| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Sylvia M Boesch, Christian Wolf, Klaus Seppi, Stephan Felber, Gregor K Wenning, Michael Schock. Differentiation of SCA2 from MSA-C using proton magnetic resonance spectroscopic imaging. Journal of magnetic resonance imaging : JMRI. vol 25. issue 3. 2007-04-19. PMID:17326083. |
to assess and compare biochemical and volumetric features of the cerebellum in patients with spinocerebellar ataxia type 2 (sca2) and patients with the cerebellar variant of multiple system atrophy (msa-c). |
2007-04-19 |
2023-08-12 |
Not clear |
| Melissa J Nirenberg, Jenny Libien, Jean-Paul Vonsattel, Stanley Fah. Multiple system atrophy in a patient with the spinocerebellar ataxia 3 gene mutation. Movement disorders : official journal of the Movement Disorder Society. vol 22. issue 2. 2007-03-23. PMID:17133518. |
the cerebellar variant of multiple system atrophy (msa-c) has overlapping clinical features with the hereditary spinocerebellar ataxias (scas), but can usually be distinguished on a clinical basis. |
2007-03-23 |
2023-08-12 |
Not clear |
| Hiroshi Morita, Kunihiro Yoshida, Kayo Suzuki, Shu-Ichi Iked. A Japanese case of SCA14 with the Gly128Asp mutation. Journal of human genetics. vol 51. issue 12. 2007-02-27. PMID:17024314. |
spinocerebellar ataxia type 14 (sca14) is a rare form of autosomal dominant cerebellar ataxias caused by mutations in the protein kinase cgamma gene (prkcg). |
2007-02-27 |
2023-08-12 |
Not clear |
| b' Jos\\xc3\\xa9 Gazulla, Mari A Tintor\\xc3\\xa. The P/Q-type voltage-dependent calcium channel as pharmacological target in spinocerebellar ataxia type 6: gabapentin and pregabalin may be of therapeutic benefit. Medical hypotheses. vol 68. issue 1. 2007-01-30. PMID:16899342.' |
spinocerebellar ataxia type 6 (sca 6) is an autosomal dominant cerebellar degeneration that shares neuropathological findings with late-onset cortical cerebellar atrophy (cca). |
2007-01-30 |
2023-08-12 |
xenopus_laevis |
| Carsten Lukas, Ludger Schöls, Barbara Bellenberg, Udo Rüb, Horst Przuntek, Gebhard Schmid, Odo Köster, Boris Sucha. Dissociation of grey and white matter reduction in spinocerebellar ataxia type 3 and 6: a voxel-based morphometry study. Neuroscience letters. vol 408. issue 3. 2007-01-23. PMID:17005321. |
the aim of this study was to examine the different patterns of cerebellar and/or brainstem atrophy in spinocerebellar ataxia (sca) type 3 and 6. |
2007-01-23 |
2023-08-12 |
human |
| Y Hellenbroich, K Gierga, E Reusche, E Schwinger, T Deller, R A I de Vos, C Zühlke, U Rü. Spinocerebellar ataxia type 4 (SCA4): Initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration. Journal of neural transmission (Vienna, Austria : 1996). vol 113. issue 7. 2007-01-05. PMID:16362839. |
spinocerebellar ataxia type 4 (sca4): initial pathoanatomical study reveals widespread cerebellar and brainstem degeneration. |
2007-01-05 |
2023-08-12 |
Not clear |
| K Lasek, R Lencer, C Gaser, J Hagenah, U Walter, A Wolters, N Kock, S Steinlechner, M Nagel, C Zühlke, M-F Nitschke, K Brockmann, C Klein, A Rolfs, F Binkofsk. Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17). Brain : a journal of neurology. vol 129. issue Pt 9. 2006-10-04. PMID:16760196. |
spinocerebellar ataxia 17 (sca17) is a rare genetic disorder characterized by cerebellar, extrapyramidal, pyramidal as well as psychiatric signs. |
2006-10-04 |
2023-08-12 |
Not clear |
| Yoshio Ienaga, Hiroshi Mitoma, Kohei Kubota, Sadao Morita, Hidehiro Mizusaw. Dynamic imbalance in gait ataxia. Characteristics of plantar pressure measurements. Journal of the neurological sciences. vol 246. issue 1-2. 2006-08-10. PMID:16574155. |
for this purpose, we compared the walking patterns of patients with cerebellar dominant multiple system atrophy (msac, n = 8), spinocerebellar ataxia type 6 (sca6, n = 4) and 16q-linked autosomal dominant cortical cerebellar atrophy (16q-linked adca, n = 6), and 6 normal subjects, by measuring toe and heel plantar pressures. |
2006-08-10 |
2023-08-12 |
human |
| Esther Brusse, Inge de Koning, Anneke Maat-Kievit, Ben A Oostra, Peter Heutink, John C van Swiete. Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype. Movement disorders : official journal of the Movement Disorder Society. vol 21. issue 3. 2006-08-03. PMID:16211615. |
autosomal dominant cerebellar ataxias (adcas) are genetically classified into spinocerebellar ataxias (scas). |
2006-08-03 |
2023-08-12 |
Not clear |
| U Rüb, K Gierga, E R Brunt, R A I de Vos, M Bauer, L Schöls, K Bürk, G Auburger, J Bohl, C Schultz, M Vuksic, G J Burbach, H Braak, T Delle. Spinocerebellar ataxias types 2 and 3: degeneration of the pre-cerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum. Journal of neural transmission (Vienna, Austria : 1996). vol 112. issue 11. 2006-07-27. PMID:15785863. |
