| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Piervito Lopriore, Marco Vista, Alessandra Tessa, Martina Giuntini, Elena Caldarazzo Ienco, Michelangelo Mancuso, Gabriele Siciliano, Filippo Maria Santorelli, Daniele Orsucc. Primary Coenzyme Q10 Deficiency-Related Ataxias. Journal of clinical medicine. vol 13. issue 8. 2024-04-27. PMID:38673663. |
cerebellar ataxia is a neurological syndrome characterized by the imbalance (e.g., truncal ataxia, gait ataxia) and incoordination of limbs while executing a task (dysmetria), caused by the dysfunction of the cerebellum or its connections. |
2024-04-27 |
2024-04-29 |
Not clear |
| Kholood M Shalabi, Danah A Alabdulathim, Hanan M Al-Taleb, Raghad K Almarzuqi, Dalal A Alsaleh, Manar A Takroni, Rahaf M Alsaleh, Reem M Basuoda. The Effect Of Physical Therapy Intervention After Cerebellar Resection. Journal of Ayub Medical College, Abbottabad : JAMC. vol 35(Suppl 1). issue 4. 2024-02-26. PMID:38406912. |
a variety of diseases, including gait ataxia, lack of coordination, diminished dexterity, and unsteady posture, can be brought on by cerebellar dysfunction. |
2024-02-26 |
2024-02-28 |
Not clear |
| Dick Jaarsma, Maria B Birkisdóttir, Randy van Vossen, Demi W G D Oomen, Oussama Akhiyat, Wilbert P Vermeij, Sebastiaan K E Koekkoek, Chris I De Zeeuw, Laurens W J Bosma. Different Purkinje cell pathologies cause specific patterns of progressive gait ataxia in mice. Neurobiology of disease. 2024-01-29. PMID:38286390. |
gait ataxia is one of the most common and impactful consequences of cerebellar dysfunction. |
2024-01-29 |
2024-02-01 |
mouse |
| Keisuke Inoue, Meiko Asaka, Sachiko Lee, Kinya Ishikawa, Dai Yanagihar. Gait disorders induced by photothrombotic cerebellar stroke in mice. Scientific reports. vol 13. issue 1. 2023-09-22. PMID:37737224. |
previous studies in mouse models of gait ataxia, such as ho15j mice and cbln1-null mice, have shown that they have a dysfunction of parallel fiber-purkinje cell synapses in the cerebellum. |
2023-09-22 |
2023-10-07 |
mouse |
| Keisuke Inoue, Meiko Asaka, Sachiko Lee, Kinya Ishikawa, Dai Yanagihar. Gait disorders induced by photothrombotic cerebellar stroke in mice. Scientific reports. vol 13. issue 1. 2023-09-22. PMID:37737224. |
here, we performed a kinematic analysis of gait ataxia caused by a photothrombotic stroke in the medial, vermal, and intermediate regions of the cerebellum of wild-type mice. |
2023-09-22 |
2023-10-07 |
mouse |
| Mario Manto, Marios Hadjivassiliou, José Fidel Baizabal-Carvallo, Christiane S Hampe, Jerome Honnorat, Bastien Joubert, Hiroshi Mitoma, Sergio Muñiz-Castrillo, Aasef G Shaikh, Alberto Vogri. Consensus Paper: Latent Autoimmune Cerebellar Ataxia (LACA). Cerebellum (London, England). 2023-03-29. PMID:36991252. |
patients with imcas develop cerebellar symptoms, characterized mainly by gait ataxia, showing an acute or subacute clinical course. |
2023-03-29 |
2023-08-14 |
Not clear |
| Sara Fabbro, Enrico Pegolo, Daniele Piccolo, Antonio Cramaro, Maurizio Mascarin, Elisa Coassin, Miran Skrap, Francesco Tuni. Primary Leptomeningeal Medulloblastoma in Adults: A Diagnostic Challenge-Case Report and Systematic Review. Asian journal of neurosurgery. vol 17. issue 4. 2022-12-26. PMID:36570761. |
a 35-year-old woman presented with headaches, diplopia, and gait ataxia, with triventricular hydrocephalus and descent of the cerebellar tonsils beyond the foramen magnum. |
2022-12-26 |
2023-08-14 |
Not clear |
