| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Martin Köllensperger, Felix Geser, Klaus Seppi, Michaela Stampfer-Kountchev, Martin Sawires, Christoph Scherfler, Sylvia Boesch, Joerg Mueller, Vasiliki Koukouni, Niall Quinn, Maria Teresa Pellecchia, Paolo Barone, Nicole Schimke, Richard Dodel, Wolfgang Oertel, Erik Dupont, Karen Østergaard, Christine Daniels, Günther Deuschl, Tanya Gurevich, Nir Giladi, Miguel Coelho, Cristina Sampaio, Christer Nilsson, Håkan Widner, Francesca Del Sorbo, Alberto Albanese, Adriana Cardozo, Eduardo Tolosa, Michael Abele, Thomas Klockgether, Christoph Kamm, Thomas Gasser, Ruth Djaldetti, Carlo Colosimo, Giuseppe Meco, Anette Schrag, Werner Poewe, Gregor K Wennin. Red flags for multiple system atrophy. Movement disorders : official journal of the Movement Disorder Society. vol 23. issue 8. 2008-10-20. PMID:18442131. |
besides the poor response to levodopa, and the additional presence of pyramidal or cerebellar signs (ataxia) or autonomic failure as major diagnostic criteria, certain other clinical features known as "red flags" or warning signs may raise the clinical suspicion of msa. |
2008-10-20 |
2023-08-12 |
Not clear |
| Lina Rosique López, Mariano Rosique Arias, José Domingo Cubillana-Herrero, Beatriz Rodríguez-González Herrer. [Sudden-onset bilateral hearing loss: case report]. Acta otorrinolaringologica espanola. vol 59. issue 5. 2008-10-16. PMID:18501164. |
an ischaemic infarction of the anterior inferior cerebellar artery (aica) is usually associated with vertigo, hearing loss, facial palsy, nystagmus, or truncal ataxia; it is often accompanied by other brainstem or cerebellar signs. |
2008-10-16 |
2023-08-12 |
Not clear |
| L J Bour, A F van Rootselaar, J H T M Koelman, M A J Tijsse. Oculomotor abnormalities in myoclonic tremor: a comparison with spinocerebellar ataxia type 6. Brain : a journal of neurology. vol 131. issue Pt 9. 2008-10-06. PMID:18687731. |
in contrast, fcmte is clinically characterized by cortical symptomatology with a distal cortical myoclonic tremor and infrequent epileptic attacks without cerebellar dysarthria and limb ataxia. |
2008-10-06 |
2023-08-12 |
Not clear |
| Mario Manto, Nordeyn Oulad Ben Tai. A novel approach for treating cerebellar ataxias. Medical hypotheses. vol 71. issue 1. 2008-09-03. PMID:18281160. |
a novel approach for treating cerebellar ataxias. |
2008-09-03 |
2023-08-12 |
human |
| Mario Manto, Nordeyn Oulad Ben Tai. A novel approach for treating cerebellar ataxias. Medical hypotheses. vol 71. issue 1. 2008-09-03. PMID:18281160. |
the terminology of cerebellar ataxias encompasses a variety of sporadic and inherited debilitating diseases. |
2008-09-03 |
2023-08-12 |
human |
| Mario Manto, Nordeyn Oulad Ben Tai. A novel approach for treating cerebellar ataxias. Medical hypotheses. vol 71. issue 1. 2008-09-03. PMID:18281160. |
we are currently lacking effective treatments in degenerative cerebellar ataxias. |
2008-09-03 |
2023-08-12 |
human |
| Mario Manto, Nordeyn Oulad Ben Tai. A novel approach for treating cerebellar ataxias. Medical hypotheses. vol 71. issue 1. 2008-09-03. PMID:18281160. |
the hypothesis is based on the possibility that the combination of tdcs and contralateral lfrsm1 can improve human cerebellar ataxias. |
2008-09-03 |
2023-08-12 |
human |
| Mario Manto, Nordeyn Oulad Ben Tai. A novel approach for treating cerebellar ataxias. Medical hypotheses. vol 71. issue 1. 2008-09-03. PMID:18281160. |
first, patients are assessed clinically using validated scales of cerebellar ataxias and performing accepted quantified tests. |
2008-09-03 |
2023-08-12 |
human |
| Mario Manto, Nordeyn Oulad Ben Tai. A novel approach for treating cerebellar ataxias. Medical hypotheses. vol 71. issue 1. 2008-09-03. PMID:18281160. |
a successful treatment of combined neurostimulation would lead to a new and readily available approach in the management of cerebellar ataxias. |
2008-09-03 |
2023-08-12 |
human |
| J M Nielsen, S D Ingha. CEREBELLAR ATAXIAS: REPORT OF SIX CASES. California and western medicine. vol 34. issue 5. 2008-08-29. PMID:18741750. |
cerebellar ataxias: report of six cases. |
2008-08-29 |
2023-08-12 |
Not clear |
| Michel Mittelbronn, David Capper, Benedikt Bader, Jens Schittenhelm, Johannes Haybaeck, Petra Weber, Richard Meyermann, Hans A Kretzschmar, Horst Wietholte. Severe hypoxia and multiple infarctions resembling Creutzfeldt-Jakob disease. Folia neuropathologica. vol 46. issue 2. 2008-08-20. PMID:18587709. |
