| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Janel Johnson, Nicholas Wood, Paola Giunti, Henry Houlde. Clinical and genetic analysis of spinocerebellar ataxia type 11. Cerebellum (London, England). vol 7. issue 2. 2009-05-15. PMID:18418680. |
the autosomal dominant cerebellar ataxias (adcas) are a genetically heterogeneous group of disorders. |
2009-05-15 |
2023-08-12 |
Not clear |
| D Genis, I Ferrer, J Valls Solé, J Corral, V Volpini, H San Nicolás, J Gich, L Ramió-Torrentà, M Ferrándiz, J Puig, F Márque. A kindred with cerebellar ataxia and thermoanalgesia. Journal of neurology, neurosurgery, and psychiatry. vol 80. issue 5. 2009-05-08. PMID:18710877. |
to characterise the clinical, neurophysiological, neuropathological and genetic features of a family with cerebellar autosomal dominant ataxia. |
2009-05-08 |
2023-08-12 |
Not clear |
| Nilgul Yardimci, Salih Gulsen, Aynur Yilmaz Avci, Nur Altinors, Turgut Zileli, Ufuk Ca. Can subdural hematoma be a trigger for Guillain-Barré syndrome? The International journal of neuroscience. vol 119. issue 3. 2009-04-09. PMID:19116843. |
we believe that gbs results from an aberrant immune response following trauma that somehow mistakenly attacks the nerve tissue of its host, and we discuss the effects of the trauma of head injury on cellular and humoral immunities and the absence of antiganglioside antibody (anti-gd1b igg, which is accused of ataxia and cerebellar symptoms) in this case report. |
2009-04-09 |
2023-08-12 |
Not clear |
| Lisa L Giles, Melissa P DelBello, Donald L Gilbert, Kevin E Stanford, Paula K Shear, Stephen M Strakowsk. Cerebellar ataxia in youths at risk for bipolar disorder. Bipolar disorders. vol 10. issue 6. 2009-04-08. PMID:18837868. |
the present study examined cerebellar function in youths who were at familial risk for bd by comparing ataxia battery scores of youths with a bipolar parent to those of healthy youths. |
2009-04-08 |
2023-08-12 |
Not clear |
| P C A van Broekhoven, M A Frens, P A Sillevis Smitt, J N van der Gees. Eye movements as a marker for cerebellar damage in paraneoplastic neurological syndromes. Parkinsonism & related disorders. vol 13 Suppl 3. 2009-04-01. PMID:18267253. |
cerebellar disturbances can induce a variety of motor deficits, ranging from severe ataxia to mild deficits of fine motor control. |
2009-04-01 |
2023-08-12 |
Not clear |
| Thomas Klockgethe. Parkinsonism & related disorders. Ataxias. Parkinsonism & related disorders. vol 13 Suppl 3. 2009-04-01. PMID:18267270. |
the non-hereditary ataxias are separated into the acquired ataxias, such as alcoholic cerebellar degeneration or paraneoplastic cerebellar degeneration, and the sporadic degenerative ataxias, such as multiple system atrophy or sporadic adult onset ataxia. |
2009-04-01 |
2023-08-12 |
Not clear |
| Dandan Jia, Hong Jiang, Beisha Tan. [Recent advances in molecular genetics of spinocerebellar ataxia type 3/Machado-Joseph disease]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. vol 25. issue 6. 2009-03-25. PMID:19065526. |
to date, nearly 28 distinct genetic loci of autosomal dominant cerebellar ataxias have been identified, among them 18 disease-causing genes have been cloned. |
2009-03-25 |
2023-08-12 |
Not clear |
| Miho Oue, Kazuhiro Mitsumura, Takashi Torashima, Chiho Koyama, Haruyasu Yamaguchi, Nobuhiko Furuya, Hirokazu Hira. Characterization of mutant mice that express polyglutamine in cerebellar Purkinje cells. Brain research. vol 1255. 2009-03-18. PMID:19103174. |
the polyq mice showed inclusion body formation, cerebellar atrophy and severe ataxia. |
2009-03-18 |
2023-08-12 |
mouse |
| Elvis J Hermann, Marion Rittierodt, Joachim K Kraus. Combined transventricular and supracerebellar infratentorial approach preserving the vermis in giant pediatric posterior fossa midline tumors. Neurosurgery. vol 63. issue 1 Suppl 1. 2009-03-16. PMID:18728601. |
children with sequelae such as cerebellar mutism and ataxia experience a compromise in their quality of life. |
2009-03-16 |
2023-08-12 |
Not clear |
| D Guerrero, N Martínez-Velilla, M C Caballero, M T Mendióroz, T Tuñón, J Masdeu, A Rodríguez, J Armstrong, I Ferre. A patient with MV2 subtype of sporadic Creutzfeldt-Jakob disease and atypical clinical presentation. Clinical neuropathology. vol 27. issue 6. 2009-02-10. PMID:19130739. |
we report the case of a 71-year-old woman with progressive dementia over the course of 4 years, characterized by prominent pyramidal signs and by the lack of ataxia and other cerebellar signs. |
2009-02-10 |
2023-08-12 |
Not clear |