| Mustafa Al-Chalabi, Nicholas R DelCimmuto, Azizullah Beran, Pratyush Pavan Devarasetty, Asmaa Mhanna, Naeem Mahfooz, Ajaz Sheik. Clinical characteristics, management, and outcomes of CLIPPERS: A comprehensive systematic review of 140 patients from 100 studies. Multiple sclerosis and related disorders. vol 68. 2022-08-27. PMID:36029706. |
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (clippers) is a rare inflammatory disorder of the central nervous system, characterized by symptoms referable to the brainstem and cerebellum such as, diplopia, gait ataxia and cerebellar dysarthria. |
2022-08-27 |
2023-08-14 |
Not clear |
| Catharina Schirmer, Mark A Abboud, Samuel C Lee, John S Bass, Arindam G Mazumder, Jessica L Kamen, Vaishnav Krishna. Home-cage behavior in the Stargazer mutant mouse. Scientific reports. vol 12. issue 1. 2022-07-27. PMID:35896608. |
in the stargazer mutant mouse, genetic disruptions of cacng2 result in absence-like spike-wave seizures, cerebellar gait ataxia and vestibular dysfunction, which limit traditional approaches to behavioral phenotyping. |
2022-07-27 |
2023-08-14 |
mouse |
| Lazaros C Triarhou, Mario Mant. Nothnagel Syndrome. Cerebellum (London, England). 2022-07-11. PMID:35817948. |
between 1879 and 1889, he reported four cases of tectal tumors that clinically manifested with bilateral ophthalmoplegia and unilateral gait ataxia, culminating in the cerebellar classic highlighted here. |
2022-07-11 |
2023-08-14 |
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 |
| 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 |
| Devi P Patra, Evelyn L Turcotte, Bernard R Bendo. Microsurgical Resection of Dorsal Pontine Cavernous Malformation: The Telovelar Approach Augmented by the Tonsillouvular Fissure Exposure: 2-Dimensional Operative Video. Operative neurosurgery (Hagerstown, Md.). vol 21. issue 4. 2021-10-23. PMID:34332499. |
surgical approaches to lesions of the fourth ventricle (fv) have been modified over the years to reduce the complications associated with splitting the inferior cerebellar vermis (icv) and disrupting the brainstem and critical surrounding structures.1-4 two common approaches to lesions of this region include the transvermian approach (tva) and telovelar approach (teva).2 the tva was initially considered the conventional route of access to lesions of the fv1 but has been associated with significant risks, including possible gait ataxia and dysarthria.3 the teva is advantageous, as it involves dissection along natural clefts and division of non-neural tissue and provides good exposure of the superolateral recess with modest exposure of the rostral fv. |
2021-10-23 |
2023-08-13 |
Not clear |
| Danuta Z Loesch, David L Duffy, Nicholas G Martin, Flora Tassone, Anna Atkinson, Elsdon Store. 'Essential Tremor' Phenotype in FMR1 Premutation/Gray Zone Sibling Series: Exploring Possible Genetic Modifiers. Twin research and human genetics : the official journal of the International Society for Twin Studies. vol 24. issue 2. 2021-09-17. PMID:33757613. |
major features comprise kinetic tremor, gait ataxia, cognitive decline and cerebellar peduncular white matter lesions, but atypical/incomplete fxtas may occur. |
2021-09-17 |
2023-08-13 |
Not clear |
| Joan A O'Keefe, Deborah Bang, Erin E Robertson, Alexandras Biskis, Bichun Ouyang, Yuanqing Liu, Gian Pal, Elizabeth Berry-Kravis, Deborah A Hal. Prodromal Markers of Upper Limb Deficits in Movement disorders clinical practice. vol 7. issue 7. 2021-08-30. PMID:33043077. |
