| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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 |
| John H Pula, Christopher M Gomez, Jorge C Katta. Ophthalmologic features of the common spinocerebellar ataxias. Current opinion in ophthalmology. vol 21. issue 6. 2010-11-22. PMID:20811282. |
the spinocerebellar ataxias (scas) are a phenotypically and genetically diverse group of autosomal dominant disorders that cause pathological degeneration in the cerebellum, brainstem, and retina, resulting in a wide variety of ophthalmologic signs and symptoms. |
2010-11-22 |
2023-08-12 |
Not clear |
| Gülin Oz, Diane Hutter, Ivan Tkác, H Brent Clark, Myron D Gross, Hong Jiang, Lynn E Eberly, Khalaf O Bushara, Christopher M Gome. Neurochemical alterations in spinocerebellar ataxia type 1 and their correlations with clinical status. Movement disorders : official journal of the Movement Disorder Society. vol 25. issue 9. 2010-11-04. PMID:20310029. |
here we tested the sensitivity of high field (4 tesla) proton magnetic resonance spectroscopy ((1)h mrs) to neurochemical alterations in the cerebellum and brainstem in spinocerebellar ataxia type 1 (sca1). |
2010-11-04 |
2023-08-12 |
human |
| Ulf Edener, Janine Wöllner, Ute Hehr, Zacharias Kohl, Stefan Schilling, Friedmar Kreuz, Peter Bauer, Veronica Bernard, Gabriele Gillessen-Kaesbach, Christine Zühlk. Early onset and slow progression of SCA28, a rare dominant ataxia in a large four-generation family with a novel AFG3L2 mutation. European journal of human genetics : EJHG. vol 18. issue 8. 2010-11-01. PMID:20354562. |
autosomal dominantly inherited spinocerebellar ataxias (scas) are a heterogeneous group of neurodegenerative disorders primarily affecting the cerebellum. |
2010-11-01 |
2023-08-12 |
Not clear |
| Ruth Elizabeth Brooke, Laura Corns, Ian James Edwards, Jim Deuchar. Kv3.3 immunoreactivity in the vestibular nuclear complex of the rat with focus on the medial vestibular nucleus: targeting of Kv3.3 neurones by terminals positive for vesicular glutamate transporter 1. Brain research. vol 1345. 2010-10-21. PMID:20471378. |
furthermore, mutations in this gene have been linked to the human disease spinocerebellar ataxia 13, associated with cerebellar and extra-cerebellar symptoms such as imbalance and nystagmus. |
2010-10-21 |
2023-08-12 |
mouse |
| Yuan Yuan, Xin Zhou, Feng Ding, Yumin Liu, Jiancheng T. Molecular genetic analysis of a new form of spinocerebellar ataxia in a Chinese Han family. Neuroscience letters. vol 479. issue 3. 2010-09-27. PMID:20641168. |
the pathological changes of spinocerebellar ataxias (scas), mainly include the degeneration of the cerebellum, spinal cord and brainstem. |
2010-09-27 |
2023-08-12 |
Not clear |
| Alexandra Dur. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond. The Lancet. Neurology. vol 9. issue 9. 2010-09-13. PMID:20723845. |
the designation of the loci, sca for spinocerebellar ataxia, indicates the involvement of at least two systems: the spinal cord and the cerebellum. |
2010-09-13 |
2023-08-12 |
Not clear |
| Antoni Matilla-Dueñas, Ivelisse Sánchez, Marc Corral-Juan, Antoni Dávalos, Ramiro Alvarez, Pilar Latorr. Cellular and molecular pathways triggering neurodegeneration in the spinocerebellar ataxias. Cerebellum (London, England). vol 9. issue 2. 2010-08-12. PMID:19890685. |
the autosomal dominant spinocerebellar ataxias (scas) are a group of progressive neurodegenerative diseases characterised by loss of balance and motor coordination due to the primary dysfunction of the cerebellum. |
2010-08-12 |
2023-08-12 |
Not clear |
| Joyce van de Leemput, Fabienne Wavrant-De Vrièze, Ian Rafferty, Jose M Bras, Paola Giunti, Elizabeth M C Fisher, John A Hardy, Andrew B Singleton, Henry Houlde. Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series. Movement disorders : official journal of the Movement Disorder Society. vol 25. issue 6. 2010-07-28. PMID:20437544. |
spinocerebellar ataxia type 15 and 16 (sca15/16) are autosomal dominant cerebellar ataxias that are slowly progressive with a predominantly pure ataxia phenotype (adca iii). |
2010-07-28 |
2023-08-12 |
Not clear |
| Taiji Tsunemi, Kinya Ishikawa, Kei Tsukui, Takuro Sumi, Ken Kitamura, Hidehiro Mizusaw. The effect of 3,4-diaminopyridine on the patients with hereditary pure cerebellar ataxia. Journal of the neurological sciences. vol 292. issue 1-2. 2010-06-14. PMID:20181362. |
downbeat nystagmus (dbn) is often seen in patients with pure cerebellar type of spinocerebellar ataxia (sca) like spinocerebellar ataxia type 6 (sca6). |
2010-06-14 |
2023-08-12 |
Not clear |