All Relations between Ataxia and cerebellum

Publication Sentence Publish Date Extraction Date Species
A Tennsted. [Contribution to the Louis-Bar syndrome (ataxia telangiectasia) (author's transl)]. Zentralblatt fur allgemeine Pathologie u. pathologische Anatomie. vol 122. issue 5. 1979-02-12. PMID:726701. we are considering the syndrome as a special form of hereditary ataxias which is morphologically belonging to the systematic atrophies of the cerebellum and, above all, combined with oculo-cutaneous telangiectasia and an immunopathy. 1979-02-12 2023-08-11 Not clear
L M Bahiga, N A Kotb, E A El-Dessouke. Neurological syndromes produced by some toxic metals encountered industrially or environmentally. Zeitschrift fur Ernahrungswissenschaft. vol 17. issue 2. 1978-10-25. PMID:356438. 4) cerebellar disturbances: in the form of ataxia in organic mercury. 1978-10-25 2023-08-11 Not clear
T Kronevi, K Ostensson, J Lesse. A case of partial cerebellar hypoplasia in a cat. Nordisk veterinaermedicin. vol 30. issue 4-5. 1978-09-01. PMID:662593. a case of spontaneous ataxia accompanied by partial cerebellar hypoplasia in a two month old siamese kitten is described. 1978-09-01 2023-08-11 cat
C M Fishe. Ataxic hemiparesis. A pathologic study. Archives of neurology. vol 35. issue 3. 1978-04-26. PMID:629655. this study demonstrates that a lesion of the basis pontis may be associated with a contralateral ataxia that is cerebellar in character. 1978-04-26 2023-08-11 Not clear
R M Welsh, P W Lampert, M B Oldston. Prevention of virus-induced cerebellar diseases by defective-interfering lymphocytic choriomeningitis virus. The Journal of infectious diseases. vol 136. issue 3. 1977-11-25. PMID:903677. standard lcmv injected into lewis rats two days after birth produced a disorder distinguishable clinically by weight loss and ataxia and histologically by infiltration of mononuclear cells and necrosis of the cerebellum. 1977-11-25 2023-08-11 rat
A M Shevchenk. [Clinical picture and pathogenesis of the Refsum syndrome]. Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952). vol 77. issue 6. 1977-10-20. PMID:70917. the clinical picture was characterized by a recurrent syndrome of polyradiculoneurites with a slight protein cellular dissociation in the csf, an expressed sensitive ataxia with elements of cerebellar disorders, a drop in the acuity of sight, audition, intellectual level and a deformation of the talipes of the friedreich type. 1977-10-20 2023-08-11 Not clear
H Stible. Crossed immunoelectrofocusing for identification of normal and abnormal cerebrospinal fluid proteins. A preliminary report. Journal of the neurological sciences. vol 32. issue 3. 1977-09-22. PMID:886359. in addition the unusual csf protein abnormalities occurring in marie-sanger-brown's ataxia and alcoholic cerebellar degeneration have been shown to represent increases of different microheterogeneous forms of transferrin. 1977-09-22 2023-08-11 Not clear
E Boltshauser, W Isle. Joubert syndrome: episodic hyperpnea, abnormal eye movements, retardation and ataxia, associated with dysplasia of the cerebellar vermis. Neuropadiatrie. vol 8. issue 1. 1977-05-12. PMID:576733. a unique syndrome consisting of episodic hyperpnea, abnormal eye movements, ataxia and mental retardation, associated with agenesis of the cerebellar vermis, has been delineated in four siblings by joubert et al. 1977-05-12 2023-08-11 Not clear
L R Northu. Additive effects of ethanol and Purkinje cell loss in the production of ataxia in mice. Psychopharmacology. vol 48. issue 2. 1977-02-24. PMID:826930. the result sindicate a primarily additive effect of ethanol and cerebellar pathology in the production of ataxia. 1977-02-24 2023-08-11 mouse
G Remillard, F Andermann, L Blitzer, E Anderman. Electroencephalographic findings in Friedreich's ataxia. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques. vol 3. issue 4. 1977-02-16. PMID:1000414. impaired function of brain stem inhibitory mechanism may be responsible for the slightly raised incidence of seizures in patients with friedreich's ataxia and other cerebellar degenerations. 1977-02-16 2023-08-11 Not clear