spinocerebellar ataxias types 2 and 3: degeneration of the pre-cerebellar nuclei isolates the three phylogenetically defined regions of the cerebellum. |
2006-07-27 |
2023-08-12 |
Not clear |
| Jayaprakash A Gosalakkal, Puttamadaiah Mallikarjuna Swam. Infantile spinocerebellar ataxia type 6: relationship to episodic ataxia type 6. Pediatric neurology. vol 34. issue 4. 2006-07-20. PMID:16638506. |
spinocerebellar ataxia type 6 is one of the hereditary progressive cerebellar ataxias first described in 1997. |
2006-07-20 |
2023-08-12 |
Not clear |
| M E Ioffe, K I Ustinova, L A Chernikova, M A Kuliko. Supervised learning of postural tasks in patients with poststroke hemiparesis, Parkinson's disease or cerebellar ataxia. Experimental brain research. vol 168. issue 3. 2006-07-06. PMID:16175360. |
supervised learning of different postural tasks in patients with lesions of the motor cortex or pyramidal system (poststroke hemiparesis: 20 patients), nigro-striatal system (parkinson's disease: 33 patients) and cerebellum (spinocerebellar ataxia: 37 patients) was studied. |
2006-07-06 |
2023-08-12 |
human |
| Antoni Matilla Dueñas, Robert Goold, Paola Giunt. Molecular pathogenesis of spinocerebellar ataxias. Brain : a journal of neurology. vol 129. issue Pt 6. 2006-06-19. PMID:16613893. |
the autosomal dominant spinocerebellar ataxias (scas) are a group of neurodegenerative diseases, clinically and genetically heterogeneous, characterized by loss of balance and motor coordination due to dysfunction of the cerebellum and its afferent and efferent connections. |
2006-06-19 |
2023-08-12 |
Not clear |
| Paula Coutinho, Vítor T Cruz, Assunção Tuna, Sérgio E Silva, João Guimarãe. Cerebellar ataxia with spasmodic cough: a new form of dominant ataxia. Archives of neurology. vol 63. issue 4. 2006-05-22. PMID:16606768. |
although mentioned in most series, "pure" autosomal dominant cerebellar ataxias, except spinocerebellar ataxia type 6, are difficult to differentiate on clinical grounds. |
2006-05-22 |
2023-08-12 |
Not clear |
| B A Crum, K A Joseph. Varied electrophysiologic patterns in spinocerebellar ataxia type 2. European journal of neurology. vol 13. issue 2. 2006-05-09. PMID:16490053. |
spinocerebellar ataxia type 2 (sca2) is one of many autosomal dominant cerebellar ataxias. |
2006-05-09 |
2023-08-12 |
Not clear |
| M Tsirigotis, M Y Tang, M Beyers, M Zhang, J Woulfe, D A Gra. Delayed spinocerebellar ataxia in transgenic mice expressing mutant ubiquitin. Neuropathology and applied neurobiology. vol 32. issue 1. 2006-03-14. PMID:16409551. |
spinocerebellar ataxia type 1 (sca1) is an incurable neurodegenerative disease resulting from loss of purkinje neurones within the cerebellum. |
2006-03-14 |
2023-08-12 |
mouse |
| Anna-Lena Ström, Lars Forsgren, Monica Holmber. A role for both wild-type and expanded ataxin-7 in transcriptional regulation. Neurobiology of disease. vol 20. issue 3. 2006-03-09. PMID:15936949. |
spinocerebellar ataxia type 7 (sca7) is a neurodegenerative disease primarily affecting the brainstem, retina and purkinje cells of the cerebellum. |
2006-03-09 |
2023-08-12 |
Not clear |
| Michito Adachi, Toru Kawanami, Humi Ohshima, Takaaki Hosoy. Cerebellar atrophy attributed to cerebellitis in two patients. Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine. vol 4. issue 2. 2006-02-23. PMID:16340165. |
the patients were negative for the spinocerebellar ataxia (sca) genes and had no symptoms of hypothyroidism, history of malignant tumors, or history of alcohol and drug (phenytoin) abuse, which may cause cerebellar atrophy. |
2006-02-23 |
2023-08-12 |
Not clear |
| Marcus Gerwig, Karim Hajjar, Albena Dimitrova, Matthias Maschke, Florian P Kolb, Markus Frings, Alfred F Thilmann, Michael Forsting, Hans Christoph Diener, Dagmar Timman. Timing of conditioned eyeblink responses is impaired in cerebellar patients. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 25. issue 15. 2006-02-13. PMID:15829644. |
sixteen patients with pure cortical cerebellar degeneration (spinocerebellar ataxia type 6 and idiopathic cerebellar ataxia), 14 patients with lesions within the territory of the superior cerebellar artery, and 13 patients with infarctions within the territory of the posterior inferior cerebellar artery were included. |
2006-02-13 |
2023-08-12 |
Not clear |
| Anna-Lena Ström, Lars Forsgren, Monica Holmber. Identification and characterization of Spinocerebellar Ataxia Type 7 (SCA7) isoform SCA7b in mice. Biochimica et biophysica acta. vol 1731. issue 3. 2006-02-03. PMID:16297465. |
spinocerebellar ataxia type 7 (sca7) is a neurodegenerative disease primarily affecting the cerebellum, brainstem and retina. |
2006-02-03 |
2023-08-12 |
mouse |