| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Bruno Lopes Santos-Lobato, Jéssica Santos de Souza Rocha, Luciano Chaves Roch. Case report: Cerebellar sparing in juvenile Huntington's disease. Frontiers in neurology. vol 13. 2023-01-30. PMID:36712421. |
the role of the cerebellum in huntington's disease has been reevaluated, based on the presence of ataxia and findings on the impact of the disease on cerebellar volume. |
2023-01-30 |
2023-08-14 |
Not clear |
| Demet Oender, Jennifer Faber, Carlo Wilke, Tamara Schaprian, Asadeh Lakghomi, David Mengel, Ludger Schöls, Andreas Traschütz, Zofia Fleszar, Claudia Dufke, Stefan Vielhaber, Judith Machts, Ilaria Giordano, Marcus Grobe-Einsler, Thomas Klopstock, Claudia Stendel, Sylvia Boesch, Wolfgang Nachbauer, Dagmar Timmann-Braun, Andreas Gustafsson Thieme, Christoph Kamm, Ales Dudesek, Chantal Tallaksen, Iselin Wedding, Alessandro Filla, Matthias Schmid, Matthis Synofzik, Thomas Klockgethe. Evolution of Clinical Outcome Measures and Biomarkers in Sporadic Adult-Onset Degenerative Ataxia. Movement disorders : official journal of the Movement Disorder Society. 2023-01-25. PMID:36695111. |
sporadic adult-onset ataxias without known genetic or acquired cause are subdivided into multiple system atrophy of cerebellar type (msa-c) and sporadic adult-onset ataxia of unknown etiology (saoa). |
2023-01-25 |
2023-08-14 |
Not clear |
| Vittorio Riso, Tommaso Filippo Nicoletti, Salvatore Rossi, Maria Gabriella Vita, Perna Alessia, Daniele Di Natale, Gabriella Silvestr. Neurological Erdheim-Chester Disease Manifesting with Subacute or Progressive Cerebellar Ataxia: Novel Case Series and Review of the Literature. Brain sciences. vol 13. issue 1. 2023-01-21. PMID:36672008. |
in this latter case, patients manifest with a slowly progressive cerebellar ataxia, variably associated with other non-specific neurological signs, infratentorial leukoencephalopathy, and cerebellar atrophy, possibly mimicking either adult-onset degenerative or immune-mediated ataxia. |
2023-01-21 |
2023-08-14 |
Not clear |
| Chunsaier Wang, Yi Yang, Zhen He, Xuejing Wei, Shutian Zhang, Jiugang Son. High-grade B-cell lymphoma with gastroduodenal involvement showing paraneoplastic cerebellar degeneration: a case report. Translational cancer research. vol 11. issue 12. 2023-01-16. PMID:36644173. |
paraneoplastic cerebellar degeneration (pcd), which displays ataxia and other cerebellar symptoms, is the most common paraneoplastic neurological syndrome (pns). |
2023-01-16 |
2023-08-14 |
Not clear |
| Pooja Sharma, Akhilesh Kumar Sonakar, Nishu Tyagi, Varun Suroliya, Manish Kumar, Rintu Kutum, Vivekananda Asokchandran, Sakshi Ambawat, Uzma Shamim, Avni Anand, Ishtaq Ahmad, Sunil Shakya, Bharathram Uppili, Aradhana Mathur, Shaista Parveen, Shweta Jain, Jyotsna Singh, Malika Seth, Sana Zahra, Aditi Joshi, Divya Goel, Shweta Sahni, Asangla Kamai, Saruchi Wadhwa, Aparna Murali, Sheeba Saifi, Debashish Chowdhury, Sanjay Pandey, Kuljeet Singh Anand, Ranganathan Lakshmi Narasimhan, Sanghamitra Laskar, Suman Kushwaha, Mukesh Kumar, Cheruvallill Velayudhan Shaji, Madakasira Vasantha Padma Srivastava, Achal K Srivastava, Mohammed Faru. Genetics of Ataxias in Indian Population: A Collative Insight from a Common Genetic Screening Tool. Advanced genetics (Hoboken, N.J.). vol 3. issue 2. 2023-01-09. PMID:36618024. |
