| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| S Kondo, M Tanaka, X Sun, Y Sakai, S Hira. [Study of patients with spinocerebellar degeneration using positron emission tomography]. Rinsho shinkeigaku = Clinical neurology. vol 33. issue 10. 1994-03-02. PMID:8293603. |
cbf/mcbf and cmro2/mcmro2 were significantly decreased in patients with olivopontocerebellar atrophy (opca) and menzel type of hereditary ataxia (menzel type) in the cerebellar hemispheres, cerebellar vermis, and brainstem, whereas patients with late cortical cerebellar atrophy (lcca) and holmes type of hereditary ataxia (holmes type) revealed a significant decrease of cbf/mcbf and cmro2/mcmro2 in the cerebellar hemispheres and cerebellar vermis, but not in the brainstem. |
1994-03-02 |
2023-08-12 |
human |
| S Kondo, M Tanaka, X Sun, Y Sakai, S Hira. [Study of patients with spinocerebellar degeneration using positron emission tomography]. Rinsho shinkeigaku = Clinical neurology. vol 33. issue 10. 1994-03-02. PMID:8293603. |
in patients with lcca and holmes type, the severity of upper limb ataxia and dysdiadochokinesis were significantly correlated with cbf/mcbf and cmro2/mcmro2 in the cerebellar hemispheres and brainstem. |
1994-03-02 |
2023-08-12 |
human |
| M Gorassini, A Prochazka, J L Taylo. Cerebellar ataxia and muscle spindle sensitivity. Journal of neurophysiology. vol 70. issue 5. 1994-02-25. PMID:8294959. |
little direct information is available on animals or humans performing voluntary movements and exhibiting ataxia or other cerebellar symptoms. |
1994-02-25 |
2023-08-12 |
Not clear |
| A S Najim al-Din, J V Trontelj, M Anderson, O Eeg-Olofsso. Ataxia and areflexia in SOAA. Acta neurologica Scandinavica. vol 88. issue 5. 1994-02-25. PMID:8296537. |
all showed features of cerebellar rather than sensory ataxia. |
1994-02-25 |
2023-08-12 |
Not clear |
| G Stevanin, E Le Guern, N Ravisé, H Chneiweiss, A Dürr, G Cancel, A Vignal, A L Boch, M Ruberg, C Pene. A third locus for autosomal dominant cerebellar ataxia type I maps to chromosome 14q24.3-qter: evidence for the existence of a fourth locus. American journal of human genetics. vol 54. issue 1. 1994-02-04. PMID:8279460. |
the autosomal dominant cerebellar ataxias (adca) type i are a group of neurological disorders that are clinically and genetically heterogeneous. |
1994-02-04 |
2023-08-12 |
Not clear |
| M S Liebling, T J Starc, W H McAlister, C B Ruzal-Shapiro, S J Abramson, W E Berdo. ACTH induced adrenal enlargement in infants treated for infantile spasms and acute cerebellar encephalopathy. Pediatric radiology. vol 23. issue 6. 1994-01-13. PMID:8255650. |
acth is used in childhood to treat infantile spasms and acute cerebellar encephalopathy (opsoclonus-cerebellar ataxia syndrome). |
1994-01-13 |
2023-08-12 |
Not clear |
| P Keswani, R Gupta, K P Singh, P Juneja, P Chablan. Unilateral ataxia following herpes zoster of spinal C4 segment. The Journal of the Association of Physicians of India. vol 41. issue 3. 1993-12-07. PMID:8226607. |
a 55 year old male developed cerebellar speech, right sided ataxia and intention tremor, three weeks after herpes zoster of right spinal c4 segment. |
1993-12-07 |
2023-08-12 |
Not clear |
| A Wittkämper, K Wessel, H Brückman. CT in autosomal dominant and idiopathic cerebellar ataxia. Neuroradiology. vol 35. issue 7. 1993-12-03. PMID:8232880. |
atrophy on ct often fails to differentiate autosomal dominant or idiopathic cerebellar ataxias in ca or opca: patients with ca can also have atrophy of the brain stem and patients with opca do not necessarily show brain stem atrophy. |
1993-12-03 |
2023-08-12 |
Not clear |
| C Hübner, G F Hoffmann, C Charpentier, K M Gibson, B Finckh, H Puhl, H A Lehr, A Kohlschütte. Decreased plasma ubiquinone-10 concentration in patients with mevalonate kinase deficiency. Pediatric research. vol 34. issue 2. 1993-12-03. PMID:8233712. |
patients with mevalonate kinase deficiency suffer from psychomotor retardation, ataxia with progredient cerebellar atrophy, and myopathy. |
1993-12-03 |
2023-08-12 |
Not clear |
| A Wakisaka, H Sasak. [Recent progress of research on hereditary spinocerebellar degeneration]. Nihon rinsho. Japanese journal of clinical medicine. vol 51. issue 9. 1993-11-22. PMID:8411730. |
