All Relations between Spinocerebellar Ataxias and cerebellum

Reference Sentence Publish Date Extraction Date Species
Haruka Ouchi, Hideaki Ishiguro, Ken Shibano, Kenju Hara, Masashiro Sugawara, Katsuhiko Enomoto, Hajime Miyat. Primary degeneration of oculomotor, motor, and somatosensory systems and auditory and visual pathways in spinocerebellar ataxia type 7: A clinicopathological study in a Japanese autopsy case. Neuropathology : official journal of the Japanese Society of Neuropathology vol issue 2022 36168676 spinocerebellar ataxia type 7 (sca7) is an autosomal dominant neurodegenerative disorder characterized by progressive cerebellar ataxia associated with retinal degeneration. 2022-09-28 2022-09-29 Not clear
Libera Siciliano, Giusy Olivito, Nicole Urbini, Maria Caterina Silveri, Maria Leggi. \" Biomedicines vol 10 issue 9 2022 36140267 accordingly, this study aims to investigate whether motor reserve (mr), likely to be boosted by exercise engagement in a lifetime, affects motor symptom severity, cognitive functioning, and functional brain networks in spinocerebellar ataxia type 2 (sca2)-a cerebellar neurodegenerative disease. 2022-09-23 2022-09-29 Not clear
Satoshi Zeniya, Nobuo Sanjo, Hiroya Kuwahara, Kinya Ishikawa, Miwa Higashi, Akiko Matsunaga, Makoto Yoneda, Hidehiro Mizusawa, Takanori Yokot. Spinocerebellar Ataxia Type 31 Exacerbated by Anti-amino Terminal of Alpha-enolase Autoantibodies. Internal medicine (Tokyo, Japan) vol 61 issue 18 2022 36104177 this is the first report of cerebellar ataxia associated with genetic spinocerebellar ataxia with concomitant cerebellar type he. 2022-09-16 2022-09-20 Not clear
Anna A Cook, Sriram Jayabal, Jacky Sheng, Eviatar Fields, Tsz Chui Sophia Leung, Sabrina Quilez, Eileen McNicholas, Lois Lau, Shixia Huang, Alanna J Wat. Activation of TrkB-Akt signaling rescues deficits in a mouse model of SCA6. Science advances vol 8 issue 37 2022 36112675 spinocerebellar ataxia type 6 (sca6) is a neurodegenerative disease resulting in motor coordination deficits and cerebellar pathology. 2022-09-16 2022-09-29 Not clear
E P Nuzhnyi, N Yu Abramycheva, I A Chkhartishvili, A O Protopopova, E Yu Fedotova, S N Illarioshki. [Spinocerebellar ataxia type 8 in Russian patients]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova vol 122 issue 8 2022 36036411 to assess the incidence of spinocerebellar ataxia type 8 (sca8) in patients with progressive cerebellar ataxia and describe the clinical features of the sca8 phenotype in russian patients. 2022-08-29 2022-08-31 Not clear
Szilvia E Mezey, Josef P Kapfhammer, Etsuko Shimobayash. Transcriptome Profile of a New Mouse Model of Spinocerebellar Ataxia Type 14 Implies Changes in Cerebellar Development. Genes vol 13 issue 8 2022 36011327 transcriptome profile of a new mouse model of spinocerebellar ataxia type 14 implies changes in cerebellar development. 2022-08-26 2022-08-29 Not clear
Ilaria Balbo, Francesca Montarolo, Federica Genovese, Filippo Tempia, Eriola Hoxh. Effects of the administration of Elovl5-dependent fatty acids on a spino-cerebellar ataxia 38 mouse model. Behavioral and brain functions : BBF vol 18 issue 1 2022 35933444 spinocerebellar ataxia 38 (sca38) is a rare autosomal neurological disorder characterized by ataxia and cerebellar atrophy. 2022-08-06 2022-08-08 Not clear
Ming-Che Kuo, Chun-Hwei Tai, Sheng-Hong Tseng, Ruey-Meei W. Long-term efficacy of bilateral subthalamic deep brain stimulation in the parkinsonism of SCA 3: A rare case report. European journal of neurology vol 29 issue 8 2022 35837753 spinocerebellar ataxia type 3 (sca3) is an autosomal dominant inherited disorder that manifests as a mixture of cerebellar ataxia, parkinsonism, and polyneuropathy; in type iv sca3, pure parkinsonism is the only symptom. 2022-07-15 2022-07-19 Not clear
David D Bushart, Vikram G Shakkotta. Vulnerability of Human Cerebellar Neurons to Degeneration in Ataxia-Causing Channelopathies. Frontiers in systems neuroscience vol 16 issue 2022 35757096 we also speculate on the vulnerability of cerebellar neurons to degeneration in mouse models of spinocerebellar ataxia (sca) where ion channel transcript dysregulation has recently been implicated in disease pathogenesis. 2022-06-27 2022-07-04 Not clear
Hung-Chieh Chen, Li-Hua Lee, Jiing-Feng Lirng, Bing-Wen Soon. Radiological hints for differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia. Scientific reports vol 12 issue 1 2022 35732792 radiological hints for differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia. 2022-06-22 2022-06-27 Not clear
Hung-Chieh Chen, Li-Hua Lee, Jiing-Feng Lirng, Bing-Wen Soon. Radiological hints for differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia. Scientific reports vol 12 issue 1 2022 35732792 differentiation cerebellar multiple systemic atrophy (msa-c) from spinocerebellar ataxia (sca) is important. 2022-06-22 2022-06-27 Not clear
