| 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. |
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 |
| L Serlenga, F Falco, V Castaldo, M Caldarazzo, A Federic. [Eye movement disorders in hereditary degenerative ataxia. Electro-oculographic study of 11 cases]. Acta neurologica. vol 14. issue 4-6. 1993-04-08. PMID:1293987. |
an electro-oculographic study has been performed in 11 patients affected by hereditary degenerative ataxias (5 friedreich's ataxias, 4 olivopontocerebellar atrophies and 2 late onset cerebellar ataxias). |
1993-04-08 |
2023-08-11 |
Not clear |