| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Sara Satolli, Salvatore Rossi, Elisa Vegezzi, David Pellerin, Maria Laura Manca, Melissa Barghigiani, Carla Battisti, Giusi Bilancieri, Giorgia Bruno, Elena Capacci, Carlo Casali, Roberto Ceravolo, Sirio Cocozza, Stefano Cotti Piccinelli, Chiara Criscuolo, Matt C Danzi, Rosa De Micco, Giuseppe De Michele, Marie-Josée Dicaire, Grazia Maria Igea Falcone, Roberto Fancellu, Yasmine Ferchichi, Camilla Ferrari, Alessandro Filla, Nicola Fini, Alessandra Govoni, Filomena Lo Vecchio, Alessandro Malandrini, Andrea Mignarri, Olimpia Musumeci, Claudia Nesti, Sabina Pappatà, Maria Teresa Pellecchia, Alessia Perna, Antonio Petrucci, Maria Grazia Pomponi, Roberta Ravenni, Ivana Ricca, Alessandra Rufa, Elisabetta Tabolacci, Alessandra Tessa, Alessandro Tessitore, Stephan Zuchner, Gabriella Silvestri, Andrea Cortese, Bernard Brais, Filippo M Santorell. Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an Italian cohort. Journal of neurology. 2024-06-17. PMID:38886208. |
spinocerebellar ataxia 27b: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an italian cohort. |
2024-06-17 |
2024-06-21 |
Not clear |
| Xinyi Dong, Bing Liu, Weijie Huang, Haojie Chen, Yunhao Zhang, Zeshan Yao, Amir Shmuel, Aocai Yang, Zhengjia Dai, Guolin Ma, Ni Sh. Disrupted cerebellar structural connectome in spinocerebellar ataxia type 3 and its association with transcriptional profiles. Cerebral cortex (New York, N.Y. : 1991). vol 34. issue 6. 2024-06-08. PMID:38850215. |
disrupted cerebellar structural connectome in spinocerebellar ataxia type 3 and its association with transcriptional profiles. |
2024-06-08 |
2024-06-11 |
human |
| Xinyi Dong, Bing Liu, Weijie Huang, Haojie Chen, Yunhao Zhang, Zeshan Yao, Amir Shmuel, Aocai Yang, Zhengjia Dai, Guolin Ma, Ni Sh. Disrupted cerebellar structural connectome in spinocerebellar ataxia type 3 and its association with transcriptional profiles. Cerebral cortex (New York, N.Y. : 1991). vol 34. issue 6. 2024-06-08. PMID:38850215. |
spinocerebellar ataxia type 3 (sca3) is primarily characterized by progressive cerebellar degeneration, including gray matter atrophy and disrupted anatomical and functional connectivity. |
2024-06-08 |
2024-06-11 |
human |
| Jennifer L Fessler, Megan A Stiles, Martin-Paul Agbaga, Mohiuddin Ahmad, David M Sherr. The Spinocerebellar Ataxia 34-Causing W246G ELOVL4 Mutation Does Not Alter Cerebellar Neuron Populations in a Rat Model. Cerebellum (London, England). 2024-06-08. PMID:38850484. |
the spinocerebellar ataxia 34-causing w246g elovl4 mutation does not alter cerebellar neuron populations in a rat model. |
2024-06-08 |
2024-06-11 |
human |
| Katherine Hamel, Emmanuel Labrada Moncada, Carrie Sheeler, Juao-Guilherme Rosa, Stephen Gilliat, Ying Zhang, Marija Cvetanovi. Cerebellar Heterogeneity and Selective vulnerability in Spinocerebellar Ataxia Type 1 (SCA1). Neurobiology of disease. vol 197. 2024-05-21. PMID:38750673. |
cerebellar heterogeneity and selective vulnerability in spinocerebellar ataxia type 1 (sca1). |
2024-05-21 |
2024-05-27 |
mouse |
| Katherine Hamel, Emmanuel Labrada Moncada, Carrie Sheeler, Juao-Guilherme Rosa, Stephen Gilliat, Ying Zhang, Marija Cvetanovi. Cerebellar Heterogeneity and Selective vulnerability in Spinocerebellar Ataxia Type 1 (SCA1). Neurobiology of disease. vol 197. 2024-05-21. PMID:38750673. |
here we describe molecular, cellular and functional heterogeneity in the context of healthy cerebellum as well as in cerebellar disease spinocerebellar ataxia type 1 (sca1). |
