| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| A Castrioto, P Prontera, E Di Gregorio, V Rossi, L Parnetti, A Rossi, E Donti, A Brusco, P Calabresi, N Tambasc. A novel spinocerebellar ataxia type 15 family with involuntary movements and cognitive decline. European journal of neurology. vol 18. issue 10. 2012-06-19. PMID:21382133. |
sca15 is a recently identified spinocerebellar ataxia with pure cerebellar involvement. |
2012-06-19 |
2023-08-12 |
Not clear |
| M Traoré, T Coulibaly, K G Meilleur, A La Pean, M Sangaré, G Landouré, F Mochel, M Karambé, C O Guinto, K H Fischbec. Clinical and genetic analysis of spinocerebellar ataxia in Mali. European journal of neurology. vol 18. issue 10. 2012-06-19. PMID:21418439. |
autosomal dominant cerebellar ataxia, currently denominated spinocerebellar ataxia (scas), represents a heterogeneous group of neurodegenerative disorders affecting the cerebellum and its connections. |
2012-06-19 |
2023-08-12 |
Not clear |
| Keiko Shimojima, Akihisa Okumura, Jun Natsume, Kaori Aiba, Hirokazu Kurahashi, Tetsuo Kubota, Kenji Yokochi, Toshiyuki Yamamot. Spinocerebellar ataxias type 27 derived from a disruption of the fibroblast growth factor 14 gene with mimicking phenotype of paroxysmal non-kinesigenic dyskinesia. Brain & development. vol 34. issue 3. 2012-06-04. PMID:21600715. |
many types of spinocerebellar ataxias (scas) manifest as progressive disorders with cerebellar involvement. |
2012-06-04 |
2023-08-12 |
Not clear |
| Freya E Cooper, Manon Grube, Katharina Von Kriegstein, Sukhbinder Kumar, Philip English, Thomas P Kelly, Patrick F Chinnery, Timothy D Griffith. Distinct critical cerebellar subregions for components of verbal working memory. Neuropsychologia. vol 50. issue 1. 2012-05-24. PMID:22133495. |
in this study we examined the correlation between cognitive performance and cerebellar integrity in a specific degeneration of the cerebellar cortex: spinocerebellar ataxia type 6 (sca6). |
2012-05-24 |
2023-08-12 |
Not clear |
| Antoni Matilla-Dueñas, Marc Corral-Juan, Victor Volpini, Ivelisse Sanche. The spinocerebellar ataxias: clinical aspects and molecular genetics. Advances in experimental medicine and biology. vol 724. 2012-04-10. PMID:22411256. |
spinocerebellar ataxias (scas) are a highly heterogeneous group of inherited neurological disorders, based on clinical characterization alone with variable degrees of cerebellar ataxia often accompanied by additional cerebellar and noncerebellar symptoms which in most cases defy differentiation. |
2012-04-10 |
2023-08-12 |
Not clear |
| Caroline Kizilyaprak, Danièle Spehner, Didier Devys, Patrick Schult. The linker histone H1C contributes to the SCA7 nuclear phenotype. Nucleus (Austin, Tex.). vol 2. issue 5. 2012-03-06. PMID:21970987. |
spinocerebellar ataxia type 7 (sca7) is a neurodegenerative disease caused by a polyglutamine expansion in ataxin-7, a subunit of the saga coactivator, which leads to progressive neuronal dysfunction and cell death in cerebellum, brainstem and retina. |
2012-03-06 |
2023-08-12 |
mouse |
| Hélio A G Teive, Renato P Munhoz, Tetsuo Ashizaw. Spinocerebellar ataxia type 10: disproportionate cerebellar symptoms among at-risk subjects induced by small amounts of alcohol. Arquivos de neuro-psiquiatria. vol 69. issue 5. 2012-02-10. PMID:22042193. |
spinocerebellar ataxia type 10: disproportionate cerebellar symptoms among at-risk subjects induced by small amounts of alcohol. |
