All Relations between Ataxia and cerebellum

Publication Sentence Publish Date Extraction Date Species
Jonathan Doan, Irfan Sheikh, Lawrence Elmer, Mehmood Rashi. Video Representation of Dopamine-Responsive Multiple System Atrophy Cerebellar Type. The American journal of case reports. vol 22. 2021-11-16. PMID:34776506. background multiple system atrophy cerebellar type (msa-c) is a subtype of msa that presents with predominant ataxia along with lesser signs of parkinsonism and autonomic dysfunction. 2021-11-16 2023-08-13 Not clear
Ahmet Cevdet Ceylan, Elif Acar Arslan, Haktan Bağış Erdem, Haluk Kavus, Mutluay Arslan, Haluk Topaloğl. Autosomal recessive spinocerebellar ataxia 18 caused by homozygous exon 14 duplication in GRID2 and review of the literature. Acta neurologica Belgica. vol 121. issue 6. 2021-11-15. PMID:32170608. autosomal recessive cerebellar ataxias (arca) are characterized by the abnormal structure of the cerebellum and spinal cord. 2021-11-15 2023-08-13 Not clear
José Luiz Pedroso, Thiago Cardoso Vale, Sophia Caldas Gonzaga da Costa, Mariana Santos, Isabel Alonso, Orlando Graziani Povoas Barsottin. Complex Movement Disorders in Ataxia with Oculomotor Apraxia Type 1: Beyond the Cerebellar Syndrome. Tremor and other hyperkinetic movements (New York, N.Y.). vol 10. 2021-11-15. PMID:33101765. complex movement disorders in ataxia with oculomotor apraxia type 1: beyond the cerebellar syndrome. 2021-11-15 2023-08-13 Not clear
Nadia Amokrane, Chi-Ying R Lin, Natasha A Desai, Sheng-Han Ku. The Impact of Compulsivity and Impulsivity in Cerebellar Ataxia: A Case Series. Tremor and other hyperkinetic movements (New York, N.Y.). vol 10. 2021-11-15. PMID:33133767. the cerebellum has recently been identified to have a key role in reward processing, and individuals with ataxia have been found to be more impulsive and compulsive as part of cerebellum-related cognitive and behavioral disturbances. 2021-11-15 2023-08-13 Not clear
I Rouco Axpe, A Loyola Irulegui, B Ruiz de la Peña, E Izarzugaza Iturriza. Hereditary cerebellar ataxias and hereditary spastic paraplegias: experience of disease from the patient's perspective. Neurologia (Barcelona, Spain). vol 36. issue 9. 2021-11-15. PMID:34294581. hereditary cerebellar ataxias and hereditary spastic paraplegias: experience of disease from the patient's perspective. 2021-11-15 2023-08-13 Not clear
Sara Nuovo, Valentina Baglioni, Roberta De Mori, Silvia Tardivo, Caterina Caputi, Monia Ginevrino, Alessia Micalizzi, Laura Masuelli, Giulia Federici, Antonella Casella, Elisa Lorefice, Danila Anello, Manuela Tolve, Donatella Farini, Enrico Bertini, Ginevra Zanni, Lorena Travaglini, Gessica Vasco, Claudio Sette, Carla Carducci, Enza M Valente, Vincenzo Leuzz. Clinical variability at the mild end of BRAT1-related spectrum: Evidence from two families with genotype-phenotype discordance. Human mutation. 2021-11-15. PMID:34747546. two siblings displayed nonprogressive congenital ataxia and shrunken cerebellum on magnetic resonance imaging. 2021-11-15 2023-08-13 Not clear
Angela Sanna, Paolo Follesa, Paolo Tacconi, Mariangela Serra, Maria Giuseppina Pisu, Viola Cocco, Michela Figorilli, Giovanni Defazio, Monica Pulighedd. Therapeutic Use of Cerebellar Intermittent Theta Burst Stimulation (iTBS) in a Sardinian Family Affected by Spinocerebellar Ataxia 38 (SCA 38). Cerebellum (London, England). 2021-11-11. PMID:34410614. afterwards, patients were exposed to ten sessions of cerebellar real and sham itbs in a cross-over study and clinical symptoms were evaluated before and after treatment by modified international cooperative ataxia rating scale (micars). 2021-11-11 2023-08-13 Not clear
