| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Thomas Wirth, Céline Bonnet, Clarisse Delvallée, David Pellerin, Thomas Bogdan, Guillemette Clément, Audrey Schalk, Jean-Baptiste Chanson, Marie-Céline Fleury, Amélie Piton, Nadège Calmels, Izzie Jacques Namer, Stéphane Kremer, Bernard Brais, Christine Tranchant, Mathilde Renaud, Mathieu Anhei. Does Spinocerebellar ataxia 27B mimic cerebellar multiple system atrophy? Journal of neurology. 2024-01-24. PMID:38263489. |
whether spinocerebellar ataxia 27b (sca27b) may present as a cerebellar multiple system atrophy (msa-c) mimic remains undetermined. |
2024-01-24 |
2024-01-26 |
Not clear |
| José Alberto Álvarez-Cuesta, Camilo Mora-Batista, Ramón Reyes-Carreto, Frank Jesus Carrillo-Rodes, Sergio J Torralbaz Fitz, Yanetza González-Zaldivar, Cruz Vargas-De-Leó. On the Cut-Off Value of the Anteroposterior Diameter of the Midbrain Atrophy in Spinocerebellar Ataxia Type 2 Patients. Brain sciences. vol 14. issue 1. 2024-01-22. PMID:38248268. |
(1) background: spinocerebellar ataxias (sca) is a term that refers to a group of hereditary ataxias, which are neurological diseases characterized by degeneration of the cells that constitute the cerebellum. |
2024-01-22 |
2024-01-24 |
human |
| Kenjiro Nakayama, Kiyotaka Nemoto, Tetsuaki Ara. Nucleus accumbens degeneration in spinocerebellar ataxia type 2: a preliminary study. Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society. 2024-01-20. PMID:38243757. |
spinocerebellar ataxia type 2 (sca2) exhibits mainly cerebellar and oculomotor dysfunctions but also, frequently, cognitive impairment and neuropsychological symptoms. |
2024-01-20 |
2024-01-22 |
Not clear |
| Diana Avila-Jaque, Fernanda Martin, M Leonor Bustamante, Mariana Luna Álvarez, José Manuel Fernández, David José Dávila Ortiz de Montellano, Rosa Pardo, Diego Varela, Marcelo Mirand. The Phenotypic Spectrum of Spinocerebellar Ataxia Type 19 in a Series of Latin American Patients. Cerebellum (London, England). 2024-01-05. PMID:38180701. |
spinocerebellar ataxia 19 (sca19) represents a rare autosomal dominant genetic disorder resulting in progressive ataxia and cerebellar atrophy. |
2024-01-05 |
2024-01-07 |
Not clear |
| Giorgi Batsikadze, Johanna Pakusch, Michael Klein, Thomas Michael Ernst, Andreas Thieme, Seyed Ali Nicksirat, Katharina Marie Steiner, Enzo Nio, Erhan Genc, Stefan Maderwald, Cornelius Deuschl, Christian Josef Merz, Harald H Quick, Melanie D Mark, Dagmar Timman. Mild deficits in fear learning: Evidence from humans and mice with cerebellar cortical degeneration. eNeuro. 2024-01-04. PMID:38176906. |
similarly, mice with cerebellar cortical degeneration (spinocerebellar ataxia type 6, sca6) were able to learn the fear association, but retrieval of fear memory was reduced. |
2024-01-04 |
2024-01-07 |
mouse |
| Louisa P Selvadurai, Susan L Perlman, Tetsuo Ashizawa, George R Wilmot, Chiadi U Onyike, Liana S Rosenthal, Vikram G Shakkottai, Henry L Paulson, Sub H Subramony, Khalaf O Bushara, Sheng-Han Kuo, Cameron Dietiker, Michael D Geschwind, Alexandra B Nelson, Christopher M Gomez, Puneet Opal, Theresa A Zesiewicz, Trevor Hawkins, Talene A Yacoubian, Peggy C Nopoulos, Sharon J Sha, Peter E Morrison, Karla P Figueroa, Stefan M Pulst, Jeremy D Schmahman. The Cerebellar Cognitive Affective/Schmahmann Syndrome Scale in Spinocerebellar Ataxias. Cerebellum (London, England). 2024-01-02. PMID:38165578. |
the cerebellar cognitive affective/schmahmann syndrome scale in spinocerebellar ataxias. |