2012-02-10 |
2023-08-12 |
human |
| Federico D'Agata, Paola Caroppo, Bruno Baudino, Marcella Caglio, Michela Croce, Mauro Bergui, Marco Tamietto, Paolo Mortara, Laura Ors. The recognition of facial emotions in spinocerebellar ataxia patients. Cerebellum (London, England). vol 10. issue 3. 2012-01-13. PMID:21503592. |
this pattern has been confirmed in many genotypes of spinocerebellar ataxias (sca), a group of genetically defined pathologies characterized by the degeneration of the cerebellum and its connections. |
2012-01-13 |
2023-08-12 |
Not clear |
| Stephanie A Furrer, Mathini S Mohanachandran, Sarah M Waldherr, Christopher Chang, Vincent A Damian, Bryce L Sopher, Gwenn A Garden, Albert R La Spad. Spinocerebellar ataxia type 7 cerebellar disease requires the coordinated action of mutant ataxin-7 in neurons and glia, and displays non-cell-autonomous bergmann glia degeneration. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 31. issue 45. 2012-01-04. PMID:22072678. |
spinocerebellar ataxia type 7 (sca7) is a dominantly inherited disorder characterized by cerebellum and brainstem neurodegeneration. |
2012-01-04 |
2023-08-12 |
mouse |
| Kerri M Carlson, Laura Melcher, Shaojuan Lai, Huda Y Zoghbi, H Brent Clark, Harry T Or. Characterization of the zebrafish atxn1/axh gene family. Journal of neurogenetics. vol 23. issue 3. 2011-12-27. PMID:19085187. |
expansion of the polyglutamine tract in atxn1 causes the neurodegenerative disease, spinocerebellar ataxia type 1 (sca1) with prominent cerebellar pathology. |
2011-12-27 |
2023-08-12 |
human |
| Gülin Oz, Manda L Vollmers, Christopher D Nelson, Ryan Shanley, Lynn E Eberly, Harry T Orr, H Brent Clar. In vivo monitoring of recovery from neurodegeneration in conditional transgenic SCA1 mice. Experimental neurology. vol 232. issue 2. 2011-12-20. PMID:21963649. |
here we assessed the sensitivity of high field proton magnetic resonance spectroscopy ((1)h mrs) to monitor reversal of neurodegeneration by taking advantage of a well characterized conditional mouse model of spinocerebellar ataxia type 1 (sca1), where the cerebellar pathology and ataxic phenotype are reversible by doxycycline administration. |
2011-12-20 |
2023-08-12 |
mouse |
| José L Pedroso, Pedro Braga-Neto, André C Felício, Camila C H Aquino, Lucila B Fernandes do Prado, Gilmar Fernandes do Prado, Orlando G P Barsottin. Sleep disorders in cerebellar ataxias. Arquivos de neuro-psiquiatria. vol 69. issue 2A. 2011-12-16. PMID:21537570. |
recently, a large body of evidence has demonstrated a high frequency of non-motor manifestations in cerebellar ataxias, specially in autosomal dominant spinocerebellar ataxias (sca). |
2011-12-16 |
2023-08-12 |
Not clear |
| Federico D'Agata, Paola Caroppo, Andrea Boghi, Mario Coriasco, Marcella Caglio, Bruno Baudino, Katiuscia Sacco, Franco Cauda, Elisabetta Geda, Mauro Bergui, Giuliano Geminiani, Gianni Boris Bradac, Laura Orsi, Paolo Mortar. Linking coordinative and executive dysfunctions to atrophy in spinocerebellar ataxia 2 patients. Brain structure & function. vol 216. issue 3. 2011-12-12. PMID:21461742. |
spinocerebellar ataxias type 2 (sca2) is a rare genetic disorder characterised by the degeneration of the cerebellum, its connections and many brainstem areas. |
2011-12-12 |
2023-08-12 |
Not clear |
