Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
Ming Li, Qianqian Ma, Xing Zhao, Can Wang, Huijie Wu, Jinyao Li, Wei Yan. Dilemma of multiple system atrophy and spinocerebellar ataxias. Journal of neurology. vol 265. issue 12. 2018-12-27. PMID:29700645. |
multiple system atrophy (msa) and spinocerebellar ataxias (scas) are both progressive neurodegenerative disorders, which can manifest cerebellar dysfunctions and parkinsonism-related symptoms, although the former is sporadic and the latter is autosomal dominant disease. |
2018-12-27 |
2023-08-13 |
Not clear |
Carlos Roberto Martins Junior, Alberto Rolim Muro Martinez, Ingrid Faber Vasconcelos, Thiago Junqueira Ribeiro de Rezende, Raphael Fernandes Casseb, Jose Luiz Pedroso, Orlando Graziani Povoas Barsottini, Íscia Lopes-Cendes, Marcondes Cavalcante Franç. Structural signature in SCA1: clinical correlates, determinants and natural history. Journal of neurology. vol 265. issue 12. 2018-12-27. PMID:30324307. |
spinocerebellar ataxia type 1 is an autosomal dominant disorder caused by a cag repeat expansion in atxn1, characterized by progressive cerebellar and extracerebellar symptoms. |
2018-12-27 |
2023-08-13 |
Not clear |
Hiroyuki Yahikozawa, Satoko Miyatake, Toshiaki Sakai, Takeshi Uehara, Mitsunori Yamada, Norinao Hanyu, Yasuhiro Futatsugi, Hiroshi Doi, Shigeru Koyano, Fumiaki Tanaka, Atsushi Suzuki, Naomichi Matsumoto, Kunihiro Yoshid. A Japanese Family of Spinocerebellar Ataxia Type 21: Clinical and Neuropathological Studies. Cerebellum (London, England). vol 17. issue 5. 2018-11-06. PMID:29687291. |
spinocerebellar ataxia type 21 (sca21) is a rare subtype of autosomal dominant cerebellar ataxias, which was first identified in a french family and has been reported almost exclusively in french ancestry so far. |
2018-11-06 |
2023-08-13 |
Not clear |
Stefania Squadrone, Paola Brizio, Cecilia Mancini, Maria Cesarina Abete, Alfredo Brusc. Altered homeostasis of trace elements in the blood of SCA2 patients. Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS). vol 47. 2018-10-05. PMID:29544796. |
spinocerebellar ataxia type 2 (sca2) is a neurological disorder characterized by cerebellar dysfunction. |
2018-10-05 |
2023-08-13 |
Not clear |
Carlo Wilke, Friedemann Bender, Stefanie N Hayer, Kathrin Brockmann, Ludger Schöls, Jens Kuhle, Matthis Synofzi. Serum neurofilament light is increased in multiple system atrophy of cerebellar type and in repeat-expansion spinocerebellar ataxias: a pilot study. Journal of neurology. vol 265. issue 7. 2018-10-04. PMID:29737427. |
serum neurofilament light is increased in multiple system atrophy of cerebellar type and in repeat-expansion spinocerebellar ataxias: a pilot study. |
2018-10-04 |
2023-08-13 |
human |
Carlo Wilke, Friedemann Bender, Stefanie N Hayer, Kathrin Brockmann, Ludger Schöls, Jens Kuhle, Matthis Synofzi. Serum neurofilament light is increased in multiple system atrophy of cerebellar type and in repeat-expansion spinocerebellar ataxias: a pilot study. Journal of neurology. vol 265. issue 7. 2018-10-04. PMID:29737427. |
specifically, as a marker of neuronal damage, nfl might (1) help to differentiate multiple system atrophy of cerebellar type (msa-c) from sporadic adult-onset ataxia (saoa), and (2) show increases in repeat-expansion spinocerebellar ataxias (scas) which might be amenable to treatment in the future. |
2018-10-04 |
2023-08-13 |
human |
Etsuko Shimobayashi, Josef P Kapfhamme. Calcium Signaling, PKC Gamma, IP3R1 and CAR8 Link Spinocerebellar Ataxias and Purkinje Cell Dendritic Development. Current neuropharmacology. vol 16. issue 2. 2018-10-01. PMID:28554312. |
spinocerebellar ataxias (scas) are a group of cerebellar diseases characterized by progressive ataxia and cerebellar atrophy. |
2018-10-01 |
2023-08-13 |
Not clear |
James P Orengo, Meike E van der Heijden, Shuang Hao, Jianrong Tang, Harry T Orr, Huda Y Zoghb. Motor neuron degeneration correlates with respiratory dysfunction in SCA1. Disease models & mechanisms. vol 11. issue 2. 2018-10-01. PMID:29419414. |
spinocerebellar ataxia type 1 (sca1) is characterized by adult-onset cerebellar degeneration with attendant loss of motor coordination. |
2018-10-01 |
2023-08-13 |
Not clear |
Arnulf H Koeppe. The neuropathology of the adult cerebellum. Handbook of clinical neurology. vol 154. 2018-09-28. PMID:29903436. |
the cerebellum is a prominent target of several sporadic and hereditary neurodegenerative diseases, including multiple system atrophy, spinocerebellar ataxia, and friedreich ataxia. |
2018-09-28 |
2023-08-13 |
Not clear |
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 |