All Relations between cerebellum and Ataxia

Publication Sentence Publish Date Extraction Date Species
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
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