2024-05-21 |
2024-05-27 |
mouse |
| Hak-In Lee, Eunjin Kwon, Eungseok Oh, Seong-Hae Jeon. Antisaccades in Spinocerebellar Ataxia Type 17 With Middle Cerebellar Peduncle Hyperintensities Without Hot-Cross-Bun Sign. Journal of clinical neurology (Seoul, Korea). vol 20. issue 3. 2024-05-10. PMID:38713080. |
antisaccades in spinocerebellar ataxia type 17 with middle cerebellar peduncle hyperintensities without hot-cross-bun sign. |
2024-05-10 |
2024-05-27 |
Not clear |
| Sharan Paul, Warunee Dansithong, Mandi Gandelman, Karla P Figueroa, Daniel R Scoles, Stefan M Puls. Cerebellar Micro-RNA Profile in a Mouse Model of Spinocerebellar Ataxia Type 2. Neurology. Genetics. vol 10. issue 2. 2024-05-08. PMID:38715656. |
cerebellar micro-rna profile in a mouse model of spinocerebellar ataxia type 2. |
2024-05-08 |
2024-05-27 |
mouse |
| Rodrigo Brito, João Victor Fabrício, Aurine Araujo, Gabriel Barreto, Adriana Baltar, Kátia Monte-Silv. Single-Session Cerebellar Transcranial Direct Current Stimulation Improves Postural Stability and Reduces Ataxia Symptoms in Spinocerebellar Ataxia. Cerebellum (London, England). 2024-05-01. PMID:38693314. |
single-session cerebellar transcranial direct current stimulation improves postural stability and reduces ataxia symptoms in spinocerebellar ataxia. |
2024-05-01 |
2024-05-04 |
human |
| Hung-Chieh Chen, Li-Hua Lee, Jiing-Feng Lirng, Bing-Wen Soon. MRl and MRS hints for the differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia type II. Heliyon. vol 10. issue 7. 2024-04-11. PMID:38601670. |
mrl and mrs hints for the differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia type ii. |
2024-04-11 |
2024-04-13 |
Not clear |
| Hung-Chieh Chen, Li-Hua Lee, Jiing-Feng Lirng, Bing-Wen Soon. MRl and MRS hints for the differentiation of cerebellar multiple system atrophy from spinocerebellar ataxia type II. Heliyon. vol 10. issue 7. 2024-04-11. PMID:38601670. |
the differentiation of spinocerebellar ataxia type ii (sca 2) from idiopathic multiple systemic atrophy of the cerebellar type (msa-c) is often difficult in patients with cerebellar ataxia when molecular testing is not available. |
2024-04-11 |
2024-04-13 |
Not clear |
| Olga S Belozor, Alex Vasilev, Alexandra G Mileiko, Lyudmila D Mosina, Ilya G Mikhailov, Darius A Ox, Elizaveta B Boitsova, Andrey N Shuvaev, Anja G Teschemacher, Sergey Kasparov, Anton N Shuvae. Memantine suppresses the excitotoxicity but fails to rescue the ataxic phenotype in SCA1 model mice. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. vol 174. 2024-04-04. PMID:38574621. |
spinocerebellar ataxia type 1 (sca1) is a debilitating neurodegenerative disorder of the cerebellum and brainstem. |
2024-04-04 |
2024-04-07 |
mouse |
| Mafalda Raposo, Jeannette Hübener-Schmid, Rebecca Tagett, Ana F Ferreira, Ana Rosa Vieira Melo, João Vasconcelos, Paula Pires, Teresa Kay, Hector Garcia-Moreno, Paola Giunti, Magda M Santana, Luis Pereira de Almeida, Jon Infante, Bart P van de Warrenburg, Jeroen J de Vries, Jennifer Faber, Thomas Klockgether, Nicolas Casadei, Jakob Admard, Ludger Schöls, Olaf Riess, Maria do Carmo Costa, Manuela Lim. Blood and cerebellar abundance of ATXN3 splice variants in spinocerebellar ataxia type 3/Machado-Joseph disease. Neurobiology of disease. 2024-02-29. PMID:38423193. |
blood and cerebellar abundance of atxn3 splice variants in spinocerebellar ataxia type 3/machado-joseph disease. |
2024-02-29 |
