| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Brent L Fogel, Hane Lee, Joshua L Deignan, Samuel P Strom, Sibel Kantarci, Xizhe Wang, Fabiola Quintero-Rivera, Eric Vilain, Wayne W Grody, Susan Perlman, Daniel H Geschwind, Stanley F Nelso. Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia. JAMA neurology. vol 71. issue 10. 2015-02-02. PMID:25133958. |
cerebellar ataxias are a diverse collection of neurologic disorders with causes ranging from common acquired etiologies to rare genetic conditions. |
2015-02-02 |
2023-08-13 |
Not clear |
| Minerva Martínez-Alfaro, Alfonso Cárabez-Trejo, Francisca Sandoval-Zapata, Verónica Morales-Tlalpan, Lourdes Palma-Tirad. Subsurface cistern (SSC) proliferation in Purkinje cells of the rat cerebellum in response to acute and chronic exposure to paint thinner: A light and electron microscopy study. Experimental and toxicologic pathology : official journal of the Gesellschaft fur Toxikologische Pathologie. vol 66. issue 7. 2015-01-30. PMID:24820124. |
these changes are probably related to behavioral manifestations of cerebellar alterations, such as imbalance and ataxia, consistent with the suggested involvement of increases in sscs in ataxia in rats and humans. |
2015-01-30 |
2023-08-13 |
rat |
| Solaf M Elsayed, Raoul Heller, Michaela Thoenes, Maha S Zaki, Daniel Swan, Ezzat Elsobky, Christine Zühlke, Inga Ebermann, Gudrun Nürnberg, Peter Nürnberg, Hanno J Bol. Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations. European journal of human genetics : EJHG. vol 22. issue 2. 2015-01-20. PMID:23838597. |
although many genes have been identified for the autosomal recessive cerebellar ataxias (arcas), several patients are unlinked to the respective loci, suggesting further genetic heterogeneity. |
2015-01-20 |
2023-08-12 |
mouse |
| Manoj Kumar, Zsolt Csaba, Stéphane Peineau, Rupali Srivastava, Sowmyalakshmi Rasika, Shyamala Mani, Pierre Gressens, Vincent El Ghouzz. Endogenous cerebellar neurogenesis in adult mice with progressive ataxia. Annals of clinical and translational neurology. vol 1. issue 12. 2015-01-09. PMID:25574472. |
endogenous cerebellar neurogenesis in adult mice with progressive ataxia. |
2015-01-09 |
2023-08-13 |
mouse |
| J Schwabova, T Maly, J Laczo, A Zumrova, V Komarek, Z Musova, F Zahalk. Application of a Scale for the Assessment and Rating of Ataxia (SARA) in Friedreich's ataxia patients according to posturography is limited. Journal of the neurological sciences. vol 341. issue 1-2. 2014-12-30. PMID:24768059. |
a scale for the assessment and rating of ataxia (sara) was developed for evaluation of autosomal dominant cerebellar ataxias (adca) and was also recommended for clinical trials of friedreich's ataxia patients (frda). |
2014-12-30 |
2023-08-13 |
Not clear |
| Carmen Rodríguez-Cueto, Cristina Benito, Julián Romero, Mariluz Hernández-Gálvez, María Gómez-Ruiz, Javier Fernández-Rui. Endocannabinoid-hydrolysing enzymes in the post-mortem cerebellum of humans affected by hereditary autosomal dominant ataxias. Pathobiology : journal of immunopathology, molecular and cellular biology. vol 81. issue 3. 2014-12-17. PMID:24642775. |
endocannabinoid-hydrolysing enzymes in the post-mortem cerebellum of humans affected by hereditary autosomal dominant ataxias. |
2014-12-17 |
2023-08-12 |
Not clear |
