| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Piervito Lopriore, Marco Vista, Alessandra Tessa, Martina Giuntini, Elena Caldarazzo Ienco, Michelangelo Mancuso, Gabriele Siciliano, Filippo Maria Santorelli, Daniele Orsucc. Primary Coenzyme Q10 Deficiency-Related Ataxias. Journal of clinical medicine. vol 13. issue 8. 2024-04-27. PMID:38673663. |
cerebellar ataxia is a neurological syndrome characterized by the imbalance (e.g., truncal ataxia, gait ataxia) and incoordination of limbs while executing a task (dysmetria), caused by the dysfunction of the cerebellum or its connections. |
2024-04-27 |
2024-04-29 |
Not clear |
| Thomas Mignan, Martí Pumarola, Simon Platt, Matthew James, Marta Pereira, Antonia Morey-Matamalas, Alfredo Reci. Granuloprival cerebellar cortical degeneration in a Yorkshire Terrier and Lagotto Romagnolo dog. Journal of veterinary internal medicine. 2024-04-25. PMID:38662636. |
a 3-month-old yorkshire terrier and a 7-month-old lagotto romagnolo dog were presented with a history of progressive cerebellar dysfunction including wide-based stance, cerebellar ataxia, intention tremors, and loss of menace response despite normal vision. |
2024-04-25 |
2024-04-28 |
dog |
| 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 |
| Gajendra Kumar, Zhanhong Zhou, Zhihua Wang, Kin Ming Kwan, Chung Tin, Chi Him Eddie M. Real-time field-programmable gate array-based closed-loop deep brain stimulation platform targeting cerebellar circuitry rescues motor deficits in a mouse model of cerebellar ataxia. CNS neuroscience & therapeutics. vol 30. issue 3. 2024-03-15. PMID:38488445. |
real-time field-programmable gate array-based closed-loop deep brain stimulation platform targeting cerebellar circuitry rescues motor deficits in a mouse model of cerebellar ataxia. |
2024-03-15 |
2024-03-17 |
mouse |
| Jung Hwan Shin, Heejung Kim, So Yeon Lee, Won Tae Yoon, Sun-Won Park, Sangmin Park, Dallah Yoo, Jee-Young Le. Impaired cognitive flexibility and disrupted cognitive cerebellum in degenerative cerebellar ataxias. Brain communications. vol 6. issue 2. 2024-03-08. PMID:38454963. |
we investigated cognitive flexibility in degenerative cerebellar ataxia patients and aim to identify the pathophysiological correlates of cognitive dysfunction in relation to cerebellar cognitive circuits. |
2024-03-08 |
2024-03-10 |
human |
| Kensuke Ikeda, Ayane Tamagake, Takafumi Kubota, Rumiko Izumi, Tatsuo Yamaguchi, Kumiko Yanagi, Tatsuro Misu, Yoko Aoki, Tadashi Kaname, Masashi Aok. Case Report: An Adult Case of Poretti-Boltshauser Syndrome Diagnosed by Medical Checkup. Cerebellum (London, England). 2024-02-29. PMID:38421477. |
these findings suggest that ptbhs should be considered in not only pediatric cerebellar dysplasia but also adult cerebellar ataxia with mild presentation. |
2024-02-29 |
2024-03-02 |
Not clear |
| Fumitaka Shimiz. [Blood-brain barrier breakdown and autoimmune cerebellar ataxia]. Rinsho shinkeigaku = Clinical neurology. 2024-02-25. PMID:38403685. |
autoimmune cerebellar ataxia is a disease entity that affects the cerebellum and is induced by autoimmune mechanisms. |
2024-02-25 |
2024-02-28 |
Not clear |
| Fumitaka Shimiz. [Blood-brain barrier breakdown and autoimmune cerebellar ataxia]. Rinsho shinkeigaku = Clinical neurology. 2024-02-25. PMID:38403685. |
the disease is classified into several etiologies, including gluten ataxia, anti-glutamate decarboxylase (gad) ataxia, paraneoplastic cerebellar degeneration, primary autoimmune cerebellar ataxia and postinfectious cerebellar ataxia. |
2024-02-25 |
2024-02-28 |
Not clear |
| Fumitaka Shimiz. [Blood-brain barrier breakdown and autoimmune cerebellar ataxia]. Rinsho shinkeigaku = Clinical neurology. 2024-02-25. PMID:38403685. |
breakdown of the blood‒brain barrier (bbb) could potentially explain the vulnerability of the cerebellum during the development of autoimmune cerebellar ataxia, as it gives rise to the entry of pathogenic autoantibodies or lymphocytes into the cerebellum. |
2024-02-25 |
2024-02-28 |
Not clear |
| Fumitaka Shimiz. [Blood-brain barrier breakdown and autoimmune cerebellar ataxia]. Rinsho shinkeigaku = Clinical neurology. 2024-02-25. PMID:38403685. |
we recently identified glucose-regulated protein (grp) 78 antibodies in paraneoplastic cerebellar degeneration and lambert-eaton myasthenic syndrome, and grp78 antibodies induced by cross-reactivity with tumors can disrupt the bbb and penetrate anti-p/q type voltage-gated calcium channel (vgcc) antibodies into the cerebellum, thus leading to cerebellar ataxia in this disease. |
