| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| J Roger, J F Pellissier, C Dravet, M Bureau-Paillas, M Arnoux, J L Larrie. [Spinocerebellar degeneration, optic atrophy, epilepsy, myoclonus and mitochondrial myopathy: a case report (author's transl)]. Revue neurologique. vol 138. issue 3. 1982-10-12. PMID:6810437. |
diagnosis was established as myoclonic cerebellar dyssynergy with spastic hereditary ataxia and leber's disease. |
1982-10-12 |
2023-08-12 |
Not clear |
| A E Hardin. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'. Brain : a journal of neurology. vol 105. issue Pt 1. 1982-06-21. PMID:7066668. |
the clinical features and classification of the late onset autosomal dominant cerebellar ataxias. |
1982-06-21 |
2023-08-12 |
Not clear |
| A E Hardin. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'. Brain : a journal of neurology. vol 105. issue Pt 1. 1982-06-21. PMID:7066668. |
the three other families contained patients with clinically distinct syndromes which were: cerebellar ataxia with pigmentary retinal degeneration; a later onset (over 60 years) 'pure' cerebellar syndrome; and an ataxia disorder associated with myoclonus and deafness. |
1982-06-21 |
2023-08-12 |
Not clear |
| A E Hardin. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'. Brain : a journal of neurology. vol 105. issue Pt 1. 1982-06-21. PMID:7066668. |
a simple classification of the autosomal dominant cerebellar ataxias is proposed and discussed in relation to previous attempts to classify these disorders on clinical and pathological grounds. |
1982-06-21 |
2023-08-12 |
Not clear |
| L R Caplan, J A Goodwi. Lateral tegmental brainstem hemorrhages. Neurology. vol 32. issue 3. 1982-05-12. PMID:7199635. |
the syndrome is relatively consistent and includes (1) ipsilateral conjugate gaze palsy, (2) ipsilateral internuclear ophthalmoplegia, (3) small reactive pupils with a smaller pupil ipsilateral to the lesion, (4) limb ataxia of the cerebellar type (often greater ipsilaterally), (5) contralateral hemiplegia, and (6) contralateral severe hemisensory loss. |
1982-05-12 |
2023-08-12 |
Not clear |
| N Sunohara, M Mukoyama, Y Mano, E Toyoshima, E Satoyosh. [Frontal pseudoataxia, discussion on its mechanism (author's transl)]. Rinsho shinkeigaku = Clinical neurology. vol 21. issue 8. 1982-04-20. PMID:7326887. |
pseudoataxia of this patient differed from the typical cerebellar or vestibular ataxia. |
1982-04-20 |
2023-08-12 |
Not clear |
| H Bachmann, J Lössne. [Hereditary ataxia-problems in the classification, genetics and genetic counseling]. Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete. vol 36. issue 11. 1982-01-20. PMID:7303765. |
own observations of two of the most important hereditary forms of ataxia, of friedreich's disease and of the autosomal dominant cerebellar ataxias (pierre marie) make clear the problems of the diagnostic limitation and of the genetic advice. |
1982-01-20 |
2023-08-12 |
Not clear |
| K Kondo, K Hirota, T Katagir. Genetic and clinical patterns of heritable cerebellar ataxias in adults. II. Clinical manifestations. Journal of medical genetics. vol 18. issue 4. 1981-11-24. PMID:7277421. |
genetic and clinical patterns of heritable cerebellar ataxias in adults. |
1981-11-24 |
2023-08-12 |
Not clear |
| A E Hardin. "Idiopathic" late onset cerebellar ataxia. A clinical and genetic study of 36 cases. Journal of the neurological sciences. vol 51. issue 2. 1981-11-22. PMID:7276977. |
the first was composed of 12 cases in whom truncal ataxia was more marked than limb ataxia and onset was relatively late (mean 54.75 years); these correspond to the marie-foix-alajouanine type of cerebellar degeneration. |
1981-11-22 |
2023-08-12 |
Not clear |
| L C Cork, J C Troncoso, D L Pric. Canine inherited ataxia. Annals of neurology. vol 9. issue 5. 1981-10-14. PMID:7271243. |
a previously unrecognized canine disorder consists of familial cortical cerebellar degeneration with many characteristics that are similar to inherited ataxias in humans. |
