| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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. 2022-11-07. PMID:36339795. |
cerebellar ataxias cause profound and characteristic abnormalities in smooth pursuit, saccades, and fixation. |
2022-11-07 |
2023-08-14 |
human |
| 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. 2022-11-04. PMID:36329776. |
spinocerebellar ataxias (scas) comprise a large heterogeneous group of autosomal dominant cerebellar ataxias. |
2022-11-04 |
2023-08-14 |
Not clear |
| Mohammad Banazadeh, Sepehr Olangian-Tehrani, Melika Sharifi, Mohammadreza Malek-Ahmadi, Farhad Nikzad, Nooria Doozandeh-Nargesi, Alireza Mohammadi, Gary J Stephens, Mohammad Shaban. Mechanisms of COVID-19-induced cerebellitis. Current medical research and opinion. 2022-10-28. PMID:36305796. |
damage to the cerebellum can lead to incoordination and ataxia. |
2022-10-28 |
2023-08-14 |
Not clear |
| Zeferino Demartini, Guilherme H W Ceccato, Érico S G G da Trindade, Luis A B Borb. Multimodal treatment of a pediatric posterior fossa arteriovenous malformation employing endovascular and microsurgical techniques. Neurosurgical focus: Video. vol 4. issue 1. 2022-10-26. PMID:36284618. |
the authors present a case of a 7-year-old girl with headache, vomiting, dysmetria, and ataxia due to a ruptured cerebellar grade iii avm. |
2022-10-26 |
2023-08-14 |
Not clear |
| Satoshi Kiyofuji, Harry J Cloft, Colin L W Driscoll, Michael J Lin. Hemangioblastoma of the pons and middle cerebellar peduncle. Neurosurgical focus: Video. vol 1. issue 2. 2022-10-26. PMID:36284873. |
a 60-year-old man with a history of four prior operations for a left cerebellar/middle cerebellar peduncle hemangioblastoma presented with hearing loss, imbalance, and ataxia (de la monte and horowitz, 1989). |
2022-10-26 |
2023-08-14 |
Not clear |
| Cheng Cheng, James Cleak, Lan Weiss, Heather Cater, Michelle Stewart, Sara Wells, Rod Carlo Columbres, Alyaa Shmara, C Alejandra Morato Torres, Faria Zafar, Birgitt Schüle, Jonathan Neumann, Eli Hatchwell, Virginia Kimoni. Early embryonic lethality in complex I associated p.L104P Nubpl mutant mice. Orphanet journal of rare diseases. vol 17. issue 1. 2022-10-25. PMID:36280881. |
patients affected by complex i deficiency harboring homozygous nubpl variants typically have neurological problems including seizures, intellectual disability, and ataxia associated with cerebellar hypoplasia. |
2022-10-25 |
2023-08-14 |
mouse |
| Zahra Aghighi, Zeynab Ghorbani, Meysam Hassani Moghaddam, Mobina Fathi, Mohammad-Amin Abdollahifar, Mansoureh Soleimani, Fariba Karimzadeh, Homa Rasoolijazi, Abbas Aliaghae. Melittin ameliorates motor function and prevents autophagy-induced cell death and astrogliosis in rat models of cerebellar ataxia induced by 3-acetylpyridine. Neuropeptides. 2022-10-24. PMID:36280441. |
cerebellar ataxia (ca) is a form of ataxia that adversely affects the cerebellum. |
2022-10-24 |
2023-08-14 |
rat |
| Lavinia C Dumitrache, Peter J McKinno. Out of LINE: Transposons, genome integrity, and neurodegeneration. Neuron. vol 110. issue 20. 2022-10-20. PMID:36265437. |
(2022) show that l1 hyperactivity occurs in the neurodegenerative syndrome ataxia telangiectasia and causes ataxia and cerebellar degeneration in mice. |
2022-10-20 |
2023-08-14 |
mouse |
| 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. 2022-10-19. PMID: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 |
2023-08-14 |
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. 2022-10-14. PMID: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 |
2023-08-14 |
Not clear |
