All Relations between Spinocerebellar Ataxias and cerebellum

Reference Sentence Publish Date Extraction Date Species
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
Siddharth Nath, Nicholas S Caron, Linda May, Oxana B Gluscencova, Jill Kolesar, Lauren Brady, Brett A Kaufman, Gabrielle L Boulianne, Amadeo R Rodriguez, Mark A Tarnopolsky, Ray Truan. Functional characterization of variants of unknown significance in a spinocerebellar ataxia patient using an unsupervised machine learning pipeline. Human genome variation vol 9 issue 1 2022 35422034 cag-expanded atxn7 has been previously defined in the pathogenesis of spinocerebellar ataxia type 7 (sca7), a polyglutamine expansion autosomal dominant cerebellar ataxia. 2022-04-15 2022-04-18 Not clear
Jiaqi Wang, Atsuhiko Sugiyama, Hajime Yokota, Shigeki Hirano, Graham Cooper, Hiroki Mukai, Kenji Ohira, Kyosuke Koide, Shoichi Ito, Carsten Finke, Alexander U Brandt, Friedemann Paul, Satoshi Kuwabar. Diagnostic efficacy of the magnetic resonance T1w/T2w ratio for the middle cerebellar peduncle in multiple system atrophy and spinocerebellar ataxia: A preliminary study. PloS one vol 17 issue 4 2022 35427382 diagnostic efficacy of the magnetic resonance t1w/t2w ratio for the middle cerebellar peduncle in multiple system atrophy and spinocerebellar ataxia: a preliminary study. 2022-04-15 2022-04-18 Not clear
Karen Jansen-West, Tiffany W Todd, Lillian M Daughrity, Mei Yue, Jimei Tong, Yari Carlomagno, Giulia Del Rosso, Aishe Kurti, Caroline Y Jones, Judith A Dunmore, Monica Castanedes-Casey, Dennis W Dickson, Zbigniew K Wszolek, John D Fryer, Leonard Petrucelli, Mercedes Prudenci. Plasma PolyQ-ATXN3 Levels Associate With Cerebellar Degeneration and Behavioral Abnormalities in a New AAV-Based SCA3 Mouse Model. Frontiers in cell and developmental biology vol 10 issue 2022 35386195 spinocerebellar ataxia type 3 (sca3) is a dominantly inherited cerebellar ataxia caused by the expansion of a polyglutamine (polyq) repeat in the gene encoding atxn3. 2022-04-07 2022-04-14 Not clear
Hiroshi Mitoma, Kazuhiko Yamaguchi, Jerome Honnorat, Mario Mant. The Clinical Concept of LTDpathy: Is Dysregulated LTD Responsible for Prodromal Cerebellar Symptoms? Brain sciences vol 12 issue 3 2022 35326260 on the other hand, in some types of spinocerebellar ataxia (sca), dysfunction in pf-pc ltd, and impairments of pf-pc ltd-related adaptive behaviors (including vestibulo-ocular reflex (vor) and prism adaptation) appear during the prodromal stage, well before the manifestations of obvious cas and cerebellar atrophy. 2022-03-25 2022-04-14 Not clear
Marc Corral-Juan, Pilar Casquero, Natalia Giraldo-Restrepo, Steve Laurie, Alicia Martinez-Pi\\xc3\\xb1eiro, Raidili Cristina Mateo-Montero, Lourdes Ispierto, Dolores Vilas, Eduardo Tolosa, Victor Volpini, Ramiro Alvarez-Ramo, Ivelisse S\\xc3\\xa1nchez, Antoni Matilla-Due\\xc3\\xb1a. New spinocerebellar ataxia subtype caused by Brain communications vol 4 issue 2 2022 35310830 new spinocerebellar ataxia subtype caused by spinocerebellar ataxias consist of a highly heterogeneous group of inherited movement disorders clinically characterized by progressive cerebellar ataxia variably associated with additional distinctive clinical signs. 2022-03-21 2022-04-14 Not clear
Marc Corral-Juan, Pilar Casquero, Natalia Giraldo-Restrepo, Steve Laurie, Alicia Martinez-Pi\\xc3\\xb1eiro, Raidili Cristina Mateo-Montero, Lourdes Ispierto, Dolores Vilas, Eduardo Tolosa, Victor Volpini, Ramiro Alvarez-Ramo, Ivelisse S\\xc3\\xa1nchez, Antoni Matilla-Due\\xc3\\xb1a. New spinocerebellar ataxia subtype caused by Brain communications vol 4 issue 2 2022 35310830 in this study, we describe a new spinocerebellar ataxia subtype in nine members of a spanish five-generation family from menorca with affected individuals variably presenting with ataxia, nystagmus, dysarthria, polyneuropathy, pyramidal signs, cerebellar atrophy and distinctive cerebral demyelination. 2022-03-21 2022-04-14 Not clear
Andreas Deistung, Dominik J\\xc3\\xa4schke, Rossitza Draganova, Viktor Pfaffenrot, Thomas Hulst, Katharina M Steiner, Andreas Thieme, Ilaria A Giordano, Thomas Klockgether, Sinem Tunc, Alexander M\\xc3\\xbcnchau, Martina Minnerop, Sophia L G\\xc3\\xb6ricke, J\\xc3\\xbcrgen R Reichenbach, Dagmar Timman. Quantitative susceptibility mapping reveals alterations of dentate nuclei in common types of degenerative cerebellar ataxias. Brain communications vol 4 issue 1 2022 35291442 spinocerebellar ataxia of type 1 and multiple system atrophy, cerebellar type patients showed higher susceptibilities in large parts of the dentate nucleus but unaltered susceptibility masses compared with controls. 2022-03-16 2022-04-14 Not clear
