| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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 |
| Gülin Oz, Isabelle Iltis, Diane Hutter, William Thomas, Khalaf O Bushara, Christopher M Gome. Distinct neurochemical profiles of spinocerebellar ataxias 1, 2, 6, and cerebellar multiple system atrophy. Cerebellum (London, England). vol 10. issue 2. 2011-11-10. PMID:20838948. |
distinct neurochemical profiles of spinocerebellar ataxias 1, 2, 6, and cerebellar multiple system atrophy. |
2011-11-10 |
2023-08-12 |
human |
| Gülin Oz, Isabelle Iltis, Diane Hutter, William Thomas, Khalaf O Bushara, Christopher M Gome. Distinct neurochemical profiles of spinocerebellar ataxias 1, 2, 6, and cerebellar multiple system atrophy. Cerebellum (London, England). vol 10. issue 2. 2011-11-10. PMID:20838948. |
we compared cerebellar and brainstem neurochemical profiles measured at 4 t from 26 patients with spinocerebellar ataxias (sca1, n = 9; sca2, n = 7; sca6, n = 5) or cerebellar multiple system atrophy (msa-c, n = 5) and 15 age-matched healthy controls. |
2011-11-10 |
2023-08-12 |
human |
| Ana Solodkin, Eitan Peri, E Elinor Chen, Eshel Ben-Jacob, Christopher M Gome. Loss of intrinsic organization of cerebellar networks in spinocerebellar ataxia type 1: correlates with disease severity and duration. Cerebellum (London, England). vol 10. issue 2. 2011-11-10. PMID:20886327. |
loss of intrinsic organization of cerebellar networks in spinocerebellar ataxia type 1: correlates with disease severity and duration. |
2011-11-10 |
2023-08-12 |
Not clear |
| Ana Solodkin, Eitan Peri, E Elinor Chen, Eshel Ben-Jacob, Christopher M Gome. Loss of intrinsic organization of cerebellar networks in spinocerebellar ataxia type 1: correlates with disease severity and duration. Cerebellum (London, England). vol 10. issue 2. 2011-11-10. PMID:20886327. |
the spinocerebellar ataxias (scas) are a genetically heterogeneous group of cerebellar degenerative disorders, characterized by progressive gait unsteadiness, hand incoordination, and dysarthria. |
2011-11-10 |
2023-08-12 |
Not clear |
| Martin Bares, Ovidiu V Lungu, Tao Liu, Tobias Waechter, Christopher M Gomez, James Ash. The neural substrate of predictive motor timing in spinocerebellar ataxia. Cerebellum (London, England). vol 10. issue 2. 2011-11-10. PMID:21110147. |
we examined the role of the cerebellum and striatum in predictive motor timing in a target interception task in healthy (n = 12) individuals and in subjects (n = 9) with spinocerebellar ataxia types 6 and 8. |
2011-11-10 |
2023-08-12 |
human |
| Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Julio Cesar García-Rodríguez, Luis Enrique Almaguer-Mederos, Tania Cruz-Mariño, José Miguel Laffita-Mes. A comprehensive review of spinocerebellar ataxia type 2 in Cuba. Cerebellum (London, England). vol 10. issue 2. 2011-11-10. PMID:21399888. |
spinocerebellar ataxia type 2 (sca2) is an autosomal dominant cerebellar ataxia characterized by a progressive cerebellar syndrome associated to saccadic slowing, peripheral neuropathy, cognitive disorders, and other multisystem features. |
2011-11-10 |
2023-08-12 |
human |
| Vikram G Shakkottai, Maria do Carmo Costa, James M Dell'Orco, Ananthakrishnan Sankaranarayanan, Heike Wulff, Henry L Paulso. Early changes in cerebellar physiology accompany motor dysfunction in the polyglutamine disease spinocerebellar ataxia type 3. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 31. issue 36. 2011-10-31. PMID:21900579. |
early changes in cerebellar physiology accompany motor dysfunction in the polyglutamine disease spinocerebellar ataxia type 3. |
2011-10-31 |
2023-08-12 |
mouse |
| Vikram G Shakkottai, Maria do Carmo Costa, James M Dell'Orco, Ananthakrishnan Sankaranarayanan, Heike Wulff, Henry L Paulso. Early changes in cerebellar physiology accompany motor dysfunction in the polyglutamine disease spinocerebellar ataxia type 3. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 31. issue 36. 2011-10-31. PMID:21900579. |
