All Relations between Spinocerebellar Ataxias and cerebellum

Publication Sentence Publish Date Extraction Date Species
Kyota Bando, Takeru Honda, Kinya Ishikawa, Yuji Takahashi, Hidehiro Mizusawa, Takashi Hanakaw. Impaired Adaptive Motor Learning Is Correlated With Cerebellar Hemispheric Gray Matter Atrophy in Spinocerebellar Ataxia Patients: A Voxel-Based Morphometry Study. Frontiers in neurology. vol 10. 2020-10-01. PMID:31803128. impaired adaptive motor learning is correlated with cerebellar hemispheric gray matter atrophy in spinocerebellar ataxia patients: a voxel-based morphometry study. 2020-10-01 2023-08-13 Not clear
Cara Kraus-Perrotta, Sarita Lagalwa. Expansion, mosaicism and interruption: mechanisms of the CAG repeat mutation in spinocerebellar ataxia type 1. Cerebellum & ataxias. vol 3. 2020-09-30. PMID:27895927. spinocerebellar ataxia type 1 (sca1) is an autosomal dominant neurodegenerative disorder that primarily affects the cerebellum and brainstem. 2020-09-30 2023-08-13 cat
Mohamed F Ibrahim, Emmet M Power, Kay Potapov, Ruth M Empso. Motor and Cerebellar Architectural Abnormalities during the Early Progression of Ataxia in a Mouse Model of SCA1 and How Early Prevention Leads to a Better Outcome Later in Life. Frontiers in cellular neuroscience. vol 11. 2020-09-30. PMID:28979190. exposing developing cerebellar purkinje neurons (pns) to mutant ataxin1 (atxn1) in 82q spinocerebellar ataxia type 1 (sca1) mice disrupts motor behavior and cerebellar climbing fiber (cf) architecture from as early as 4 weeks of age. 2020-09-30 2023-08-13 mouse
Yoji Okahara, Kouji Takano, Tetsuo Komori, Masahiro Nagao, Yasuo Iwadate, Kenji Kansak. Operation of a P300-based brain-computer interface by patients with spinocerebellar ataxia. Clinical neurophysiology practice. vol 2. 2020-09-30. PMID:30214988. we investigated the efficacy of a p300-based brain-computer interface (bci) for patients with spinocerebellar ataxia (sca), which is often accompanied by cerebellar impairment. 2020-09-30 2023-08-13 Not clear
Kentaro Kawamura, Seiji Etoh, Megumi Shimodozon. Transcranial magnetic stimulation for diplopia in a patient with spinocerebellar ataxia type 6: a case report. Cerebellum & ataxias. vol 5. 2020-09-30. PMID:30479783. in patients with spinocerebellar ataxia type 6 (sca6) are often treated by transcranial magnetic stimulation (tms) over the motor cortex and cerebellum. 2020-09-30 2023-08-13 Not clear
María Gómez-Ruiz, Carmen Rodríguez-Cueto, Eva Luna-Piñel, Mariluz Hernández-Gálvez, Javier Fernández-Rui. Endocannabinoid System in Spinocerebellar Ataxia Type-3 and Other Autosomal-Dominant Cerebellar Ataxias: Potential Role in Pathogenesis and Expected Relevance as Neuroprotective Targets. Frontiers in molecular neuroscience. vol 12. 2020-09-30. PMID:31068788. endocannabinoid system in spinocerebellar ataxia type-3 and other autosomal-dominant cerebellar ataxias: potential role in pathogenesis and expected relevance as neuroprotective targets. 2020-09-30 2023-08-13 Not clear
