| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Nicolaas J M Arts, Maud E G van Dorst, Sandra H Vos, Roy P C Kessel. Coordination and Cognition in Pure Nutritional Wernicke's Encephalopathy with Cerebellar Degeneration after COVID-19 Infection: A Unique Case Report. Journal of clinical medicine. vol 12. issue 7. 2023-04-13. PMID:37048595. |
however, a similar degeneration may also develop after non-alcoholic malnutrition, but evidence for a lasting ataxia of stance and gait and lasting abnormalities in the cerebellum is lacking in the few patients described with purely nutritional cerebellar degeneration (ncd). |
2023-04-13 |
2023-08-14 |
Not clear |
| Dmitry Yu Isaev, Roza M Vlasova, J Matias Di Martino, Christopher D Stephen, Jeremy D Schmahmann, Guillermo Sapiro, Anoopum S Gupt. Uncertainty of Vowel Predictions as a Digital Biomarker for Ataxic Dysarthria. Cerebellum (London, England). 2023-04-11. PMID:37039956. |
dysarthria is a common manifestation across cerebellar ataxias leading to impairments in communication, reduced social connections, and decreased quality of life. |
2023-04-11 |
2023-08-14 |
human |
| Andreas Traschütz, Astrid D Adarmes-Gomez, Mathieu Anheim, Jonathan Baets, Björn H Falkenburger, Janina Gburek-Augustat, Sarah Doss, Christoph Kamm, Peter Klivenyi, Marcus Grobe-Einsler, Thomas Klopstock, Martina Minnerop, Alexander Münchau, Chiara Pane, Mathilde Renaud, Filippo M Santorelli, Ludger Schöls, Dagmar Timmann, Stefan Vielhaber, Tobias B Haack, Bart P van de Warrenburg, Ginevra Zanni, Matthis Synofzi. Autosomal Recessive Cerebellar Ataxias in Europe: Frequency, Onset, and Severity in 677 Patients. Movement disorders : official journal of the Movement Disorder Society. 2023-04-07. PMID:37027459. |
autosomal recessive cerebellar ataxias in europe: frequency, onset, and severity in 677 patients. |
2023-04-07 |
2023-08-14 |
Not clear |
| Anhar Hassa. Episodic Ataxias: Primary and Secondary Etiologies, Treatment, and Classification Approaches. Tremor and other hyperkinetic movements (New York, N.Y.). vol 13. 2023-04-03. PMID:37008993. |
episodic ataxia (ea), characterized by recurrent attacks of cerebellar dysfunction, is the manifestation of a group of rare autosomal dominant inherited disorders. |
2023-04-03 |
2023-08-14 |
Not clear |
| Keisuke Ishii, Takao Kohno, Mitsuharu Hattor. Postnatal injection of Reelin protein into the cerebellum ameliorates the motor functions in reeler mouse. Neuroscience research. 2023-04-03. PMID:37011786. |
in both humans and mice, the lack of reelin gene causes cerebellar hypoplasia and ataxia. |
2023-04-03 |
2023-08-14 |
mouse |
| Mehri Salari, Masoud Etemadifar, Ronak Rashedi, Sayna Mardan. A Review of Ocular Movement Abnormalities in Hereditary Cerebellar Ataxias. Cerebellum (London, England). 2023-03-31. PMID:37000369. |
a review of ocular movement abnormalities in hereditary cerebellar ataxias. |
2023-03-31 |
2023-08-14 |
Not clear |
| Mehri Salari, Masoud Etemadifar, Ronak Rashedi, Sayna Mardan. A Review of Ocular Movement Abnormalities in Hereditary Cerebellar Ataxias. Cerebellum (London, England). 2023-03-31. PMID:37000369. |
