| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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 |
| 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 |