prodromal markers of upper limb deficits in fragile x-associated tremor/ataxia syndrome (fxtas) is a rare, late-onset neurodegenerative disorder characterized by tremor and cerebellar gait ataxia, affecting premutation carriers (pmc) of cgg expansions (range, 55-200) in the fragile x mental retardation 1 ( |
2021-08-30 |
2023-08-13 |
Not clear |
| John M Ringman, Yuchuan Qiao, Alexander Garbin, Beth E Fisher, Brent Fogel, Kecia Watari Knoell, Helena C Chui, Yonggang Shi, Jessica E Rexac. Emotional detachment, gait ataxia, and cerebellar dysconnectivity associated with compound heterozygous mutations in the Neurocase. vol 26. issue 5. 2021-08-20. PMID:32893728. |
emotional detachment, gait ataxia, and cerebellar dysconnectivity associated with compound heterozygous mutations in the we report a patient with autism-like deficits in emotional connectedness, executive dysfunction, and ataxia beginning at age 39. he had compound heterozygous variants in spg7 (a510v and 1552+1 g>t substitutions), mutation of which is classically associated with spastic paraparesis. diffusion mri demonstrated abnormalities in the cerebellar outflow tracts. transcranial magnetic stimulation showed a prolonged cortical silent period representing exaggerated cortical inhibition, as previously described with pure cerebellar degeneration. the acquired cerebellar cognitive affective syndrome in association with specific anatomic and neurophysiological abnormalities in the cerebellum expand the spectrum of spg7-related neurodegeneration and support a role for cerebellar output in socio-emotional behavior. |
2021-08-20 |
2023-08-13 |
Not clear |
| Elan D Louis, Phyllis L Faus. Essential Tremor Within the Broader Context of Other Forms of Cerebellar Degeneration. Cerebellum (London, England). vol 19. issue 6. 2021-08-19. PMID:32666285. |
other features of cerebellar dysfunction, gait ataxia and eye motion abnormalities, are seen to a mild degree in et and more markedly in scas. |
2021-08-19 |
2023-08-13 |
Not clear |
| Zubir Rentiya, Robert Hutnik, Yolunna Q Mekkam, Junun Ba. The Pathophysiology and Clinical Manifestations of Spinocerebellar Ataxia Type 6. Cerebellum (London, England). vol 19. issue 3. 2021-03-15. PMID:32125675. |
in addition to basic cerebellar dysfunction symptoms, patients with sca develop gait ataxia, dysphagia, dysarthria, oculomotor disturbances, pyramidal and extrapyramidal disease signs, rigidity, bradycardia, sensory deficits, and mild cognitive and executive function decline. |
2021-03-15 |
2023-08-13 |
Not clear |
| Eduardo Freitas, Octávia Costa, Sofia Roch. A New Phenotype of Ataxia With Oculomotor Apraxia Type 4. Cureus. vol 13. issue 2. 2021-03-05. PMID:33654647. |
in this case report, we describe two sisters, who were 52- and 58-years-old, with cerebellar dysarthria, oculomotor apraxia, dystonia, and gait ataxia. |
2021-03-05 |
2023-08-13 |
Not clear |
| Piotr Alster, Dariusz M Koziorowski, Mirosław Za Bek, Sebastian Dzierzȩcki, Jacek Ma Dry, Karolina Duszyńska-Wa S, Hanna Grygarowicz, Justyna Zielonko, Leszek Królicki, Andrzej Friedma. Making a Difference-Positive Effect of Unilateral VIM Gamma Knife Thalamotomy in the Therapy of Tremor in Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS). Frontiers in neurology. vol 9. 2020-10-01. PMID:29997574. |
the symptoms include action tremor and cerebellar gait ataxia. |
2020-10-01 |
2023-08-13 |
Not clear |