| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Élise Morlet, Franz Hozer, Jean-François Costemale-Lacost. Neuroprotective effects of lithium: what are the implications in humans with neurodegenerative disorders? Geriatrie et psychologie neuropsychiatrie du vieillissement. vol 16. issue 1. 2018-09-27. PMID:29400298. |
in spinocerebellar ataxia, introduction of lithium may be of benefits in terms of improvement of cerebellar symptoms. |
2018-09-27 |
2023-08-13 |
Not clear |
| Sowmya Devatha Venkatesh, Mahesh Kandasamy, Nagaraj S Moily, Radhika Vaidyanathan, Lakshmi Narayanan Kota, Syama Adhikarla, Ravi Yadav, Pramod Kumar Pal, Sanjeev Jain, Meera Purushotta. Genetic testing for clinically suspected spinocerebellar ataxias: report from a tertiary referral centre in India. Journal of genetics. vol 97. issue 1. 2018-09-17. PMID:29666341. |
spinocerebellar ataxias (scas) are a heterogeneous group of neurodegenerative syndromes, characterized by a wide range of muscular weakness and motor deficits, caused due to cerebellar degeneration. |
2018-09-17 |
2023-08-13 |
human |
| Luis Velázquez-Pérez, Gilberto Sánchez-Cruz, Roberto Rodríguez-Labrada, Mercedes Velázquez-Manresa, Ricardo Hechavarría-Pupo, Luis E Almaguer-Medero. Postural Instability in Prodromal Spinocerebellar Ataxia Type 2: Insights into Cerebellar Involvement Before Onset of Permanent Ataxia. Cerebellum (London, England). vol 16. issue 1. 2018-09-13. PMID:26956609. |
postural instability in prodromal spinocerebellar ataxia type 2: insights into cerebellar involvement before onset of permanent ataxia. |
2018-09-13 |
2023-08-13 |
Not clear |
| G Olivito, M Lupo, C Iacobacci, S Clausi, S Romano, M Masciullo, M Molinari, M Cercignani, M Bozzali, M Leggi. Structural cerebellar correlates of cognitive functions in spinocerebellar ataxia type 2. Journal of neurology. vol 265. issue 3. 2018-08-23. PMID:29356974. |
structural cerebellar correlates of cognitive functions in spinocerebellar ataxia type 2. |
2018-08-23 |
2023-08-13 |
Not clear |
| G Olivito, M Lupo, C Iacobacci, S Clausi, S Romano, M Masciullo, M Molinari, M Cercignani, M Bozzali, M Leggi. Structural cerebellar correlates of cognitive functions in spinocerebellar ataxia type 2. Journal of neurology. vol 265. issue 3. 2018-08-23. PMID:29356974. |
spinocerebellar ataxia type 2 (sca2) is an autosomal dominant neurodegenerative disease involving the cerebellum and characterized by a typical motor syndrome. |
2018-08-23 |
2023-08-13 |
Not clear |
| Feng Jing, Dan Yang, Tao Che. [Advance in research on spinocerebellar ataxia 2]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. vol 35. issue 2. 2018-08-23. PMID:29653012. |
spinocerebellar ataxia type 2 (sca2) is a rare autosomal dominant progressive degenerative disease of the nervous system, which is characterized by a progressive cerebellar syndrome associated with saccadic eye scan, peripheral neuropathy, cognitive disorders, and other multisystem features. |
2018-08-23 |
2023-08-13 |
Not clear |
| Vincent Huin, Isabelle Strubi-Vuillaume, Kathy Dujardin, Marine Brion, Marie Delliaux, Delphine Dellacherie, Jean-Christophe Cuvellier, Jean-Marie Cuisset, Audrey Riquet, Caroline Moreau, Luc Defebvre, Bernard Sablonnière, David Devo. Expanding the phenotype of SCA19/22: Parkinsonism, cognitive impairment and epilepsy. Parkinsonism & related disorders. vol 45. 2018-08-06. PMID:28947073. |
spinocerebellar ataxia types 19 and 22 (sca19/22) are rare conditions in which relatively isolated cerebellar involvement is frequently associated with cognitive impairment. |
2018-08-06 |
2023-08-13 |
Not clear |
| Andrew Mundwiler, Vikram G Shakkotta. Autosomal-dominant cerebellar ataxias. Handbook of clinical neurology. vol 147. 2018-07-26. PMID:29325610. |
spinocerebellar ataxias (scas) are a genetically diverse group of dominantly inherited disorders that share clinical features that result from dysfunction and degeneration of the cerebellum and its associated pathways. |
2018-07-26 |
2023-08-13 |
Not clear |
| Jeanne Hsieh, Jen-Wei Liu, Horng-Jyh Harn, Kuo-Wei Hsueh, Karthyayani Rajamani, Yu-Chen Deng, Chih-Min Chia, Woei-Cheang Shyu, Shinn-Zong Lin, Tzyy-Wen Chio. Human Olfactory Ensheathing Cell Transplantation Improves Motor Function in a Mouse Model of Type 3 Spinocerebellar Ataxia. Cell transplantation. vol 26. issue 10. 2018-07-19. PMID:29251109. |
spinocerebellar ataxia (sca) is a progressive neurodegenerative disease that affects the cerebellum and spinal cord. |
2018-07-19 |
2023-08-13 |
mouse |
| Judit M Pérez Ortiz, Harry T Or. Spinocerebellar Ataxia Type 1: Molecular Mechanisms of Neurodegeneration and Preclinical Studies. Advances in experimental medicine and biology. vol 1049. 2018-07-09. PMID:29427101. |
spinocerebellar ataxia type 1 (sca1) is an adult-onset, inherited disease that leads to degeneration of purkinje cells of the cerebellum and culminates in death 10-30 years after disease onset. |
