| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Yasuo Terao, Hideki Fukuda, Shin-Ichi Tokushige, Satomi Inomata-Terada, Akihiro Yugeta, Masashi Hamada, Yoshikazu Ugaw. Distinguishing spinocerebellar ataxia with pure cerebellar manifestation from multiple system atrophy (MSA-C) through saccade profiles. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. vol 128. issue 1. 2017-05-31. PMID:27866117. |
distinguishing spinocerebellar ataxia with pure cerebellar manifestation from multiple system atrophy (msa-c) through saccade profiles. |
2017-05-31 |
2023-08-13 |
Not clear |
| Yasuo Terao, Hideki Fukuda, Shin-Ichi Tokushige, Satomi Inomata-Terada, Akihiro Yugeta, Masashi Hamada, Yoshikazu Ugaw. Distinguishing spinocerebellar ataxia with pure cerebellar manifestation from multiple system atrophy (MSA-C) through saccade profiles. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. vol 128. issue 1. 2017-05-31. PMID:27866117. |
patients with spinocerebellar ataxia with pure cerebellar presentation (scd) and multiple system atrophy (msa-c) show similar symptoms at early stages, although cerebellofugal pathology predominates in scd, and cerebellopetal pathology in msa-c. we studied whether saccade velocity profiles, which reflect the accelerating and braking functions of the cerebellum, can differentiate these two disorders. |
2017-05-31 |
2023-08-13 |
Not clear |
| Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Reidenis Torres-Vega, Jacqueline Medrano Montero, Yaimeé Vázquez-Mojena, Georg Auburger, Ulf Zieman. Abnormal corticospinal tract function and motor cortex excitability in non-ataxic SCA2 mutation carriers: A TMS study. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. vol 127. issue 8. 2017-05-26. PMID:27417041. |
to evaluate if the corticospinal tract is affected in the prodromal stage of spinocerebellar ataxia type 2 (sca2), prior to development of the cerebellar syndrome. |
2017-05-26 |
2023-08-13 |
Not clear |
| 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 |