| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| b' Olivera Tama\\xc5\\xa1, Gorica Mari\\xc4\\x87, Milutin Kosti\\xc4\\x87, Andona Milovanovi\\xc4\\x87, Katarina \\xc4\\x90ur\\xc4\\x91evi\\xc4\\x87, Biljana Salak \\xc4\\x90oki\\xc4\\x87, Elka Stefanova, Tatjana Pekmezovi\\xc4\\x87, Nata\\xc5\\xa1a Draga\\xc5\\xa1evi\\xc4\\x87-Mi\\xc5\\xa1kovi\\xc4\\x8. The Impact of Demographic and Clinical Factors on the Quality of Life in Patients with Neurodegenerative Cerebellar Ataxias. Brain sciences. vol 14. issue 1. 2024-01-26. PMID:38275506.' |
we included a total of 107 patients with cerebellar degenerative ataxia. |
2024-01-26 |
2024-01-28 |
Not clear |
| b' Olivera Tama\\xc5\\xa1, Gorica Mari\\xc4\\x87, Milutin Kosti\\xc4\\x87, Andona Milovanovi\\xc4\\x87, Katarina \\xc4\\x90ur\\xc4\\x91evi\\xc4\\x87, Biljana Salak \\xc4\\x90oki\\xc4\\x87, Elka Stefanova, Tatjana Pekmezovi\\xc4\\x87, Nata\\xc5\\xa1a Draga\\xc5\\xa1evi\\xc4\\x87-Mi\\xc5\\xa1kovi\\xc4\\x8. The Impact of Demographic and Clinical Factors on the Quality of Life in Patients with Neurodegenerative Cerebellar Ataxias. Brain sciences. vol 14. issue 1. 2024-01-26. PMID:38275506.' |
the most frequent types of neurodegenerative cerebellar ataxias were autosomal dominant ataxias (38.3%) and sporadic ataxias (32.7%). |
2024-01-26 |
2024-01-28 |
Not clear |
| Andrea Ciricugno, Viola Oldrati, Zaira Cattaneo, Maria Leggio, Cosimo Urgesi, Giusy Olivit. Cerebellar Neurostimulation for Boosting Social and Affective Functions: Implications for the Rehabilitation of Hereditary Ataxia Patients. Cerebellum (London, England). 2024-01-25. PMID:38270782. |
cerebellar neurostimulation for boosting social and affective functions: implications for the rehabilitation of hereditary ataxia patients. |
2024-01-25 |
2024-01-27 |
Not clear |
| Emilie R Lowell, James C Borders, Sarah E Perry, Avery E Dakin, Jordanna S Sevitz, Sheng-Han Kuo, Michelle S Troch. Sensorimotor Cough Dysfunction in Cerebellar Ataxias. Cerebellum (London, England). 2024-01-24. PMID:38032397. |
sensorimotor cough dysfunction in cerebellar ataxias. |
2024-01-24 |
2024-01-26 |
human |
| Emilie R Lowell, James C Borders, Sarah E Perry, Avery E Dakin, Jordanna S Sevitz, Sheng-Han Kuo, Michelle S Troch. Sensorimotor Cough Dysfunction in Cerebellar Ataxias. Cerebellum (London, England). 2024-01-24. PMID:38032397. |
cerebellar ataxias are neurological conditions with a high prevalence of aspiration pneumonia and dysphagia. |
2024-01-24 |
2024-01-26 |
human |
| Emilie R Lowell, James C Borders, Sarah E Perry, Avery E Dakin, Jordanna S Sevitz, Sheng-Han Kuo, Michelle S Troch. Sensorimotor Cough Dysfunction in Cerebellar Ataxias. Cerebellum (London, England). 2024-01-24. PMID:38032397. |
results indicate that voluntary and reflex cough sensorimotor dysfunction is present in cerebellar ataxias and that increased severity of ataxia symptoms may impact voluntary cough function. |
2024-01-24 |
2024-01-26 |
human |
| Igor Y Iskusnykh, Anastasia A Zakharova, Evgenii D Kryl'skii, Tatyana N Popov. Aging, Neurodegenerative Disorders, and Cerebellum. International journal of molecular sciences. vol 25. issue 2. 2024-01-23. PMID:38256091. |
diminished cerebellar function results in the motor and cognitive impairment observed in patients with neurodegenerative disorders such as alzheimer's disease (ad), vascular dementia (vd), parkinson's disease (pd), huntington's disease (hd), spinal muscular atrophy (sma), amyotrophic lateral sclerosis (als), friedreich's ataxia (frda), and multiple sclerosis (ms), and even during the normal aging process. |
2024-01-23 |
2024-01-25 |
Not clear |
| David J Szmulewicz, Rocco Galli, Alexander A Tarnutze. Patient-Related Outcome Measures for Oculomotor Symptoms in the Cerebellar Ataxias: Insights from Non-Cerebellar Disorders. Cerebellum (London, England). 2024-01-12. PMID:38214833. |
patient-related outcome measures for oculomotor symptoms in the cerebellar ataxias: insights from non-cerebellar disorders. |
2024-01-12 |
2024-01-14 |
human |
| 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 |
| Giacomo Argenziano, Francesco Cavallieri, Andrea Castellucci, Valentina Fioravanti, Giulia Di Rauso, Annalisa Gessani, Isabella Campanini, Andrea Merlo, Manuela Napoli, Sara Grisanti, Jessica Rossi, Giulia Toschi, Chiara Zini, Angelo Ghidini, Franco Valzani. Vestibular Hypofunction in ARSACS Syndrome: A Possible Pitfall in the Differential Diagnosis of Recessive Cerebellar and Afferent Ataxias. Neurology. Clinical practice. vol 14. issue 1. 2023-12-28. PMID:38152064. |
vestibular hypofunction in arsacs syndrome: a possible pitfall in the differential diagnosis of recessive cerebellar and afferent ataxias. |