Joana Damásio, Mariana Santos, Raquel Samões, Maria Araújo, Mafalda Macedo, Ana Sardoeira, Sara Cavaco, Joel Freitas, José Barros, Jorge Oliveira, Jorge Sequeiro. Novel KMT2B mutation causes cerebellar ataxia: Expanding the clinical phenotype. Clinical genetics. vol 100. issue 6. 2021-11-11. PMID:34477219. hereditary cerebellar ataxias comprise a heterogeneous group of neurodegenerative disorders affecting the cerebellum and/or cerebellar pathways. 2021-11-11 2023-08-13 Not clear
Joana Damásio, Mariana Santos, Raquel Samões, Maria Araújo, Mafalda Macedo, Ana Sardoeira, Sara Cavaco, Joel Freitas, José Barros, Jorge Oliveira, Jorge Sequeiro. Novel KMT2B mutation causes cerebellar ataxia: Expanding the clinical phenotype. Clinical genetics. vol 100. issue 6. 2021-11-11. PMID:34477219. our findings highlight the possible role of kmt2b as a gene involved in hereditary cerebellar ataxias. 2021-11-11 2023-08-13 Not clear
Srikrishna V Malayala, Praveena Jaidev, Rachana Vanaparthy, Taranjeet S Joll. Acute COVID-19 Cerebellitis: A Rare Neurological Manifestation of COVID-19 Infection. Cureus. vol 13. issue 10. 2021-11-11. PMID:34754665. neurological exam was consistent with cerebellar symptoms like broad bases gait, truncal ataxia and subsequent imaging revealed white matter degeneration and edema of the cerebellar hemispheres. 2021-11-11 2023-08-13 Not clear
Aparna S Chivukula, Mariia Suslova, Daniel Kortzak, Peter Kovermann, Christoph Fahlk. Functional consequences of SLC1A3 mutations associated with episodic ataxia 6. Human mutation. vol 41. issue 11. 2021-11-10. PMID:32741053. the episodic ataxias (ea) are a group of inherited neurological diseases characterized by paroxysmal cerebellar incoordination. 2021-11-10 2023-08-13 Not clear
M Hadjivassiliou, P G Sarrigiannis, P D Shanmugarajah, D S Sanders, R A Grünewald, P Zis, N Hoggar. Clinical Characteristics and Management of 50 Patients with Anti-GAD Ataxia: Gluten-Free Diet Has a Major Impact. Cerebellum (London, England). vol 20. issue 2. 2021-11-05. PMID:33084997. gaze-evoked nystagmus was present in 26%, cerebellar dysarthria in 26%, limb ataxia in 44% and gait ataxia in 100%. 2021-11-05 2023-08-13 Not clear
Owen P Morgan, Mitchell B Slapik, Katherine G Iannuzzelli, Stephen M LaConte, Jonathan M Lisinski, Peg C Nopoulos, Ashley M Cochran, Sharif I Kronemer, Liana S Rosenthal, Cherie L Marve. The Cerebellum and Implicit Sequencing: Evidence from Cerebellar Ataxia. Cerebellum (London, England). vol 20. issue 2. 2021-11-05. PMID:33123963. for example, when cognitive and motor functions relied on cerebellar function simultaneously, the ataxia group's motor function was unaffected, in contrast to that of controls whose motor performance declined as a function of cognitive load. 2021-11-05 2023-08-13 Not clear
Abhimanyu Mahajan, Lyndsey Schroder, Aleksander Rekhtman, Alok K Dwivedi, Lily L Wang, Alberto J Espa. Tremor-Dominant Cervical Dystonia: a Cerebellar Syndrome. Cerebellum (London, England). vol 20. issue 2. 2021-11-05. PMID:33161481. all patients were evaluated for cerebellar disability using the scale for the assessment and rating of ataxia (sara), gait variability using protokinetics zeno walkway, and cerebellar volume analysis extracted from brain magnetic resonance imaging (mri) using a semiquantitative scale. 2021-11-05 2023-08-13 Not clear
