All Relations between Spinocerebellar Ataxias and cerebellum

Publication Sentence Publish Date Extraction Date Species
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
Kaisu Nikali, Anu Suomalainen, Juha Saharinen, Mikko Kuokkanen, Johannes N Spelbrink, Tuula Lönnqvist, Leena Peltone. Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky. Human molecular genetics. vol 14. issue 20. 2006-01-12. PMID:16135556. infantile onset spinocerebellar ataxia (iosca) (mim 271245) is a severe autosomal recessively inherited neurodegenerative disorder characterized by progressive atrophy of the cerebellum, brain stem and spinal cord and sensory axonal neuropathy. 2006-01-12 2023-08-12 Not clear
Ullrich Wüllner, Michael Reimold, Michael Abele, Katrin Bürk, Martina Minnerop, Bernd-Michael Dohmen, Hans-Juergen Machulla, Roland Bares, Thomas Klockgethe. Dopamine transporter positron emission tomography in spinocerebellar ataxias type 1, 2, 3, and 6. Archives of neurology. vol 62. issue 8. 2005-09-08. PMID:16087769. the spinocerebellar ataxias (scas) are a genetically heterogeneous group of autosomal dominant ataxias: some mutations, including sca1, sca2, and sca3, are multisystemic disorders characterized by a variety of noncerebellar symptoms while others, like sca6, give rise to a pure cerebellar syndrome. 2005-09-08 2023-08-12 Not clear
Victor Hugo Cervantes-Kardasch, Esperanza García-Martíne. [Molecular physiopathology of the spinocerebellar ataxia type 6 (SCA6)]. Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. vol 56. issue 3. 2005-03-29. PMID:15612520. spinocerebellar ataxia type 6 (sca6) is a neurodegenerative, monogenic, and autosomic dominant disease which is characterized by a global cerebellar atrophy. 2005-03-29 2023-08-12 Not clear