| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| K Gustaw, K Beltowska, M M Studzińsk. Neurological and psychological symptoms after the severe acute neuroborreliosis. Annals of agricultural and environmental medicine : AAEM. vol 8. issue 1. 2001-08-23. PMID:11426930. |
the neurological examination showed that 36.4% of the patients experienced such cerebellum integrity disturbances as abnormalities in gait and coordination or even mild ataxia. |
2001-08-23 |
2023-08-12 |
Not clear |
| J Megna, M O'del. Ataxia from lithium toxicity successfully treated with high-dose buspirone: a single-case experimental design. Archives of physical medicine and rehabilitation. vol 82. issue 8. 2001-08-23. PMID:11494197. |
injury to the cerebellum commonly results in clumsiness or uncoordinated movement, which is referred to as ataxia. |
2001-08-23 |
2023-08-12 |
Not clear |
| K Aoki, A Kawata, M Suda, S Hira. [Clinical features of autosomal dominant spinocerebellar ataxias genetically unclassified into any known triplet-repeat diseases]. Rinsho shinkeigaku = Clinical neurology. vol 41. issue 1. 2001-08-09. PMID:11433762. |
based on these, 17 patients from 13 families showed late-onset (mean age at onset: 46 years old) and slowly progressive truncal and limb ataxias of cerebellar origin. |
2001-08-09 |
2023-08-12 |
Not clear |
| W Soong B, C Lu Y, B Choo K, Y Lee . Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6. Archives of neurology. vol 58. issue 7. 2001-08-02. PMID:11448300. |
frequency analysis of autosomal dominant cerebellar ataxias in taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6. |
2001-08-02 |
2023-08-12 |
Not clear |
| H J Schelhaas, P F Ippel, G Hageman, R J Sinke, E N van der Laan, F A Beeme. Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia. Journal of neurology. vol 248. issue 2. 2001-07-26. PMID:11284128. |
the autosomal dominant cerebellar ataxias (adcas) are a heterogeneous group of neurodegenerative disorders characterised by progressive cerebellar dysfunction in combination with a variety of other associative features. |
2001-07-26 |
2023-08-12 |
Not clear |
| M Selim, D A Drachma. Ataxia associated with Hashimoto's disease: progressive non-familial adult onset cerebellar degeneration with autoimmune thyroiditis. Journal of neurology, neurosurgery, and psychiatry. vol 71. issue 1. 2001-07-26. PMID:11413268. |
ataxia associated with hashimoto's disease: progressive non-familial adult onset cerebellar degeneration with autoimmune thyroiditis. |
2001-07-26 |
2023-08-12 |
Not clear |
| H K Naran. A critical review of atypical cerebellum-type Creutzfeldt-Jakob disease: its relationship to "new variant" CJD and bovine spongiform encephalopathy. Experimental biology and medicine (Maywood, N.J.). vol 226. issue 7. 2001-07-19. PMID:11444099. |
for nvcjd, initially, difficulty with balancing and ataxia occurs, confluent spongiform changes are seen in the cerebellum, and a large number of prp plaques are seen. |
2001-07-19 |
2023-08-12 |
cattle |
| K L Quick, L L Duga. Superoxide stress identifies neurons at risk in a model of ataxia-telangiectasia. Annals of neurology. vol 49. issue 5. 2001-06-14. PMID:11357953. |
however, the hallmark of a-t is fulminant degeneration of cerebellar purkinje cells accompanied by a progressive ataxia with features of both cerebellar and basal ganglia dysfunction. |
2001-06-14 |
2023-08-12 |
mouse |
| M White, R Lalonde, T Botez-Marquar. Neuropsychologic and neuropsychiatric characteristics of patients with Friedreich's ataxia. Acta neurologica Scandinavica. vol 102. issue 4. 2001-05-31. PMID:11071106. |
objectives and materials and methods: due to recent evidence of frontal-lobe related dysfunctions in patients with cerebellar atrophy, patients with friedreich's ataxia were compared to normal subjects controlled for age, gender, and educational level on tests measuring information processing speed, visuospatial organization, selective attention, executive functions, and mood. |
2001-05-31 |
2023-08-12 |
human |
| K Bürk, S Bösch, C A Müller, A Melms, C Zühlke, M Stern, I Besenthal, M Skalej, P Ruck, S Ferber, T Klockgether, J Dichgan. Sporadic cerebellar ataxia associated with gluten sensitivity. Brain : a journal of neurology. vol 124. issue Pt 5. 2001-05-31. PMID:11335703. |
