 4 cases of machado-joseph disease (mjd), and 21 cases of friedreich's ataxia (fa). |
1999-07-27 |
2023-08-12 |
Not clear |
| A H Koeppen, A C Dickson, J B Lamarche, Y Robitaill. Synapses in the hereditary ataxias. Journal of neuropathology and experimental neurology. vol 58. issue 7. 1999-07-27. PMID:10411345. |
the inexorable clinical progression of the hereditary ataxias could not be attributed to synaptic loss in a single anatomic structure of cerebellum, brain stem, or spinal cord. |
1999-07-27 |
2023-08-12 |
Not clear |
| D K Jin, M R Oh, S M Song, S W Koh, M Lee, G M Kim, W Y Lee, C S Chung, K H Lee, J H Im, M J Lee, J W Kim, M S Le. Frequency of spinocerebellar ataxia types 1,2,3,6,7 and dentatorubral pallidoluysian atrophy mutations in Korean patients with spinocerebellar ataxia. Journal of neurology. vol 246. issue 3. 1999-07-14. PMID:10323319. |
autosomal dominant cerebellar ataxias (adcas) are a heterogeneous group of disorders characterized by degenerative symptoms in the cerebellum, spinal cord, and brain stem. |
1999-07-14 |
2023-08-12 |
Not clear |
| N Zecevic, A Milosevic, B E Ehrlic. Calcium signaling molecules in human cerebellum at midgestation and in ataxia. Early human development. vol 54. issue 2. 1999-07-13. PMID:10213289. |
calcium signaling molecules in human cerebellum at midgestation and in ataxia. |
1999-07-13 |
2023-08-12 |
human |
| N Kubis, A Dürr, M Gugenheim, H Chneiweiss, P Mazzetti, A Brice, P Bouch. Polyneuropathy in autosomal dominant cerebellar ataxias: phenotype-genotype correlation. Muscle & nerve. vol 22. issue 6. 1999-07-07. PMID:10366224. |
polyneuropathy in autosomal dominant cerebellar ataxias: phenotype-genotype correlation. |
1999-07-07 |
2023-08-12 |
Not clear |
| N Kubis, A Dürr, M Gugenheim, H Chneiweiss, P Mazzetti, A Brice, P Bouch. Polyneuropathy in autosomal dominant cerebellar ataxias: phenotype-genotype correlation. Muscle & nerve. vol 22. issue 6. 1999-07-07. PMID:10366224. |
autosomal dominant cerebellar ataxias (adcas) are clinically and genetically heterogeneous neurodegenerative disorders. |
1999-07-07 |
2023-08-12 |
Not clear |
| J Quintern, I Immisch, H Albrecht, W Pöllmann, S Glasauer, A Straub. Influence of visual and proprioceptive afferences on upper limb ataxia in patients with multiple sclerosis. Journal of the neurological sciences. vol 163. issue 1. 1999-06-10. PMID:10223413. |
our objective was to investigate how cooling of the arm and vision influence pointing movements in healthy subjects and patients with cerebellar limb ataxia due to clinically proven multiple sclerosis. |
1999-06-10 |
2023-08-12 |
human |
| b' E Bertini, J Campos-Castell\\xc3\\xb. [Congenital ataxias of genetic origin with structural anomalies of the cerebellum]. Revista de neurologia. vol 28. issue 1. 1999-06-07. PMID:10101768.' |
[congenital ataxias of genetic origin with structural anomalies of the cerebellum]. |
1999-06-07 |
2023-08-12 |
Not clear |
| b' E Bertini, J Campos-Castell\\xc3\\xb. [Congenital ataxias of genetic origin with structural anomalies of the cerebellum]. Revista de neurologia. vol 28. issue 1. 1999-06-07. PMID:10101768.' |
after a brief description on the normal development of the cerebellum, we present an extensive review on the neurological disorders due to malformations or metabolic disorders associated with hypoplasia of the cerebellum and congenital ataxia. |
1999-06-07 |
2023-08-12 |
Not clear |
