| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| I Bruck, S A Antoniuk, A D Carvalho Neto, A Spessatt. Cerebellar vermis hypoplasia - non progressive congenital ataxia: clinical and radiological findings in a pair of siblings. Arquivos de neuro-psiquiatria. vol 58. issue 3B. 2001-01-11. PMID:11018828. |
these siblings meet many of the criteria described in non-progressive congenital ataxia in which can occur familial cases with cerebellar atrophy, including vermis hypoplasia. |
2001-01-11 |
2023-08-12 |
Not clear |
| M Jäger, F von Rosen, G Fesl, T Gasse. [Typical anticipation in type 7 spinocerebellar ataxia]. Der Nervenarzt. vol 71. issue 10. 2001-01-11. PMID:11082815. |
spinocerebellar ataxia type 7 (sca7) belongs to the category of autosomal dominant cerebellar ataxias (adca). |
2001-01-11 |
2023-08-12 |
Not clear |
| A Durr, A Bric. Clinical and genetic aspects of spinocerebellar degeneration. Current opinion in neurology. vol 13. issue 4. 2000-12-22. PMID:10970057. |
the unstable mutations caused by trinucleotide repeat expansions are responsible for a growing number of inherited cerebellar ataxias. |
2000-12-22 |
2023-08-12 |
Not clear |
| Y G Jeong, B H Hyu. Abnormal synaptic organization between granule cells and Purkinje cells in the new ataxic mutant mouse, pogo. Neuroscience letters. vol 294. issue 2. 2000-12-22. PMID:11058791. |
this correlation between the presence of altered synaptic organization in the cerebellum and ataxia in pogo/pogo mutant mice warrants further investigation. |
2000-12-22 |
2023-08-12 |
mouse |
| A H Németh, E Bochukova, E Dunne, S M Huson, J Elston, M A Hannan, M Jackson, C J Chapman, A M Taylo. Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34. American journal of human genetics. vol 67. issue 5. 2000-12-14. PMID:11022012. |
this work will ultimately allow the disease gene to be identified and its relevance to other types of autosomal recessive cerebellar ataxias to be determined. |
2000-12-14 |
2023-08-12 |
Not clear |
| E V Sullivan, A Deshmukh, J E Desmond, K O Lim, A Pfefferbau. Cerebellar volume decline in normal aging, alcoholism, and Korsakoff's syndrome: relation to ataxia. Neuropsychology. vol 14. issue 3. 2000-11-30. PMID:10928737. |
cerebellar volume decline in normal aging, alcoholism, and korsakoff's syndrome: relation to ataxia. |
2000-11-30 |
2023-08-12 |
Not clear |
| E V Sullivan, A Deshmukh, J E Desmond, K O Lim, A Pfefferbau. Cerebellar volume decline in normal aging, alcoholism, and Korsakoff's syndrome: relation to ataxia. Neuropsychology. vol 14. issue 3. 2000-11-30. PMID:10928737. |
regional distribution but not severity of cerebellar volume deficits is similar in alcoholic individuals whether or not complicated by ks and relates to ataxia. |
2000-11-30 |
2023-08-12 |
Not clear |
| N T Potter, M A Nanc. Genetic testing for ataxia in North America. Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology. vol 5. issue 2. 2000-11-21. PMID:11066010. |
the ataxia molecular diagnostics testing group was established to generate quantitative proficiency and outcomes data regarding molecular testing for the autosomal dominant cerebellar ataxias (spinocerebellar ataxia types 1 [sca-1] through -3, -6, and -7, and dentatorubral-pallidoluysian atrophy) in north america. |
2000-11-21 |
2023-08-12 |
Not clear |
| L Schöls, S Szymanski, S Peters, H Przuntek, J T Epplen, C Hardt, O Ries. Genetic background of apparently idiopathic sporadic cerebellar ataxia. Human genetics. vol 107. issue 2. 2000-10-27. PMID:11030410. |
however, no molecular pathogenic factor is known to cause idiopathic cerebellar ataxias. |
2000-10-27 |
2023-08-12 |
Not clear |
| H Fujigasaki, T Uchihara, S Koyano, K Iwabuchi, S Yagishita, T Makifuchi, A Nakamura, K Ishida, S Toru, S Hirai, K Ishikawa, T Tanabe, H Mizusaw. Ataxin-3 is translocated into the nucleus for the formation of intranuclear inclusions in normal and Machado-Joseph disease brains. Experimental neurology. vol 165. issue 2. 2000-10-26. PMID:10993685. |
machado-joseph disease (mjd)/spinocerebellar ataxia type 3 (sca3) is one of the dominantly inherited cerebellar ataxias. |
2000-10-26 |
2023-08-12 |
Not clear |
| L C Castillo, F Gracia, G C Román, P Levine, W C Reeves, J Kapla. Spinocerebellar syndrome in patients infected with human T-lymphotropic virus types I and II (HTLV-I/HTLV-II): report of 3 cases from Panama. Acta neurologica Scandinavica. vol 101. issue 6. 2000-10-20. PMID:10877159. |
