| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Sung Ho Jang, Hyeok Gyu Kwo. Improvement of ataxia in a patient with cerebellar infarction by recovery of injured cortico-ponto-cerebellar tract and dentato-rubro-thalamic tract: a diffusion tensor tractography study. Neural regeneration research. vol 14. issue 8. 2020-09-30. PMID:30964075. |
improvement of ataxia in a patient with cerebellar infarction by recovery of injured cortico-ponto-cerebellar tract and dentato-rubro-thalamic tract: a diffusion tensor tractography study. |
2020-09-30 |
2023-08-13 |
Not clear |
| María Gómez-Ruiz, Carmen Rodríguez-Cueto, Eva Luna-Piñel, Mariluz Hernández-Gálvez, Javier Fernández-Rui. Endocannabinoid System in Spinocerebellar Ataxia Type-3 and Other Autosomal-Dominant Cerebellar Ataxias: Potential Role in Pathogenesis and Expected Relevance as Neuroprotective Targets. Frontiers in molecular neuroscience. vol 12. 2020-09-30. PMID:31068788. |
endocannabinoid system in spinocerebellar ataxia type-3 and other autosomal-dominant cerebellar ataxias: potential role in pathogenesis and expected relevance as neuroprotective targets. |
2020-09-30 |
2023-08-13 |
Not clear |
| Masaaki Nakamura, Masafumi Bekki, Youko Miura, Mina Itatani, Liu Xiao Ji. Cerebellar Transcranial Magnetic Stimulation Improves Ataxia in Minamata Disease. Case reports in neurology. vol 11. issue 2. 2020-09-30. PMID:31543798. |
cerebellar transcranial magnetic stimulation improves ataxia in minamata disease. |
2020-09-30 |
2023-08-13 |
Not clear |
| Salil Manek, Mark F. Le. Gait and Balance Dysfunction in Adults. Current treatment options in neurology. vol 5. issue 2. 2020-09-29. PMID:12628066. |
another important cause of gait disturbance in adults is the cerebellar ataxias. |
2020-09-29 |
2023-08-12 |
Not clear |
| Parvaneh Karimzadeh, Simin Khayatzadeh Kakhki, Shaghayegh Sadat Esmail Nejad, Masood Houshmand, Mohammad Ghofran. Ataxia Oculomotor Apraxia Type 1 in the Siblings of a Family: A Novel Mutation. Iranian journal of child neurology. vol 11. issue 1. 2020-09-29. PMID:28277561. |
although aoa1 (ataxia oculomotor apraxia1) is one of the most common causes of autosomal recessive cerebellar ataxias in japanese population, it is reported from all over the world. |
2020-09-29 |
2023-08-13 |
human |
| Parvaneh Karimzadeh, Simin Khayatzadeh Kakhki, Shaghayegh Sadat Esmail Nejad, Masood Houshmand, Mohammad Ghofran. Ataxia Oculomotor Apraxia Type 1 in the Siblings of a Family: A Novel Mutation. Iranian journal of child neurology. vol 11. issue 1. 2020-09-29. PMID:28277561. |
the clinical manifestations are similar to ataxia telangiectasia in which non-neurological manifestations are absent and include almost 10% of autosomal recessive cerebellar ataxias. |
2020-09-29 |
2023-08-13 |
human |
| Florian Bodranghien, Nordeyn Oulad Ben Taib, Lionel Van Maldergem, Mario Mant. A Postural Tremor Highly Responsive to Transcranial Cerebello-Cerebral DCS in ARCA3. Frontiers in neurology. vol 8. 2020-09-29. PMID:28316589. |
cerebellar ataxias are disabling disorders that impact the quality of life of patients. |
2020-09-29 |
2023-08-13 |
Not clear |
| Jessie C Jacobsen, Whitney Whitford, Brendan Swan, Juliet Taylor, Donald R Love, Rosamund Hill, Sarah Molyneux, Peter M George, Richard Mackay, Stephen P Robertson, Russell G Snell, Klaus Lehner. Compound Heterozygous Inheritance of Mutations in Coenzyme Q8A Results in Autosomal Recessive Cerebellar Ataxia and Coenzyme Q JIMD reports. vol 42. 2020-09-29. PMID:29159460. |
compound heterozygous inheritance of mutations in coenzyme q8a results in autosomal recessive cerebellar ataxia and coenzyme q autosomal recessive ataxias are characterised by a fundamental loss in coordination of gait with associated atrophy of the cerebellum. |
2020-09-29 |
2023-08-13 |
Not clear |
| Malcolm Proudfoot, Alastair Wilkin. Treatment of Cerebellar Ataxia in the Context of Systemic Diseases. Current treatment options in neurology. vol 19. issue 12. 2020-09-29. PMID:29177818. |
purpose of review the purpose of this review is to assess the evidence behind treatment regimens for cerebellar ataxias occurring in the context of systemic disease. |
2020-09-29 |
2023-08-13 |
Not clear |
| Malcolm Proudfoot, Alastair Wilkin. Treatment of Cerebellar Ataxia in the Context of Systemic Diseases. Current treatment options in neurology. vol 19. issue 12. 2020-09-29. PMID:29177818. |
summary despite their rarity, cerebellar ataxias occurring in the context of systemic disease cause significant morbidity and better therapies are required to improve outcomes associated with these conditions. |
2020-09-29 |
2023-08-13 |
Not clear |
| Faruk Incecik, Ozlem M Herguner, Patrick Willems, Neslihan O Munga. Spinocerebellar Ataxia-21 in a Turkish Child. Annals of Indian Academy of Neurology. vol 21. issue 1. 2020-09-29. PMID:29720801. |