2024-02-25 |
2024-02-28 |
Not clear |
| Maryam Raoofi Nejad, Elham Siasi, Mohammad Amin Abdollahifar, Abbas Aliaghaei, Elham Sias. Elderberry diet enhances motor performance and reduces neuroinflammation-induced cell death in cerebellar ataxia rat models. Journal of chemical neuroanatomy. 2024-02-24. PMID:38401660. |
cerebellar ataxia (ca) is a condition in which cerebellar dysfunction results in movement disorders such as dysmetria, synergy and dysdiadochokinesia. |
2024-02-24 |
2024-02-27 |
rat |
| İlknur Sürücü Kara, Engin Köse, Büşranur Çavdarlı, Fatma Tuba Eminoğl. Neuronal ceroid lipofuscinosis type 11 diagnosed patient with bi-allelic variants in GNR gene: case report and review of literature. Journal of pediatric endocrinology & metabolism : JPEM. 2024-01-22. PMID:38253347. |
neuronal ceroid lipofuscinosis type 11 (ncl11) is a rare disease that presents with progressive cognitive decline, epilepsy, visual impairment, retinal atrophy, cerebellar ataxia and cerebellar atrophy. |
2024-01-22 |
2024-01-25 |
Not clear |
| Maria Júnia Lira E Silva, João Eudes Magalhãe. Cerebellar ataxia and primary Sjogren's syndrome without cerebellar degeneration: a case report. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 2024-01-20. PMID:38244117. |
cerebellar ataxia and primary sjogren's syndrome without cerebellar degeneration: a case report. |
2024-01-20 |
2024-01-23 |
Not clear |
| Tainá C Atella, Jorge M Medina, Georgia C Atella, Silvana Allodi, George E G Kluc. Neuroprotective Effects of Metformin Through AMPK Activation in a Neurotoxin-Based Model of Cerebellar Ataxia. Molecular neurobiology. 2024-01-02. PMID:38165584. |
cerebellar ataxia is a heterogeneous group of neural disorders clinically characterized by cerebellar dysfunction. |
2024-01-02 |
2024-01-10 |
rat |
| Lahiru L Abeysekara, Bipasha Kashyap, Chandima Kolambahewage, Pubudu N Pathirana, Malcolm Horne, David J Szmulewic. A Study of Upper-Limb Motion using Kinematic Measures for Clinical Assessment of Cerebellar Ataxia. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference. vol 2023. 2023-12-12. PMID:38082882. |
cerebellar ataxia (ca) is a group of diseases affecting the cerebellum, which is responsible for movement coordination. |
2023-12-12 |
2023-12-17 |
Not clear |
| Jonathan Nicholas, Christian Amlang, Chi-Ying R Lin, Leila Montaser-Kouhsari, Natasha Desai, Ming-Kai Pan, Sheng-Han Kuo, Daphna Shoham. The Role of the Cerebellum in Learning to Predict Reward: Evidence from Cerebellar Ataxia. Cerebellum (London, England). 2023-12-08. PMID:38066397. |
the role of the cerebellum in learning to predict reward: evidence from cerebellar ataxia. |
2023-12-08 |
2023-12-17 |
human |
| Jonathan Nicholas, Christian Amlang, Chi-Ying R Lin, Leila Montaser-Kouhsari, Natasha Desai, Ming-Kai Pan, Sheng-Han Kuo, Daphna Shoham. The Role of the Cerebellum in Learning to Predict Reward: Evidence from Cerebellar Ataxia. Cerebellum (London, England). 2023-12-08. PMID:38066397. |
here we address this gap through an investigation of multiple forms of reward learning in individuals with cerebellum dysfunction, represented by cerebellar ataxia cases. |
2023-12-08 |
2023-12-17 |
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. |
cerebellar atrophy (ca) is a frequent neuroimaging finding in paediatric neurology, usually associated with cerebellar ataxia. |
2023-11-25 |
2023-11-28 |
Not clear |
| Francis M Chen, Huixian Li, Dittman Lai-Shun Chung, Angel T L Mak, Fung Ping Leung, Ho Yin Edwin Chan, Wing Tak Won. IL-4/STAT6 axis observed to reverse proliferative defect in SCA3 patient-derived neural progenitor cells. Clinical and experimental pharmacology & physiology. 2023-11-07. PMID:37933553. |
spinocerebellar ataxia 3 (sca3) is an incurable, neurodegenerative genetic disorder that leads to progressive cerebellar ataxia and other parkinsonian-like pathologies because of loss of cerebellar neurons. |
2023-11-07 |
2023-11-08 |
Not clear |
| R G Harrell, A R Cassidy, B N Klatt, P Hovareshti, S L Whitne. Vestibular rehabilitation in cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS)- A case report. Journal of otology. vol 18. issue 4. 2023-10-26. PMID:37877066. |
cerebellar ataxia, neuropathy, and vestibular areflexia syndrome (canvas) is a neurodegenerative disease of the cerebellum. |
2023-10-26 |
2023-11-08 |
Not clear |