| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| D Collins, J M Angles, J Christodoulou, D Spielman, S A Lindsay, J Boyd, M B Krockenberge. Severe subacute necrotizing encephalopathy (Leigh-like syndrome) in American Staffordshire bull terrier dogs. Journal of comparative pathology. vol 148. issue 4. 2013-11-08. PMID:23123128. |
previously reported hereditary ataxias in the breed, including l-2 hydroxyglutaric aciduria and cerebellar cortical degeneration, as well as thiamine deficiency, were excluded. |
2013-11-08 |
2023-08-12 |
Not clear |
| Susan Elizabeth Tomlinson, Sanjeev Rajakulendran, Stella Veronica Tan, Tracey Dawn Graves, Doris-Eva Bamiou, Robyn W Labrum, David Burke, Carolyn M Sue, Paola Giunti, Stephanie Schorge, Dimitri M Kullmann, Michael G Hann. Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1. Journal of neurology, neurosurgery, and psychiatry. vol 84. issue 10. 2013-11-08. PMID:23349320. |
heterozygous mutations in kcna1 cause episodic ataxia type 1 (ea1), an ion channel disorder characterised by brief paroxysms of cerebellar dysfunction and persistent neuromyotonia. |
2013-11-08 |
2023-08-12 |
Not clear |
| Udo Rüb, Ludger Schöls, Henry Paulson, Georg Auburger, Pawel Kermer, Joanna C Jen, Kay Seidel, Horst-Werner Korf, Thomas Delle. Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7. Progress in neurobiology. vol 104. 2013-11-05. PMID:23438480. |
the spinocerebellar ataxias type 1 (sca1), 2 (sca2), 3 (sca3), 6 (sca6) and 7 (sca7) are genetically defined autosomal dominantly inherited progressive cerebellar ataxias (adcas). |
2013-11-05 |
2023-08-12 |
Not clear |
| L Vedolin, G Gonzalez, C F Souza, C Lourenço, A J Barkovic. Inherited cerebellar ataxia in childhood: a pattern-recognition approach using brain MRI. AJNR. American journal of neuroradiology. vol 34. issue 5. 2013-11-04. PMID:22595899. |
ataxias caused by dysfunction of the cerebellum occur in acute, intermittent, and progressive disorders. |
2013-11-04 |
2023-08-12 |
Not clear |
| Shingo Miyamoto, Soichiro Ikushima, Minoru Inomata, Ryutaro Nomura, Ichiro Suzuk. [Emergency oncology cases for whom stereotactic radiotherapy by cyberknife proved effective for cerebellar metastasis of lung cancer]. Gan to kagaku ryoho. Cancer & chemotherapy. vol 40. issue 8. 2013-10-29. PMID:23986054. |
cerebellar metastasis sometimes causes symptoms such as ataxia and dizziness, or hydrocephalus by compression of the fourth ventricle, making emergency treatment necessary. |
2013-10-29 |
2023-08-12 |
Not clear |
| Shadi Al-Afif, Mareike Staden, Joachim K Krauss, Kerstin Schwabe, Elvis J Herman. Splitting of the cerebellar vermis in juvenile rats--effects on social behavior, vocalization and motor activity. Behavioural brain research. vol 250. 2013-10-25. PMID:23685319. |
postoperative neurological deficits, such as cerebellar mutism and ataxia have been attributed to splitting of the cerebellar vermis to remove these tumors. |
2013-10-25 |
2023-08-12 |
human |
| Roman Schniepp, Veronika Jakl, Max Wuehr, Joachim Havla, Tanja Kümpfel, Marianne Dieterich, Michael Strupp, Klaus Jah. Treatment with 4-aminopyridine improves upper limb tremor of a patient with multiple sclerosis: a video case report. Multiple sclerosis (Houndmills, Basingstoke, England). vol 19. issue 4. 2013-10-23. PMID:23069878. |
the reversible potassium channel blocker 4-aminopyridine is effective in the treatment of numerous cerebellar dysfunctions, such as episodic ataxia type 2 and downbeat nystagmus syndrome. |
2013-10-23 |
2023-08-12 |
Not clear |
| Elena Martín-García, Francesco Mannara, Javier Gutiérrez-Cuesta, Lidia Sabater, Josep Dalmau, Rafael Maldonado, Francesc Grau. Intrathecal injection of P/Q type voltage-gated calcium channel antibodies from paraneoplastic cerebellar degeneration cause ataxia in mice. Journal of neuroimmunology. vol 261. issue 1-2. 2013-10-17. PMID:23726906. |
intrathecal injection of p/q type voltage-gated calcium channel antibodies from paraneoplastic cerebellar degeneration cause ataxia in mice. |
2013-10-17 |
2023-08-12 |
mouse |
| Takeyuki Sugawara, Chihiro Hisatsune, Tung Dinh Le, Tsutomu Hashikawa, Moritoshi Hirono, Mitsuharu Hattori, Soichi Nagao, Katsuhiko Mikoshib. Type 1 inositol trisphosphate receptor regulates cerebellar circuits by maintaining the spine morphology of purkinje cells in adult mice. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 33. issue 30. 2013-10-17. PMID:23884927. |
in addition, the abnormally rearranged pf-pc synaptic circuits in mature cerebellum caused unexpectedly severe ataxia in adult l7-cre;itpr1(flox/flox) mice. |
2013-10-17 |
2023-08-12 |
mouse |
| Chia-Feng Lu, Bing-Wen Soong, Hsiu-Mei Wu, Shin Teng, Po-Shan Wang, Yu-Te W. Disrupted cerebellar connectivity reduces whole-brain network efficiency in multiple system atrophy. Movement disorders : official journal of the Movement Disorder Society. vol 28. issue 3. 2013-09-20. PMID:23325625. |