cerebellar ataxias are a wide heterogeneous group of disorders that may present with fine motor deficits as well as gait and balance disturbances that have a significant influence on everyday activities. |
2023-03-31 |
2023-08-14 |
Not clear |
| Mehri Salari, Masoud Etemadifar, Ronak Rashedi, Sayna Mardan. A Review of Ocular Movement Abnormalities in Hereditary Cerebellar Ataxias. Cerebellum (London, England). 2023-03-31. PMID:37000369. |
to review the ocular movements in cerebellar ataxias in order to improve the clinical knowledge of cerebellar ataxias and related subtypes. |
2023-03-31 |
2023-08-14 |
Not clear |
| Nicole M Eklund, Jessey Ouillon, Vineet Pandey, Christopher D Stephen, Jeremy D Schmahmann, Jeremy Edgerton, Krzysztof Z Gajos, Anoopum S Gupt. Real-life ankle submovements and computer mouse use reflect patient-reported function in adult ataxias. Brain communications. vol 5. issue 2. 2023-03-30. PMID:36993945. |
thirty-four individuals with degenerative ataxias (spinocerebellar ataxia types 1, 2, 3 and 6 and multiple system atrophy of the cerebellar type) and eight age-matched controls completed the cross-sectional study. |
2023-03-30 |
2023-08-14 |
mouse |
| Toshio Fukutak. [Non-cerebellar ataxias: posterior column-like ataxia and cerebellar-like ataxia]. Rinsho shinkeigaku = Clinical neurology. 2023-03-29. PMID:36990780. |
ataxia is not only due to cerebellar lesions, but also due to non-cerebellar lesions such as those in the brain, spinal cord, dorsal root (dr), peripheral nerve. |
2023-03-29 |
2023-08-14 |
Not clear |
| Toshio Fukutak. [Non-cerebellar ataxias: posterior column-like ataxia and cerebellar-like ataxia]. Rinsho shinkeigaku = Clinical neurology. 2023-03-29. PMID:36990780. |
from these viewpoints, i here describe various non-cerebellar ataxia in some disorders such as tabes dorsalis and sensory neuropathies and emphasize a role of a peripheral sensory input to the cerebellum via the dr ganglia and spinocerebellar tract for sensory ataxia because there is the international consensus (2016) that the ataxia in miller fisher syndrome is suggested cerebellar-like clinicophysiologically. |
2023-03-29 |
2023-08-14 |
Not clear |
| Mario Manto, Marios Hadjivassiliou, José Fidel Baizabal-Carvallo, Christiane S Hampe, Jerome Honnorat, Bastien Joubert, Hiroshi Mitoma, Sergio Muñiz-Castrillo, Aasef G Shaikh, Alberto Vogri. Consensus Paper: Latent Autoimmune Cerebellar Ataxia (LACA). Cerebellum (London, England). 2023-03-29. PMID:36991252. |
immune-mediated cerebellar ataxias (imcas) have diverse etiologies. |
2023-03-29 |
2023-08-14 |
Not clear |
| Sunmi Yoon, Napissara Boonpraman, Chae Young Kim, Jong-Seok Moon, Sun Shin Y. Reduction of fetuin-A levels contributes to impairment of Purkinje cells in cerebella of patients with Parkinson's disease. BMB reports. 2023-03-20. PMID:36935573. |
phenotypic features such as ataxia and loss of motor function, which are characteristics of parkinson's disease (pd), are expected to be very closely related to cerebellum function. |
2023-03-20 |
2023-08-14 |
mouse |
