| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Michelle A Farrar, Steve Vucic, Garth Nicholson, Matthew C Kierna. Motor cortical dysfunction develops in spinocerebellar ataxia type 3. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. vol 127. issue 11. 2017-05-24. PMID:27689815. |
spinocerebellar ataxia type 3 (sca3) is an inherited neurodegenerative disorder characterized by cerebellar ataxia and variable expression of clinical features beyond the cerebellum. |
2017-05-24 |
2023-08-13 |
Not clear |
| Robert J Ure, Sanveer Dhanju, Anthony E Lang, Alfonso Fasan. Unusual tremor syndromes: know in order to recognise. Journal of neurology, neurosurgery, and psychiatry. vol 87. issue 11. 2017-05-17. PMID:26985048. |
the review includes fragile x-associated tremor/ataxia syndrome, spinocerebellar ataxia type 12, tremors caused by autosomal recessive cerebellar ataxias, myorhythmia, isolated tongue tremor, wilson's disease, slow orthostatic tremor, peripheral trauma-induced tremor, tardive tremor and rabbit syndrome, paroxysmal tremors (hereditary chin tremor, bilateral high-frequency synchronous discharges, head tremor, limb-shaking transient ischaemic attack), bobble-head doll syndrome, spasmus nutans and shuddering attacks. |
2017-05-17 |
2023-08-13 |
rabbit |
| Gerson da Silva Carvalho, Jonas Alex Morales Saute, Clarissa Branco Haas, Vitor Rocco Torrez, Andressa Wigner Brochier, Gabriele Nunes Souza, Gabriel Vasata Furtado, Tailise Gheno, Aline Russo, Thais Lampert Monte, Artur Schumacher-Schuh, Rui D'Avila, Karina Carvalho Donis, Raphael Machado Castilhos, Diogo Onofre Souza, Maria Luiza Saraiva-Pereira, Vanessa Leotti Torman, Suzi Camey, Luis Valmor Portela, Laura Bannach Jardi. Cytokines in Machado Joseph Disease/Spinocerebellar Ataxia 3. Cerebellum (London, England). vol 15. issue 4. 2017-03-06. PMID:26395908. |
age at onset, disease duration, and clinical scales scale for the assessment and rating of ataxia (sara), neurological examination score for spinocerebellar ataxias (nessca), sca functional index (scafi), and composite cerebellar functional score (ccfs) were obtained from the symptomatic carriers. |
2017-03-06 |
2023-08-13 |
Not clear |
| Mario Manto, Christophe Haba. Cerebellar disorders: clinical/radiologic findings and modern imaging tools. Handbook of clinical neurology. vol 135. 2017-02-10. PMID:27432679. |
genetic ataxias include mainly four groups of disorders: autosomal-recessive cerebellar ataxias, autosomal-dominant ataxias (spinocerebellar ataxias and episodic ataxias), mitochondrial disorders, and x-linked ataxias. |
2017-02-10 |
2023-08-13 |
Not clear |
| Anju Shukla, Priyanka Upadhyai, Jhanvi Shah, K Neethukrishna, Stephanie Bielas, K M Girish. Autosomal recessive spinocerebellar ataxia 20: Report of a new patient and review of literature. European journal of medical genetics. vol 60. issue 2. 2017-02-10. PMID:27913285. |
autosomal recessive spinocerebellar ataxia 20 (scar20) is a recently described disorder characterized by intellectual disability, ataxia, coarse facial features, progressive loss of purkinje cells in the cerebellum and often hearing loss and skeletal abnormalities. |
2017-02-10 |
2023-08-13 |
Not clear |
| Irene Paradisi, Vassiliki Ikonomu, Sergio Aria. Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent. Journal of human genetics. vol 61. issue 3. 2016-12-30. PMID:26538302. |
dominantly inherited ataxias (spinocerebellar ataxias, scas) are a genetically heterogeneous group of neurologic diseases characterized by progressive cerebellar and spinal tract degeneration with ataxia and other signs, common to all known subtypes. |
2016-12-30 |
2023-08-13 |
Not clear |
| Carlos R Hernandez-Castillo, Victor Galvez, Rosalinda Diaz, Juan Fernandez-Rui. Specific cerebellar and cortical degeneration correlates with ataxia severity in spinocerebellar ataxia type 7. Brain imaging and behavior. vol 10. issue 1. 2016-12-13. PMID:25917872. |
specific cerebellar and cortical degeneration correlates with ataxia severity in spinocerebellar ataxia type 7. |
2016-12-13 |
2023-08-13 |
human |
| Zhen Yang, Chuyang Ye, John A Bogovic, Aaron Carass, Bruno M Jedynak, Sarah H Ying, Jerry L Princ. Automated cerebellar lobule segmentation with application to cerebellar structural analysis in cerebellar disease. NeuroImage. vol 127. 2016-12-13. PMID:26408861. |
the proposed method was then applied to 77 subjects to study the region-specific cerebellar structural differences in three spinocerebellar ataxia (sca) genetic subtypes. |
2016-12-13 |
2023-08-13 |
human |