2024-03-03 |
human |
| Christopher Douthwaite, Christoph Tietje, XiaoQian Ye, Sabine Liebsche. Probing cerebellar circuit dysfunction in rodent models of spinocerebellar ataxia by means of in vivo two-photon calcium imaging. STAR protocols. vol 5. issue 1. 2024-02-27. PMID:38412102. |
probing cerebellar circuit dysfunction in rodent models of spinocerebellar ataxia by means of in vivo two-photon calcium imaging. |
2024-02-27 |
2024-03-01 |
mouse |
| Christopher Douthwaite, Christoph Tietje, XiaoQian Ye, Sabine Liebsche. Probing cerebellar circuit dysfunction in rodent models of spinocerebellar ataxia by means of in vivo two-photon calcium imaging. STAR protocols. vol 5. issue 1. 2024-02-27. PMID:38412102. |
purkinje neuron degeneration characterizes spinocerebellar ataxia type 1, yet the comprehension of the impact on the broader cerebellar circuit remains incomplete. |
2024-02-27 |
2024-03-01 |
mouse |
| Marina Sanchez-Flores, Marc Corral-Juan, Esther Gasch-Navalón, Davide Cirillo, Ivelisse Sanchez, Antoni Matilla-Dueña. Novel genotype-phenotype correlations, differential cerebellar allele-specific methylation, and a common origin of the (ATTTC) Human genetics. 2024-02-24. PMID:38396267. |
novel genotype-phenotype correlations, differential cerebellar allele-specific methylation, and a common origin of the (atttc) spinocerebellar ataxia subtype 37 (sca37) is a rare disease originally identified in ataxia patients from the iberian peninsula with a pure cerebellar syndrome. |
2024-02-24 |
2024-02-26 |
Not clear |
| Xinyuan Liu, Jing Guo, Zhouyu Jiang, Xingli Liu, Hui Chen, Yuhan Zhang, Jian Wang, Chen Liu, Qing Gao, Huafu Che. Compressed cerebellar functional connectome hierarchy in spinocerebellar ataxia type 3. Human brain mapping. vol 45. issue 3. 2024-02-20. PMID:38376240. |
compressed cerebellar functional connectome hierarchy in spinocerebellar ataxia type 3. |
2024-02-20 |
2024-02-22 |
Not clear |
| Mónica Ferreira, Tamara Schaprian, David Kügler, Martin Reuter, Katharina Deike-Hoffmann, Dagmar Timmann, Thomas M Ernst, Paola Giunti, Hector Garcia-Moreno, Bart van de Warrenburg, Judith van Gaalen, Jeroen de Vries, Heike Jacobi, Katharina Marie Steiner, Gülin Öz, James M Joers, Chiadi Onyike, Michal Povazan, Kathrin Reetz, Sandro Romanzetti, Thomas Klockgether, Jennifer Fabe. Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and Duration. Cerebellum (London, England). 2024-02-16. PMID:38363498. |
in this study, we aim to identify volume differences in the cerebellum between spinocerebellar ataxia type 1 (sca1), sca3 and sca6 as well as multiple system atrophy of cerebellar type (msa-c). |
2024-02-16 |
2024-02-18 |
Not clear |
| Camila C Lobo, Guilherme S O Wertheimer, Gabriel S Schmitt, Paula C A A P Matos, Thiago J R Rezende, Joyce M Silva, Fabrício C Borba, Fabrício D Lima, Alberto R M Martinez, Orlando G P Barsottini, José Luiz Pedroso, Wilson Marques, Marcondes C Franç. Cranial Nerve Thinning Distinguishes RFC1-Related Disorder from Other Late-Onset Ataxias. Movement disorders clinical practice. vol 11. issue 1. 2024-01-31. PMID:38291837. |
rfc1-related disorder (rfc1/canvas) shares clinical features with other late-onset ataxias, such as spinocerebellar ataxias (sca) and multiple system atrophy cerebellar type (msa-c). |
2024-01-31 |
2024-02-02 |
Not clear |
| 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. |
does spinocerebellar ataxia 27b mimic cerebellar multiple system atrophy? |
2024-01-24 |
2024-01-26 |
Not clear |