the fact that the disease is strongly associated with the same hla haplotypes found in coeliac disease not only demonstrates coeliac disease and ataxia with gluten sensitivity to be part of the same disease entity but supports the hypothesis of an immunological pathogenesis of cerebellar degeneration. |
2001-05-31 |
2023-08-12 |
human |
| H Takegoshi, T Murofush. Vestibular evoked myogenic potentials in patients with spinocerebellar degeneration. Acta oto-laryngologica. vol 120. issue 7. 2001-04-12. PMID:11132714. |
the patients with scd were classified into three groups: those with olivo-ponto-cerebellar ataxia (opca; n = 10); those with cortical cerebellar atrophy (cca; n = 3); and those with machado-joseph disease (mjd; n = 3). |
2001-04-12 |
2023-08-12 |
human |
| D Devos, S Schraen-Maschke, I Vuillaume, K Dujardin, P Nazé, C Willoteaux, A Destée, B Sablonnièr. Clinical features and genetic analysis of a new form of spinocerebellar ataxia. Neurology. vol 56. issue 2. 2001-04-05. PMID:11160961. |
the autosomal dominant cerebellar ataxias (adca) are a clinically heterogeneous group of disorders. |
2001-04-05 |
2023-08-12 |
Not clear |
| Y Ikeda, M Shizuka-Ikeda, M Watanabe, M Schmitt, K Okamoto, M Shoj. Asymptomatic CTG expansion at the SCA8 locus is associated with cerebellar atrophy on MRI. Journal of the neurological sciences. vol 182. issue 1. 2001-03-01. PMID:11102643. |
the ataxia patient showed almost pure cerebellar symptoms, and a cerebral mri of the patient demonstrated significant atrophy of the cerebellar vermis and hemispheres with preservation of brainstem and cerebrum. |
2001-03-01 |
2023-08-12 |
Not clear |
| J Jonasson, V Juvonen, P Sistonen, J Ignatius, D Johansson, E J Björck, J Wahlström, A Melberg, G Holmgren, L Forsgren, M Holmber. Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia. European journal of human genetics : EJHG. vol 8. issue 12. 2001-02-22. PMID:11175279. |
sca7 is one of the least common genetically verified autosomal dominant cerebellar ataxias (adcas) in the world (4.5 to 11.6%), but in sweden and finland sca7 is the most commonly identified form of adca. |
2001-02-22 |
2023-08-12 |
Not clear |
| N Oba, H Horikaw. [A case of midbrain infarction with acute bilateral cerebellar ataxia]. Rinsho shinkeigaku = Clinical neurology. vol 40. issue 6. 2001-02-02. PMID:11086404. |
we consider that bilateral ataxia of the present case was caused by the lesion at the decussation of the superior cerebellar peduncle. |
2001-02-02 |
2023-08-12 |
Not clear |
| N Matsuoka, T Harada, S Kitae, S Nakamura, M Sanomura, K Ishikaw. [Hypothyroidism with severe cerebellar atrophy and ataxia]. Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine. vol 89. issue 8. 2001-01-26. PMID:11062918. |
[hypothyroidism with severe cerebellar atrophy and ataxia]. |
2001-01-26 |
2023-08-12 |
Not clear |
| T Klockgether, U Wüllner, A Spauschus, B Ever. The molecular biology of the autosomal-dominant cerebellar ataxias. Movement disorders : official journal of the Movement Disorder Society. vol 15. issue 4. 2001-01-11. PMID:10928570. |
the molecular biology of the autosomal-dominant cerebellar ataxias. |
2001-01-11 |
2023-08-12 |
Not clear |
| T Klockgether, U Wüllner, A Spauschus, B Ever. The molecular biology of the autosomal-dominant cerebellar ataxias. Movement disorders : official journal of the Movement Disorder Society. vol 15. issue 4. 2001-01-11. PMID:10928570. |
autosomal-dominant cerebellar ataxias (adca) may present as progressive or paroxysmal disorders. |
2001-01-11 |
2023-08-12 |
Not clear |
| C Park, C M Longo, S L Ackerma. Genetic and physical mapping of the cerebellar deficient folia (cdf) locus on mouse chromosome 6. Genomics. vol 69. issue 1. 2001-01-11. PMID:11013084. |
cerebellar deficient folia (cdf) is a recessive mouse mutation causing ataxia and cerebellar cytoarchitectural abnormalities, including hypoplasia, foliation defects, and purkinje cell ectopia. |
2001-01-11 |
2023-08-12 |
mouse |
| I Bruck, S A Antoniuk, A D Carvalho Neto, A Spessatt. Cerebellar vermis hypoplasia - non progressive congenital ataxia: clinical and radiological findings in a pair of siblings. Arquivos de neuro-psiquiatria. vol 58. issue 3B. 2001-01-11. PMID:11018828. |
cerebellar vermis hypoplasia - non progressive congenital ataxia: clinical and radiological findings in a pair of siblings. |
2001-01-11 |
2023-08-12 |
Not clear |