Andreas Deistung, Dominik J\\xc3\\xa4schke, Rossitza Draganova, Viktor Pfaffenrot, Thomas Hulst, Katharina M Steiner, Andreas Thieme, Ilaria A Giordano, Thomas Klockgether, Sinem Tunc, Alexander M\\xc3\\xbcnchau, Martina Minnerop, Sophia L G\\xc3\\xb6ricke, J\\xc3\\xbcrgen R Reichenbach, Dagmar Timman. Quantitative susceptibility mapping reveals alterations of dentate nuclei in common types of degenerative cerebellar ataxias. Brain communications vol 4 issue 1 2022 35291442 the most striking changes in susceptibility were found in spinocerebellar ataxia of type 1, multiple system atrophy, cerebellar type and spinocerebellar ataxia of type 6. 2022-03-16 2022-04-14 Not clear
Andreas Deistung, Dominik J\\xc3\\xa4schke, Rossitza Draganova, Viktor Pfaffenrot, Thomas Hulst, Katharina M Steiner, Andreas Thieme, Ilaria A Giordano, Thomas Klockgether, Sinem Tunc, Alexander M\\xc3\\xbcnchau, Martina Minnerop, Sophia L G\\xc3\\xb6ricke, J\\xc3\\xbcrgen R Reichenbach, Dagmar Timman. Quantitative susceptibility mapping reveals alterations of dentate nuclei in common types of degenerative cerebellar ataxias. Brain communications vol 4 issue 1 2022 35291442 because iron content is known to be high in glial cells but not in neurons of the cerebellar nuclei, the higher susceptibility in spinocerebellar ataxia of type 1 and multiple system atrophy, cerebellar type may be explained by a reduction of neurons (increase in iron concentration) and/or an increase in iron-rich glial cells, e.g. 2022-03-16 2022-04-14 Not clear
Nannan Qian, Taohua Wei, Wenming Yang, Jiuxiang Wang, Shijie Zhang, Shan Jin, Wei Dong, Wenjie Hao, Yue Yang, Ru Huan. Case Report: Late-Onset Autosomal Recessive Cerebellar Ataxia Associated With Frontiers in genetics vol 13 issue 2022 35281832 case report: late-onset autosomal recessive cerebellar ataxia associated with autosomal recessive cerebellar ataxia type 1 (arca-1), also known as autosomal recessive spinocerebellar ataxia type 8 (scar8), is caused by spectrin repeat containing nuclear envelope protein 1 ( 2022-03-14 2022-04-14 Not clear
Ping-I Chiang, Ting-Wei Liao, Chiung-Mei Che. A Novel SETX Mutation in a Taiwanese Patient with Autosomal Recessive Cerebellar Ataxia Detected by Targeted Next-Generation Sequencing, and a Literature Review. Brain sciences vol 12 issue 2 2022 35203940 ataxia with oculomotor apraxia type 2 (aoa2), also known as autosomal recessive spinocerebellar ataxia with axonal neuropathy-2 (scan2) (omim #606002), is a neurodegenerative disorder characterized by early-onset progressive cerebellar ataxia, polyneuropathy, and elevated levels of alpha-fetoprotein. 2022-02-25 2022-02-27 Not clear
Javier Miranda, Esther Cub. Spinocerebellar ataxia type 3: response to levodopa infusion in two cases. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol issue 2022 35199253 spinocerebellar ataxia type 3 (sca-atxn3) is a genetic neurodegenerative disease characterized by progressive cerebellar ataxia and other variable findings, including parkinsonian syndrome. 2022-02-24 2022-02-27 Not clear
Athena Zachou, Danai Palaiologou, Emmanouil Kanavakis, Evangelos Anagnosto. Retrocollis as the cardinal feature in a de novo ITRP1 variant. Brain & development vol issue 2022 35148930 itpr1 gene variants, through a loss-of-function mechanism, have been found to be related with the manifestation of spinocerebellar ataxia (sca) 15, an adult-onset slow progressive cerebellar ataxia, sca 29, a rare non-progressive congenital cerebellar ataxia and gillepsie syndrome (sca 29 phenotype plus aniridia). 2022-02-12 2022-02-13 Not clear
Raghavendra Y Nagaraja, David M Sherry, Jennifer L Fessler, Megan A Stiles, Feng Li, Karanpreet Multani, Albert Orock, Mohiuddin Ahmad, Richard S Brush, Robert E Anderson, Martin-Paul Agbaga, Ferenc De\\xc3\\xa1. W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and Climbing Fibers and Causes Motor Defects in a Rat Model of SCA34. Molecular neurobiology vol 58 issue 10 2021 34227061 spinocerebellar ataxia (sca) is a neurodegenerative disorder characterized by ataxia and cerebellar atrophy. 2022-02-03 2022-01-13 Not clear
Qing Lin, Yichen Chang, Peng Liu, Jeffery A Jones, Xi Chen, Danhua Peng, Mingyuan Chen, Chao Wu, Hanjun Li. Cerebellar Continuous Theta Burst Stimulation Facilitates Auditory-Vocal Integration in Spinocerebellar Ataxia. Cerebral cortex (New York, N.Y. : 1991) vol issue 2021 34240142 cerebellar continuous theta burst stimulation facilitates auditory-vocal integration in spinocerebellar ataxia. 2022-02-01 2022-01-13 Not clear
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