in the japanese, olivo-ponto-cerebellar atrophy (opca), machado-joseph disease (mjd) and dominant cortical cerebellar atrophy (cca) are the most popular forms of ataxia. |
1993-11-22 |
2023-08-12 |
Not clear |
| J M Stevens, W A Serva, B E Kendall, A R Valentine, J R Ponsfor. Chiari malformation in adults: relation of morphological aspects to clinical features and operative outcome. Journal of neurology, neurosurgery, and psychiatry. vol 56. issue 10. 1993-11-19. PMID:8410004. |
patients with the most severe cerebellar malformation, defined as descent of the cerebellar tonsils to or below the axis, had disabling ataxia and nystagmus more frequently. |
1993-11-19 |
2023-08-12 |
Not clear |
| S Gispert, R Twells, G Orozco, A Brice, J Weber, L Heredero, K Scheufler, B Riley, R Allotey, C Nother. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1. Nature genetics. vol 4. issue 3. 1993-09-24. PMID:8358438. |
the autosomal dominant cerebellar ataxias (adca) are a group of neurodegenerative disorders characterized by onset with gait ataxia, dysarthria, dysmetria and dysdiadochokinesia. |
1993-09-24 |
2023-08-12 |
Not clear |
| P Trouilla. The cerebellar serotoninergic system and its possible involvement in cerebellar ataxia. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. vol 20 Suppl 3. 1993-08-26. PMID:8334597. |
in human heredoataxias (friedreich's ataxia and cerebellar cortical atrophy), serotoninergic disturbances have been observed in the csf, including low 5-hiaa values and an increased serotoninergic turnover. |
1993-08-26 |
2023-08-12 |
human |
| A Plaitaki. Modulation of monoaminergic and amino acid transmission as a means for therapeutic intervention in ataxia. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. vol 20 Suppl 3. 1993-08-26. PMID:8392900. |
of the monoamines, serotonin has been proposed as a neuromodulator in the cerebellum and is thought to play a role in the pathophysiology of ataxia in animal models, and human cerebellar disorders. |
1993-08-26 |
2023-08-12 |
human |
| J A Zwart, G Bovim, H J Johnsen, H Schrade. [Mononucleosis and neurological manifestations]. Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. vol 113. issue 12. 1993-08-16. PMID:7741803. |
2 had cerebellar symptoms, with ataxia and disturbance of gait. |
1993-08-16 |
2023-08-12 |
Not clear |
| A Chiò, L Orsi, P Mortara, D Schiffe. Early onset cerebellar ataxia with retained tendon reflexes: prevalence and gene frequency in an Italian population. Clinical genetics. vol 43. issue 4. 1993-08-16. PMID:8330454. |
a genetic epidemiologic analysis of early onset cerebellar ataxias (eoca) with retained tendon reflexes was performed in a defined area of northwestern italy. |
1993-08-16 |
2023-08-12 |
Not clear |
| R Lalonde, C C Joyal, J M Guastavino, M I Bote. Hole poking and motor coordination in lurcher mutant mice. Physiology & behavior. vol 54. issue 1. 1993-08-12. PMID:8327607. |
lurcher mutant mice, a cerebellar mutant displaying ataxia and equilibrium deficits, had fewer hole pokes in a 16-hole matrix than normal mice. |
1993-08-12 |
2023-08-12 |
mouse |
| D M Juriloff, M J Harris, M L Harrod, T M Gunn, J E Mille. Ataxia and a cerebellar defect in the exencephaly-prone SELH/Bc mouse stock. Teratology. vol 47. issue 4. 1993-08-05. PMID:8322227. |
ataxia and a cerebellar defect in the exencephaly-prone selh/bc mouse stock. |
1993-08-05 |
2023-08-12 |
mouse |
| A Bonni, R del Carpio-O'Donovan, Y Robitaille, E Andermann, F Andermann, D A Arnol. Magnetic resonance imaging in the diagnosis of dominantly inherited cerebello-olivary atrophy: a clinicopathologic study. Canadian Association of Radiologists journal = Journal l'Association canadienne des radiologistes. vol 44. issue 3. 1993-07-07. PMID:8504332. |
the affected members of each family demonstrated a stereotyped, progressive, "pure" cerebellar syndrome, which began with gait ataxia followed years later by dysarthria and limb ataxia. |
1993-07-07 |
2023-08-12 |
Not clear |
| F Hentati, C Ben Hamida, M Zeghal, M Kamoun, B Fezaa, M Ben Hamid. Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum. Neuromuscular disorders : NMD. vol 2. issue 5-6. 1993-05-27. PMID:1300184. |
in addition, in the three oldest patients there were cerebellar signs, ataxia and babinski signs. |
1993-05-27 |
2023-08-11 |
Not clear |