María Gómez-Ruiz, Carmen Rodríguez-Cueto, Eva Luna-Piñel, Mariluz Hernández-Gálvez, Javier Fernández-Rui. Endocannabinoid System in Spinocerebellar Ataxia Type-3 and Other Autosomal-Dominant Cerebellar Ataxias: Potential Role in Pathogenesis and Expected Relevance as Neuroprotective Targets. Frontiers in molecular neuroscience. vol 12. 2020-09-30. PMID:31068788. spinocerebellar ataxias (scas) are a group of hereditary and progressive neurological disorders characterized by a loss of balance and motor coordination typically associated with cerebellar atrophy. 2020-09-30 2023-08-13 Not clear
Corey Bolton, Maureen Lac. Comparison of cognitive profiles in spinocerebellar ataxia subtypes: a case series. Cerebellum & ataxias. vol 6. 2020-09-30. PMID:31548897. the spinocerebellar ataxias (sca) are a heterogeneous group of progressive neurodegenerative disorders that are associated with diffuse cerebellar atrophy. 2020-09-30 2023-08-13 Not clear
Chi-Wen Jao, Bing-Wen Soong, Chao-Wen Huang, Chien-An Duan, Chih-Chun Wu, Yu-Te Wu, Po-Shan Wan. Diffusion Tensor Magnetic Resonance Imaging for Differentiating Multiple System Atrophy Cerebellar Type and Spinocerebellar Ataxia Type 3. Brain sciences. vol 9. issue 12. 2020-09-28. PMID:31817016. diffusion tensor magnetic resonance imaging for differentiating multiple system atrophy cerebellar type and spinocerebellar ataxia type 3. 2020-09-28 2023-08-13 Not clear
Chi-Wen Jao, Bing-Wen Soong, Chao-Wen Huang, Chien-An Duan, Chih-Chun Wu, Yu-Te Wu, Po-Shan Wan. Diffusion Tensor Magnetic Resonance Imaging for Differentiating Multiple System Atrophy Cerebellar Type and Spinocerebellar Ataxia Type 3. Brain sciences. vol 9. issue 12. 2020-09-28. PMID:31817016. multiple system atrophy cerebellar type (msa-c) and spinocerebellar ataxia type 3 (sca3) demonstrate similar manifestations, including ataxia, pyramidal and extrapyramidal signs, as well as atrophy and signal intensity changes in the cerebellum and brainstem. 2020-09-28 2023-08-13 Not clear
Francesca Binda, Carla Pernaci, Smita Saxen. Cerebellar Development and Circuit Maturation: A Common Framework for Spinocerebellar Ataxias. Frontiers in neuroscience. vol 14. 2020-09-28. PMID:32300292. cerebellar development and circuit maturation: a common framework for spinocerebellar ataxias. 2020-09-28 2023-08-13 Not clear
Francesca Binda, Carla Pernaci, Smita Saxen. Cerebellar Development and Circuit Maturation: A Common Framework for Spinocerebellar Ataxias. Frontiers in neuroscience. vol 14. 2020-09-28. PMID:32300292. spinocerebellar ataxias (scas) affect the cerebellum and its afferent and efferent systems that degenerate during disease progression. 2020-09-28 2023-08-13 Not clear
Shuo Han, Yufan He, Aaron Carass, Sarah H Ying, Jerry L Princ. Cerebellum Parcellation with Convolutional Neural Networks. Proceedings of SPIE--the International Society for Optical Engineering. vol 10949. 2020-09-28. PMID:32394999. such studies have revealed that different spinocerebellar ataxia (sca) subtypes have different patterns of cerebellar atrophy and that atrophy of different cerebellar regions is correlated with specific functional losses. 2020-09-28 2023-08-13 human
Katherine J Robinson, Maxinne Watchon, Angela S Lair. Aberrant Cerebellar Circuitry in the Spinocerebellar Ataxias. Frontiers in neuroscience. vol 14. 2020-09-28. PMID:32765211. aberrant cerebellar circuitry in the spinocerebellar ataxias. 2020-09-28 2023-08-13 Not clear
