| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Intissar Barbouch, Amina Ali Kako, Yassine Mebrou. Comprehensive Evaluation of Sporadic Late-Onset Cerebellar Ataxias: Clinical Presentation, Diagnostic Challenges, and Treatment Outcomes. Cureus. vol 16. issue 6. 2024-07-22. PMID:39036235. |
comprehensive evaluation of sporadic late-onset cerebellar ataxias: clinical presentation, diagnostic challenges, and treatment outcomes. |
2024-07-22 |
2024-07-24 |
Not clear |
| Intissar Barbouch, Amina Ali Kako, Yassine Mebrou. Comprehensive Evaluation of Sporadic Late-Onset Cerebellar Ataxias: Clinical Presentation, Diagnostic Challenges, and Treatment Outcomes. Cureus. vol 16. issue 6. 2024-07-22. PMID:39036235. |
sporadic late-onset cerebellar ataxias (sloca) present a diagnostic challenge due to their heterogeneous etiologies and complex clinical manifestations. |
2024-07-22 |
2024-07-24 |
Not clear |
| Albert J Fenoy, Zili D Chu, Robert J Ritter, Christopher R Conner, Stephen F Krali. Evaluating functional connectivity differences between DBS ON/OFF states in essential tremor. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics. vol 21. issue 4. 2024-07-13. PMID:38824101. |
a sub-group analysis of patients with greater ataxia had significantly decreased functional connectivity between multiple rois in the cortex and cerebellum when dbs was on compared to off. |
2024-07-13 |
2024-07-16 |
Not clear |
| Marian Y Girgis, Eman Mahfouz, Alshaimaa Abdellatif, Farah Taha, Walaa ElNagga. Cerebral Folate Transport Deficiency in 2 Cases with Intractable Myoclonic Epilepsy. Journal of epilepsy research. vol 14. issue 1. 2024-07-10. PMID:38978529. |
in conclusion, cerebral folate transport deficiency should be suspected in every child with global developmental delay, intractable myoclonic epilepsy, ataxia with neuroimaging suggesting cerebellar atrophy and brain calcifications. |
2024-07-10 |
2024-07-12 |
Not clear |
| Marie Beaudin, Nicolas Dupre, Mario Mant. The importance of synthetic pharmacotherapy for recessive cerebellar ataxias. Expert review of neurotherapeutics. 2024-07-09. PMID:38980086. |
the importance of synthetic pharmacotherapy for recessive cerebellar ataxias. |
2024-07-09 |
2024-07-12 |
Not clear |
| Sareh Hosseinpour, Maryam Bemanalizadeh, Pouria Mohammadi, Mahmoud Reza Ashrafi, Morteza Heidar. An overview of early-onset cerebellar ataxia: a practical guideline. Acta neurologica Belgica. 2024-07-01. PMID:38951452. |
they are mainly manifested by degeneration or abnormal development of the cerebellum occurring before the age of 25 years and typically the pattern of inheritance is autosomal recessive.the diagnosis of autosomal recessive cerebellar ataxias (arcas) is confirmed by the clinical, laboratory, electrophysiological examination, neuroimaging findings, and mutation analysis when the causative gene is detected. |
2024-07-01 |
2024-07-04 |
Not clear |
| Eboni M V Bucknor, Errin Johnson, Stephanie Efthymiou, Javeria R Alvi, Tipu Sultan, Henry Houlden, Reza Maroofian, Ehsan G Karimiani, Mattéa J Finelli, Peter L Olive. Neuroinflammation and Lysosomal Abnormalities Characterise the Essential Role for Oxidation Resistance 1 in the Developing and Adult Cerebellum. Antioxidants (Basel, Switzerland). vol 13. issue 6. 2024-06-27. PMID:38929124. |
loss-of-function mutations in the tldc family of proteins cause a range of severe childhood-onset neurological disorders with common clinical features that include cerebellar neurodegeneration, ataxia and epilepsy. |
2024-06-27 |
2024-06-29 |
mouse |
| Sudan Zhu, Yuting Shi, Zhao Chen, Zhe Long, Linlin Wan, Daji Chen, Xinrong Yuan, You Fu, Feiyan Deng, Xiafei Long, Kefang Du, Rong Qiu, Beisha Tang, Chunrong Wang, Hong Jian. The characteristic and biomarker value of transcranial sonography in cerebellar ataxia. Annals of clinical and translational neurology. 2024-06-26. PMID:38924300. |
we aimed to assess the potential value of tcs in patients with cerebellar ataxias for disease diagnosis and severity assessment. |
2024-06-26 |
2024-06-29 |
Not clear |
| Adreesh Mukherjee, Sanjay Pande. Tremor in Spinocerebellar Ataxia: A Scoping Review. Tremor and other hyperkinetic movements (New York, N.Y.). vol 14. 2024-06-24. PMID:38911333. |
spinocerebellar ataxia (sca) denotes an expanding list of autosomal dominant cerebellar ataxias. |
2024-06-24 |
2024-06-26 |
Not clear |
| Armin Adibi, Ali Rastegar-Kashkouli, Pourya Yousefi, Iman Adibi, Elahe Ahmadi, Saba Naghav. Plasmapheresis and IVIG for Treatment of Non-Tumor Anti-Tr/DNER Antibody-Associated Ataxia: A Case Report. Cerebellum (London, England). 2024-06-14. PMID:38874737. |
autoimmune cerebellar ataxia (aca) is a condition characterized by progressive ataxia resulting from an immune-mediated attack on cerebellar structures. |
2024-06-14 |
2024-06-16 |
Not clear |
