| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Mónica Ferreira, Tamara Schaprian, David Kügler, Martin Reuter, Katerina Deike-Hoffmann, Dagmar Timmann, Thomas 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. Research square. 2023-11-28. PMID:38014351. |
cerebellar volumetry in ataxias: relation to ataxia severity and duration. |
2023-11-28 |
2023-11-29 |
Not clear |
| Poornima Jayadev Menon, Tan Xin Yi, Sharon Moran, Richard A Walsh, Sinéad M Murphy, Petya Bogdanova-Mihaylov. Health-Related Quality of Life in Patients with Inherited Ataxia in Ireland. Cerebellum (London, England). 2023-11-27. PMID:38010570. |
inherited cerebellar ataxias (ca) are heterogeneous progressive neurological conditions associated with significant functional limitations. |
2023-11-27 |
2023-11-29 |
human |
| Dolores Martínez-Rubio, Isabel Hinarejos, Herminia Argente-Escrig, Clara Marco-Marín, María Ana Lozano, Nerea Gorría-Redondo, Vincenzo Lupo, Itxaso Martí-Carrera, Concepción Miranda, María Vázquez-López, Asunción García-Pérez, Ana Victoria Marco-Hernández, Miguel Tomás-Vila, Sergio Aguilera-Albesa, Carmen Espinó. Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy. International journal of molecular sciences. vol 24. issue 22. 2023-11-25. PMID:38003592. |
we investigated ten cases with early-onset cerebellar involvement with and without ataxia by exome sequencing or by a targeted panel with 363 genes involved in ataxia or spastic paraplegia. |
2023-11-25 |
2023-11-28 |
Not clear |
| Katharina Feil, Tim W Rattay, Adedolapo Kamaldeen Adeyemi, Nicolina Goldschagg, Michael Leo Strup. [What's behind cerebellar dizziness? - News on diagnosis and therapy]. Laryngo- rhino- otologie. 2023-11-21. PMID:37989215. |
typical clinical cerebellar signs, including gait and limb ataxia or dysarthria, were found less frequently. |
2023-11-21 |
2023-11-29 |
Not clear |
| Silvia Maria Marchese, Fulvia Palesi, Anna Nigri, Maria Grazia Bruzzone, Chiara Pantaleoni, Claudia A M Gandini Wheeler-Kingshott, Stefano D'Arrigo, Egidio D'Angelo, Paolo Cavallar. Structural and connectivity parameters reveal spared connectivity in young patients with non-progressive compared to slow-progressive cerebellar ataxia. Frontiers in neurology. vol 14. 2023-11-15. PMID:37965172. |
within pediatric cerebellar ataxias (pcas), patients with non-progressive ataxia (nonp) surprisingly show postural motor behavior comparable to that of healthy controls, differently to slow-progressive ataxia patients (slowp). |
2023-11-15 |
2023-11-20 |
Not clear |
| Sang-Seok Yeo, Seung-Min Nam, In-Hee Ch. Injury of the Vestibulocerebellar Tract and Signs of Ataxia in Patients with Cerebellar Stroke. Journal of clinical medicine. vol 12. issue 21. 2023-11-14. PMID:37959342. |
injury of the vestibulocerebellar tract and signs of ataxia in patients with cerebellar stroke. |
2023-11-14 |
2023-11-20 |
Not clear |
| Giulia Ferrera, Rossella Izzo, Daniele Ghezzi, Lorenzo Nanetti, Eleonora Lamantea, Anna Ardisson. A novel pathogenic variant in the SCA25-related gene expanding the etiology of early-onset and progressive cerebellar ataxia in childhood. Neuropediatrics. 2023-11-07. PMID:37935417. |
we report for the first time cerebellar gray matter hyperintensities, suggesting that sca25 should be included in the differential diagnosis of cerebellar ataxias associated with such brain imaging features. |
2023-11-07 |
2023-11-20 |
Not clear |
| Takuya Watanabe, Yuki Kakinuma, Keiko Watanabe, Ryuta Kinn. Acute cerebellitis following COVID-19 infection associated with autoantibodies to glutamate receptors: a case report. Journal of neurovirology. 2023-11-06. PMID:37930583. |
about 2 weeks after these symptoms improved, she showed cerebellar symptoms such as ocular overshoot and ataxia when presenting to our hospital. |
2023-11-06 |
2023-11-08 |
Not clear |
| Zeus T Dominguez-Vega, Mariano Bernaldo de Quiros, Jan Willem J Elting, Deborah A Sival, Natasha M Maurit. Instrumented Gait Classification Using Meaningful Features in Patients with Impaired Coordination. Sensors (Basel, Switzerland). vol 23. issue 20. 2023-10-30. PMID:37896504. |
early onset ataxia (eoa) and developmental coordination disorder (dcd) both affect cerebellar functioning in children, making the clinical distinction challenging. |
2023-10-30 |
2023-11-08 |
human |