Minkyeong Kim, Seung Hwan Oh, Jae Wook Cho, Jae-Hyeok Le. Spinocerebellar Ataxia 13 Presenting with Pure Cerebellar Syndrome in a Korean Family. Journal of movement disorders. vol 13. issue 3. 2020-09-28. PMID:32894899. spinocerebellar ataxia 13 presenting with pure cerebellar syndrome in a korean family. 2020-09-28 2023-08-13 Not clear
Norlinah Mohamed Ibrahim, Yue Hui Lau, Noorasyikin Ariffin, Siti Hajar Md Desa, Elena Azizan, Long Kha Chin, Shahrul Azmin Md Rani, Yusnita Yakob, Santhi Datuk Puvanarajah, Bart van de Warrenbur. Frequency of Spinocerebellar Ataxia type 1, 2, 3,6 and 7 and clinical profile of Spinocerebellar Ataxia type 3 in Malaysia. Cerebellum & ataxias. vol 7. 2020-09-28. PMID:32922823. spinocerebellar ataxias (sca) are highly heterogenous group of neurodegenerative diseases causing progressive cerebellar dysfunction. 2020-09-28 2023-08-13 Not clear
Jun Young Park, Kwangsic Joo, Se Joon Wo. Ophthalmic Manifestations and Genetics of the Polyglutamine Autosomal Dominant Spinocerebellar Ataxias: A Review. Frontiers in neuroscience. vol 14. 2020-09-28. PMID:32973440. spinocerebellar ataxia (sca) is a part of the cerebellar neurodegenerative disease group that is diverse in genetics and phenotypes. 2020-09-28 2023-08-13 Not clear
Atsuhiko Sugiyama, Noriko Sato, Yukio Kimura, Hiroyuki Fujii, Norihide Maikusa, Yoko Shigemoto, Fumio Suzuki, Emiko Morimoto, Kyosuke Koide, Yuji Takahashi, Hiroshi Matsuda, Satoshi Kuwabar. Quantifying iron deposition in the cerebellar subtype of multiple system atrophy and spinocerebellar ataxia type 6 by quantitative susceptibility mapping. Journal of the neurological sciences. vol 407. 2020-09-16. PMID:31639532. quantifying iron deposition in the cerebellar subtype of multiple system atrophy and spinocerebellar ataxia type 6 by quantitative susceptibility mapping. 2020-09-16 2023-08-13 Not clear
Atsuhiko Sugiyama, Noriko Sato, Yukio Kimura, Hiroyuki Fujii, Norihide Maikusa, Yoko Shigemoto, Fumio Suzuki, Emiko Morimoto, Kyosuke Koide, Yuji Takahashi, Hiroshi Matsuda, Satoshi Kuwabar. Quantifying iron deposition in the cerebellar subtype of multiple system atrophy and spinocerebellar ataxia type 6 by quantitative susceptibility mapping. Journal of the neurological sciences. vol 407. 2020-09-16. PMID:31639532. we used quantitative susceptibility mapping (qsm) to assess the brain iron deposition in 28 patients with the cerebellar subtype of multiple system atrophy (msa-c), nine patients with spinocerebellar ataxia type 6 (sca6), and 23 healthy controls. 2020-09-16 2023-08-13 Not clear
Elan D Louis, Chloë A Kerridge, Debotri Chatterjee, Regina T Martuscello, Daniel Trujillo Diaz, Arnulf H Koeppen, Sheng-Han Kuo, Jean-Paul G Vonsattel, Peter A Sims, Phyllis L Faus. Contextualizing the pathology in the essential tremor cerebellar cortex: a patholog-omics approach. Acta neuropathologica. vol 138. issue 5. 2020-09-15. PMID:31317229. to address this, we compared the severity and patterning of degenerative changes within the cerebellar cortex in patients with et, other neurodegenerative disorders of the cerebellum (spinocerebellar ataxias (scas), multiple system atrophy (msa)], and other disorders that may involve the cerebellum [parkinson's disease (pd), dystonia]. 2020-09-15 2023-08-13 Not clear