| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Alkis M Hadjiosif, Tricia L Gibo, Maurice A Smit. The cerebellum acts as the analog to the medial temporal lobe for sensorimotor memory. bioRxiv : the preprint server for biology. 2024-04-22. PMID:38645006. |
here we studied the sensorimotor learning of individuals with severe ataxia from cerebellar degeneration. |
2024-04-22 |
2024-04-24 |
Not clear |
| G Clément, S Puisieux, D Pellerin, B Brais, C Bonnet, M Renau. Spinocerebellar ataxia 27B (SCA27B), a frequent late-onset cerebellar ataxia. Revue neurologique. 2024-04-12. PMID:38609751. |
genetic cerebellar ataxias are still a diagnostic challenge, and yet not all of them have been identified. |
2024-04-12 |
2024-04-15 |
Not clear |
| G Clément, S Puisieux, D Pellerin, B Brais, C Bonnet, M Renau. Spinocerebellar ataxia 27B (SCA27B), a frequent late-onset cerebellar ataxia. Revue neurologique. 2024-04-12. PMID:38609751. |
the core phenotype of the disease consists of slowly progressive late-onset ataxia with cerebellar syndrome, oculomotor disorders including downbeat nystagmus, and episodic symptoms such as diplopia. |
2024-04-12 |
2024-04-15 |
Not clear |
| N Déglo. Gene editing as a therapeutic strategy for spinocerebellar ataxia type-3. Revue neurologique. 2024-04-05. PMID:38580500. |
clinically, sca3 pathology is characterized by progressive ataxia leading to motor incoordination that may affect balance, gait and speech, and neuropathologically by a progressive degeneration of the spinal cord and cerebellum, as well as the cerebral cortex and basal ganglia. |
2024-04-05 |
2024-04-10 |
Not clear |
| Salma Marrakchi, Khadija Laasri, Rim Moufakkir, Yousra Guelzim, Ihssan Hadj Hsain, Zakia El Yousfi, Jamal El Fenni, Hassan En-Noual. Progressive ataxia and palatal tremor (PAPT) with hypertrophic olivary degeneration (HOD): A case report. Radiology case reports. vol 19. issue 6. 2024-03-28. PMID:38544788. |
here we report a case of a mid-adult-onset man which presents a worsening cerebellar progressive ataxia with palatal tremor, in whom imaging reveals abnormalities of the olivary nuclei with tardive cerebellar atrophy which has been diagnosed as a sporadic papt. |
2024-03-28 |
2024-03-30 |
Not clear |
| Mara-Luciana Floare, Stephen B Wharton, Julie E Simpson, Daniel Aeschlimann, Nigel Hoggard, Marios Hadjivassilio. Cerebellar degeneration in gluten ataxia is linked to microglial activation. Brain communications. vol 6. issue 2. 2024-03-21. PMID:38510211. |
cerebellar degeneration in gluten ataxia is linked to microglial activation. |
2024-03-21 |
2024-03-23 |
Not clear |
| Roberta De Mori, Silvia Tardivo, Lidia Pollara, Silvia Clara Giliani, Eltahir Ali, Lucio Giordano, Vincenzo Leuzzi, Rita Fischetto, Blanca Gener, Santo Diprima, Marco J Morelli, Maria Cristina Monti, Virginie Sottile, Enza Maria Valent. Joubert syndrome-derived induced pluripotent stem cells show altered neuronal differentiation in vitro. Cell and tissue research. 2024-03-19. PMID:38502237. |
joubert syndrome (js) is a recessively inherited congenital ataxia characterized by hypotonia, psychomotor delay, abnormal ocular movements, intellectual disability, and a peculiar cerebellar and brainstem malformation, the "molar tooth sign." |
2024-03-19 |
2024-03-23 |
Not clear |
| Chiara Briani, Andrea Visenti. Hematologic malignancies and hematopoietic stem cell transplantation. Handbook of clinical neurology. vol 200. 2024-03-17. PMID:38494294. |
high-risk antibodies are absent in most lymphoma-associated paraneoplastic neurologic syndromes, with the exception of antibodies to tr/dner in paraneoplastic cerebellar degeneration, mglur5 in limbic encephalitis, and mglur1 in some cerebellar ataxias. |
2024-03-17 |
2024-03-20 |
Not clear |
| Albert Saiz, Francesc Grau. Neuronal antibodies in nonparaneoplastic autoimmune cerebellar ataxias. Current opinion in neurology. 2024-03-14. PMID:38483149. |
neuronal antibodies in nonparaneoplastic autoimmune cerebellar ataxias. |
2024-03-14 |
2024-03-16 |
Not clear |
| Albert Saiz, Francesc Grau. Neuronal antibodies in nonparaneoplastic autoimmune cerebellar ataxias. Current opinion in neurology. 2024-03-14. PMID:38483149. |
to describe relevant advances in nonparaneoplastic autoimmune cerebellar ataxias (aca) with neuronal antibodies. |
2024-03-14 |
2024-03-16 |
Not clear |
| Jung Hwan Shin, Heejung Kim, So Yeon Lee, Won Tae Yoon, Sun-Won Park, Sangmin Park, Dallah Yoo, Jee-Young Le. Impaired cognitive flexibility and disrupted cognitive cerebellum in degenerative cerebellar ataxias. Brain communications. vol 6. issue 2. 2024-03-08. PMID:38454963. |
impaired cognitive flexibility and disrupted cognitive cerebellum in degenerative cerebellar ataxias. |
2024-03-08 |
2024-03-10 |
human |