| You-Kang Chang, Ming-Hsiang Chen, Yi-Hung Chiang, Yu-Fan Chen, Wei-Hsien Ma, Chian-You Tseng, Bin-Wen Soong, Jennifer H Ho, Oscar K Le. Mesenchymal stem cell transplantation ameliorates motor function deterioration of spinocerebellar ataxia by rescuing cerebellar Purkinje cells. Journal of biomedical science. vol 18. 2011-12-12. PMID:21824437. |
spinocerebellar ataxia (sca) refers to a disease entity in which polyglutamine aggregates are over-produced in purkinje cells (pcs) of the cerebellum as well as other neurons in the central nervous system, and the formation of intracellular polyglutamine aggregates result in the loss of neurons as well as deterioration of motor functions. |
2011-12-12 |
2023-08-12 |
human |
| Takahiro Seki, Naoko Adachi, Nana Abe-Seki, Takayuki Shimahara, Hideyuki Takahashi, Kazuhiro Yamamoto, Naoaki Saito, Norio Saka. Elucidation of the molecular mechanism and exploration of novel therapeutics for spinocerebellar ataxia caused by mutant protein kinase Cγ. Journal of pharmacological sciences. vol 116. issue 3. 2011-12-06. PMID:21666345. |
spinocerebellar ataxia (sca) is an inherited neurodegenerative disorder that is characterized by cerebellar atrophy and progressive ataxia and is classified into 31 types by the genetic locus. |
2011-12-06 |
2023-08-12 |
Not clear |
| Ana Solodkin, Christopher M Gome. Spinocerebellar ataxia type 6. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827907. |
spinocerebellar ataxia type 6 (sca6) is the prototype of a pure cerebellar ataxia, associated with a severe form of progressive ataxia and cerebellar dysfunction. |
2011-12-06 |
2023-08-12 |
Not clear |
| Giovanni Stevanin, Alexandra Dür. Spinocerebellar ataxia 13 and 25. Handbook of clinical neurology. vol 103. 2011-12-06. PMID:21827913. |
spinocerebellar ataxia (sca) types 13 and 25 are two genetic entities among the autosomal dominant cerebellar ataxias, initially mapped in two french families to chromosomes 19q and 2p, respectively. |
2011-12-06 |
2023-08-12 |
Not clear |
| Sarah Stricker, Timm Oberwahrenbrock, Hanna Zimmermann, Jan Schroeter, Matthias Endres, Alexander U Brandt, Friedemann Pau. Temporal retinal nerve fiber loss in patients with spinocerebellar ataxia type 1. PloS one. vol 6. issue 7. 2011-12-06. PMID:21829579. |
autosomal dominant spinocerebellar ataxia type 1 is an adult onset progressive disorder with well characterized neurodegeneration in the cerebellum and brainstem. |
2011-12-06 |
2023-08-12 |
Not clear |
| Alessandra Rufa, Pamela Federigh. Fast versus slow: different saccadic behavior in cerebellar ataxias. Annals of the New York Academy of Sciences. vol 1233. 2011-11-30. PMID:21950987. |
spinocerebellar ataxia type 2 (sca2) is a genetic neurodegenerative disorder primarily characterized by involvement of the brainstem and cerebellum, basal ganglia, spinal cord, cerebral cortex, but white matter is also involved. |
2011-11-30 |
2023-08-12 |
Not clear |
| Ulf Edener, Veronica Bernard, Yorck Hellenbroich, Gabriele Gillessen-Kaesbach, Christine Zühlk. Two dominantly inherited ataxias linked to chromosome 16q22.1: SCA4 and SCA31 are not allelic. Journal of neurology. vol 258. issue 7. 2011-11-15. PMID:21267591. |
autosomal dominant spinocerebellar ataxias (scas) are heterogeneous neurological disorders characterised by cerebellar dysfunction mostly due to purkinje cell degeneration. |
2011-11-15 |
2023-08-12 |
Not clear |