| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| G Stevanin, A Dürr, A Bric. Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology. European journal of human genetics : EJHG. vol 8. issue 1. 2000-04-14. PMID:10713882. |
clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology. |
2000-04-14 |
2023-08-12 |
Not clear |
| G Stevanin, A Dürr, A Bric. Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathology. European journal of human genetics : EJHG. vol 8. issue 1. 2000-04-14. PMID:10713882. |
major advances have been made in the understanding of autosomal dominant cerebellar ataxias since genetic markers came into use in the 1980s. |
2000-04-14 |
2023-08-12 |
Not clear |
| Q Saleem, S Choudhry, M Mukerji, L Bashyam, M V Padma, A Chakravarthy, M C Maheshwari, S Jain, S K Brahmachar. Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation. Human genetics. vol 106. issue 2. 2000-04-13. PMID:10746559. |
expansion of ctg/cag trinucleotide repeats has been shown to cause a number of autosomal dominant cerebellar ataxias (adca) such as sca1, sca2, sca3/ mjd, sca6, sca7, sca8 and drpla. |
2000-04-13 |
2023-08-12 |
Not clear |
| D Timmann, S Watts, J Hor. Causes of left-right ball inaccuracy in overarm throws made by cerebellar patients. Experimental brain research. vol 130. issue 4. 2000-04-05. PMID:10717787. |
cerebellar patients throw inaccurately in the left-right direction but the cause of this multijoint ataxia is unclear. |
2000-04-05 |
2023-08-12 |
human |
| E Maserati, A Verri, L Seghezzi, R Tupler, A Federico, L Tiepolo, P Maraschi. Cerebellar dysgenesis and mental retardation associated with a complex chromosome rearrangement. Annales de genetique. vol 42. issue 4. 2000-03-06. PMID:10674160. |
cerebellar hypoplasia, mild mental retardation, skeletal abnormalities, and ataxia were present in a 40 years old patient with a complex chromosome rearrangement (ccr). |
2000-03-06 |
2023-08-12 |
Not clear |
| F J Carod-Artal, M C del Negro, A P Vargas, I Rizz. [Cerebellar syndrome and peripheral neuropathy as manifestations of infection by HTLV-1 human T-cell lymphotropic virus]. Revista de neurologia. vol 29. issue 10. 2000-02-22. PMID:10637843. |
much less frequently it may precede, or give rise to, a cerebellar syndrome with ataxia and intention tremor. |
2000-02-22 |
2023-08-12 |
human |
| K Phanthumchind. Syndrome of progressive ataxia and palatal myoclonus: a case report. Journal of the Medical Association of Thailand = Chotmaihet thangphaet. vol 82. issue 11. 2000-02-18. PMID:10659552. |
physical examination revealed palatal and tongue myoclonus, cerebellar gait, limb ataxia and spasticity of the lower extremities. |
2000-02-18 |
2023-08-12 |
Not clear |
| C Mauger, J Del-Favero, C Ceuterick, U Lübke, C van Broeckhoven, J Marti. Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibody. Brain research. Molecular brain research. vol 74. issue 1-2. 2000-02-15. PMID:10640674. |
autosomal dominant cerebellar ataxias (adcas) are a complex group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. |
2000-02-15 |
2023-08-12 |
Not clear |
| b' M Svetel, N Vojvodi\\xc4\\x87, S R Filipovi\\xc4\\x87, N Dragasevi\\xc4\\x87, N Sterni\\xc4\\x87, V S Kosti\\xc4\\x8. [Buspirone in the treatment of cerebellar ataxia]. Srpski arhiv za celokupno lekarstvo. vol 127. issue 9-10. 2000-02-10. PMID:10649900.' |
it was found that patients exhibiting mild ataxia showed a better improvement in comparison to the patients who had marked cerebellar symptoms at the beginning of the treatment (table 2). |
2000-02-10 |
2023-08-12 |
Not clear |
| B Schaller, P Bernhard, P Graber, A J Stec. [Cerebellar syndrome after varicella infection without virus identification in cerebrospinal fluid--an important differential ataxia diagnosis]. Praxis. vol 88. issue 46. 2000-01-31. PMID:10593144. |
[cerebellar syndrome after varicella infection without virus identification in cerebrospinal fluid--an important differential ataxia diagnosis]. |
2000-01-31 |
2023-08-12 |
Not clear |
| B Schaller, P Bernhard, P Graber, A J Stec. [Cerebellar syndrome after varicella infection without virus identification in cerebrospinal fluid--an important differential ataxia diagnosis]. Praxis. vol 88. issue 46. 2000-01-31. PMID:10593144. |
