All Relations between Dysarthria and cerebellum
| 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. | it is frequently associated with other signs of cerebellar dysfunction, including abnormal eye movements, dysmetria, kinetic tremor, dysarthria, and/or dysphagia. | 2024-04-27 | 2024-04-29 | Not clear |
| Jiajie Chen, Lingchun Liu, Hongyan Zhu, Jinming Han, Rong Li, Xiarong Gong, Hao Fu, Jingjing Long, Haixia Li, Qiang Men. Autoimmune nodopathy with anti-contactin 1 antibody characterized by cerebellar dysarthria: a case report and literature review. Frontiers in immunology. vol 15. 2024-03-25. PMID:38524138. | autoimmune nodopathy with anti-contactin 1 antibody characterized by cerebellar dysarthria: a case report and literature review. | 2024-03-25 | 2024-03-27 | Not clear |
| Jiajie Chen, Lingchun Liu, Hongyan Zhu, Jinming Han, Rong Li, Xiarong Gong, Hao Fu, Jingjing Long, Haixia Li, Qiang Men. Autoimmune nodopathy with anti-contactin 1 antibody characterized by cerebellar dysarthria: a case report and literature review. Frontiers in immunology. vol 15. 2024-03-25. PMID:38524138. | in this study, we reported a rare case of an with cntn1 antibodies characterized by the presence of cntn1 antibodies in both serum and cerebrospinal fluid, which is associated with cerebellar dysarthria. | 2024-03-25 | 2024-03-27 | Not clear |
| Devid Damiani, Matteo Baggiani, Stefania Della Vecchia, Valentina Naef, Filippo Maria Santorell. Pluripotent Stem Cells as a Preclinical Cellular Model for Studying Hereditary Spastic Paraplegias. International journal of molecular sciences. vol 25. issue 5. 2024-03-13. PMID:38473862. | depending on the gene and mutation involved, the disease could present as a pure form with limb spasticity, or a complex form associated with cerebellar and/or cortical signs such as ataxia, dysarthria, epilepsy, and intellectual disability. | 2024-03-13 | 2024-03-15 | Not clear |
| Daisuke Kuzume, Yuko Morimoto, Satoshi Tsutsumi, Masahiro Yamasaki, Naohisa Hosom. [A case of bilateral middle cerebellar peduncle infarction with hot cross bun sign]. Rinsho shinkeigaku = Clinical neurology. 2024-02-18. PMID:38369329. | neurological examination revealed dysarthria and cerebellar truncal ataxia. | 2024-02-18 | 2024-02-21 | 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 |
| 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 |
| Arundhati Negi, M Mukhyaprana Prabh. Rapidly Progressive Dementia in an Elderly Male: Perseverance Becomes the Key to a Rare Diagnosis. Cureus. vol 15. issue 10. 2023-12-01. PMID:38021635. | neurological examination revealed fast saccades, cerebellar dysarthria, hypertonia, and normal power in all four limbs, brisk reflexes, past pointing, intentional tremors, resting myoclonic jerks, and ataxic gait. | 2023-12-01 | 2023-12-07 | Not clear |
| Arundhati Negi, M Mukhyaprana Prabh. Rapidly Progressive Dementia in an Elderly Male: Perseverance Becomes the Key to a Rare Diagnosis. Cureus. vol 15. issue 10. 2023-12-01. PMID:38021635. | neurological examination revealed fast saccades, cerebellar dysarthria, hypertonia, and normal power in all four limbs, brisk reflexes, past pointing, intentional tremors, resting myoclonic jerks, and ataxic gait. | 2023-11-29 | 2023-12-07 | Not clear |
| R Kravljanac, A Golubovic, B Vucetic Tadic, S Ostojic, I Cerovic, J Savki. "The Red Flags" in Clinical Approach to Acute Ataxia-the Experience in Cohort of 76 Children. Cerebellum (London, England). 2023-11-26. PMID:38008790. | clinical presentation was divided into two categories: (1) isolated cerebellar signs (cs): ataxic gait, dysmetria, dysdiadochokinesia, intention tremor, dysarthria, and nystagmus; (2) cs-plus symptoms which included cs associated with any of other symptoms such as encephalopathy (gcs < 15), awareness disturbances, vomiting, headache, a new onset limb or facial paresis, torticollis, hypotonia, and opsoclonus. | 2023-11-26 | 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 |