Fan Wu, Xu Wang, Xiaohan Li, Huidi Teng, Tao Tian, Jing Ba. Spinocerebellar ataxia type 23 (SCA23): a review. Journal of neurology. vol 268. issue 12. 2021-11-04. PMID:33175256. spinocerebellar ataxias (scas), formerly known as autosomal dominant cerebellar ataxias (adcas), are a group of hereditary heterogeneous neurodegenerative diseases. 2021-11-04 2023-08-13 Not clear
Michaela Dankova, Jaroslav Jerabek, Dylan J Jester, Alena Zumrova, Jaroslava Paulasova Schwabova, Rudolf Cerny, Silvia Kmetonyova, Martin Vyhnale. Clinical dynamic visual acuity in patients with cerebellar ataxia and vestibulopathy. PloS one. vol 16. issue 7. 2021-11-03. PMID:34324564. deterioration of dynamic visual acuity (dva) as a result of impaired vestibulo-ocular reflex (vor) has been well described in peripheral vestibulopathies, however, changes in dva in patients with degenerative cerebellar ataxias (ca) and its relation to vor impairment in these patients has not yet been evaluated. 2021-11-03 2023-08-13 human
Danielle E Whittaker, Roberto Oleari, Louise C Gregory, Polona Le Quesne Stabej, Hywel J Williams, John G Torpiano, Nancy Formosa, Mario J Cachia, Daniel Field, Antonella Lettieri, Louise A Ocaka, Alyssa Jj Paganoni, Sakina H Rajabali, Kimberley Lh Riegman, Lisa B De Martini, Taro Chaya, Iain C Robinson, Takahisa Furukawa, Anna Cariboni, M Albert Basson, Mehul T Dattan. A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia. The Journal of clinical investigation. 2021-11-03. PMID:34730112. patients exhibited intellectual disability, ataxia with cerebellar hypoplasia, scoliosis and delayed puberty with congenital hypogonadotropic hypogonadism (chh). 2021-11-03 2023-08-13 mouse
Chenguang Zhou, Zhiqiang Xu, Botao Huang, Yuanhong He, Yinghui Zhu, Yuanzheng Zhao, Peng Wan. Caudal paramedian midbrain infarction: a clinical study of imaging, clinical features and stroke mechanisms. Acta neurologica Belgica. vol 121. issue 2. 2021-11-01. PMID:31456122. all patients presented with bilateral cerebellar dysfunction which included dysarthric speech, truncal or gait ataxia and four-limb ataxia. 2021-11-01 2023-08-13 Not clear
Shu-Mei Wang, Ying-Wa Chan, Yiu-On Tsui, Fong-Yung Ch. Effects of Anodal Cerebellar Transcranial Direct Current Stimulation on Movements in Patients with Cerebellar Ataxias: A Systematic Review. International journal of environmental research and public health. vol 18. issue 20. 2021-11-01. PMID:34682435. effects of anodal cerebellar transcranial direct current stimulation on movements in patients with cerebellar ataxias: a systematic review. 2021-11-01 2023-08-13 human
Shu-Mei Wang, Ying-Wa Chan, Yiu-On Tsui, Fong-Yung Ch. Effects of Anodal Cerebellar Transcranial Direct Current Stimulation on Movements in Patients with Cerebellar Ataxias: A Systematic Review. International journal of environmental research and public health. vol 18. issue 20. 2021-11-01. PMID:34682435. cerebellar transcranial direct current stimulation (cerebellar tdcs) is a promising therapy for cerebellar ataxias and has attracted increasing attention from researchers and clinicians. 2021-11-01 2023-08-13 human