| Patrícia Áurea Andreucci Martins Bonilha, Beatriz Cassarotti, Thabata Emanuelle Martins Nunes, Hélio Afonso Ghizoni Teiv. Frontal ataxia: historical aspects and clinical definition. Arquivos de neuro-psiquiatria. 2023-10-29. PMID:37899045. |
the goal of the present study is to recall the historical aspects of this condition, to draw attention to the importance of this clinical finding for the differential diagnosis of ataxias and to review the main semiological differences between primary ataxias (frontal, cerebellar, and sensory ataxia). |
2023-10-29 |
2023-11-08 |
Not clear |
| Evan Hy Einstein, Juliana Corlier, Cole Matthews, Doan Ngo, Michael K Leuchter, Cole Citrenbaum, Nikita Vince-Cruz, Bhavna Ramesh, Aaron Slan, Scott A Wilke, Nathaniel Ginder, Thomas Strouse, Andrew F Leuchte. Bilateral Cerebellar Repetitive Transcranial Magnetic Stimulation for Chronic Ataxia After Hemorrhagic Stroke: a Case Report. Cerebellum (London, England). 2023-10-21. PMID:37864649. |
bilateral cerebellar repetitive transcranial magnetic stimulation for chronic ataxia after hemorrhagic stroke: a case report. |
2023-10-21 |
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 |
| Camilla Aurora Franchino, Martina Brughera, Valentina Baderna, Daniele De Ritis, Alessandra Rocco, Sara Seneca, Luc Regal, Paola Podini, Maurizio D'Antonio, Camilo Toro, Angelo Quattrini, Emmanuel Scalais, Francesca Maltecc. Sustained OMA1-mediated integrated stress response is beneficial for spastic ataxia type 5. Brain : a journal of neurology. 2023-10-07. PMID:37804316. |
pharmacological tuning of the isr may represent a future therapeutic strategy for spax5 and other cerebellar ataxias caused by impaired mitochondrial proteostasis. |
2023-10-07 |
2023-10-15 |
mouse |
| Hélio A G Teive, Léo Coutinho, Alex T Meira, Gustavo L Franklin, Carlos Henrique F Camargo, Renato Puppi Munho. Autosomal Recessive Cerebellar Ataxias: New Acronyms, Old Eponyms, and the Butterfly Life Cycle. Movement disorders clinical practice. vol 10. issue 9. 2023-09-29. PMID:37772306. |
autosomal recessive cerebellar ataxias: new acronyms, old eponyms, and the butterfly life cycle. |
2023-09-29 |
2023-10-07 |
Not clear |
| Mario Manto, Jan Cendelin, Michael Strupp, Hiroshi Mitom. Advances in cerebellar disorders: pre-clinical models, therapeutic targets and challenges. Expert opinion on therapeutic targets. 2023-09-28. PMID:37768297. |
cerebellar ataxias (cas) represent neurological disorders with multiple etiologies and a high phenotypic variability. |
2023-09-28 |
2023-10-07 |
Not clear |
| 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 |
| Alex T Meira, Marianna P M de Moraes, Matheus G Ferreira, Gustavo L Franklin, Flávio M Rezende Filho, Hélio A G Teive, Orlando G P Barsottini, José Luiz Pedros. Immune-mediated ataxias: Guide to clinicians. Parkinsonism & related disorders. 2023-09-25. PMID:37748994. |
immune-mediated cerebellar ataxias were initially described as a clinical entity in the 1980s, and since then, an expanding body of evidence has contributed to our understanding of this topic. |
2023-09-25 |
2023-10-07 |
Not clear |
| Alex T Meira, Marianna P M de Moraes, Matheus G Ferreira, Gustavo L Franklin, Flávio M Rezende Filho, Hélio A G Teive, Orlando G P Barsottini, José Luiz Pedros. Immune-mediated ataxias: Guide to clinicians. Parkinsonism & related disorders. 2023-09-25. PMID:37748994. |
these ataxias encompass various etiologies, including postinfectious cerebellar ataxia, gluten ataxia, paraneoplastic cerebellar degeneration, opsoclonus-myoclonus-ataxia syndrome and primary autoimmune cerebellar ataxia. |
2023-09-25 |
2023-10-07 |
Not clear |
| Mahesh Kamate, Thanuja Basavanagowd. ARV1 Gene: A Novel Cause of Autosomal Recessive Cerebellar Ataxia with Elevated Alpha Fetoprotein. Cerebellum (London, England). 2023-09-25. PMID:37749428. |
we report a case of arv1 mutation presenting with ataxia, ocular abnormalities, and elevated alpha-fetoprotein levels, thus mimicking autosomal recessive cerebellar ataxias. |
2023-09-25 |
2023-10-07 |
Not clear |
| Haloom Rafehi, Mark F Bennett, Melanie Bahl. Detection and discovery of repeat expansions in ataxia enabled by next-generation sequencing: present and future. Emerging topics in life sciences. 2023-09-21. PMID:37733280. |
hereditary cerebellar ataxias are a heterogenous group of progressive neurological disorders that are disproportionately caused by repeat expansions (res) of short tandem repeats (strs). |
2023-09-21 |
2023-10-07 |
Not clear |