All Relations between Ataxia and cerebellum

Publication Sentence Publish Date Extraction Date Species
Mario Mascalch. MRI CNS Atrophy Pattern and the Etiologies of Progressive Ataxias. Tomography (Ann Arbor, Mich.). vol 8. issue 1. 2022-02-24. PMID:35202200. mri shows the three archetypal patterns of cns volume loss underlying progressive ataxias in vivo, namely spinal atrophy (sa), cortical cerebellar atrophy (cca) and olivopontocerebellar atrophy (opca). 2022-02-24 2023-08-13 Not clear
Ian H Harding, Phillip G D War. Brain susceptibility imaging provides valuable Brain communications. vol 4. issue 1. 2022-02-18. PMID:35178517. brain susceptibility imaging provides valuable this scientific commentary relates to: 'quantitative susceptibility mapping reveals alterations of dentate nuclei in common types of degenerative cerebellar ataxias' by deistung 2022-02-18 2023-08-13 Not clear
Izumi Aida, Tetsuo Ozawa, Kentaro Ohta, Hidehiko Fujinaka, Kiyoe Goto, Takashi Nakajim. Autosomal Recessive Spinocerebellar Ataxia Type 10: A Report of a New Case in Japan. Internal medicine (Tokyo, Japan). 2022-02-03. PMID:35110481. this case presented with adult-onset slowly progressive spastic ataxia with cerebellar atrophy and mild cognitive decline. 2022-02-03 2023-08-13 Not clear
Benjamin Roeben, Eva Bültmann, Claudia Stendel, Matthis Synofzi. Cerebellar Bottom of Fissure Hyperintensities in MT-ATP6-associated Ataxia. Annals of neurology. 2022-01-30. PMID:35094430. cerebellar bottom of fissure hyperintensities in mt-atp6-associated ataxia. 2022-01-30 2023-08-13 Not clear
Hiroshi Mitoma, Mario Mant. Advances in the Pathogenesis of Auto-antibody-Induced Cerebellar Synaptopathies. Cerebellum (London, England). 2022-01-22. PMID:35064896. the presence of auto-antibodies that target synaptic machinery proteins was documented recently in immune-mediated cerebellar ataxias. 2022-01-22 2023-08-13 Not clear
Natale Maiorana, Matteo Guidetti, Michelangelo Dini, Alberto Priori, Roberta Ferrucc. Cerebellar tDCS as Therapy for Cerebellar Ataxias. Cerebellum (London, England). 2022-01-21. PMID:35060077. cerebellar tdcs as therapy for cerebellar ataxias. 2022-01-21 2023-08-13 Not clear
Natale Maiorana, Matteo Guidetti, Michelangelo Dini, Alberto Priori, Roberta Ferrucc. Cerebellar tDCS as Therapy for Cerebellar Ataxias. Cerebellum (London, England). 2022-01-21. PMID:35060077. cerebellar ataxias (cas) represent the prototypical clinical manifestation of cerebellar alterations, but other movement disorders, such as parkinson's disease, essential tremor, and dystonia have also been associated with alterations of networks which include the cerebellum, or of the cerebellum itself. 2022-01-21 2023-08-13 Not clear
Sergio Muñiz-Castrillo, Alberto Vogrig, Nicolás Lundahl Ciano-Petersen, Macarena Villagrán-García, Bastien Joubert, Jérôme Honnora. Novelties in Autoimmune and Paraneoplastic Cerebellar Ataxias: Twenty Years of Progresses. Cerebellum (London, England). 2022-01-12. PMID:35020135. novelties in autoimmune and paraneoplastic cerebellar ataxias: twenty years of progresses. 2022-01-12 2023-08-13 Not clear
Sergio Muñiz-Castrillo, Alberto Vogrig, Nicolás Lundahl Ciano-Petersen, Macarena Villagrán-García, Bastien Joubert, Jérôme Honnora. Novelties in Autoimmune and Paraneoplastic Cerebellar Ataxias: Twenty Years of Progresses. Cerebellum (London, England). 2022-01-12. PMID:35020135. major advances in our knowledge concerning autoimmune and paraneoplastic cerebellar ataxias have occurred in the last 20 years. 2022-01-12 2023-08-13 Not clear
Sergio Muñiz-Castrillo, Alberto Vogrig, Nicolás Lundahl Ciano-Petersen, Macarena Villagrán-García, Bastien Joubert, Jérôme Honnora. Novelties in Autoimmune and Paraneoplastic Cerebellar Ataxias: Twenty Years of Progresses. Cerebellum (London, England). 2022-01-12. PMID:35020135. moreover, important advances in our understanding of the pathogenesis of cerebellar ataxias include the description of antibody effects, especially those targeting cell-surface antigens, and first attempts to isolate antigen-specific t-cells. 2022-01-12 2023-08-13 Not clear
Sergio Muñiz-Castrillo, Alberto Vogrig, Nicolás Lundahl Ciano-Petersen, Macarena Villagrán-García, Bastien Joubert, Jérôme Honnora. Novelties in Autoimmune and Paraneoplastic Cerebellar Ataxias: Twenty Years of Progresses. Cerebellum (London, England). 2022-01-12. PMID:35020135. herein, we review the principal novelties of the last 20 years regarding autoimmune and paraneoplastic cerebellar ataxias. 2022-01-12 2023-08-13 Not clear