cerebellar ataxias (cas) represent a group of autosomal dominant and recessive neurodegenerative disorders affecting cerebellum with or without spinal cord. |
2023-01-09 |
2023-08-14 |
Not clear |
| Jooheon Kong, Sun-Uk Lee, Sungwook Yu, Ji-Soo Ki. Isolated Bilateral Superior Cerebellar Peduncular Lesion Presenting Square-Wave Jerks and Ataxia. Journal of clinical neurology (Seoul, Korea). vol 19. issue 1. 2023-01-06. PMID:36606652. |
isolated bilateral superior cerebellar peduncular lesion presenting square-wave jerks and ataxia. |
2023-01-06 |
2023-08-14 |
Not clear |
| Elan D Louis, Regina T Martuscello, John T Gionco, Whitney G Hartstone, Jessica B Musacchio, Marisa Portenti, Morgan McCreary, Sheng-Han Kuo, Jean-Paul G Vonsattel, Phyllis L Faus. Histopathology of the cerebellar cortex in essential tremor and other neurodegenerative motor disorders: comparative analysis of 320 brains. Acta neuropathologica. 2023-01-06. PMID:36607423. |
building off our prior study and now doubling the sample size, we conducted comparative analyses in a postmortem series of 320 brains on the severity and patterning of cerebellar cortex degenerative changes in et (n = 100), other neurodegenerative disorders of the cerebellum [spinocerebellar ataxias (scas, n = 47, including 13 sca3 and 34 sca1, 2, 6, 7, 8, 14); friedreich's ataxia (fa, n = 13); multiple system atrophy (msa), n = 29], and other disorders that may involve the cerebellum [parkinson's disease (pd), n = 62; dystonia, n = 19] versus controls (n = 50). |
2023-01-06 |
2023-08-14 |
Not clear |
| Yi-Tong Qiu, Yi Chen, Hui-Xin Tan, Wei Su, Qi-Fan Guo, Qiang Ga. Efficacy and Safety of Repetitive Transcranial Magnetic Stimulation in Cerebellar Ataxia: a Systematic Review and Meta-analysis. Cerebellum (London, England). 2023-01-05. PMID:36604400. |
comparing real and sham-rtms interventions, the utilization of rtms on cerebellum improved the scale for the assessment and rating of ataxia (sara) (smd - 0.87, 95% ci - 1.41 to - 0.34; p = 0.001; i |
2023-01-05 |
2023-08-14 |
Not clear |
| Jacob Saucier, Mohammad Al-Qadi, Mouna Ben Amor, Kinya Ishikawa, Ludivine Chamard-Witkowsk. Spinocerebellar ataxia type 31: A clinical and radiological literature review. Journal of the neurological sciences. vol 444. 2022-12-23. PMID:36563608. |
spinocerebellar ataxia type 31 (sca31) is an autosomal dominant disease, classified amongst pure cerebellar ataxias (adca type 3). |
2022-12-23 |
2023-08-14 |
Not clear |
| Raquel Baviera-Muñoz, Lidón Carretero-Vilarroig, Juan Francisco Vázquez-Costa, Carlos Morata-Martínez, Marina Campins-Romeu, Nuria Muelas, Isabel Sastre-Bataller, Irene Martínez-Torres, Julia Pérez-García, Rafael Sivera, Teresa Sevilla, Juan J Vilchez, Teresa Jaijo, Carmen Espinós, Jose M Millán, Luis Bataller, Elena Alle. Diagnostic Efficacy of Genetic Studies in a Series of Hereditary Cerebellar Ataxias in Eastern Spain. Neurology. Genetics. vol 8. issue 6. 2022-12-19. PMID:36530930. |
diagnostic efficacy of genetic studies in a series of hereditary cerebellar ataxias in eastern spain. |
2022-12-19 |