here we present a 73-year-old female patient presenting with rapid cognitive decline, visual, acoustic and cerebellar disturbances, ataxia and eeg changes compatible with early cjd stages. |
2008-08-20 |
2023-08-12 |
Not clear |
| Marguerite Harding, Brian Brophy, Timothy Geak. Malignant cerebellar ganglioglioma. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. vol 15. issue 5. 2008-08-13. PMID:18313924. |
we present a 62-year-old man with a high-grade cerebellar ganglioglioma with ataxia. |
2008-08-13 |
2023-08-12 |
Not clear |
| Hai-xia Lu, Hannah Levis, Nabil Melhem, Terry Parke. Toxin-produced Purkinje cell death: a model for neural stem cell transplantation studies. Brain research. vol 1207. 2008-08-13. PMID:18374311. |
purkinje cell loss is the hallmark of the cerebellar ataxias. |
2008-08-13 |
2023-08-12 |
rat |
| Takashi Torashima, Chiho Koyama, Akira Iizuka, Kazuhiro Mitsumura, Kiyohiko Takayama, Shigeru Yanagi, Miho Oue, Haruyasu Yamaguchi, Hirokazu Hira. Lentivector-mediated rescue from cerebellar ataxia in a mouse model of spinocerebellar ataxia. EMBO reports. vol 9. issue 4. 2008-08-11. PMID:18344973. |
the model mice showed poor dendritic arborization of purkinje cells, a markedly atrophied cerebellum and severe ataxia. |
2008-08-11 |
2023-08-12 |
mouse |
| Mathieu Anheim, Marie-Celine Fleury, Jerome Franques, Maria-Ceu Moreira, Jean-Pierre Delaunoy, Dominique Stoppa-Lyonnet, Michel Koenig, Christine Tranchan. Clinical and molecular findings of ataxia with oculomotor apraxia type 2 in 4 families. Archives of neurology. vol 65. issue 7. 2008-08-04. PMID:18625865. |
ataxia with oculomotor apraxia type 2 (aoa2) is an autosomal recessive disease caused by setx mutations in 9q34 resulting in cerebellar ataxia in association with peripheral neuropathy, cerebellar atrophy on imaging, an elevated alpha-fetoprotein (afp) serum level, and occasional oculomotor apraxia. |
2008-08-04 |
2023-08-12 |
Not clear |
| An-Hsun Chou, Tu-Hsueh Yeh, Pin Ouyang, Ying-Ling Chen, Si-Ying Chen, Hung-Li Wan. Polyglutamine-expanded ataxin-3 causes cerebellar dysfunction of SCA3 transgenic mice by inducing transcriptional dysregulation. Neurobiology of disease. vol 31. issue 1. 2008-07-29. PMID:18502140. |
a prominent neuronal loss was not found in the cerebellum of 10 to 11-month-old ataxin-3-q79 mice displaying pronounced ataxic symptoms, suggesting that instead of neuronal demise, ataxin-3-q79 causes neuronal dysfunction of the cerebellum and resulting ataxia. |
2008-07-29 |
2023-08-12 |
mouse |
| An-Hsun Chou, Tu-Hsueh Yeh, Pin Ouyang, Ying-Ling Chen, Si-Ying Chen, Hung-Li Wan. Polyglutamine-expanded ataxin-3 causes cerebellar dysfunction of SCA3 transgenic mice by inducing transcriptional dysregulation. Neurobiology of disease. vol 31. issue 1. 2008-07-29. PMID:18502140. |
our study suggests that polyglutamine-expanded ataxin-3 causes cerebellar dysfunction and ataxia by disrupting the normal pattern of gene transcriptions. |
2008-07-29 |
2023-08-12 |
mouse |
| Jan Cendelín, Ivana Korelusová, Frantisek Voze. The effect of repeated rotarod training on motor skills and spatial learning ability in Lurcher mutant mice. Behavioural brain research. vol 189. issue 1. 2008-07-01. PMID:18243354. |
due to loss of purkinje cells, they suffer from functional cerebellar decortication resulting in ataxia and deterioration of cognitive functions. |
2008-07-01 |
2023-08-12 |
mouse |
| Yukiko Tomioka, Taisuke Miyazaki, Satoshi Taharaguchi, Saori Yoshino, Masami Morimatsu, Toshimitsu Uede, Etsuro Ono, Masahiko Watanab. Cerebellar pathology in transgenic mice expressing the pseudorabies virus immediate-early protein IE180. The European journal of neuroscience. vol 27. issue 8. 2008-07-01. PMID:18412631. |
previously, we reported that transgenic expression of ie180 in mice causes severe ataxia and cerebellar deformity. |
2008-07-01 |
2023-08-12 |
mouse |
| Yukiko Tomioka, Taisuke Miyazaki, Satoshi Taharaguchi, Saori Yoshino, Masami Morimatsu, Toshimitsu Uede, Etsuro Ono, Masahiko Watanab. Cerebellar pathology in transgenic mice expressing the pseudorabies virus immediate-early protein IE180. The European journal of neuroscience. vol 27. issue 8. 2008-07-01. PMID:18412631. |
despite similar expression levels of the transgenes, ataxia and cerebellar defects were only manifested in the dlc1081 transgenic mice but their phenotypes were milder compared with the ie180 transgenic mice. |
2008-07-01 |
2023-08-12 |
mouse |