the relationship between cerebellar dysfunction, motor symptoms, and neuronal loss in the inherited ataxias, including the polyglutamine disease spinocerebellar ataxia type 3 (sca3), remains poorly understood. |
2011-10-31 |
2023-08-12 |
mouse |
| L Eichler, B Bellenberg, H K Hahn, O Köster, L Schöls, C Luka. Quantitative assessment of brain stem and cerebellar atrophy in spinocerebellar ataxia types 3 and 6: impact on clinical status. AJNR. American journal of neuroradiology. vol 32. issue 5. 2011-09-29. PMID:21372168. |
quantitative assessment of brain stem and cerebellar atrophy in spinocerebellar ataxia types 3 and 6: impact on clinical status. |
2011-09-29 |
2023-08-12 |
Not clear |
| Carsten Lukas, Barbara Bellenberg, Odo Köster, Sebastian Greschner, Horst K Hah. A new sulcus-corrected approach for assessing cerebellar volume in spinocerebellar ataxia. Psychiatry research. vol 193. issue 2. 2011-08-23. PMID:21680158. |
a new sulcus-corrected approach for assessing cerebellar volume in spinocerebellar ataxia. |
2011-08-23 |
2023-08-12 |
human |
| Carsten Lukas, Barbara Bellenberg, Odo Köster, Sebastian Greschner, Horst K Hah. A new sulcus-corrected approach for assessing cerebellar volume in spinocerebellar ataxia. Psychiatry research. vol 193. issue 2. 2011-08-23. PMID:21680158. |
we present a new fast and reliable sulcus-corrected approach for quantitative assessment of cerebellar atrophy, evaluated on patients with spinocerebellar ataxia (sca). |
2011-08-23 |
2023-08-12 |
human |
| Fadi A Issa, Christopher Mazzochi, Allan F Mock, Diane M Papazia. Spinocerebellar ataxia type 13 mutant potassium channel alters neuronal excitability and causes locomotor deficits in zebrafish. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 31. issue 18. 2011-08-05. PMID:21543613. |
mutations in the kv3.3 voltage-gated k(+) channel cause spinocerebellar ataxia type 13 (sca13), a human autosomal-dominant disease characterized by locomotor impairment and the death of cerebellar neurons. |
2011-08-05 |
2023-08-12 |
human |
| Ellis Chan, Perrine Charles, Pascale Ribai, Cyril Goizet, Cecilia Marelli, Carlo-Maria Vincitorio, Alice Le Bayon, Lucie Guyant-Maréchal, Nadia Vandenberghe, Mathieu Anheim, David Devos, Leorah Freeman, Isabelle Le Ber, Karine N'Guyen, Maya Tchikviladzé, Pierre Labauge, Didier Hannequin, Alexis Brice, Alexandra Durr, Sophie Tezenas du Montce. Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxias. Movement disorders : official journal of the Movement Disorder Society. vol 26. issue 3. 2011-07-29. PMID:21287600. |
quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxias. |
2011-07-29 |
2023-08-12 |
Not clear |
| Susan L Perlma. Spinocerebellar degenerations. Handbook of clinical neurology. vol 100. 2011-07-12. PMID:21496573. |
the spinocerebellar ataxias (sca) are a large group of inherited disorders affecting the cerebellum and its afferent and efferent pathways. |
2011-07-12 |
2023-08-12 |
Not clear |
| Pamela Federighi, Gabriele Cevenini, Maria T Dotti, Francesca Rosini, Elena Pretegiani, Antonio Federico, Alessandra Ruf. Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias. Brain : a journal of neurology. vol 134. issue Pt 3. 2011-04-15. PMID:21354979. |
differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias. |
2011-04-15 |
2023-08-12 |
human |
| Pamela Federighi, Gabriele Cevenini, Maria T Dotti, Francesca Rosini, Elena Pretegiani, Antonio Federico, Alessandra Ruf. Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias. Brain : a journal of neurology. vol 134. issue Pt 3. 2011-04-15. PMID:21354979. |
we investigated the different extent of saccade dynamic abnormalities in spinocerebellar ataxia type 2 and late-onset cerebellar ataxias, genetically undefined and with prevalent cerebellar atrophy. |
2011-04-15 |
2023-08-12 |
human |