| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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 |
| 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. |
genetic and laboratory screening for spinocerebellar ataxias and other forms of late-onset cerebellar ataxias were also performed. |
2011-04-15 |
2023-08-12 |
human |
| Yosuke Miyaji, Hiroshi Doi, Shigeru Koyano, Yasuhisa Baba, Yume Suzuki, Yoshiyuki Kuroiw. [A case of spinocerebellar ataxia type 2 presenting with a clinical course similar to spastic paraparesis]. Rinsho shinkeigaku = Clinical neurology. vol 50. issue 9. 2010-12-13. PMID:20960929. |
because brain mri showed mild atrophy of the cerebellar vermis, genetic analysis for spinocerebellar ataxia types 1, 2, 3, 6, 7, 8, 12, and 17, and dentatorubral-pallidoluysian atrophy was performed. |
2010-12-13 |
2023-08-12 |
Not clear |
| Freya E Cooper, Manon Grube, Kelly J Elsegood, John L Welch, Thomas P Kelly, Patrick F Chinnery, Timothy D Griffith. The contribution of the cerebellum to cognition in Spinocerebellar Ataxia Type 6. Behavioural neurology. vol 23. issue 1-2. 2010-12-02. PMID:20714057. |
the contribution of the cerebellum to cognition in spinocerebellar ataxia type 6. |
2010-12-02 |
2023-08-12 |
Not clear |
| Freya E Cooper, Manon Grube, Kelly J Elsegood, John L Welch, Thomas P Kelly, Patrick F Chinnery, Timothy D Griffith. The contribution of the cerebellum to cognition in Spinocerebellar Ataxia Type 6. Behavioural neurology. vol 23. issue 1-2. 2010-12-02. PMID:20714057. |
this study sought evidence for a specific cerebellar contribution to cognition by characterising the cognitive phenotype of spinocerebellar ataxia type 6 (sca-6); an autosomal dominant genetic disease which causes a highly specific late-onset cerebellar degeneration. |
2010-12-02 |
2023-08-12 |
Not clear |