we report on a 35 year old female with a 26 day history of an intermittent cerebellar syndrome (dysarthria, ataxia of extremities, gait and trunk, nystagmus), mild meningism, cephalgia, recurrent emesis and nausea. |
2000-01-31 |
2023-08-12 |
Not clear |
| J W Kim, S H Kim, J K Ch. Pseudochoreoathetosis in four patients with hypesthetic ataxic hemiparesis in a thalamic lesion. Journal of neurology. vol 246. issue 11. 2000-01-27. PMID:10631641. |
all the patients had both cerebellar and sensory ataxia. |
2000-01-27 |
2023-08-12 |
Not clear |
| E O Berglund, K K Murai, B Fredette, G Sekerková, B Marturano, L Weber, E Mugnaini, B Ransch. Ataxia and abnormal cerebellar microorganization in mice with ablated contactin gene expression. Neuron. vol 24. issue 3. 2000-01-04. PMID:10595523. |
ataxia and abnormal cerebellar microorganization in mice with ablated contactin gene expression. |
2000-01-04 |
2023-08-12 |
mouse |
| K Sawada, S Komatsu, H Haga, S Oda, Y Fuku. Abnormal expression of tyrosine hydroxylase immunoreactivity in Purkinje cells precedes the onset of ataxia in dilute-lethal mice. Brain research. vol 844. issue 1-2. 1999-12-10. PMID:10536275. |
expression of tyrosine hydroxylase (th) immunostaining in the cerebellum was examined in dilute-lethal mice (dl) prior to and following the onset of ataxia. |
1999-12-10 |
2023-08-12 |
mouse |
| I Samman, W J Schulz-Schaeffer, J C Wöhrle, A Sommer, H A Kretzschmar, M Henneric. Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2. Journal of neurology, neurosurgery, and psychiatry. vol 67. issue 5. 1999-11-19. PMID:10519881. |
a 68 year old woman with sporadic creutzfeldt-jakob disease is described, who neither showed characteristic eeg abnormalities nor a positive test of the neuronal protein 14-3-3 or neuron specific enolase (nse) in csf, despite a clinical presentation with ataxia of cerebellar type, rapidly progressive dementia, myoclonus, and marked hyperintense signal abnormalities in the deep cortical layers and the basal ganglia on t2 and diffusion weighted mri. |
1999-11-19 |
2023-08-12 |
Not clear |
| R C Stern, C M Hulett. Paraneoplastic limbic encephalitis associated with small cell carcinoma of the prostate. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. vol 12. issue 8. 1999-10-28. PMID:10463484. |
a 76-year-old man with primary small cell carcinoma of the prostate died after a subacute illness marked by memory loss and truncal ataxia post-mortem examination of the central nervous system was consistent with limbic encephalitis and cerebellar degeneration. |
1999-10-28 |
2023-08-12 |
Not clear |
| M Hsieh, S Y Li, C J Tsai, Y Y Chen, C S Liu, C Y Chang, L S Ro, D F Chen, S S Chen, C L. Identification of five spinocerebellar ataxia type 2 pedigrees in patients with autosomal dominant cerebellar ataxia in Taiwan. Acta neurologica Scandinavica. vol 100. issue 3. 1999-10-20. PMID:10478584. |
the autosomal dominant cerebellar ataxias (adcas) are a group of genetically diverse neurological conditions linked by progressive deterioration in balance and coordination. |
1999-10-20 |
2023-08-12 |
Not clear |
| D Tentler, P Gustavsson, J Leisti, M Schueler, J Chelly, E Timonen, G Annerén, H F Willard, N Dah. Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia. European journal of human genetics : EJHG. vol 7. issue 5. 1999-10-19. PMID:10439959. |
deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxia. |
1999-10-19 |
2023-08-12 |
Not clear |
| M Matsumoto, E Nagat. Type 1 inositol 1,4,5-trisphosphate receptor knock-out mice: their phenotypes and their meaning in neuroscience and clinical practice. Journal of molecular medicine (Berlin, Germany). vol 77. issue 5. 1999-09-22. PMID:10426189. |
animals exhibited severe neurological symptoms, ataxia and epilepsy, and were shown to be deficient in the cerebellar long-term depression. |
1999-09-22 |
2023-08-12 |
mouse |
| M A Pujana, J Corral, M Gratacòs, O Combarros, J Berciano, D Genís, I Banchs, X Estivill, V Volpin. Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases. The Ataxia Study Group. Human genetics. vol 104. issue 6. 1999-09-02. PMID:10453742. |
autosomal dominant cerebellar ataxias (adca) are a clinically heterogeneous group of neurodegenerative disorders caused by unstable cag repeat expansions encoding polyglutamine tracts. |
1999-09-02 |
2023-08-12 |
cat |