| Flavio Fenzi, Nicolò Rizzut. Ataxia and migraine-like headache in a girl with a cerebellar developmental venous anomaly. Journal of the neurological sciences. vol 273. issue 1-2. 2009-02-06. PMID:18620709. |
ataxia and migraine-like headache in a girl with a cerebellar developmental venous anomaly. |
2009-02-06 |
2023-08-12 |
Not clear |
| Mario Mascalch. Spinocerebellar ataxias. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 29 Suppl 3. 2009-02-03. PMID:18941720. |
conventional mri in patients presenting with progressive ataxia demonstrates the three main patterns of macroscopic damage, namely spinal atrophy, olivopontocerebellar atrophy and cortical cerebellar atrophy. |
2009-02-03 |
2023-08-12 |
Not clear |
| Michael Strupp, Roger Kalla, Stefan Glasauer, Judith Wagner, Katharina Hüfner, Klaus Jahn, Thomas Brand. Aminopyridines for the treatment of cerebellar and ocular motor disorders. Progress in brain research. vol 171. 2009-01-15. PMID:18718350. |
on the basis of these assumptions, we evaluated the efficacy and underlying mechanisms of aminopyridines in dbn and ubn as well as in another cerebellar disorder with an impaired pc function: episodic ataxia type 2 (ea2), which is caused by mutations of the pq-calcium channel. |
2009-01-15 |
2023-08-12 |
mouse |
| K Sambasivaiah, S Samson, Ramakrishna, V Prasanna, A Hari Shanka. Vermian metastasis causing truncal ataxia and hydrocephalus as initial presentation of carcinoma stomach. Tropical gastroenterology : official journal of the Digestive Diseases Foundation. vol 29. issue 2. 2009-01-13. PMID:18972771. |
carcinoma stomach, where the primary is silent, and which presents with truncal ataxia and features of hydrocephalus due to isolated metastatic deposit in the cerebellar vermis is exceptionally rare. |
2009-01-13 |
2023-08-12 |
Not clear |
| Matthias Löhle, Wiebke Schrempf, Martin Wolz, Heinz Reichmann, Alexander Storc. Potassium channel blocker 4-aminopyridine is effective in interictal cerebellar symptoms in episodic ataxia type 2--a video case report. Movement disorders : official journal of the Movement Disorder Society. vol 23. issue 9. 2009-01-12. PMID:18442126. |
potassium channel blocker 4-aminopyridine is effective in interictal cerebellar symptoms in episodic ataxia type 2--a video case report. |
2009-01-12 |
2023-08-12 |
Not clear |
| Mark D Lopez, Cristin Wis. Acute ataxia in a 4-year-old boy: a case of Lyme disease neuroborreliosis. The American journal of emergency medicine. vol 26. issue 9. 2009-01-08. PMID:19091290. |
ataxia is a rare but known manifestation of cerebellar involvement in lyme disease. |
2009-01-08 |
2023-08-12 |
Not clear |
| N Taslim, S Al-Rejaie, M Saeed Da. Attenuation of ethanol-induced ataxia by alpha(4)beta(2) nicotinic acetylcholine receptor subtype in mouse cerebellum: a functional interaction. Neuroscience. vol 157. issue 1. 2009-01-05. PMID:18812210. |
attenuation of ethanol-induced ataxia by alpha(4)beta(2) nicotinic acetylcholine receptor subtype in mouse cerebellum: a functional interaction. |
2009-01-05 |
2023-08-12 |
mouse |
| Joon Kim, Suguna Rani Krishnaswami, Joseph G Gleeso. CEP290 interacts with the centriolar satellite component PCM-1 and is required for Rab8 localization to the primary cilium. Human molecular genetics. vol 17. issue 23. 2008-12-29. PMID:18772192. |
joubert syndrome (js) is a developmental brain disorder characterized by cerebellar vermis hypoplasia, abnormal eye movement, ataxia and mental retardation. |
2008-12-29 |
2023-08-12 |
Not clear |
| Karen Menuz, Roger A Nicol. Loss of inhibitory neuron AMPA receptors contributes to ataxia and epilepsy in stargazer mice. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 28. issue 42. 2008-10-29. PMID:18923036. |
additionally, although stargazer ataxia has been attributed to loss of ampars from cerebellar granule cells, other cerebellar neurons have not been examined. |
2008-10-29 |
2023-08-12 |
mouse |
| Shigeki Hirano, Hitoshi Shinotoh, Kimihito Arai, Akiyo Aotsuka, Fumihiko Yasuno, Noriko Tanaka, Tsuneyoshi Ota, Koichi Sato, Kiyoshi Fukushi, Shuji Tanada, Takamichi Hattori, Toshiaki Iri. PET study of brain acetylcholinesterase in cerebellar degenerative disorders. Movement disorders : official journal of the Movement Disorder Society. vol 23. issue 8. 2008-10-20. PMID:18412283. |
reduction of ache activities in the thalamus and cerebellum in msa and in the thalamus in sca-3 suggest that cholinergic modulating drugs may have a role in the treatment of ataxia and other symptoms in these disorders. |
2008-10-20 |
2023-08-12 |
human |