hereditary cerebellar ataxias are genetically heterogeneous disorders. |
2020-09-29 |
2023-08-13 |
Not clear |
| Rosella Abeti, Alexander F Brown, Marta Maiolino, Sandip Patel, Paola Giunt. Calcium Deregulation: Novel Insights to Understand Friedreich's Ataxia Pathophysiology. Frontiers in cellular neuroscience. vol 12. 2020-09-29. PMID:30333728. |
friedreich's ataxia (frda) is a neurodegenerative disorder, characterized by degeneration of dorsal root ganglia, cerebellum and cardiomyopathy. |
2020-09-29 |
2023-08-13 |
Not clear |
| Lisandra Martins, Diogo Galvão, Anaísa Silva, Bárbara Vieira, Óscar Reis, Rita Vitorino, Paula Pire. Paraneoplastic opsoclonus-myoclonus syndrome as a rare presentation of breast cancer. Journal of surgical case reports. vol 2019. issue 2. 2020-09-29. PMID:30788093. |
opsoclonus-myoclonus paraneoplastic syndrome is a medical condition that includes opsoclonus along with diffuse or focal body myoclonus and truncal titubation with or without ataxia and other cerebellar signs. |
2020-09-29 |
2023-08-13 |
Not clear |
| Pramod Theetha Kariyanna, Alix Charles, Muhammad Faizan Ahmed, Apoorva Jayarangaiah, Sushruth Das, Mohammed Al-Sadawi, Madina Abduraimova, Samy I McFarlan. Rare Case of Bilateral Cerebellar Hemorrhage in a Male Boxer. American journal of medical case reports. vol 7. issue 10. 2020-09-29. PMID:31457070. |
our report highlights the need to consider cerebellar bleed in boxers who present after ataxia after boxing/knocked out. |
2020-09-29 |
2023-08-13 |
Not clear |
| Chi-Wen Jao, Bing-Wen Soong, Chao-Wen Huang, Chien-An Duan, Chih-Chun Wu, Yu-Te Wu, Po-Shan Wan. Diffusion Tensor Magnetic Resonance Imaging for Differentiating Multiple System Atrophy Cerebellar Type and Spinocerebellar Ataxia Type 3. Brain sciences. vol 9. issue 12. 2020-09-28. PMID:31817016. |
our results may suggest that fa and md can be effectively used for differentiating sca3 and msa-c, both of which are cerebellar ataxias and have many common atrophied regions in the cerebral and cerebellar cortex. |
2020-09-28 |
2023-08-13 |
Not clear |
| Hiroshi Mitoma, Mario Manto, Jordi Gandin. Recent Advances in the Treatment of Cerebellar Disorders. Brain sciences. vol 10. issue 1. 2020-09-28. PMID:31878024. |
various etiopathologies affect the cerebellum, resulting in the development of cerebellar ataxias (cas), a heterogeneous group of disorders characterized clinically by movement incoordination, affective dysregulation, and cognitive dysmetria. |
2020-09-28 |
2023-08-13 |
Not clear |
| Rosa Campopiano, Rosangela Ferese, Fabio Buttari, Cinzia Femiano, Diego Centonze, Francesco Fornai, Francesca Biagioni, Maria Antonietta Chiaravalloti, Mauro Magnani, Emiliano Giardina, Anna Ruzzo, Stefano Gambardell. A Novel Homozygous Variant in the Fork-Head-Associated Domain of Polynucleotide Kinase Phosphatase in a Patient Affected by Late-Onset Ataxia With Oculomotor Apraxia Type 4. Frontiers in neurology. vol 10. 2020-09-28. PMID:32010037. |
ataxia with oculomotor apraxia (aoa) is a clinical syndrome featuring a group of genetic diseases including at least four separate autosomal-recessive cerebellar ataxias. |
2020-09-28 |
2023-08-13 |
Not clear |
| Majid Zaki-Dizaji, Mohammad Tajdini, Fatemeh Kiaee, Hossein Shojaaldini, Reza Shervin Badv, Hassan Abolhassani, Asghar Aghamohammad. Dystonia in Ataxia Telangiectasia: A Case Report with Novel Mutations. Oman medical journal. vol 35. issue 1. 2020-09-28. PMID:32095276. |
ataxia telangiectasia (a-t) is a common, genetically inherited cause of early childhood-onset ataxia that is classically characterized by progressive cerebellar malfunction, oculocutaneous telangiectasia, genome instability, and immunodeficiency. |
2020-09-28 |
2023-08-13 |
Not clear |
| Michela Lupo, Giusy Olivito, Silvia Clausi, Libera Siciliano, Vittorio Riso, Marco Bozzali, Filippo M Santorelli, Gabriella Silvestri, Maria Leggi. Cerebello-Cortical Alterations Linked to Cognitive and Social Problems in Patients With Spastic Paraplegia Type 7: A Preliminary Study. Frontiers in neurology. vol 11. 2020-09-28. PMID:32161564. |
spastic paraplegia type 7 (spg7), which represents one of the most common forms of autosomal recessive spastic paraplegia (mim#607259), often manifests with a complicated phenotype, characterized by progressive spastic ataxia with evidence of cerebellar atrophy on brain mri. |
2020-09-28 |
2023-08-13 |
human |
| Valentina Cerrat. Cerebellar Astrocytes: Much More Than Passive Bystanders In Ataxia Pathophysiology. Journal of clinical medicine. vol 9. issue 3. 2020-09-28. PMID:32168822. |
cerebellar astrocytes: much more than passive bystanders in ataxia pathophysiology. |
2020-09-28 |
2023-08-13 |
Not clear |