| b' Cak Ciss\\xc3\\xa9, L Ciss\\xc3\\xa9, O Samass\\xc3\\xa9kou, H O Ba, T Coulibaly, S H Diallo, S Diallo, A Tam\\xc3\\xa9ga, S Diarra, A B Ma\\xc3\\xafga, F Kan\\xc3\\xa9, A Yalcouy\\xc3\\xa9, A Bocoum, M E Demb\\xc3\\xa9l\\xc3\\xa9, O Traor\\xc3\\xa9, A Simaga, S F Traor\\xc3\\xa9, M Keita, K Fischbeck, M Traor\\xc3\\xa9, C O Guinto, G Landour\\xc3\\xa. Clinical, paraclinical and genetic aspects of autosomal recessive cerebellar ataxias (ARCA) in Mali. Le Mali medical. vol 37. issue 4. 2023-03-15. PMID:36919030.' |
clinical, paraclinical and genetic aspects of autosomal recessive cerebellar ataxias (arca) in mali. |
2023-03-15 |
2023-08-14 |
Not clear |
| b' Cak Ciss\\xc3\\xa9, L Ciss\\xc3\\xa9, O Samass\\xc3\\xa9kou, H O Ba, T Coulibaly, S H Diallo, S Diallo, A Tam\\xc3\\xa9ga, S Diarra, A B Ma\\xc3\\xafga, F Kan\\xc3\\xa9, A Yalcouy\\xc3\\xa9, A Bocoum, M E Demb\\xc3\\xa9l\\xc3\\xa9, O Traor\\xc3\\xa9, A Simaga, S F Traor\\xc3\\xa9, M Keita, K Fischbeck, M Traor\\xc3\\xa9, C O Guinto, G Landour\\xc3\\xa. Clinical, paraclinical and genetic aspects of autosomal recessive cerebellar ataxias (ARCA) in Mali. Le Mali medical. vol 37. issue 4. 2023-03-15. PMID:36919030.' |
autosomal recessive cerebellar ataxias (arca) are a group of rare and heterogynous neurodegenerative diseases mainly characterized by unbalance and walking difficulty and movement incoordination. |
2023-03-15 |
2023-08-14 |
Not clear |
| Hoda Ranjbar, Monavareh Soti, Kristi A Kohlmeier, Mahyar Janahmadi, Mohammad Shaban. Pharmacologic antagonism of CB1 receptors improves electrophysiological alterations in Purkinje cells exposed to 3-AP. BMC neuroscience. vol 24. issue 1. 2023-03-03. PMID:36869289. |
although ataxia is associated with cerebellar dysfunction, little is known about the effects of 3-ap exposure on purkinje cell electrophysiological properties. |
2023-03-03 |
2023-08-14 |
Not clear |
| Chi-Ying R Lin, Sheng-Han Ku. Ataxias: Hereditary, Acquired, and Reversible Etiologies. Seminars in neurology. 2023-02-24. PMID:36828010. |
a variety of etiologies can cause cerebellar dysfunction, leading to ataxia symptoms. |
2023-02-24 |
2023-08-14 |
Not clear |
| Thomas Klockgethe. [Gene Therapy for Ataxias]. Fortschritte der Neurologie-Psychiatrie. 2023-02-22. PMID:36806180. |
ataxias are progressive diseases that are usually the result of cerebellar degeneration. |
2023-02-22 |
2023-08-14 |
Not clear |
| Eduardo Benarroc. What Is the Role of Norepinephrine in Cerebellar Modulation and Stress-Induced Episodic Ataxia? Neurology. vol 100. issue 8. 2023-02-22. PMID:36806456. |
what is the role of norepinephrine in cerebellar modulation and stress-induced episodic ataxia? |
2023-02-22 |
2023-08-14 |
Not clear |
| Sophie Tezenas du Montcel, Emilien Petit, Titilayo Olubajo, Jennifer Faber, Pauline Lallemant-Dudek, Khalaf Bushara, Susan Perlman, Sub H Subramony, David Morgan, Brianna Jackman, Henry Lauris Paulson, Gülin Öz, Thomas Klockgether, Alexandra Durr, Tetsuo Ashizaw. Baseline Clinical and Blood Biomarker in Patients With Preataxic and Early-Stage Disease Spinocerebellar Ataxia 1 and 3. Neurology. 2023-02-16. PMID:36797067. |
in spinocerebellar ataxia, ataxia onset can be preceded by mild clinical manifestation, cerebellar and/or brainstem alterations or biomarkers modifications. |
2023-02-16 |
2023-08-14 |
Not clear |