| C J L M Smeets, D S Verbee. Climbing fibers in spinocerebellar ataxia: A mechanism for the loss of motor control. Neurobiology of disease. vol 88. 2016-12-13. PMID:26792399. |
the spinocerebellar ataxias (scas) form an ever-growing group of neurodegenerative disorders causing dysfunction of the cerebellum and loss of motor control in patients. |
2016-12-13 |
2023-08-13 |
Not clear |
| Lipin Liang, Tao Chen, Yan W. The electrophysiology of spinocerebellar ataxias. Neurophysiologie clinique = Clinical neurophysiology. vol 46. issue 1. 2016-12-13. PMID:26947625. |
spinocerebellar ataxias (scas) are a group of autosomal dominantly inherited neurodegenerative diseases, involving the cerebellum and the brainstem. |
2016-12-13 |
2023-08-13 |
Not clear |
| Adele G Marthaler, Alisa Tubsuwan, Benjamin Schmid, Ulla B Poulsen, Poul Hyttel, Jørgen E Nielsen, Troels T Nielsen, Bjørn Hols. Generation of spinocerebellar ataxia type 2 patient-derived iPSC line H271. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345803. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Adele G Marthaler, Benjamin Schmid, Alisa Tubsuwan, Ulla B Poulsen, Alexander F Engelbrecht, Ulrike A Mau-Holzmann, Poul Hyttel, Jørgen E Nielsen, Troels T Nielsen, Bjørn Hols. Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H196. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345804. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Adele G Marthaler, Benjamin Schmid, Alisa Tubsuwan, Ulla B Poulsen, Poul Hyttel, Troels T Nielsen, Jørgen E Nielsen, Bjørn Hols. Generation of spinocerebellar ataxia type 2 patient-derived iPSC line H266. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345805. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Adele G Marthaler, Benjamin Schmid, Alisa Tubsuwan, Ulla B Poulsen, Alexander F Engelbrecht, Ulrike A Mau-Holzmann, Poul Hyttel, Jørgen E Nielsen, Troels T Nielsen, Bjørn Hols. Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H271. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345809. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Adele G Marthaler, Benjamin Schmid, Alisa Tubsuwan, Ulla B Poulsen, Poul Hyttel, Troels T Nielsen, Jørgen E Nielsen, Bjørn Hols. Generation of spinocerebellar ataxia type 2 patient-derived iPSC line H196. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345814. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Adele G Marthaler, Alisa Tubsuwan, Benjamin Schmid, Ulla B Poulsen, Alexander F Engelbrecht, Ulrike A Mau-Holzmann, Poul Hyttel, Troels T Nielsen, Jørgen E Nielsen, Bjørn Hols. Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H266. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345815. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Harini Sarva, William Lawrence Severt, Nuri Jacoby, Seth L Pullman, Rachel Saunders-Pullma. Secondary orthostatic tremor in the setting of cerebellar degeneration. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. vol 27. 2016-11-07. PMID:26765757. |
we present two patients with ot and cerebellar degeneration, one of whom had spinocerebellar ataxia type 2 and a good treatment response. |
2016-11-07 |
2023-08-13 |
Not clear |
| Giselle Melo Fontes Silva, José Luiz Pedroso, Diogo Fernandes Dos Santos, Pedro Braga-Neto, Lucila Bizari Fernandes Do Prado, Luciane Bizari Coin De Carvalho, Orlando G P Barsottini, Gilmar Fernandes Do Prad. NREM-related parasomnias in Machado-Joseph disease: clinical and polysomnographic evaluation. Journal of sleep research. vol 25. issue 1. 2016-10-28. PMID:26359123. |
spinocerebellar ataxias (sca) are autosomal dominant neurodegenerative disorders that affect the cerebellum and its connections, and have a marked clinical and genetic variability. |
2016-10-28 |
2023-08-13 |
human |
| Jan Cendeli. Transplantation and Stem Cell Therapy for Cerebellar Degenerations. Cerebellum (London, England). vol 15. issue 1. 2016-10-21. PMID:26155762. |
in purkinje cell degeneration mice, lurcher mutant mice and mouse models of spinocerebellar ataxia type 1 and type 2 and niemann-pick disease type c. despite the lack of direct comparative studies, it appears that there might be differences in graft development and functioning between various types of cerebellar degeneration. |
2016-10-21 |
2023-08-13 |
mouse |
| Sriram Jayabal, Lovisa Ljungberg, Thomas Erwes, Alexander Cormier, Sabrina Quilez, Sara El Jaouhari, Alanna J Wat. Rapid Onset of Motor Deficits in a Mouse Model of Spinocerebellar Ataxia Type 6 Precedes Late Cerebellar Degeneration. eNeuro. vol 2. issue 6. 2016-09-20. PMID:26730403. |
rapid onset of motor deficits in a mouse model of spinocerebellar ataxia type 6 precedes late cerebellar degeneration. |
2016-09-20 |
2023-08-13 |
mouse |