1981-10-14 |
2023-08-12 |
human |
| T N Seyfried, T Itoh, G H Glaser, N Miyazawa, R K Y. Cerebellar gangliosides and phospholipids in mutant mice with ataxia and epilepsy: the Tottering/Leaner syndrome. Brain research. vol 216. issue 2. 1981-09-25. PMID:7248784. |
cerebellar gangliosides and phospholipids in mutant mice with ataxia and epilepsy: the tottering/leaner syndrome. |
1981-09-25 |
2023-08-12 |
mouse |
| J P Willner, G A Grabowski, R E Gordon, A N Bender, R J Desnic. Chronic GM2 gangliosidosis masquerading as atypical Friedreich ataxia: clinical, morphologic, and biochemical studies of nine cases. Neurology. vol 31. issue 7. 1981-08-27. PMID:6454083. |
symptoms included early onset of cerebellar signs (tremor, incoordination, and dysarthia) and, with maturity, the development of upper and lower motor neuron disorders, marked dysarthia, and ataxia. |
1981-08-27 |
2023-08-12 |
Not clear |
| I R Livingstone, F L Mastaglia, R J Pennington, C Skilbec. Choline chloride in the treatment of cerebellar and spinocerebellar ataxia. Journal of the neurological sciences. vol 50. issue 2. 1981-07-23. PMID:7229661. |
the use of orally administered choline chloride in the treatment of cerebellar and spinocerebellar ataxia was investigated by a short-term double-blind crossover trial in 20 patients with ataxia. |
1981-07-23 |
2023-08-12 |
Not clear |
| I R Livingstone, F L Mastaglia, R J Pennington, C Skilbec. Choline chloride in the treatment of cerebellar and spinocerebellar ataxia. Journal of the neurological sciences. vol 50. issue 2. 1981-07-23. PMID:7229661. |
mild but significant improvement in upper limb co-ordination was noted in 3 patients with friedreich's ataxia, 3 with mixed ataxia and 4 patients with primary cerebellar degeneration. |
1981-07-23 |
2023-08-12 |
Not clear |
| S Goldber. Principles of neurologic localization. American family physician. vol 23. issue 4. 1981-05-21. PMID:6259916. |
higher level, organized dysfunction points to the cerebrum; ataxia during intentional movements indicates cerebellar involvement, and sudden, unintended movements suggest basal ganglia disorders. |
1981-05-21 |
2023-08-12 |
Not clear |
| K Kondo, I Sobu. Genetic and clinical patterns of heritable cerebellar ataxias in adults. I. Genetic analyses. Journal of medical genetics. vol 17. issue 6. 1981-05-21. PMID:7205427. |
genetic and clinical patterns of heritable cerebellar ataxias in adults. |
1981-05-21 |
2023-08-12 |
Not clear |
| R G Miller, H J Freun. Cerebellar dyssynergia in humans--a quantitative analysis. Annals of neurology. vol 8. issue 6. 1981-05-21. PMID:7212645. |
patients with cerebellar lesions and limb ataxia performed two types of continuous tracking tasks involving flexion and extension of the index finger. |
1981-05-21 |
2023-08-12 |
human |
| J Lapresle, A Annab. [Congenital and sporadic atrophy of the granular layer of the cerebellum with secondary pontocerebellar degeneration (author's transl)]. Revue neurologique. vol 135. issue 12. 1981-04-13. PMID:7466115. |
by analogy with herringham and andrewes cat ataxia due to a perinatal virus infection (margolis and kilham), it can be hypothesized that granular cerebellar atrophy in man is related to an injury incurred at a "favorable" moment in histogenesis, that is, between the 3rd and 6th month of fetal life. |
1981-04-13 |
2023-08-12 |
cat |
| R M Barlo. Morphogenesis of cerebellar lesions in bovine familial convulsions and ataxia. Veterinary pathology. vol 18. issue 2. 1981-04-13. PMID:7467075. |
morphogenesis of cerebellar lesions in bovine familial convulsions and ataxia. |
1981-04-13 |
2023-08-12 |
cattle |
| R M Barlo. Morphogenesis of cerebellar lesions in bovine familial convulsions and ataxia. Veterinary pathology. vol 18. issue 2. 1981-04-13. PMID:7467075. |
cerebellar lesions develop in a heritable disorder characterized by recurrent episodic seizures in newborn and young calves and by ataxia in survivors of several bouts of convulsions. |
1981-04-13 |
2023-08-12 |
cattle |