| Dolores Martínez-Rubio, Isabel Hinarejos, Paula Sancho, Nerea Gorría-Redondo, Raquel Bernadó-Fonz, Cristina Tello, Clara Marco-Marín, Itxaso Martí-Carrera, María Jesús Martínez-González, Ainhoa García-Ribes, Raquel Baviera-Muñoz, Isabel Sastre-Bataller, Irene Martínez-Torres, Anna Duat-Rodríguez, Patrícia Janeiro, Esther Moreno, Leticia Pías-Peleteiro, Mar O'Callaghan Gordo, Ángeles Ruiz-Gómez, Esteban Muñoz, Maria Josep Martí, Ana Sánchez-Monteagudo, Candela Fuster, Amparo Andrés-Bordería, Roser Maria Pons, Silvia Jesús-Maestre, Pablo Mir, Vincenzo Lupo, Belén Pérez-Dueñas, Alejandra Darling, Sergio Aguilera-Albesa, Carmen Espinó. Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias. International journal of molecular sciences. vol 23. issue 19. 2022-10-14. PMID:36233161. |
our clinical series comprises 124 patients with movement disorders (mds) and/or ataxia with cerebellar atrophy (ca), many of them showing signs of neurodegeneration with brain iron accumulation (nbia). |
2022-10-14 |
2023-08-14 |
Not clear |
| Yi Jin, Yuchao Chen, Dan Li, Mengqiu Qiu, Menglu Zhou, Zhouyao Hu, Qiusi Cai, Xulin Weng, Xiaodong Lu, Bin W. Autonomic dysfunction as the initial presentation in spinocerebellar ataxia type 3: A case report and review of the literature. Frontiers in neurology. vol 13. 2022-10-14. PMID:36237609. |
combination of early and autonomic abnormalities and ataxia would be more characteristic of the cerebellar type of multiple system atrophy (msa-c), the patient's positive family history and identification of an |
2022-10-14 |
2023-08-14 |
Not clear |
| Sylvie Picker-Minh, Ilaria Luperi, Ethiraj Ravindran, Nadine Kraemer, Sami Zaqout, Gisela Stoltenburg-Didinger, Olaf Ninnemann, Luis R Hernandez-Miranda, Shyamala Mani, Angela M Kaind. PTRH2 is Necessary for Purkinje Cell Differentiation and Survival and its Loss Recapitulates Progressive Cerebellar Atrophy and Ataxia Seen in IMNEPD Patients. Cerebellum (London, England). 2022-10-11. PMID:36219306. |
ptrh2 is necessary for purkinje cell differentiation and survival and its loss recapitulates progressive cerebellar atrophy and ataxia seen in imnepd patients. |
2022-10-11 |
2023-08-14 |
Not clear |
| Leslie J Roberts, Michael McVeigh, Linda Seiderer, Ian H Harding, Louise A Corben, Martin Delatycki, David J Szmulewic. Overview of the Clinical Approach to Individuals With Cerebellar Ataxia and Neuropathy. Neurology. Genetics. vol 8. issue 5. 2022-10-03. PMID:36187726. |
based on the evolving available literature and experience, we outline a clinical approach to the diagnosis of adult-onset ataxia where a combination of cerebellar and peripheral or cranial nerve pathology exists. |
2022-10-03 |
2023-08-14 |
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. 2022-10-03. PMID:36190665. |
cerebellar ataxias (cas) comprise a rare group of neurological disorders characterized by extensive phenotypic and genetic heterogeneity. |
2022-10-03 |
2023-08-14 |
Not clear |
| Marjolaine Tremblay, Laura Girard-Côté, 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. 2022-10-01. PMID: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 |
2023-08-14 |
Not clear |
| Giulia Coarelli, Thomas Wirth, Christine Tranchant, Michel Koenig, Alexandra Durr, Mathieu Anhei. The inherited cerebellar ataxias: an update. Journal of neurology. 2022-09-24. PMID:36152050. |
the inherited cerebellar ataxias: an update. |
2022-09-24 |
2023-08-14 |
Not clear |
| Giulia Coarelli, Thomas Wirth, Christine Tranchant, Michel Koenig, Alexandra Durr, Mathieu Anhei. The inherited cerebellar ataxias: an update. Journal of neurology. 2022-09-24. PMID: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 |
2023-08-14 |
Not clear |
| Giulia Coarelli, Thomas Wirth, Christine Tranchant, Michel Koenig, Alexandra Durr, Mathieu Anhei. The inherited cerebellar ataxias: an update. Journal of neurology. 2022-09-24. PMID:36152050. |
to guide diagnosis, several algorithms and a new genetic nomenclature for recessive cerebellar ataxias have been proposed. |
2022-09-24 |
2023-08-14 |
Not clear |
| Marios Hadjivassiliou, Mario Manto, Hiroshi Mitom. Rare Etiologies in Immune-Mediated Cerebellar Ataxias: Diagnostic Challenges. Brain sciences. vol 12. issue 9. 2022-09-23. PMID:36138901. |
rare etiologies in immune-mediated cerebellar ataxias: diagnostic challenges. |
2022-09-23 |
2023-08-14 |
Not clear |