| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| A Barth, J Bogousslavsky, F Regl. Infarcts in the territory of the lateral branch of the posterior inferior cerebellar artery. Journal of neurology, neurosurgery, and psychiatry. vol 57. issue 9. 1994-10-17. PMID:8089672. |
unilateral limb ataxia without dysarthria or vestibular signs suggests isolated 1pica territory infarction and should allow its differentiation from other cerebellar infarcts. |
1994-10-17 |
2023-08-12 |
Not clear |
| R Sandyk, K Derpapa. Magnetic fields normalize visual evoked potentials and brainstem auditory evoked potentials in multiple sclerosis. The International journal of neuroscience. vol 68. issue 3-4. 1994-09-19. PMID:8063529. |
the present communication concerns a 46 year old woman with a 10 year history of chronic progressive multiple sclerosis (ms) in whom external application of magnetic fields (mf) (7.5 picotesla; 5 hz) during a period of remission resulted in a rapid and dramatic improvement in symptoms including vision, cerebellar symptomatology (ataxia and dysarthria), mood, sleep, bowel and bladder functions as well as fatigue. |
1994-09-19 |
2023-08-12 |
Not clear |
| S Belal, G Cancel, G Stevanin, F Hentati, C Khati, C Ben Hamida, G Auburger, Y Agid, M Ben Hamida, A Bric. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus. Neurology. vol 44. issue 8. 1994-09-12. PMID:8058142. |
autosomal dominant cerebellar ataxias (adca) type 1 are a clinically and genetically heterogeneous group of neurodegenerative disorders. |
1994-09-12 |
2023-08-12 |
Not clear |
| L G Gouw, K B Digre, C P Harris, J H Haines, L J Ptace. Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindred. Neurology. vol 44. issue 8. 1994-09-12. PMID:8058146. |
the autosomal dominant cerebellar ataxias (adca) comprise a heterogeneous group of neurologic disorders characterized by degeneration of the cerebellum, spinal cord, and brainstem. |
1994-09-12 |
2023-08-12 |
Not clear |
| S N al-Din, M Anderson, O Eeg-Olofsson, J V Trontel. Neuro-ophthalmic manifestations of the syndrome of ophthalmoplegia, ataxia and areflexia: a review. Acta neurologica Scandinavica. vol 89. issue 3. 1994-08-08. PMID:8030396. |
the ophthalmoplegia was remarkable in its constant association with a cerebellar type ataxia. |
1994-08-08 |
2023-08-12 |
Not clear |
| Y Ugawa, K Genba-Shimizu, J C Rothwell, M Iwata, I Kanazaw. Suppression of motor cortical excitability by electrical stimulation over the cerebellum in ataxia. Annals of neurology. vol 36. issue 1. 1994-07-29. PMID:8024268. |
suppression of motor cortical excitability by electrical stimulation over the cerebellum in ataxia. |
1994-07-29 |
2023-08-12 |
human |
| Y Ugawa, K Genba-Shimizu, J C Rothwell, M Iwata, I Kanazaw. Suppression of motor cortical excitability by electrical stimulation over the cerebellum in ataxia. Annals of neurology. vol 36. issue 1. 1994-07-29. PMID:8024268. |
we studied the effect of electrical stimulation over the cerebellum on electromyographic responses evoked by magnetic stimulation over the cerebral motor cortex in 41 normal volunteers and 32 patients with ataxia due to various disorders. |
1994-07-29 |
2023-08-12 |
human |
| Y Ugawa, K Genba-Shimizu, J C Rothwell, M Iwata, I Kanazaw. Suppression of motor cortical excitability by electrical stimulation over the cerebellum in ataxia. Annals of neurology. vol 36. issue 1. 1994-07-29. PMID:8024268. |
the technique described here would be useful for distinguishing ataxia due to lesions of cerebellar afferent pathway from other types of cerebellar ataxia. |
1994-07-29 |
2023-08-12 |
human |
| Y Ugawa, R Hanajima, I Kanazaw. Motor cortex inhibition in patients with ataxia. Electroencephalography and clinical neurophysiology. vol 93. issue 3. 1994-07-12. PMID:7515799. |
in all patients with degenerative ataxias and patients with a lesion in the cerebellar thalamus, the "cortico-cortical" inhibition was normal and the "cerebellar" inhibition was absent. |
1994-07-12 |
2023-08-12 |
human |
| H Stibler, G Blennow, B Kristiansson, H Lindehammer, B Hagber. Carbohydrate-deficient glycoprotein syndrome: clinical expression in adults with a new metabolic disease. Journal of neurology, neurosurgery, and psychiatry. vol 57. issue 5. 1994-07-07. PMID:8201322. |
after the age of 15 the disease was mainly characterised by neurological symptoms consisting of non-progressive ataxia associated with cerebellar hypoplasia, stable mental retardation, variable peripheral neuropathy, and strabismus. |
1994-07-07 |
2023-08-12 |
Not clear |
| E Atti. Parieto-cerebellar loop impairment in ataxic hemiparesis: proposed pathophysiology based on an analysis of cerebral blood flow. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. vol 21. issue 1. 1994-06-15. PMID:8180898. |
ataxia of the cerebellar type was unilateral in 15 patients and bilateral in 1 with similar, deep, bilateral causative lesions. |
1994-06-15 |
2023-08-12 |
human |
| S Kojim. [Clinical types of spinocerebellar degeneration and evaluation with MR imaging]. Rinsho shinkeigaku = Clinical neurology. vol 33. issue 12. 1994-06-06. PMID:8174328. |
the second pattern largely included late cortical cerebellar atrophy and hereditary ataxia of holmes type. |
1994-06-06 |
2023-08-12 |
Not clear |
| R Twells, P T Yenchitsomanus, C Sirinavin, R Allotey, N Poungvarin, A Viriyavejakul, C Cemal, J Weber, M Farrall, P Rodpraser. Autosomal dominant cerebellar ataxia with dementia: evidence for a fourth disease locus. Human molecular genetics. vol 3. issue 1. 1994-05-23. PMID:8162021. |
the autosomal dominant cerebellar ataxias have proved particularly difficult to classify due to the lack of phenotypic concordance both within and between families. |
1994-05-23 |
2023-08-12 |
Not clear |
| J S Fain, F H Tomlinson, B W Scheithauer, J E Parisi, G P Fletcher, P J Kelly, G M Mille. Symptomatic glial cysts of the pineal gland. Journal of neurosurgery. vol 80. issue 3. 1994-03-30. PMID:8113858. |
postoperative follow-up review in all 24 cases (range 3 months to 10 years) revealed no complications in 21, mild ocular movement deficit in one, gradually resolving parinaud's syndrome in one, and radiographic evidence of a postoperative venous infarct of the superior cerebellum with ataxia of 1 week's duration in one. |
1994-03-30 |
2023-08-12 |
Not clear |
| 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 |