2018-07-09 |
2023-08-13 |
mouse |
| Xiaofei Du, Christopher Manuel Gome. Spinocerebellar [corrected] Ataxia Type 6: Molecular Mechanisms and Calcium Channel Genetics. Advances in experimental medicine and biology. vol 1049. 2018-07-09. PMID:29427102. |
spinocerebellar ataxia (sca) type 6 is an autosomal dominant disease affecting cerebellar degeneration. |
2018-07-09 |
2023-08-13 |
Not clear |
| G Olivito, M Lupo, C Iacobacci, S Clausi, S Romano, M Masciullo, M Molinari, M Cercignani, M Bozzali, M Leggi. Microstructural MRI Basis of the Cognitive Functions in Patients with Spinocerebellar Ataxia Type 2. Neuroscience. vol 366. 2018-06-29. PMID:29031602. |
spinocerebellar ataxia type 2 (sca2) is an autosomal dominant neurodegenerative disease involving the cerebellum. |
2018-06-29 |
2023-08-13 |
Not clear |
| Arunmozhi Elavarasi, Deepa Dash, Manjari Tripathi, Rohit Bhati. Cerebellar ataxia and neuropathy as presenting features of hepatitis-B related cirrhosis and portal hypertension. BMJ case reports. vol 2017. 2018-06-14. PMID:29054954. |
adult onset cerebellar dysfunction with neuropathy is a commonly encountered condition and is usually due to genetic causes such as spinocerebellar ataxia, gluten ataxia, alcohol related, toxic, degenerative, immune mediated, paraneoplastic causes and so on. |
2018-06-14 |
2023-08-13 |
Not clear |
| Koji Ab. [An early history of Japanese amyotrophic lateral sclerosis (ALS)-related diseases and the current development]. Rinsho shinkeigaku = Clinical neurology. vol 58. issue 3. 2018-06-07. PMID:29491329. |
in relation to foreign previous reports, five topics are introduced and discussed on als with dementia, als/parkinsonism dementia complex (als/pdc), familial als (fals), spinal bulbar muscular atrophy (sbma), and multisystem involvement especially in cerebellar system of als including als/sca (spinocerebellar ataxia) crossroad mutation asidan. |
2018-06-07 |
2023-08-13 |
Not clear |
| Sriram Jayabal, Hui Ho Vanessa Chang, Kathleen E Cullen, Alanna J Wat. 4-aminopyridine reverses ataxia and cerebellar firing deficiency in a mouse model of spinocerebellar ataxia type 6. Scientific reports. vol 6. 2018-06-04. PMID:27381005. |
4-aminopyridine reverses ataxia and cerebellar firing deficiency in a mouse model of spinocerebellar ataxia type 6. |
2018-06-04 |
2023-08-13 |
mouse |
| Etsuko Shimobayashi, Josef P Kapfhamme. Increased biological activity of protein Kinase C gamma is not required in Spinocerebellar ataxia 14. Molecular brain. vol 10. issue 1. 2018-05-07. PMID:28738819. |
spinocerebellar ataxia (sca) is an autosomal dominant neurodegenerative disorder characterized by slowly progressive cerebellar dysfunction. |
2018-05-07 |
2023-08-13 |
Not clear |
| Wenhui Qu, Andrea Johnson, Joo Hyun Kim, Abigail Lukowicz, Daniel Svedberg, Marija Cvetanovi. Inhibition of colony-stimulating factor 1 receptor early in disease ameliorates motor deficits in SCA1 mice. Journal of neuroinflammation. vol 14. issue 1. 2018-03-26. PMID:28545543. |
polyglutamine (polyq) expansion in the protein ataxin-1 (atxn1) causes spinocerebellar ataxia type 1 (sca1), a fatal dominantly inherited neurodegenerative disease characterized by motor deficits, cerebellar neurodegeneration, and gliosis. |
2018-03-26 |
2023-08-13 |
mouse |
| Chiharu Isono, Makito Hirano, Hikaru Sakamoto, Shuichi Ueno, Susumu Kusunoki, Yusaku Nakamur. Progression of Dysphagia in Spinocerebellar Ataxia Type 6. Dysphagia. vol 32. issue 3. 2018-03-12. PMID:28042641. |
spinocerebellar ataxia type 6 (sca6), an autosomal dominant triplet repeat disease, predominantly affects the cerebellum with a late onset and generally good prognosis. |
2018-03-12 |
2023-08-13 |
Not clear |
| Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, José Miguel Laffita-Mes. Prodromal spinocerebellar ataxia type 2: Prospects for early interventions and ethical challenges. Movement disorders : official journal of the Movement Disorder Society. vol 32. issue 5. 2018-02-06. PMID:28256108. |
research during the past 3 decades in spinocerebellar ataxia type 2 has revealed a large body of evidence suggesting that many disease features precede the manifest cerebellar syndrome, which delineates the prodromal stage of this disorder. |
2018-02-06 |
2023-08-13 |
Not clear |
| Lulin Choubtum, Pirada Witoonpanich, Kongkiat Kulkantrakorn, Suchat Hanchaiphiboolkul, Sunsanee Pongpakdee, Somsak Tiamkao, Teeratorn Pulke. Trinucleotide repeat expansion of TATA-binding protein gene associated with Parkinson's disease: A Thai multicenter study. Parkinsonism & related disorders. vol 28. 2018-02-05. PMID:27172828. |
spinocerebellar ataxia type 17 (sca17) is an inherited cerebellar degeneration associated with trinucleotide repeat expansions in the tata-binding protein gene (tbp). |
2018-02-05 |
2023-08-13 |
Not clear |