2023-08-14 |
Not clear |
| b' Filip Milosavljevi\\xc4\\x87, Irene Brusini, Andrea Atanasov, Marina Manojlovi\\xc4\\x87, Marija Vu\\xc4\\x8di\\xc4\\x87, Zorana Ore\\xc5\\xa1\\xc4\\x8danin-Du\\xc5\\xa1i\\xc4\\x87, Jelena Brklja\\xc4\\x8di\\xc4\\x87, \\xc4\\x8cedo Miljevi\\xc4\\x87, Aleksandra Nikoli\\xc4\\x87-Koki\\xc4\\x87, Du\\xc5\\xa1ko Blagojevi\\xc4\\x87, Chunliang Wang, Peter Damberg, Vesna Pe\\xc5\\xa1i\\xc4\\x87, Rachel F Tyndale, Magnus Ingelman-Sundberg, Marin M Juki\\xc4\\x8. The humanized CYP2C19 transgenic mouse exhibits cerebellar atrophy and movement impairment reminiscent of ataxia. Neuropathology and applied neurobiology. 2022-12-19. PMID:36536486.' |
the humanized cyp2c19 transgenic mouse exhibits cerebellar atrophy and movement impairment reminiscent of ataxia. |
2022-12-19 |
2023-08-14 |
mouse |
| Arif Sikandar, Xia-Hua Liu, Hao-Ling Xu, Ying Li, Yun-Qing Lin, Xin-Yuan Chen, Gui-He Li, Min-Ting Lin, Ning Wang, Wan-Jin Chen, Guo-Xin Ni, Shi-Rui Ga. Short-term efficacy of repetitive transcranial magnetic stimulation in SCA3: A prospective, randomized, double-blind, sham-controlled study. Parkinsonism & related disorders. vol 106. 2022-12-18. PMID:36529111. |
repetitive transcranial magnetic stimulation (rtms) is a non-invasive form of brain stimulation, demonstrated to improve symptoms in patients with neurodegenerative cerebellar ataxias. |
2022-12-18 |
2023-08-14 |
Not clear |
| Arif Sikandar, Xia-Hua Liu, Hao-Ling Xu, Ying Li, Yun-Qing Lin, Xin-Yuan Chen, Gui-He Li, Min-Ting Lin, Ning Wang, Wan-Jin Chen, Guo-Xin Ni, Shi-Rui Ga. Short-term efficacy of repetitive transcranial magnetic stimulation in SCA3: A prospective, randomized, double-blind, sham-controlled study. Parkinsonism & related disorders. vol 106. 2022-12-18. PMID:36529111. |
the present study investigated whether treatment with rtms over the cerebellum for 15 consecutive days improved measures of ataxia in sca3 patients. |
2022-12-18 |
2023-08-14 |
Not clear |
| David Pellerin, Matt C Danzi, Carlo Wilke, Mathilde Renaud, Sarah Fazal, Marie-Josée Dicaire, Carolin K Scriba, Catherine Ashton, Christopher Yanick, Danique Beijer, Adriana Rebelo, Clarissa Rocca, Zane Jaunmuktane, Joshua A Sonnen, Roxanne Larivière, David Genís, Laura Molina Porcel, Karine Choquet, Rawan Sakalla, Sylvie Provost, Rebecca Robertson, Xavier Allard-Chamard, Martine Tétreault, Sarah J Reiling, Sara Nagy, Vikas Nishadham, Meera Purushottam, Seena Vengalil, Mainak Bardhan, Atchayaram Nalini, Zhongbo Chen, Jean Mathieu, Rami Massie, Colin H Chalk, Anne-Louise Lafontaine, François Evoy, Marie-France Rioux, Jiannis Ragoussis, Kym M Boycott, Marie-Pierre Dubé, Antoine Duquette, Henry Houlden, Gianina Ravenscroft, Nigel G Laing, Phillipa J Lamont, Mario A Saporta, Rebecca Schüle, Ludger Schöls, Roberta La Piana, Matthis Synofzik, Stephan Zuchner, Bernard Brai. Deep Intronic The New England journal of medicine. 2022-12-14. PMID:36516086. |
deep intronic the late-onset cerebellar ataxias (locas) have largely resisted molecular diagnosis. |
2022-12-14 |
2023-08-14 |
Not clear |
| Mario Mant. The underpinnings of cerebellar ataxias. Clinical neurophysiology practice. vol 7. 2022-12-12. PMID:36504687. |
the underpinnings of cerebellar ataxias. |