finally, we found that the reductions in nodal efficiency of the cerebellar lobules and bilateral sensorimotor, prefrontal, and basal ganglia regions negatively correlated with the severity of ataxia for the cerebellar-type multiple system atrophy patients. |
2013-09-20 |
2023-08-12 |
Not clear |
| Abdul Qayyum Rana, A N Rana, Ashfique Adlu. Acute ataxia due to anti-Yo antibody paraneoplastic cerebellar degeneration 4 months prior to diagnosis of uterine carcinoma. Acta neurologica Belgica. vol 112. issue 3. 2013-09-19. PMID:22426676. |
acute ataxia due to anti-yo antibody paraneoplastic cerebellar degeneration 4 months prior to diagnosis of uterine carcinoma. |
2013-09-19 |
2023-08-12 |
Not clear |
| S Kammermeier, J F Kleine, T Eggert, S Krafczyk, U Büttne. Disturbed vestibular-neck interaction in cerebellar disease. Journal of neurology. vol 260. issue 3. 2013-09-19. PMID:23081756. |
cerebellar dysfunction results in ataxia including postural deficits. |
2013-09-19 |
2023-08-12 |
Not clear |
| Xiaofei Du, Jun Wang, Haipeng Zhu, Lorenzo Rinaldo, Kay-Marie Lamar, Ann C Palmenberg, Christian Hansel, Christopher M Gome. Second cistron in CACNA1A gene encodes a transcription factor mediating cerebellar development and SCA6. Cell. vol 154. issue 1. 2013-09-17. PMID:23827678. |
when expressed as an independent polypeptide, α1act-bearing an expanded polyq tract-lacks transcription factor function and neurite outgrowth properties, causes cell death in culture, and leads to ataxia and cerebellar atrophy in transgenic mice. |
2013-09-17 |
2023-08-12 |
mouse |
| Hiroshi Mitoma, Hidehiro Mizusaw. [Autoantibodies to GAD and autoimmune-mediated neurological diseases]. Nihon rinsho. Japanese journal of clinical medicine. vol 71. issue 5. 2013-08-22. PMID:23777105. |
in rat cerebellar slices, the cerebrospinal fluid (csf) from gad-ab-positive ataxia acted on the terminals of gabaergic interneurons to depress the gaba release on purkinje cells. |
2013-08-22 |
2023-08-12 |
rat |
| C Tranchan. [Have centers of rare neurological diseases changed their practices and management of the hereditary cerebellar ataxias?]. Revue neurologique. vol 169 Suppl 1. 2013-08-16. PMID:23452767. |
[have centers of rare neurological diseases changed their practices and management of the hereditary cerebellar ataxias?]. |
2013-08-16 |
2023-08-12 |
Not clear |
| C Tranchan. [Have centers of rare neurological diseases changed their practices and management of the hereditary cerebellar ataxias?]. Revue neurologique. vol 169 Suppl 1. 2013-08-16. PMID:23452767. |
the classification and management of hereditary cerebellar ataxias have been considerably changed by advances made in the field of genetics. |
2013-08-16 |
2023-08-12 |
Not clear |
| Udo Rüb, Franziska Hoche, Ewout R Brunt, Helmut Heinsen, Kay Seidel, Domenico Del Turco, Henry L Paulson, Jürgen Bohl, Charlotte von Gall, Jean-Paul Vonsattel, Horst-Werner Korf, Wilfred F den Dunne. Degeneration of the cerebellum in Huntington's disease (HD): possible relevance for the clinical picture and potential gateway to pathological mechanisms of the disease process. Brain pathology (Zurich, Switzerland). vol 23. issue 2. 2013-08-15. PMID:22925167. |
degeneration of the cerebellum might contribute significantly to poorly understood symptoms occurring in hd such as impaired rapid alternating movements and fine motor skills, dysarthria, ataxia and postural instability, gait and stance imbalance, broad-based gait and stance, while the morphological alterations (ie ballooned neurons, torpedo-like axonal inclusions) observed in the majority of surviving nerve cells may represent a gateway to the unknown mechanisms of the pathological process of hd. |
2013-08-15 |
2023-08-12 |
Not clear |
| Rita B Morais, Inês Sousa, Maria J Leiria, Conceição Marques, José C Ferreira, Pedro Cabra. Pseudotumoral acute hemicerebellitis in a child. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. vol 17. issue 2. 2013-08-12. PMID:22771177. |
acute cerebellitis is an inflammatory disorder usually involving both sides of the cerebellum and presenting with localized signs such as ataxia. |
2013-08-12 |
2023-08-12 |
Not clear |
| Steven K Charles, Allison M Okamura, Amy J Bastia. Does a basic deficit in force control underlie cerebellar ataxia? Journal of neurophysiology. vol 109. issue 4. 2013-08-09. PMID:23175807. |
here we tested whether the cerebellum is involved in controlling force separate from estimating limb dynamics and whether ataxia could result from a deficit in force control. |
2013-08-09 |
2023-08-12 |
human |
| Hiroshi Mitoma, Kazunori Nanr. [Autoantibodies associated with autoimmune-mediated cerebellar ataxia]. Brain and nerve = Shinkei kenkyu no shinpo. vol 65. issue 4. 2013-08-07. PMID:23568983. |
these results suggest that pathogenic abs elicit cerebellar synaptic dysfunction, and thereby cause ataxia in patients. |
2013-08-07 |
2023-08-12 |
Not clear |