a prospective study of neurological disorders in panama (1985-1990) revealed 13 patients with tsp and 3 with htlv-i/ii-associated spinocerebellar syndrome (hscs) presenting at onset loss of balance, wide-based stance and gait, truncal instability, and mild leg ataxia (vermian cerebellar syndrome), with absent upper limb dysmetria but with postural tremor, downbeat nystagmus, and dysarthria. |
2000-10-20 |
2023-08-12 |
human |
| G Drost, A Verrips, H O Thijssen, Gabreël. Cerebellar involvement as a rare complication of pneumococcal meningitis. Neuropediatrics. vol 31. issue 2. 2000-10-04. PMID:10832585. |
cerebellar involvement after regaining consciousness consisted of a symmetrical ataxia and mutism. |
2000-10-04 |
2023-08-12 |
Not clear |
| R Singh, R A Macdonell, I E Scheffer, K M Crossland, S F Berkovi. Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanisms. Epileptic disorders : international epilepsy journal with videotape. vol 1. issue 2. 2000-09-07. PMID:10937138. |
in family wf, there was a co-occurrence of epilepsy (benign infantile convulsions, idiopathic generalized epilepsy), episodic ataxia (with cerebellar atrophy and without myokymia) and common migraine. |
2000-09-07 |
2023-08-12 |
Not clear |
| S Di Donat. The complex clinical and genetic classification of inherited ataxias. I. Dominant ataxias. Italian journal of neurological sciences. vol 19. issue 6. 2000-08-30. PMID:10935827. |
the clinical classification of autosomal dominant cerebellar ataxias (adcas) is intricate due to the variable and unpredictable association of signs and symptoms of central nervous system (cns) and peripheral nervous system (pns) deterioration during the life of a patient. |
2000-08-30 |
2023-08-12 |
Not clear |
| R Rizzi, V Carelli, L Monari, M Mochi, R Liguori, M Sensi, S Cocozza, A Filla, P Montagn. Cerebellar ataxia, hypogonadism and chorioretinopathy: molecular analysis of an Italian family. Italian journal of neurological sciences. vol 19. issue 1. 2000-08-29. PMID:10935859. |
our findings confirm that ahcr is a distinct disease within the inherited cerebellar ataxias. |
2000-08-29 |
2023-08-12 |
Not clear |
| N Hadj-Sahraoui, F Frédéric, N Delhaye-Bouchaud, J Marian. Gender effect on Purkinje cell loss in the cerebellum of the heterozygous reeler mouse. Journal of neurogenetics. vol 11. issue 1-2. 2000-07-21. PMID:10876649. |
homozygous mutant mice such as staggerer (sg/sg) or reeler (rl/rl) exhibit a marked ataxia associated with an atrophic cerebellum during the first postnatal weeks and a reduced number of purkinje cells, the deficit reaching about 75% in sg/sg and 50% in rl/rl as compared to age- and sex-matched mice from the same strain background. |
2000-07-21 |
2023-08-12 |
mouse |
| A R Mushegian, S A Vishnivetskiy, V V Gurevic. Conserved phosphoprotein interaction motif is functionally interchangeable between ataxin-7 and arrestins. Biochemistry. vol 39. issue 23. 2000-07-20. PMID:10841760. |
olivopontocerebellar atrophy with retinal degeneration is a hereditary neurodegenerative disorder that belongs to the subtype ii of the autosomal dominant cerebellar ataxias and is characterized by early-onset cerebellar and macular degeneration preceded by diagnostically useful tritan colorblindness. |
2000-07-20 |
2023-08-12 |
Not clear |
| A STRUPPLER, E SCHENC. [The so-called relaxation reflex in cerebellar & other ataxias]. Fortschritte der Neurologie, Psychiatrie, und ihrer Grenzgebiete. vol 26. issue 8. 2000-07-01. PMID:13574289. |
[the so-called relaxation reflex in cerebellar & other ataxias]. |
2000-07-01 |
2023-08-12 |
Not clear |
| S Giuffrida, S Lanza, D A Restivo, R Saponara, S C Valvo, F Le Pira, A Trovato Salinaro, F Spinella, A Nicoletti, D F Condorell. Clinical and molecular analysis of 11 Sicilian SCA2 families: influence of gender on age at onset. European journal of neurology. vol 6. issue 3. 2000-06-26. PMID:10210910. |
autosomal dominant cerebellar ataxias (adcas) are a complex group of slowly progressive neurodegenerative disorders characterized by gait and stance ataxia, dysarthria and other symptoms of nervous system involvement. |
2000-06-26 |
2023-08-12 |
Not clear |
| S Kuwahara, M Kawada, S Uga, K Mor. [A case of cerebellar meningo-encephalitis caused by Epstein-Barr virus(EBV): usefulness of Gd-enhanced MRI for detection of the lesions]. No to shinkei = Brain and nerve. vol 52. issue 1. 2000-04-18. PMID:10689689. |
a 61-year-old woman with a history of liver cirrhosis and diabetes mellitus presented with cerebellar signs such as ataxia of the trunk, bilateral upper and lower extremities and slurred speech two weeks after the acute upper respiratory inflammation for several days. |
2000-04-18 |
2023-08-12 |
Not clear |