2024-01-02 |
2024-01-10 |
Not clear |
| Gabriela Bolzan, Maria E Müller Eyng, Vanessa B Leotti, Maria L Saraiva-Pereira, Laura B Jardi. Cognitive-affective manifestations since premanifest phases of Spinocerebellar Ataxia Type 3/Machado-Joseph Disease. Cortex; a journal devoted to the study of the nervous system and behavior. vol 171. 2023-12-13. PMID:38091940. |
cognitive deficits were related to spinocerebellar ataxia type 3/machado-joseph disease (sca3/mjd), but the cerebellar cognitive affective syndrome (ccas) needs further investigation in this disorder. |
2023-12-13 |
2023-12-17 |
Not clear |
| Anna A Cook, Tsz Chui Sophia Leung, Max Rice, Maya Nachman, Élyse Zadigue-Dube, Alanna Jean Wat. Endosomal dysfunction contributes to cerebellar deficits in spinocerebellar ataxia type 6. eLife. vol 12. 2023-12-12. PMID:38084749. |
endosomal dysfunction contributes to cerebellar deficits in spinocerebellar ataxia type 6. |
2023-12-12 |
2023-12-17 |
mouse |
| Anna A Cook, Tsz Chui Sophia Leung, Max Rice, Maya Nachman, Élyse Zadigue-Dube, Alanna Jean Wat. Endosomal dysfunction contributes to cerebellar deficits in spinocerebellar ataxia type 6. eLife. vol 12. 2023-12-12. PMID:38084749. |
spinocerebellar ataxia type 6 (sca6) is a rare disease that is characterized by cerebellar dysfunction. |
2023-12-12 |
2023-12-17 |
mouse |
| Ye Tu, Zheng Li, Fei Xiong, Feng Ga. Progressive white matter degeneration in patients with spinocerebellar ataxia type 2. Neuroradiology. 2023-12-01. PMID:38040824. |
spinocerebellar ataxia type 2 (sca2) is a progressive neurodegenerative disorder characterized by cerebellar atrophy. |
2023-12-01 |
2023-12-10 |
Not clear |
| Leon Tejwani, Neal G Ravindra, Changwoo Lee, Yubao Cheng, Billy Nguyen, Kimberly Luttik, Luhan Ni, Shupei Zhang, Logan M Morrison, John Gionco, Yangfei Xiang, Jennifer Yoon, Hannah Ro, Fatema Haidery, Rosalie M Grijalva, Eunwoo Bae, Kristen Kim, Regina T Martuscello, Harry T Orr, Huda Y Zoghbi, Hayley S McLoughlin, Laura P W Ranum, Vikram G Shakkottai, Phyllis L Faust, Siyuan Wang, David van Dijk, Janghoo Li. Longitudinal single-cell transcriptional dynamics throughout neurodegeneration in SCA1. Neuron. 2023-11-28. PMID:38016472. |
to dissect how individual cell types within a heterogeneous tissue contribute to the pathogenesis and progression of a neurodegenerative disorder, we performed longitudinal single-nucleus rna sequencing of mouse and human spinocerebellar ataxia type 1 (sca1) cerebellar tissue, establishing continuous dynamic trajectories of each cell population. |
2023-11-28 |
2023-12-07 |
mouse |
| N Al-Arab, S Hannou. White matter integrity assessment in spinocerebellar ataxia type 2 (SCA2) patients. Clinical radiology. 2023-11-12. PMID:37953094. |
to assess the burden of white matter (wm) damage in the cerebrum and cerebellum of spinocerebellar ataxia type 2 (sca2) patients in an attempt to identify key regions affected by the neurodegenerative processes using diffusion tensor imaging (dti). |
2023-11-12 |
2023-11-20 |
Not clear |
| Francis M Chen, Huixian Li, Dittman Lai-Shun Chung, Angel T L Mak, Fung Ping Leung, Ho Yin Edwin Chan, Wing Tak Won. IL-4/STAT6 axis observed to reverse proliferative defect in SCA3 patient-derived neural progenitor cells. Clinical and experimental pharmacology & physiology. 2023-11-07. PMID:37933553. |
spinocerebellar ataxia 3 (sca3) is an incurable, neurodegenerative genetic disorder that leads to progressive cerebellar ataxia and other parkinsonian-like pathologies because of loss of cerebellar neurons. |