Hiroshi Mitoma, Jerome Honnorat, Kazuhiko Yamaguchi, Mario Mant. Cerebellar long-term depression and auto-immune target of auto-antibodies: the concept of LTDpathies. Molecular biomedicine. vol 2. issue 1. 2022-01-10. PMID:35006439. in immune-mediated cerebellar ataxias (imcas), various synaptic proteins, such as gad65, voltage-gated ca channel (vgcc), metabotropic glutamate receptor type 1 (mglur1), and glutamate receptor delta (glur delta) are auto-immune targets. 2022-01-10 2023-08-13 Not clear
Hiroshi Mitoma, Jerome Honnorat, Kazuhiko Yamaguchi, Mario Mant. Cerebellar long-term depression and auto-immune target of auto-antibodies: the concept of LTDpathies. Molecular biomedicine. vol 2. issue 1. 2022-01-10. PMID:35006439. we suggest that anti-vgcc, anti-mglur1, and anti-glur delta abs-associated cerebellar ataxias share one common pathophysiological mechanism: a deregulation in pf-pc ltd, which results in impairment of restoration or maintenance of the internal model and triggers cerebellar ataxias. 2022-01-10 2023-08-13 Not clear
Filip Tichane. Psychiatric-Like Impairments in Mouse Models of Spinocerebellar Ataxias. Cerebellum (London, England). 2022-01-09. PMID:35000108. in sca1 mice with complex neuropathology, some of the psychiatric-like impairments are present even before marked cerebellar degeneration and ataxia and correlate with hippocampal atrophy. 2022-01-09 2023-08-13 mouse
Filip Tichane. Psychiatric-Like Impairments in Mouse Models of Spinocerebellar Ataxias. Cerebellum (London, England). 2022-01-09. PMID:35000108. similarly, complete or partial deletion of the implicated gene (atxn1) leads to cognitive dysfunction and anxiety-like behavior, respectively, without apparent ataxia and cerebellar degeneration. 2022-01-09 2023-08-13 mouse
Reiko Ashida, Peter Walsh, Jonathan C W Brooks, Nadia L Cerminara, Richard Apps, Richard J Edward. Sensory and motor electrophysiological mapping of the cerebellum in humans. Scientific reports. vol 12. issue 1. 2022-01-08. PMID:34997137. cerebellar damage during posterior fossa surgery in children can lead to ataxia and risk of cerebellar mutism syndrome. 2022-01-08 2023-08-13 human
Polina A Egorova, Ilya B Bezprozvann. Electrophysiological Studies Support Utility of Positive Modulators of SK Channels for the Treatment of Spinocerebellar Ataxia Type 2. Cerebellum (London, England). 2022-01-03. PMID:34978024. the abnormal intrinsic pacemaking was reported in mouse models of episodic ataxia type 2 (ea2), sca1, sca2, sca3, sca6, huntington's disease (hd), and in some other murine models of the disorders associated with the cerebellar degeneration. 2022-01-03 2023-08-13 mouse
Brenda Toscano Márquez, Anna A Cook, Max Rice, Alexia Smileski, Kristen Vieira-Lomasney, François Charron, R Anne McKinney, Alanna J Wat. Molecular Identity and Location Influence Purkinje Cell Vulnerability in Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay Mice. Frontiers in cellular neuroscience. vol 15. 2021-12-31. PMID:34970120. in patients with autosomal-recessive spastic ataxia of charlevoix-saguenay (arsacs) and mouse models of arsacs, it has been observed that purkinje cells in anterior cerebellar vermis are vulnerable to degeneration while those in posterior vermis are resilient. 2021-12-31 2023-08-13 mouse
Deborah A Sival, Suus A M van Noort, Marina A J Tijssen, Tom J de Koning, Dineke S Verbee. Developmental neurobiology of cerebellar and Basal Ganglia connections. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. vol 36. 2021-12-26. PMID:34954622. the high prevalence of mixed phenotypes of early onset ataxia (eoa) with comorbid dystonia has shifted the pathogenetic concept from the cerebellum towards the interconnected cerebellar motor network. 2021-12-26 2023-08-13 Not clear
Lise Legrand, Jonathan W Weinsaft, Francoise Pousset, Claire Ewenczyk, Perrine Charles, Stéphane Hatem, Anna Heinzmann, Marie Biet, Alexandra Durr, Alban Redheui. Characterizing cardiac phenotype in Friedreich's ataxia: The CARFA study. Archives of cardiovascular diseases. 2021-12-18. PMID:34920960. friedreich's ataxia is an autosomal recessive mitochondrial disease caused by a triplet repeat expansion in the frataxin gene (fxn), exhibiting cerebellar sensory ataxia, diabetes and cardiomyopathy. 2021-12-18 2023-08-13 Not clear