| D Babovic-Vuksanovic, K Snow, M C Patterson, V V Michel. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion. American journal of medical genetics. vol 79. issue 5. 1999-06-02. PMID:9779806. |
autosomal dominant cerebellar ataxias are a heterogeneous group of neurodegenerative disorders that generally present in adulthood. |
1999-06-02 |
2023-08-12 |
Not clear |
| S Kuwabara, M Asahina, M Nakajima, M Mori, T Fukutake, T Hattori, N Yuk. Special sensory ataxia in Miller Fisher syndrome detected by postural body sway analysis. Annals of neurology. vol 45. issue 4. 1999-05-10. PMID:10211482. |
to investigate whether ataxia in miller fisher syndrome (mfs) is caused by loss of proprioception or cerebellar dysfunction, we studied the power spectrum peak of the body sway frequency in 10 mfs patients, and compared the results with those of patients with cerebellar or sensory ataxia. |
1999-05-10 |
2023-08-12 |
Not clear |
| S Kuwabara, M Asahina, M Nakajima, M Mori, T Fukutake, T Hattori, N Yuk. Special sensory ataxia in Miller Fisher syndrome detected by postural body sway analysis. Annals of neurology. vol 45. issue 4. 1999-05-10. PMID:10211482. |
the cerebellar patients had a peak at 2.4 hz, whereas sensory ataxia patients had a 1-hz peak. |
1999-05-10 |
2023-08-12 |
Not clear |
| L Zu, K P Figueroa, R Grewal, S M Puls. Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22. American journal of human genetics. vol 64. issue 2. 1999-04-13. PMID:9973298. |
the autosomal dominant cerebellar ataxias (adcas) are a clinically and genetically heterogeneous group of disorders. |
1999-04-13 |
2023-08-12 |
Not clear |
| E R Korpi, P Koikkalainen, O Y Vekovischeva, R Mäkelä, R Kleinz, M Uusi-Oukari, W Wisde. Cerebellar granule-cell-specific GABAA receptors attenuate benzodiazepine-induced ataxia: evidence from alpha 6-subunit-deficient mice. The European journal of neuroscience. vol 11. issue 1. 1999-04-01. PMID:9987027. |
cerebellar granule-cell-specific gabaa receptors attenuate benzodiazepine-induced ataxia: evidence from alpha 6-subunit-deficient mice. |
1999-04-01 |
2023-08-12 |
mouse |
| N G Daunton, F Tang, M L Corcoran, R A Fox, S Y Ma. Chronic exposure to hypergravity affects thyrotropin-releasing hormone levels in rat brainstem and cerebellum. Biological signals and receptors. vol 7. issue 6. 1999-02-22. PMID:9873155. |
these results suggest that trh may play a role in adaptation to altered gravity as it does in adaptation to altered vestibular input following labyrinthectomy, and in cerebellar and vestibular control of locomotion, as seen in studies of ataxia. |
1999-02-22 |
2023-08-12 |
rat |
| T C Yasha, A Mohanty, S Radhesh, V Santosh, S Das, S K Shanka. Infratentorial dysembryoplastic neuroepithelial tumor (DNT) associated with Arnold-Chiari malformation. Clinical neuropathology. vol 17. issue 6. 1999-02-09. PMID:9832257. |
we report the second case of dnt in the cerebellum occurring in a 20-year-old male presenting with ataxia. |
1999-02-09 |
2023-08-12 |
Not clear |
| A J Raeber, S Brandner, M A Klein, Y Benninger, C Musahl, R Frigg, C Roeckl, M B Fischer, C Weissmann, A Aguzz. Transgenic and knockout mice in research on prion diseases. Brain pathology (Zurich, Switzerland). vol 8. issue 4. 1999-01-29. PMID:9804380. |
unexpectedly, transgenic mice expressing prp with specific amino-proximal truncations spontaneously develop a neurologic syndrome presenting with ataxia and cerebellar lesions. |
1999-01-29 |
2023-08-12 |
mouse |