Pauline Bohne, Max Rybarski, Damian Boden-El Mourabit, Felix Krause, Melanie D Mar. Cerebellar contribution to threat probability in a SCA6 mouse model. Human molecular genetics vol issue 2022 35708512 in this study we investigated the cerebellar contribution in evoking appropriate defensive escape behavior using a purely cerebellar, neurodegenerative mouse model for spinocerebellar ataxia type 6 (sca6) which is caused by an expanded cag repeat in exon 47 of the p/q type calcium channel \xce\xb11a subunit. 2022-06-16 2022-06-20 Not clear
Kristin Mayoral-Palarz, Andreia Neves-Carvalho, Sara Duarte-Silva, Daniela Monteiro-Fernandes, Patr\\xc3\\xadcia Maciel, Kamran Khodakha. Cerebellar neuronal dysfunction accompanies early motor symptoms in spinocerebellar ataxia type 3. Disease models & mechanisms vol issue 2022 35660856 cerebellar neuronal dysfunction accompanies early motor symptoms in spinocerebellar ataxia type 3. 2022-06-06 2022-06-13 Not clear
Minori Furuta, Masayuki Sato, Setsuki Tsukagoshi, Yoshito Tsushima, Yoshio Iked. Criteria-unfulfilled multiple system atrophy at an initial stage exhibits laterality of middle cerebellar peduncles. Journal of the neurological sciences vol 438 issue 2022 35609364 seven msa-pc patients meeting the above condition at an initial evaluation were identified, and all the msa-pc patients later developed autonomic dysfunction and finally fulfilled the criteria for probable or possible category of msa-c. for comparison, two patients with spinocerebellar ataxia type 6 and three patients with idiopathic cerebellar ataxia who did not exhibit autonomic dysfunction for more than three years were enrolled in this study (non-msa-pc). 2022-05-24 2022-06-13 Not clear
Xin-Yuan Chen, Yan-Hua Lian, Xia-Hua Liu, Arif Sikandar, Meng-Cheng Li, Hao-Ling Xu, Jian-Ping Hu, Qun-Lin Chen, Shi-Rui Ga. Effects of Repetitive Transcranial Magnetic Stimulation on Cerebellar Metabolism in Patients With Spinocerebellar Ataxia Type 3. Frontiers in aging neuroscience vol 14 issue 2022 35547622 effects of repetitive transcranial magnetic stimulation on cerebellar metabolism in patients with spinocerebellar ataxia type 3. 2022-05-13 2022-06-13 Not clear
Roderick P P W M Maas, Steven Teerenstra, Ivan Toni, Thomas Klockgether, Dennis J L G Schutter, Bart P C van de Warrenbur. Cerebellar Transcranial Direct Current Stimulation in Spinocerebellar Ataxia Type 3: a Randomized, Double-Blind, Sham-Controlled Trial. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics vol issue 2022 35501469 cerebellar transcranial direct current stimulation in spinocerebellar ataxia type 3: a randomized, double-blind, sham-controlled trial. 2022-05-02 2022-05-06 Not clear
Roderick P P W M Maas, Steven Teerenstra, Ivan Toni, Thomas Klockgether, Dennis J L G Schutter, Bart P C van de Warrenbur. Cerebellar Transcranial Direct Current Stimulation in Spinocerebellar Ataxia Type 3: a Randomized, Double-Blind, Sham-Controlled Trial. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics vol issue 2022 35501469 the objective of this study was to investigate if a two-week regimen of daily cerebellar tdcs sessions diminishes ataxia and non-motor symptom severity and alters cerebellar-m1 connectivity in individuals with spinocerebellar ataxia type 3 (sca3). 2022-05-02 2022-05-06 Not clear
Hui Chen, Limeng Dai, Yuhan Zhang, Liu Feng, Zhenzhen Jiang, Xingang Wang, Dongjing Xie, Jing Guo, Huafu Chen, Jian Wang, Chen Li. Network Reconfiguration Among Cerebellar Visual, Frontiers in aging neuroscience vol 14 issue 2022 35478700 network reconfiguration among cerebellar visual, spinocerebellar ataxia type 3 (sca3) is a rare movement disorder characterized with ataxia. 2022-04-28 2022-04-30 Not clear
Anton N Shuvaev, Olga S Belozor, Oleg I Mozhei, Aleksandra G Mileiko, Ludmila D Mosina, Irina V Laletina, Ilia G Mikhailov, Yana V Fritsler, Andrey N Shuvaev, Anja G Teschemacher, Sergey Kasparo. Memantine Disrupts Motor Coordination through Anxiety-like Behavior in CD1 Mice. Brain sciences vol 12 issue 4 2022 35448027 we previously used memantine to prevent functional damage and to retain morphology of cerebellar neurons and bergmann glia in an optogenetic mouse model of spinocerebellar ataxia type-1 (sca1). 2022-04-21 2022-04-25 Not clear
Chengyuan Mao, Xinwei Li, Yun Su, Haiyang Luo, Liyuan Fan, Huimin Zheng, Yu Fan, Zhihua Yang, Shuo Zhang, Zhengwei Hu, Xiaoyan Hao, Changhe Shi, Yuming X. Spinocerebellar Ataxia Type 10 with Atypical Clinical Manifestation in Han Chinese. Cerebellum (London, England) vol issue 2022 35441258 spinocerebellar ataxia type 10 (sca10) is an autosomal dominant cerebellar ataxia accompanied by extracerebellar signs and other neurological disorders. 2022-04-20 2022-04-25 Not clear
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