| Armin Adibi, Ali Rastegar-Kashkouli, Pourya Yousefi, Iman Adibi, Elahe Ahmadi, Saba Naghav. Plasmapheresis and IVIG for Treatment of Non-Tumor Anti-Tr/DNER Antibody-Associated Ataxia: A Case Report. Cerebellum (London, England). 2024-06-14. PMID:38874737. |
the patient's gait improved, ataxia resolved, and cerebellar tests normalized following treatment. |
2024-06-14 |
2024-06-16 |
Not clear |
| D González-Tapia, N Vázquez-Hernández, F Urmeneta-Ortiz, N Navidad-Hernandez, M Lazo-Yepez, A Tejeda-Martínez, M Flores-Soto, I González-Burgo. 3-Acetylpyridine-induced ataxic-like motor impairments are associated with plastic changes in the Purkinje cells of the rat cerebellum. Neurologia. vol 39. issue 5. 2024-06-03. PMID:38830720. |
ataxias are characterized by aberrant movement patterns closely related to cerebellar dysfunction. |
2024-06-03 |
2024-06-06 |
rat |
| D González-Tapia, N Vázquez-Hernández, F Urmeneta-Ortiz, N Navidad-Hernandez, M Lazo-Yepez, A Tejeda-Martínez, M Flores-Soto, I González-Burgo. 3-Acetylpyridine-induced ataxic-like motor impairments are associated with plastic changes in the Purkinje cells of the rat cerebellum. Neurologia. vol 39. issue 5. 2024-06-03. PMID:38830720. |
findings suggest a limited capacity of purkinje cells to acquire and consolidate afferent excitatory inputs and an aberrant, rigid profile in the movement-related output patterns of purkinje neurons that likely contributes to the motor-related impairments characteristic of cerebellar ataxias. |
2024-06-03 |
2024-06-06 |
rat |
| Cankatika Choudhury, Akhil Sahi. Cerebellar syndrome as the presenting feature of Hashimoto encephalopathy. BMJ case reports. vol 17. issue 5. 2024-05-28. PMID:38806398. |
this highlights the importance of antithyroid antibodies testing even in cases of pure cerebellar syndrome to rule out hashimoto encephalopathy associated ataxia. |
2024-05-28 |
2024-06-03 |
Not clear |
| Hélène Cwerman-Thibault, Vassilissa Malko-Baverel, Gwendoline Le Guilloux, Edward Ratcliffe, Djmila Mouri, Isabel Torres-Cuevas, Ivan Millán, Bruno Saubaméa, Virginie Mignon, Odile Boespflug-Tanguy, Pierre Gressens, Marisol Corral-Debrinsk. Neuroglobin overexpression in cerebellar neurons of Harlequin mice improves mitochondrial homeostasis and reduces ataxic behavior. Molecular therapy : the journal of the American Society of Gene Therapy. 2024-05-26. PMID:38796706. |
consequently, harlequin mice display degeneration of the cerebellum and suffer from progressive blindness and ataxia. |
2024-05-26 |
2024-05-31 |
mouse |
| Alzahra Hamdan, Andrew C Hooker, Xiaomei Chen, Andreas Traschütz, Rebecca Schüle, Matthis Synofzik, Mats O Karlsso. Item performance of the scale for the assessment and rating of ataxia in rare and ultra-rare genetic ataxias. CPT: pharmacometrics & systems pharmacology. 2024-05-21. PMID:38769902. |
the scale for the assessment and rating of ataxia (sara) is widely used for assessing the severity and progression of genetic cerebellar ataxias. |
2024-05-21 |
2024-05-27 |
human |
| Alzahra Hamdan, Andrew C Hooker, Xiaomei Chen, Andreas Traschütz, Rebecca Schüle, Matthis Synofzik, Mats O Karlsso. Item performance of the scale for the assessment and rating of ataxia in rare and ultra-rare genetic ataxias. CPT: pharmacometrics & systems pharmacology. 2024-05-21. PMID:38769902. |
leveraging sara subscores data from 1932 visits from 990 patients of the autosomal recessive cerebellar ataxias (arca) registry, we assessed the performance of sara using irt methodology. |
2024-05-21 |
2024-05-27 |
human |
| Paolo Flace, Diana Galletta, Antonella Bizzoca, Gianfranco Gennarini, Paolo Livre. A candidate projective neuron type of the cerebellar cortex: the synarmotic neuron. European journal of histochemistry : EJH. vol 68. issue 2. 2024-05-20. PMID:38766720. |
on this basis, the present minireview mainly focuses on the morphofunctional and neurochemical data of the synarmotic neuron, and explores its potential involvement in some forms of cerebellar ataxias. |
2024-05-20 |
2024-05-27 |
Not clear |
| Laura Ivete Rudaks, Dennis Yeow, Karl Ng, Ira W Deveson, Marina L Kennerson, Kishore Raj Kuma. An Update on the Adult-Onset Hereditary Cerebellar Ataxias: Novel Genetic Causes and New Diagnostic Approaches. Cerebellum (London, England). 2024-05-17. PMID:38760634. |
an update on the adult-onset hereditary cerebellar ataxias: novel genetic causes and new diagnostic approaches. |
2024-05-17 |
2024-05-27 |
Not clear |
| Laura Ivete Rudaks, Dennis Yeow, Karl Ng, Ira W Deveson, Marina L Kennerson, Kishore Raj Kuma. An Update on the Adult-Onset Hereditary Cerebellar Ataxias: Novel Genetic Causes and New Diagnostic Approaches. Cerebellum (London, England). 2024-05-17. PMID:38760634. |
the hereditary cerebellar ataxias (hcas) are rare, progressive neurologic disorders caused by variants in many different genes. |
2024-05-17 |
2024-05-27 |
Not clear |