R C Packar. The neurologic complications of alcoholism. American family physician. vol 14. issue 3. 1976-11-01. PMID:183491. other conspicuous clinical pictures include ataxia of cerebellar origin, convulsions, acute hallucinosis, myopathy and coma. 1976-11-01 2023-08-11 Not clear
E Andermann, F Andermann, M Joubert, D Melançon, G Karpati, S Carpente. Three familial midline malformtion syndromes of the central nervous system: agenesis of the corpus callosum and anterior horn-cell disease; agenesis of cerebellar vermis; and atrophy of the cerebellar vermis. Birth defects original article series. vol 11. issue 2. 1976-09-01. PMID:1227532. in another family, mental retardation, ataxia and episodic hyperpnea were associated with agenesis of the cerebellar vermis in 4 sibs. 1976-09-01 2023-08-11 Not clear
E Andermann, F Andermann, M Joubert, D Melançon, G Karpati, S Carpente. Three familial midline malformtion syndromes of the central nervous system: agenesis of the corpus callosum and anterior horn-cell disease; agenesis of cerebellar vermis; and atrophy of the cerebellar vermis. Birth defects original article series. vol 11. issue 2. 1976-09-01. PMID:1227532. in yet another french-canadian family, atrophy of the cerebellar vermis was associated with mental retardation, ataxia and a mild pyramidal syndrome. 1976-09-01 2023-08-11 Not clear
S M Denni. Congenital defects of the nervous system of lambs. Australian veterinary journal. vol 51. issue 8. 1976-01-14. PMID:1103813. the various defects were: hydrocephalus 15, spina bifida 9, meningocoele 8, perosomus elumbis 8, cyclopia 6, cerebellar agenesis 3, aprosopia 3, cranium bifidum 3, anencephaly 2, cerebellar fusion 2, meningo-encephalocoele 2, congenital ataxia 2, micrencephaly 2, cerebellar hypoplasia 1, and acrania 1. 1976-01-14 2023-08-11 Not clear
P A Mårdh, B Ursing, K Lin. Persistent cerebellar symptoms after infection with Mycoplasma pneumoniae. Scandinavian journal of infectious diseases. vol 7. issue 2. 1975-12-29. PMID:1179170. in contrast to published cases with neurological manifestations of infection with m. pneumoniae, the patient was disabled by persistent cerebellar symptoms with generalized ataxia and atactic dysarthria. 1975-12-29 2023-08-11 Not clear
S Deura, M Fujita, S Nagasak. [Proceedings: Neural structure in cerebellar motor ataxia]. Nihon seirigaku zasshi. Journal of the Physiological Society of Japan. vol 36. issue 8-9. 1975-12-20. PMID:4478293. [proceedings: neural structure in cerebellar motor ataxia]. 1975-12-20 2023-08-11 Not clear
D Böh. [Differential diagnosis of cerebellar and spinal ataxia in horse. A case of cerebellar ataxia in a foal]. Berliner und Munchener tierarztliche Wochenschrift. vol 88. issue 5. 1975-06-12. PMID:1120060. [differential diagnosis of cerebellar and spinal ataxia in horse. 1975-06-12 2023-08-11 Not clear
R W Baloh, H R Konrad, V Honrubi. Vestibulo-ocular function in patients with cerebellar atrophy. Neurology. vol 25. issue 2. 1975-05-13. PMID:1078721. eye movement abnormalities were quantiatively assessed in four patients with clinically pure cerebellar atrophy (group a), six patients with brainstem plus cerebellar atrophy (group b), and five patients with friedreich's ataxia (group c). 1975-05-13 2023-08-11 Not clear
J Colover, M Lucas, J A Comley, A M Ro. Neurological abnormalities in the 'cri-du-chat' syndrome. Journal of neurology, neurosurgery, and psychiatry. vol 35. issue 5. 1973-01-05. PMID:5084140. an unusual case of the cri-du-chat syndrome is described in a 6½ year old boy, who, as well as attacks of stridor and choking, showed disorders of spatial perception and cerebellar signs in the form of nystagmus, clumsiness of the hands, and ataxia. 1973-01-05 2023-08-11 Not clear
M Ak. [The cerebellum and ataxia]. Nihon rinsho. Japanese journal of clinical medicine. vol 29. issue 8. 1972-08-18. PMID:4948546. [the cerebellum and ataxia]. 1972-08-18 2023-08-11 Not clear