| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Rebekah K Jobling, Mirna Assoum, Oleksandr Gakh, Susan Blaser, Julian A Raiman, Cyril Mignot, Emmanuel Roze, Alexandra Dürr, Alexis Brice, Nicolas Lévy, Chitra Prasad, Tara Paton, Andrew D Paterson, Nicole M Roslin, Christian R Marshall, Jean-Pierre Desvignes, Nathalie Roëckel-Trevisiol, Stephen W Scherer, Guy A Rouleau, André Mégarbané, Grazia Isaya, Valérie Delague, Grace Yoo. PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia. Brain : a journal of neurology. vol 138. issue Pt 6. 2015-08-07. PMID:25808372. |
non-progressive cerebellar ataxias are a rare group of disorders that comprise approximately 10% of static infantile encephalopathies. |
2015-08-07 |
2023-08-13 |
Not clear |
| Shin Hisahara, Takashi Matsushita, Mizuki Kitamura, Shinichi Mezawa, Michio Nonaka, Tomihiro Imai, Shun Shimoham. Long-term clinical and radiological improvement of chronic acquired hepatocerebral degeneration after obliteration of portosystemic shunt: Report of a case. Journal of the neurological sciences. vol 346. issue 1-2. 2015-07-23. PMID:25172193. |
we report a male patient with cirrhosis of unknown cause, who developed slowly progressive cerebellar truncal and limb ataxia and slurred speech. |
2015-07-23 |
2023-08-13 |
Not clear |
| Jean Carroll, Tristan K W Page, Shih-Chieh Chiang, Bernadett Kalmar, David Bode, Linda Greensmith, Peter J Mckinnon, Julian R Thorpe, Majid Hafezparast, Sherif F El-Khamis. Expression of a pathogenic mutation of SOD1 sensitizes aprataxin-deficient cells and mice to oxidative stress and triggers hallmarks of premature ageing. Human molecular genetics. vol 24. issue 3. 2015-07-23. PMID:25274775. |
aprataxin (aptx) deficiency causes progressive cerebellar degeneration, ataxia and oculomotor apraxia in man. |
2015-07-23 |
2023-08-13 |
mouse |
| K Solbach, O Kraff, M Minnerop, A Beck, L Schöls, E R Gizewski, M E Ladd, D Timman. Cerebellar pathology in Friedreich's ataxia: atrophied dentate nuclei with normal iron content. NeuroImage. Clinical. vol 6. 2015-07-20. PMID:25379420. |
cerebellar pathology in friedreich's ataxia: atrophied dentate nuclei with normal iron content. |
2015-07-20 |
2023-08-13 |
Not clear |
| Ugur Uygunoglu, Aysegul Gunduz, Sukriye F Menku, Basak Yilmaz, Esra Hatipoglu, Cengiz Yalcinkaya, Sabahattin Saip, Hulya Apaydi. Cerebrotendinous xanthomatosis: the effectiveness of high-dose piracetam for the treatment of cerebellar and sensorial ataxia. Cerebellum (London, England). vol 13. issue 6. 2015-07-17. PMID:25084753. |
cerebrotendinous xanthomatosis: the effectiveness of high-dose piracetam for the treatment of cerebellar and sensorial ataxia. |
2015-07-17 |
2023-08-13 |
Not clear |
| Ailish Malone, Mario Manto, Chris Has. Dissecting the links between cerebellum and dystonia. Cerebellum (London, England). vol 13. issue 6. 2015-07-17. PMID:25239288. |
so far, although dystonia has been observed in some forms of ataxia such as dominant ataxias, the link between the cerebellum and dystonia has remained unclear. |
2015-07-17 |
2023-08-13 |
human |
| Umar Akbar, Tetsuo Ashizaw. Ataxia. Neurologic clinics. vol 33. issue 1. 2015-07-15. PMID:25432731. |
ataxia is a disorder of balance and coordination resulted from dysfunctions involving cerebellum and its afferent and efferent connections. |
2015-07-15 |
2023-08-13 |
Not clear |
| Duaa B Saeed, Limci Gupt. Paraneoplastic cerebellar degeneration associated with serous adenocarcinoma of the ovary. BMJ case reports. vol 2014. 2015-07-13. PMID:25432905. |
the patient presented with progressive ataxia and dysarthria and after excluding primary cerebellar pathology, paraneoplastic syndrome was suspected and she was investigated for a malignancy. |
2015-07-13 |
2023-08-13 |
Not clear |
| Tracy M Jones, Jessica D Shaw, Kelly Sullivan, Theresa A Zesiewic. Treatment of cerebellar ataxia. Neurodegenerative disease management. vol 4. issue 5. 2015-07-07. PMID:25405651. |
symptoms of cerebellar degeneration include ataxia or wide-based gait, visual and speech dysfunction, dysmetria, and dyscoordination. |
2015-07-07 |
2023-08-13 |
Not clear |
| Naiara Akizu, Vincent Cantagrel, Maha S Zaki, Lihadh Al-Gazali, Xin Wang, Rasim Ozgur Rosti, Esra Dikoglu, Antoinette Bernabe Gelot, Basak Rosti, Keith K Vaux, Eric M Scott, Jennifer L Silhavy, Jana Schroth, Brett Copeland, Ashleigh E Schaffer, Philip L S M Gordts, Jeffrey D Esko, Matthew D Buschman, Seth J Field, Gennaro Napolitano, Ghada M Abdel-Salam, R Koksal Ozgul, Mahmut Samil Sagıroglu, Matloob Azam, Samira Ismail, Mona Aglan, Laila Selim, Iman G Mahmoud, Sawsan Abdel-Hadi, Amera El Badawy, Abdelrahim A Sadek, Faezeh Mojahedi, Hulya Kayserili, Amira Masri, Laila Bastaki, Samia Temtamy, Ulrich Müller, Isabelle Desguerre, Jean-Laurent Casanova, Ali Dursun, Murat Gunel, Stacey B Gabriel, Pascale de Lonlay, Joseph G Gleeso. Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction. Nature genetics. vol 47. issue 5. 2015-07-06. PMID:25848753. |