| Mónica Ferreira, Tamara Schaprian, David Kügler, Martin Reuter, Katharina Deike-Hoffmann, Dagmar Timmann, Thomas M Ernst, Paola Giunti, Hector Garcia-Moreno, Bart van de Warrenburg, Judith van Gaalen, Jeroen de Vries, Heike Jacobi, Katharina Marie Steiner, Gülin Öz, James M Joers, Chiadi Onyike, Michal Povazan, Kathrin Reetz, Sandro Romanzetti, Thomas Klockgether, Jennifer Fabe. Correction: Cerebellar Volumetry in Ataxias: Relation to Ataxia Severity and Duration. Cerebellum (London, England). 2024-03-06. PMID:38446346. |
correction: cerebellar volumetry in ataxias: relation to ataxia severity and duration. |
2024-03-06 |
2024-03-08 |
Not clear |
| Retraction: Very late-onset Friedreich's ataxia with rapid course mimicking as possible multiple system atrophy cerebellar type. BMJ case reports. vol 17. issue 3. 2024-03-06. PMID:38448050. |
retraction: very late-onset friedreich's ataxia with rapid course mimicking as possible multiple system atrophy cerebellar type. |
2024-03-06 |
2024-03-09 |
Not clear |
| Kalaivani Manibarathi, Tam Pham, Holger Hengel, Matthis Synofzik, Maike Nagel, Rebecca Schül. An iPSC model for POLR3A-associated spastic ataxia: Generation of three unrelated patient cell lines. Stem cell research. vol 76. 2024-03-04. PMID:38437768. |
spastic ataxias (sa) are a group of neurodegenerative disorders with combined pyramidal and cerebellar system affection, leading to an overlap phenotype between hereditary spastic paraplegias (hsp) and cerebellar ataxias (ca). |
2024-03-04 |
2024-03-07 |
human |
| Tsutomu Yasuda, Jun Shimizu, Toji Miyagawa, Yuri Tsutsumi, Takeshi Iwatsubo, Shoji Tsuj. Paraneoplastic Cerebellar Degeneration Leading to an Early Diagnosis of Peritoneal Serous Papillary Carcinoma. Internal medicine (Tokyo, Japan). 2024-03-03. PMID:38432969. |
a 77-year-old female with a subacute progression of ataxia and serum anti-yo antibodies was suspected to have paraneoplastic cerebellar degeneration (pcd). |
2024-03-03 |
2024-03-06 |
Not clear |
| Zdenka Purkartova, Kristyna Krakorova, Vaclav Babuska, Jan Tuma, Zbyněk Houdek, Nilpawan Roy Choudhury, Stepan Kapl, Yaroslav Kolinko, Martina Sucha, Elena Porras-Garcia, Milena Kralickova, Jan Cendeli. Quantification of Solid Embryonic Cerebellar Graft Volume in a Degenerative Ataxia Model. Cerebellum (London, England). 2024-03-02. PMID:38430389. |
quantification of solid embryonic cerebellar graft volume in a degenerative ataxia model. |
2024-03-02 |
2024-03-04 |
mouse |
| Zdenka Purkartova, Kristyna Krakorova, Vaclav Babuska, Jan Tuma, Zbyněk Houdek, Nilpawan Roy Choudhury, Stepan Kapl, Yaroslav Kolinko, Martina Sucha, Elena Porras-Garcia, Milena Kralickova, Jan Cendeli. Quantification of Solid Embryonic Cerebellar Graft Volume in a Degenerative Ataxia Model. Cerebellum (London, England). 2024-03-02. PMID:38430389. |
substitution of lost neurons by neurotransplantation would be a possible management of advanced degenerative cerebellar ataxias in which insufficient cerebellar reserve remains. |
2024-03-02 |
2024-03-04 |
mouse |
| Christopher D Stephen, Mark Vangel, Anoopum S Gupta, Jason P MacMore, Jeremy D Schmahman. Rates of change of pons and middle cerebellar peduncle diameters are diagnostic of multiple system atrophy of the cerebellar type. Brain communications. vol 6. issue 1. 2024-02-27. PMID:38410617. |
we measured anterior-posterior pons and middle cerebellar peduncle diameters on baseline and subsequent mris, and correlated results with brief ataxia rating scale scores. |
2024-02-27 |
2024-03-02 |
Not clear |
| Omer Gullulu, Emrah Ozcelik, Merve Tuzlakoglu Ozturk, Mustafa Safa Karagoz, Uygar Halis Tazeba. A multi-faceted approach to unravel coding and non-coding gene fusions and target chimeric proteins in ataxia. Journal of biomolecular structure & dynamics. 2024-02-27. PMID:38411012. |
ataxia represents a heterogeneous group of neurodegenerative disorders characterized by a loss of balance and coordination, often resulting from mutations in genes vital for cerebellar function and maintenance. |
2024-02-27 |
2024-03-02 |
mouse |
| Shihan Chen, Catherine Ashton, Rawan Sakalla, Guillemette Clement, Sophie Planel, Celine Bonnet, Phillipa Lamont, Karthik Kulanthaivelu, Atchayaram Nalini, Henry Houlden, Antoine Duquette, Marie-Josee Dicaire, Pablo Iruzubieta Agudo, Javier Ruiz Martinez, Enrique Marco de Lucas, Rodrigo Sutil Berjon, Jon Infante Ceberio, Elisabetta Indelicato, Sylvia Boesch, Matthis Synofzik, Benjamin Bender, Matt C Danzi, Stephan Zuchner, David Pellerin, Bernard Brais, Mathilde Renaud, Roberta La Pian. Neuroradiological findings in GAA-FGF14 ataxia (SCA27B): more than cerebellar atrophy. medRxiv : the preprint server for health sciences. 2024-02-26. PMID:38405699. |
neuroradiological findings in gaa-fgf14 ataxia (sca27b): more than cerebellar atrophy. |
2024-02-26 |
2024-02-28 |
human |