All Relations between Ataxia and cerebellum

Reference Sentence Publish Date Extraction Date Species
Shunsuke Koga, Shan Ali, Matthew C Baker, Klaas J Wierenga, Michelle Dompenciel, Dennis W Dickson, Zbigniew K Wszole. A novel clinicopathologic entity causing rapidly progressive cerebellar ataxia? Parkinsonism & related disorders vol issue 2022 36396537 these names describe key features of the disease, including degeneration limited to the cerebellar cortex (with or without secondary involvement of inferior olivary nuclei), a slowly progressive ataxia, and absence of a clear etiology, such as multiple system atrophy, as well as paraneoplastic, autoimmune, infectious and inherited ataxias. 2022-11-17 2022-11-21 Not clear
Catarina Os\\xc3\\xb3rio, Joshua J White, Heiling Lu, Gerrit C Beekhof, Francesca Romana Fiocchi, Charlotte A Andriessen, Stephanie Dijkhuizen, Laura Post, Martijn Schonewill. Pre-ataxic loss of intrinsic plasticity and motor learning in a mouse model of SCA1. Brain : a journal of neurology vol issue 2022 36352508 spinocerebellar ataxias are neurodegenerative diseases the hallmark symptom of which is the development of ataxia due to cerebellar dysfunction. 2022-11-10 2022-11-15 Not clear
Catarina Os\\xc3\\xb3rio, Joshua J White, Heiling Lu, Gerrit C Beekhof, Francesca Romana Fiocchi, Charlotte A Andriessen, Stephanie Dijkhuizen, Laura Post, Martijn Schonewill. Pre-ataxic loss of intrinsic plasticity and motor learning in a mouse model of SCA1. Brain : a journal of neurology vol issue 2022 36352508 together, our results suggest that abnormal synaptic signalling and intrinsic plasticity during the pre-ataxia stage of spinocerebellar ataxias underlie an aberrant cerebellar circuitry that anticipates the full extent of the disease severity. 2022-11-10 2022-11-15 Not clear
Naveed Malek, Chulika Makawita, Yaqub Al-Sami, Aram Aslanyan, Rajith de Silv. A Systematic Review of the Spectrum and Prevalence of Non-Motor Symptoms in Adults with Hereditary Cerebellar Ataxias. Movement disorders clinical practice vol 9 issue 8 2022 36339305 a systematic review of the spectrum and prevalence of non-motor symptoms in adults with hereditary cerebellar ataxias. 2022-11-07 2022-11-08 Not clear
Naveed Malek, Chulika Makawita, Yaqub Al-Sami, Aram Aslanyan, Rajith de Silv. A Systematic Review of the Spectrum and Prevalence of Non-Motor Symptoms in Adults with Hereditary Cerebellar Ataxias. Movement disorders clinical practice vol 9 issue 8 2022 36339305 cerebellar ataxias comprise a large group of heterogeneous disorders with both motor and non-motor symptoms (nms). 2022-11-07 2022-11-08 Not clear
Hamed Azami, Zhuoqing Chang, Steven E Arnold, Guillermo Sapiro, Anoopum S Gupt. Detection of Oculomotor Dysmetria From Mobile Phone Video of the Horizontal Saccades Task Using Signal Processing and Machine Learning Approaches. IEEE access : practical innovations, open solutions vol 10 issue 2022 36339795 cerebellar ataxias cause profound and characteristic abnormalities in smooth pursuit, saccades, and fixation. 2022-11-07 2022-11-08 Not clear
Kavyashree Kulamarva, Umesh Chikkanna, Kishore Kumar Ramakrishna, Hemant Bhargav, Selva Ganapathy Velayutham, Shivarama Varamball. Integrative Approach Improves Fall Risk and Postural Stability in Spinocerebellar Ataxia-2 - A Case Report. International journal of yoga vol 15 issue 2 2022 36329776 spinocerebellar ataxias (scas) comprise a large heterogeneous group of autosomal dominant cerebellar ataxias. 2022-11-04 2022-11-08 Not clear
Roderick P P W M Maas, Bart P C van de Warrenbur. Therapeutic Misestimation in Patients with Degenerative Ataxia: Lessons from a Randomized Controlled Trial. Movement disorders : official journal of the Movement Disorder Society vol issue 2022 36259428 the absence of effective treatments may render patients with degenerative cerebellar ataxias susceptible to a placebo response, which could affect the outcome of clinical trials. 2022-10-19 2022-10-25 Not clear
Young Woo Park, James M Joers, Bin Guo, Diane Hutter, Khalaf Bushara, Isaac M Adanyeguh, Lynn E Eberly, G\\xc3\\xbclin \\xc3\\x96z, Christophe Lengle. Corrigendum: Assessment of cerebral and cerebellar white matter microstructure in spinocerebellar ataxias 1, 2, 3, and 6 using diffusion MRI. Frontiers in neurology vol 13 issue 2022 36247785 corrigendum: assessment of cerebral and cerebellar white matter microstructure in spinocerebellar ataxias 1, 2, 3, and 6 using diffusion mri. 2022-10-17 2022-10-25 Not clear