pediatric-onset ataxias often present clinically as developmental delay and intellectual disability, with prominent cerebellar atrophy as a key neuroradiographic finding. |
2015-07-06 |
2023-08-13 |
zebrafish |
| Wahiba Hamza, Lamia Ali Pacha, Tarik Hamadouche, Jean Muller, Nathalie Drouot, Farida Ferrat, Samira Makri, Malika Chaouch, Meriem Tazir, Michel Koenig, Traki Benhassin. Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia. BMC medical genetics. vol 16. 2015-06-30. PMID:26068213. |
autosomal recessive cerebellar ataxias (arca) are a complex group of neurodegenerative disorders with great genetic and phenotypic heterogeneity, over 30 genes/loci have been associated with more than 20 different clinical forms of arca. |
2015-06-30 |
2023-08-13 |
Not clear |
| Michael Strupp, Andreas Zwergal, Katharina Feil, Tatiana Bremova, Thomas Brand. Pharmacotherapy of vestibular and cerebellar disorders and downbeat nystagmus: translational and back-translational research. Annals of the New York Academy of Sciences. vol 1343. 2015-06-24. PMID:25903394. |
there are ongoing rcts on vestibular paroxysmia with carbamazepine (vespa), acute unilateral vestibulopathy with betahistine (betavest), vestibular migraine with metoprolol (provemig), benign paroxysmal positional vertigo with vitamin d (vitd@bppv), ea2 with 4-aminopyridine versus acetazolamide (eat-2-treat), and cerebellar ataxias with acetyl-dl-leucine (alcat). |
2015-06-24 |
2023-08-13 |
Not clear |
| Lucía Calatrava-Ferreras, Rafael Gonzalo-Gobernado, Diana Reimers, Antonio S Herranz, Adriano Jiménez-Escrig, Juan José Díaz-Gil, María José Casarejos, María Teresa Montero-Vega, Eulalia Bazá. Neuroprotective role of liver growth factor "LGF" in an experimental model of cerebellar ataxia. International journal of molecular sciences. vol 15. issue 10. 2015-06-19. PMID:25338046. |
cerebellar ataxias (ca) comprise a heterogeneous group of neurodegenerative diseases characterized by a lack of motor coordination. |
2015-06-19 |
2023-08-13 |
rat |
| Lucía Calatrava-Ferreras, Rafael Gonzalo-Gobernado, Diana Reimers, Antonio S Herranz, Adriano Jiménez-Escrig, Juan José Díaz-Gil, María José Casarejos, María Teresa Montero-Vega, Eulalia Bazá. Neuroprotective role of liver growth factor "LGF" in an experimental model of cerebellar ataxia. International journal of molecular sciences. vol 15. issue 10. 2015-06-19. PMID:25338046. |
in view of these results, we propose lgf as a potential therapeutic agent in cerebellar ataxias. |
2015-06-19 |
2023-08-13 |
rat |
| Ji Sun Kim, Jin Whan Ch. Hereditary Cerebellar Ataxias: A Korean Perspective. Journal of movement disorders. vol 8. issue 2. 2015-06-19. PMID:26090078. |
hereditary cerebellar ataxias: a korean perspective. |
2015-06-19 |
2023-08-13 |
Not clear |
| Ji Sun Kim, Jin Whan Ch. Hereditary Cerebellar Ataxias: A Korean Perspective. Journal of movement disorders. vol 8. issue 2. 2015-06-19. PMID:26090078. |
more than 35 autosomal dominant cerebellar ataxias have been designated as spinocerebellar ataxia, and there are 55 recessive ataxias that have not been named systematically. |
2015-06-19 |
2023-08-13 |
Not clear |
| Yuka Miyoshi, Yoshichika Yoshioka, Kinuko Suzuki, Taisuke Miyazaki, Minako Koura, Kazumasa Saigoh, Naoko Kajimura, Yoko Monobe, Susumu Kusunoki, Junichiro Matsuda, Masahiko Watanabe, Naoto Hayasak. A new mouse allele of glutamate receptor delta 2 with cerebellar atrophy and progressive ataxia. PloS one. vol 9. issue 9. 2015-06-18. PMID:25250835. |
a new mouse allele of glutamate receptor delta 2 with cerebellar atrophy and progressive ataxia. |
2015-06-18 |
2023-08-13 |
mouse |
| Elsdon Store. Genetic cerebellar ataxias. Seminars in neurology. vol 34. issue 3. 2015-06-02. PMID:25192506. |
genetic cerebellar ataxias. |
2015-06-02 |
2023-08-13 |
Not clear |
| M Faruq, A Narang, R Kumari, R Pandey, A Garg, M Behari, D Dash, A K Srivastava, M Mukerj. Novel mutations in typical and atypical genetic loci through exome sequencing in autosomal recessive cerebellar ataxia families. Clinical genetics. vol 86. issue 4. 2015-05-25. PMID:24102492. |
nearly a thousand mutations mapping to 60 different loci have been identified in cerebellar ataxias. |
2015-05-25 |
2023-08-12 |
Not clear |
| Esther B E Becke. The Moonwalker mouse: new insights into TRPC3 function, cerebellar development, and ataxia. Cerebellum (London, England). vol 13. issue 5. 2015-05-20. PMID:24797279. |
the moonwalker mouse: new insights into trpc3 function, cerebellar development, and ataxia. |
2015-05-20 |
2023-08-13 |
mouse |