2023-11-07 |
2023-11-08 |
Not clear |
| Senmao Chai, Deyang Liu, Yajing Liu, Ming San. A novel c.3636-4 A>G mutation in the CCDC88C plays a causative role in familial spinocerebellar ataxia. Human heredity. 2023-10-29. PMID:37899026. |
spinocerebellar ataxia (sca) is an autosomal dominant genetic disease characterized by cerebellar neurological deficits. |
2023-10-29 |
2023-11-08 |
Not clear |
| Zhi-Xian Ye, Jin Bi, Liang-Liang Qiu, Xuan-Yu Chen, Meng-Cheng Li, Xin-Yuan Chen, Yu-Sen Qiu, Ru-Ying Yuan, Xin-Tong Yu, Chun-Yu Huang, Bi Cheng, Wei Lin, Wan-Jin Chen, Jian-Ping Hu, Ying Fu, Ning Wang, Shi-Rui Ga. Cognitive impairment associated with cerebellar volume loss in spinocerebellar ataxia type 3. Journal of neurology. 2023-10-17. PMID:37848650. |
cognitive impairment associated with cerebellar volume loss in spinocerebellar ataxia type 3. |
2023-10-17 |
2023-11-08 |
Not clear |
| Zhi-Xian Ye, Jin Bi, Liang-Liang Qiu, Xuan-Yu Chen, Meng-Cheng Li, Xin-Yuan Chen, Yu-Sen Qiu, Ru-Ying Yuan, Xin-Tong Yu, Chun-Yu Huang, Bi Cheng, Wei Lin, Wan-Jin Chen, Jian-Ping Hu, Ying Fu, Ning Wang, Shi-Rui Ga. Cognitive impairment associated with cerebellar volume loss in spinocerebellar ataxia type 3. Journal of neurology. 2023-10-17. PMID:37848650. |
spinocerebellar ataxia type 3 (sca3; the most common hereditary ataxia) is neuropathologically characterized by cerebellar atrophy and frequently presents with cognitive impairment. |
2023-10-17 |
2023-11-08 |
Not clear |
| Victor Olmos, Evrett Thompson, Neha Gogia, Kimberly Luttik, Vaishnavi Veeranki, Luhan Ni, Serena Sim, Kelly Chen, Diane S Krause, Janghoo Li. Dysregulation of alternative splicing in spinocerebellar ataxia type 1. Human molecular genetics. 2023-10-06. PMID:37802886. |
we performed bulk rna sequencing in mouse models of spinocerebellar ataxia type 1 and identified that mutant ataxin-1 expression abnormally leads to diverse splicing events in the mouse cerebellum of spinocerebellar ataxia type 1. |
2023-10-06 |
2023-10-15 |
mouse |
| Prashant Phulpagar, Vikram V Holla, Deepti Tomar, Nitish Kamble, Ravi Yadav, Pramod Kumar Pal, Babylakshmi Muthusam. Novel CWF19L1 mutations in patients with spinocerebellar ataxia, autosomal recessive 17. Journal of human genetics. 2023-09-26. PMID:37752213. |
spinocerebellar ataxia, autosomal recessive-17 (scar17) is a rare hereditary ataxia characterized by ataxic gait, cerebellar signs and occasionally accompanied by intellectual disability and seizures. |
2023-09-26 |
2023-10-07 |
Not clear |
| Nicole Urbini, Libera Siciliano, Giusy Olivito, Maria Leggi. Unveiling the role of cerebellar alterations in the autonomic nervous system: a systematic review of autonomic dysfunction in spinocerebellar ataxias. Journal of neurology. 2023-09-25. PMID:37749264. |
unveiling the role of cerebellar alterations in the autonomic nervous system: a systematic review of autonomic dysfunction in spinocerebellar ataxias. |
2023-09-25 |
2023-10-07 |
Not clear |
| Nicole Urbini, Libera Siciliano, Giusy Olivito, Maria Leggi. Unveiling the role of cerebellar alterations in the autonomic nervous system: a systematic review of autonomic dysfunction in spinocerebellar ataxias. Journal of neurology. 2023-09-25. PMID:37749264. |
autonomic dysfunctions are prevalent in several cerebellar disorders, but they have not been systematically investigated in spinocerebellar ataxias (scas). |
2023-09-25 |
2023-10-07 |
Not clear |