All Relations between Spinocerebellar Ataxias and cerebellum

Publication Sentence Publish Date Extraction Date Species
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
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