2023-12-28 |
2023-12-30 |
Not clear |
| Giacomo Argenziano, Francesco Cavallieri, Andrea Castellucci, Valentina Fioravanti, Giulia Di Rauso, Annalisa Gessani, Isabella Campanini, Andrea Merlo, Manuela Napoli, Sara Grisanti, Jessica Rossi, Giulia Toschi, Chiara Zini, Angelo Ghidini, Franco Valzani. Vestibular Hypofunction in ARSACS Syndrome: A Possible Pitfall in the Differential Diagnosis of Recessive Cerebellar and Afferent Ataxias. Neurology. Clinical practice. vol 14. issue 1. 2023-12-28. PMID:38152064. |
autosomal recessive spastic ataxia of charlevoix-saguenay (arsacs) is an early-onset ataxia characterized by cerebellar dysfunction, spasticity, and sensory-motor polyneuropathy due to variations in the |
2023-12-28 |
2023-12-30 |
Not clear |
| Mario Manto, Hiroshi Mitom. Recent Advances in Immune-Mediated Cerebellar Ataxias: Pathogenesis, Diagnostic Approaches, Therapies, and Future Challenges-Editorial. Brain sciences. vol 13. issue 12. 2023-12-23. PMID:38137074. |
recent advances in immune-mediated cerebellar ataxias: pathogenesis, diagnostic approaches, therapies, and future challenges-editorial. |
2023-12-23 |
2023-12-25 |
Not clear |
| Mario Manto, Hiroshi Mitom. Recent Advances in Immune-Mediated Cerebellar Ataxias: Pathogenesis, Diagnostic Approaches, Therapies, and Future Challenges-Editorial. Brain sciences. vol 13. issue 12. 2023-12-23. PMID:38137074. |
the clinical category of immune-mediated cerebellar ataxias (imcas) has been established after 3 decades of clinical and experimental research. |
2023-12-23 |
2023-12-25 |
Not clear |
| Mario Manto, Hiroshi Mitom. Recent Advances in Immune-Mediated Cerebellar Ataxias: Pathogenesis, Diagnostic Approaches, Therapies, and Future Challenges-Editorial. Brain sciences. vol 13. issue 12. 2023-12-23. PMID:38137074. |
imcas include various disorders, including gluten ataxia (ga), post-infectious cerebellitis (pic), miller fisher syndrome (mfs), paraneoplastic cerebellar degeneration (pcd), opsoclonus myoclonus syndrome (oms), and anti-gad ataxia. |
2023-12-23 |
2023-12-25 |
Not clear |
| Jitka Májovská, Igor Nestrašil, Alia Ahmed, Monica T Bondy, Jiří Klempíř, Helena Jahnová, Susanne A Schneider, Dana Horáková, Jan Krásenský, Pavel Ješina, Manuela Vaneckova, David R Nascene, Chester B Whitley, Jeanine R Jarnes, Martin Magner, Petr Duše. Quantitative brain morphometry identifies cerebellar, cortical, and subcortical gray and white matter atrophy in late-onset Tay-Sachs disease. Journal of inherited metabolic disease. 2023-12-19. PMID:38112342. |
patients with dysarthria and those initially presenting with ataxia had more severe cerebellar atrophy. |
2023-12-19 |
2023-12-23 |
Not clear |
| Meike E van der Heijden, Roy V Sillito. Cerebellar dysfunction in rodent models with dystonia, tremor, and ataxia. Dystonia. vol 2. 2023-12-19. PMID:38105800. |
cerebellar dysfunction in rodent models with dystonia, tremor, and ataxia. |
2023-12-19 |
2023-12-21 |
mouse |
| Meike E van der Heijden, Roy V Sillito. Cerebellar dysfunction in rodent models with dystonia, tremor, and ataxia. Dystonia. vol 2. 2023-12-19. PMID:38105800. |
namely, how does cerebellar pathophysiology cause the diverse motor abnormalities in dystonia, tremor, and ataxia? |
2023-12-19 |
2023-12-21 |
mouse |
| Cyrine Jeridi, Amine Rachdi, Fatma Nabli, Zacharia Saied, Rania Zouari, Dina Ben Mohamed, Mariem Ben Said, Saber Masmoudi, Samia Ben Sassi, Rim Amour. Genetic heterogeneity within a consanguineous family involving Journal of neurogenetics. 2023-12-18. PMID:38109176. |
genetic heterogeneity within a consanguineous family involving autosomal recessive cerebellar ataxias (arca) constitute a highly heterogeneous group of progressive neurodegenerative disorders that typically occur prior to adulthood. |
2023-12-18 |
2023-12-21 |
Not clear |
| Masaki Taka. [Eserine, in Crooked House and Curtain]. Brain and nerve = Shinkei kenkyu no shinpo. vol 75. issue 12. 2023-12-14. PMID:38097226. |
in clinical medicine, eserine was used as an ophthalmic treatment for glaucoma and considered as a treatment for myasthenia gravis, alzheimer's disease, and hereditary cerebellar ataxias. |
2023-12-14 |
2023-12-17 |
Not clear |
| P R Sowmini, Sivaroja Yellaturi, S Sakthi Velayutham, Mugundhan Krishna. Spinocerebellar ataxia 46 in a young female. Journal of neurosciences in rural practice. vol 14. issue 4. 2023-12-07. PMID:38059248. |
sca 46 is a rare autosomal dominant ataxia initially described in a dutch family, clinically characterized by ataxia, peripheral neuropathy, cerebellar dysarthria, and varied oculomotor abnormalities. |
2023-12-07 |
2023-12-10 |
Not clear |