Zeeshan Gauhar, Leon Tejwani, Uzma Abdullah, Sadia Saeed, Shagufta Shafique, Mazhar Badshah, Jungmin Choi, Weilai Dong, Carol Nelson-Williams, Richard P Lifton, Janghoo Lim, Ghazala K Raj. A Novel Missense Mutation in Cells vol 11 issue 19 2022 36231052 a novel missense mutation in autosomal-recessive cerebellar ataxias (arcas) are heterogeneous rare disorders mainly affecting the cerebellum and manifest as movement disorders in children and young adults. 2022-10-14 2022-10-25 Not clear
Ayush Agarwal, Pankaj, Mohd Faruq, Ajay Garg, Achal K Srivastav. Cognition in Trinucleotide Repeat Spinocerebellar Ataxias: A Review. Annals of Indian Academy of Neurology vol 25 issue 4 2022 36211141 spinocerebellar ataxias (scas) comprise a group of complex and heterogeneous hereditary neurodegenerative disorders characterized by cerebellar ataxia, with ophthalmoplegia, pyramidal and extrapyramidal features, peripheral neuropathy, motor neuron disease, pigmentary retinopathy, epilepsy, and dementia in varying proportions. 2022-10-10 2022-10-25 Not clear
Misbahuddin M Rafeeq, Muhammad Umair, Muhammad Bilal, Alaa Hamed Habib, Ahmed Waqas, Ziaullah M Sain, Mohammad Zubair Alam, Raja Hussain Al. A novel biallelic variant further delineates PRDX3-related autosomal recessive cerebellar ataxia. Neurogenetics vol issue 2022 36190665 cerebellar ataxias (cas) comprise a rare group of neurological disorders characterized by extensive phenotypic and genetic heterogeneity. 2022-10-03 2022-10-10 Not clear
Marjolaine Tremblay, Laura Girard-C\\xc3\\xb4t\\xc3\\xa9, Bernard Brais, Cynthia Gagno. Documenting manifestations and impacts of autosomal recessive spastic ataxia of Charlevoix-Saguenay to develop patient-reported outcome. Orphanet journal of rare diseases vol 17 issue 1 2022 36183078 autosomal recessive cerebellar ataxias (arca) are a group of rare inherited disorders characterized by degeneration or abnormal development of the cerebellum. 2022-10-01 2022-10-10 Not clear
Giulia Coarelli, Thomas Wirth, Christine Tranchant, Michel Koenig, Alexandra Durr, Mathieu Anhei. The inherited cerebellar ataxias: an update. Journal of neurology vol issue 2022 36152050 the inherited cerebellar ataxias: an update. 2022-09-24 2022-09-29 Not clear
Giulia Coarelli, Thomas Wirth, Christine Tranchant, Michel Koenig, Alexandra Durr, Mathieu Anhei. The inherited cerebellar ataxias: an update. Journal of neurology vol issue 2022 36152050 this narrative review aims at providing an update on the management of inherited cerebellar ataxias (icas), describing main clinical entities, genetic analysis strategies and recent therapeutic developments. 2022-09-24 2022-09-29 Not clear
Giulia Coarelli, Thomas Wirth, Christine Tranchant, Michel Koenig, Alexandra Durr, Mathieu Anhei. The inherited cerebellar ataxias: an update. Journal of neurology vol issue 2022 36152050 to guide diagnosis, several algorithms and a new genetic nomenclature for recessive cerebellar ataxias have been proposed. 2022-09-24 2022-09-29 Not clear
Marios Hadjivassiliou, Mario Manto, Hiroshi Mitom. Rare Etiologies in Immune-Mediated Cerebellar Ataxias: Diagnostic Challenges. Brain sciences vol 12 issue 9 2022 36138901 rare etiologies in immune-mediated cerebellar ataxias: diagnostic challenges. 2022-09-23 2022-09-29 Not clear
Marios Hadjivassiliou, Mario Manto, Hiroshi Mitom. Rare Etiologies in Immune-Mediated Cerebellar Ataxias: Diagnostic Challenges. Brain sciences vol 12 issue 9 2022 36138901 immune-mediated cerebellar ataxias (imcas) have diverse etiologies, such as gluten ataxia (ga), post-infectious cerebellitis (pic), miller fisher syndrome (mfs), paraneoplastic cerebellar degeneration (pcd), opsoclonus myoclonus syndrome (oms), and anti-gad ataxia. 2022-09-23 2022-09-29 Not clear
Shigeki Hirano, Atsuhiko Sugiyama, Kimihito Ara. Noradrenergic Pathway to the Cerebellum: the Study Must Go On. Cerebellum (London, England) vol issue 2022 36149525 cerebellar dysfunction and noradrenergic system may relate to tremor in parkinson disease and essential tremor, motor learning, and the vestibulo-ocular reflex in spinocerebellar ataxias. 2022-09-23 2022-09-29 Not clear
Lazaros C Triarhou, Mario Mant. The Discovery of the Monoaminergic Innervation of the Cerebellum: Convergence of Divergent and Point-to-Point Systems. Cerebellum (London, England) vol issue 2022 36149526 the discovery of noradrenergic and serotoninergic innervation of the cerebellum has been a crucial step in understanding the neurochemical relationships between brainstem nuclei and the cerebellum, and the attempts to treat cerebellar ataxias pharmacologically. 2022-09-23 2022-09-29 Not clear
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