2022-12-12 |
2023-08-14 |
human |
| Karin C Knudson, Anoopum S Gupt. Assessing Cerebellar Disorders with Wearable Inertial Sensor Data Using Time-Frequency and Autoregressive Hidden Markov Model Approaches. Sensors (Basel, Switzerland). vol 22. issue 23. 2022-12-11. PMID:36502155. |
in this paper, we use autoregressive hidden markov models and a time-frequency approach to create meaningful quantitative descriptions of behavioral characteristics of cerebellar ataxias from wearable inertial sensor data gathered during movement. |
2022-12-11 |
2023-08-14 |
human |
| Michele H Potashman, Miranda L Mize, Melissa W Beiner, Samantha Pierce, Vladimir Coric, Jeremy D Schmahman. Ataxia Rating Scales Reflect Patient Experience: an Examination of the Relationship Between Clinician Assessments of Cerebellar Ataxia and Patient-Reported Outcomes. Cerebellum (London, England). 2022-12-10. PMID:36495470. |
ataxia rating scales are observer administered clinical outcome assessments (coas) of the cerebellar motor syndrome. |
2022-12-10 |
2023-08-14 |
Not clear |
| Haloom Rafehi, Justin Read, David J Szmulewicz, Kayli C Davies, Penny Snell, Liam G Fearnley, Liam Scott, Mirja Thomsen, Greta Gillies, Kate Pope, Mark F Bennett, Jacob E Munro, Kathie J Ngo, Luke Chen, Mathew J Wallis, Ernest G Butler, Kishore R Kumar, Kathy Hc Wu, Susan E Tomlinson, Stephen Tisch, Abhishek Malhotra, Matthew Lee-Archer, Egor Dolzhenko, Michael A Eberle, Leslie J Roberts, Brent L Fogel, Norbert Brüggemann, Katja Lohmann, Martin B Delatycki, Melanie Bahlo, Paul J Lockhar. An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA50/ATX-FGF14. American journal of human genetics. 2022-12-09. PMID:36493768. |
adult-onset cerebellar ataxias are a group of neurodegenerative conditions that challenge both genetic discovery and molecular diagnosis. |
2022-12-09 |
2023-08-14 |
Not clear |
| Carolina Alvarez, Mona Grimmel, Darius Ebrahimi-Fakhari, Victoria Paul, Natalie Deininger, Angelika Riess, Tobias Haack, Elena Gardella, Rikke Møller, Allan Baya. Expansion of the phenotypic and molecular spectrum of CWF19L1-related disorder. Clinical genetics. 2022-12-01. PMID:36453471. |
the clinical spectrum was broad, including mild to profound global developmental delay; global or motor regression in infancy or adolescence; childhood-onset ataxia and cerebellar atrophy; and early-onset epilepsy. |
2022-12-01 |
2023-08-14 |
Not clear |
| Rupa Radhakrishnan, Lindsey A G Shea, Sumit Pruthi, Victoria M Silvera, Thangamadhan Bosemani, Nilesh K Desai, Donald L Gilbert, Orit A Glenn, Carolina V Guimaraes, Mai-Lan Ho, H F Samuel Lam, Mohit Maheshwari, David M Mirsky, Helen R Nadel, Sonia Partap, Gary R Schooler, Unni K Udayasankar, Matthew T Whitehead, Jason N Wright, Cynthia K Rigsb. ACR Appropriateness Criteria® Ataxia-Child. Journal of the American College of Radiology : JACR. vol 19. issue 11S. 2022-11-27. PMID:36436955. |
nonprogressive childhood ataxia suggests a congenital brain malformation or early prenatal or perinatal brain injury, and progressive childhood ataxia indicates inherited causes or acquired posterior fossa lesions that result in gradual cerebellar dysfunction. |
2022-11-27 |
2023-08-14 |
Not clear |