| Yeboah Kofi Gyening, Keren Boris, Mignot Cyril, Richard S Brush, Marie-Cécile Nassogne, Martin-Paul Agbag. A novel ELOVL4 variant, L168S, causes early childhood-onset Spinocerebellar ataxia-34 and retinal dysfunction: a case report. Acta neuropathologica communications. vol 11. issue 1. 2023-08-11. PMID:37568198. | here, we report a novel case of an early childhood onset and rapidly progressive cerebellar degeneration and retinal dysfunction in a belgian-italian girl who developed severe dysarthria and gait problems starting at about 3.5 years of age and progressed to immobility by 4.5 years of age. | 2023-08-11 | 2023-08-16 | Not clear |
| Mizuho Inoue, Soichi Oya, Tetsuo Yamaga, Takashi Tajima, Shunya Hanakit. Pearls & Oy-sters: Cognitive and Affective Dysfunction Caused by a Small Cerebellar Hemangioblastoma. Neurology. 2023-07-05. PMID:37407260. | the primary function of the cerebellum is the coordination and regulation of movement; therefore, cerebellar tumors usually present with ataxia, dysarthria, and vertigo. | 2023-07-05 | 2023-08-14 | Not clear |
| Mizuho Inoue, Soichi Oya, Tetsuo Yamaga, Takashi Tajima, Shunya Hanakit. Pearls & Oy-sters: Cognitive and Affective Dysfunction Caused by a Small Cerebellar Hemangioblastoma. Neurology. 2023-07-05. PMID:37407260. | she had no cerebellar symptoms including no coordination dysfunction or dysarthria. | 2023-07-05 | 2023-08-14 | Not clear |
| Karamazovova Simona, Matuskova Veronika, Ismail Zahinoor, Vyhnalek Marti. Neuropsychiatric symptoms in spinocerebellar ataxias and Friedreich ataxia. Neuroscience and biobehavioral reviews. 2023-05-03. PMID:37137435. | spinocerebellar ataxias (sca) and friedreich ataxia (frda) are rare neurodegenerative diseases of the cerebellum presenting mainly with a progressive loss of gait and limb coordination, dysarthria, and other motor disturbances, but also a range of cognitive and neuropsychiatric symptoms. | 2023-05-03 | 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 |
| Ketan Agarwal, Ratnadeep Biswas, Vijay Kuma. Wernekink Commissure Syndrome With Bilateral Cerebellar Signs and Holmes Tremor in a Patient With a Preexisting Movement Disorder. Cureus. vol 15. issue 3. 2023-04-03. PMID:37009377. | the patient presented with sudden onset gait instability with bilateral cerebellar signs (more prominent on the left side), holmes tremor in bilateral limbs, slurred speech, and marked dysarthria. | 2023-04-03 | 2023-08-14 | Not clear |
| Klivényi Péter, Szpisjak László, Salamon András, L Németh Viola, Szépfalusi Noémi, Zoltán Maróti, Kalmár Tibor, Zimmermann Aliz, Zádori Déne. [Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient]. Ideggyogyaszati szemle. vol 76. issue 1-2. 2023-03-09. PMID:36892293. | spinocerebellar ataxia type 48 (sca48) is an autosomal dominantly inherited disease characterized by gait and limb ataxia, cerebellar dysarthria, cognitive impairment, psychiatric abnormalities and variable types of movement disorders. |
2023-03-09 | 2023-08-14 | Not clear |
| Tingwei Song, Yuwen Zhao, Guo Wen, Juan Du, Qian X. A novel Frontiers in neurology. vol 14. 2023-02-23. PMID:36816548. | common clinical symptoms include dysarthria, cerebellar symptoms, motor deficits, and cognitive impairment. | 2023-02-23 | 2023-08-14 | Not clear |
| Dinesh M Chaudhari, Pushpendra Nath Renjen, Urusa Hasan, Nidhi Goyal, Kamal Ahma. Metronidazole-Induced Encephalopathy (MIE). Cureus. vol 14. issue 12. 2023-02-01. PMID:36721588. | it may produce different neurologic side effects like cerebellar dysfunction, peripheral neuropathy, vestibulotoxicity, visual impairment, encephalopathy, ataxic gait, seizures, dysarthria, and cochleotoxicity. | 2023-02-01 | 2023-08-14 | Not clear |