| Christos Ganos, Panagiotis Kassavetis, Roberto Erro, Mark J Edwards, John Rothwell, Kailash P Bhati. The role of the cerebellum in the pathogenesis of cortical myoclonus. Movement disorders : official journal of the Movement Disorder Society. vol 29. issue 4. 2014-12-03. PMID:24634361. |
we critically view information on cerebellar physiology with regard to motorcortical output and compare findings between hypothesized and reported neurophysiological changes in conditions with cortical myoclonus and ataxia. |
2014-12-03 |
2023-08-12 |
Not clear |
| Luis Ruano, Claudia Melo, M Carolina Silva, Paula Coutinh. The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies. Neuroepidemiology. vol 42. issue 3. 2014-11-24. PMID:24603320. |
hereditary cerebellar ataxias (hca) and hereditary spastic paraplegias (hsp) are two groups of neurodegenerative disorders that usually present with progressive gait impairment, often leading to permanent disability. |
2014-11-24 |
2023-08-12 |
Not clear |
| M Rossi, S Perez-Lloret, L Doldan, D Cerquetti, J Balej, P Millar Vernetti, H Hawkes, A Cammarota, M Merell. Autosomal dominant cerebellar ataxias: a systematic review of clinical features. European journal of neurology. vol 21. issue 4. 2014-11-06. PMID:24765663. |
autosomal dominant cerebellar ataxias: a systematic review of clinical features. |
2014-11-06 |
2023-08-13 |
Not clear |
| M Rossi, S Perez-Lloret, L Doldan, D Cerquetti, J Balej, P Millar Vernetti, H Hawkes, A Cammarota, M Merell. Autosomal dominant cerebellar ataxias: a systematic review of clinical features. European journal of neurology. vol 21. issue 4. 2014-11-06. PMID:24765663. |
to assess, through systematic review, distinctive or common clinical signs of autosomal dominant cerebellar ataxias (adcas), also referred to as spinocerebellar ataxias (scas) in genetic nomenclature. |
2014-11-06 |
2023-08-13 |
Not clear |
| M Saeed Da. Functional role for mouse cerebellar NO/cGMP/KATP pathway in ethanol-induced ataxia. Alcoholism, clinical and experimental research. vol 38. issue 1. 2014-10-09. PMID:23905929. |
functional role for mouse cerebellar no/cgmp/katp pathway in ethanol-induced ataxia. |
2014-10-09 |
2023-08-12 |
mouse |
| R Gatt. Immune dysfunction is one of many defects. Immunology today. vol 5. issue 5. 2014-10-08. PMID:25289547. |
they then begin to stagger (ataxia) and show signs of degenerating cerebellar function; by five years of age, they have dilated blood vessels (telangiectases) over the exposed bulbar conjunctiva and skin of the ear. |
2014-10-08 |
2023-08-13 |
Not clear |
| Chengzu Long, Chad E Grueter, Kunhua Song, Song Qin, Xiaoxia Qi, Y Megan Kong, John M Shelton, James A Richardson, Chun-Li Zhang, Rhonda Bassel-Duby, Eric N Olso. Ataxia and Purkinje cell degeneration in mice lacking the CAMTA1 transcription factor. Proceedings of the National Academy of Sciences of the United States of America. vol 111. issue 31. 2014-10-03. PMID:25049392. |
here, we show that global or nervous system deletion of camta1 in mice causes severe ataxia with purkinje cell degeneration and cerebellar atrophy, partially resembling the consequences of haploinsufficiency of the human camta1 locus. |
2014-10-03 |
2023-08-13 |
mouse |
| Ella M R Fonteyn, Samyra H J Keus, Carla C P Verstappen, Ludger Schöls, Imelda J M de Groot, Bart P C van de Warrenbur. The effectiveness of allied health care in patients with ataxia: a systematic review. Journal of neurology. vol 261. issue 2. 2014-09-29. PMID:23589192. |
a systematic search for clinical trials concerning allied health care in cerebellar ataxias was conducted using the electronic databases of pubmed, medline, embase, cinahl and pedro, and references lists of articles, in the time period from 1980 up to and including december 2011 in english and dutch. |
2014-09-29 |
2023-08-12 |
Not clear |
| Georgios Koutsis, Athina Kladi, Georgia Karadima, Henry Houlden, Nicholas W Wood, Kyproula Christodoulou, Marios Pana. Friedreich's ataxia and other hereditary ataxias in Greece: an 18-year perspective. Journal of the neurological sciences. vol 336. issue 1-2. 2014-09-29. PMID:24209901. |
undiagnosed dominant patients included a majority of type iii autosomal dominant cerebellar ataxias. |
2014-09-29 |
2023-08-12 |
Not clear |
| Yuting Shi, Junling Wang, Jia-Da Li, Haigang Ren, Wenjuan Guan, Miao He, Weiqian Yan, Ying Zhou, Zhengmao Hu, Jianguo Zhang, Jingjing Xiao, Zheng Su, Meizhi Dai, Jun Wang, Hong Jiang, Jifeng Guo, Yafang Zhou, Fufeng Zhang, Nan Li, Juan Du, Qian Xu, Yacen Hu, Qian Pan, Lu Shen, Guanghui Wang, Kun Xia, Zhuohua Zhang, Beisha Tan. Identification of CHIP as a novel causative gene for autosomal recessive cerebellar ataxia. PloS one. vol 8. issue 12. 2014-09-27. PMID:24312598. |
autosomal recessive cerebellar ataxias are a group of neurodegenerative disorders that are characterized by complex clinical and genetic heterogeneity. |
2014-09-27 |
2023-08-12 |
human |
| C N Prudente, E J Hess, H A Jinna. Dystonia as a network disorder: what is the role of the cerebellum? Neuroscience. vol 260. 2014-09-25. PMID:24333801. |
why are focal cerebellar lesions or degenerative cerebellar disorders more commonly associated with ataxia rather than dystonia? |
2014-09-25 |
2023-08-12 |
Not clear |
| G Grimaldi, G P Argyropoulos, A Boehringer, P Celnik, M J Edwards, R Ferrucci, J M Galea, S J Groiss, K Hiraoka, P Kassavetis, E Lesage, M Manto, R C Miall, A Priori, A Sadnicka, Y Ugawa, U Zieman. Non-invasive cerebellar stimulation--a consensus paper. Cerebellum (London, England). vol 13. issue 1. 2014-09-24. PMID:23943521. |
cerebellar tms is an effective and valuable method to evaluate the cerebello-thalamo-cortical loop functions and for the study of the pathophysiology of ataxia. |
2014-09-24 |
2023-08-12 |
Not clear |
| Kyung Yeon Lee, Yun-Jin Lee, Tae Hyoung Kim, Doo-Sung Cheon, Sang-Ook Na. Clinico-radiological spectrum in enterovirus 71 infection involving the central nervous system in children. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. vol 21. issue 3. 2014-09-23. PMID:24169271. |
five of 13 patients with lesions in the bilateral dentate nuclei of the cerebellum exhibited no cerebellar symptoms, while two with no cerebellar lesions developed ataxia. |
2014-09-23 |
2023-08-12 |
Not clear |
| Luis Velázquez-Pérez, Rigoberto González-Piña, Roberto Rodríguez-Labrada, Raul Aguilera-Rodríguez, Lourdes Galicia-Polo, Yaimeé Vázquez-Mojena, Ana M Cortés-Rubio, Marla R Trujillo-Bracamontes, Cesar M Cerecedo-Zapata, Oscar Hernández-Hernández, Bulmaro Cisneros, Jonathan J Magañ. Recessive spinocerebellar ataxia with paroxysmal cough attacks: a report of five cases. Cerebellum (London, England). vol 13. issue 2. 2014-09-12. PMID:24097205. |
hereditary ataxias are a heterogeneous group of neurological diseases characterized by progressive cerebellar syndrome and numerous other features, which result in great diversity of ataxia subtypes. |
2014-09-12 |
2023-08-12 |
Not clear |