| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Richard S Stewart, Pedro Piccardo, Bernardino Ghetti, David A Harri. Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 25. issue 13. 2006-03-23. PMID:15800202. |
these mice develop a fatal neurological illness characterized by ataxia and marked neuronal loss in the cerebellum and hippocampus. |
2006-03-23 |
2023-08-12 |
mouse |
| José Berciano, Jon Infante, Antonio García, José Miguel Polo, Victor Volpini, Onofre Combarro. Very late-onset Friedreich's ataxia with minimal GAA1 expansion mimicking multiple system atrophy of cerebellar type. Movement disorders : official journal of the Movement Disorder Society. vol 20. issue 12. 2006-03-21. PMID:16092110. |
very late-onset friedreich's ataxia with minimal gaa1 expansion mimicking multiple system atrophy of cerebellar type. |
2006-03-21 |
2023-08-12 |
Not clear |
| T Klockgethe. [Ataxias. Diagnostic procedure and treatment]. Der Nervenarzt. vol 76. issue 10. 2006-03-14. PMID:16175415. |
ataxia disorders (or ataxias) include both hereditary and nonhereditary diseases of the cerebellum and spinal cord, all of which are clinically characterized by progressive ataxia. |
2006-03-14 |
2023-08-12 |
Not clear |
| T Klockgethe. [Ataxias. Diagnostic procedure and treatment]. Der Nervenarzt. vol 76. issue 10. 2006-03-14. PMID:16175415. |
a distinction is made between ataxia disorders and focal diseases of the cerebellum (tumor, abscess, infarction, hemorrhage, demyelinating disease). |
2006-03-14 |
2023-08-12 |
Not clear |
| T Klockgethe. [Ataxias. Diagnostic procedure and treatment]. Der Nervenarzt. vol 76. issue 10. 2006-03-14. PMID:16175415. |
patients with sporadic disease starting in adulthood may have an acquired ataxia, such as alcoholic cerebellar degeneration (acd) or paraneoplastic cerebellar degeneration (pcd), or a sporadic degenerative ataxia, such as multiple system atrophy (msa) or sporadic adult-onset ataxia (saoa). |
2006-03-14 |
2023-08-12 |
Not clear |
| Stephan Klebe, Alexandra Durr, Alexander Rentschler, Valerie Hahn-Barma, Michael Abele, Naima Bouslam, Ludger Schöls, Pierre Jedynak, Sylvie Forlani, Elodie Denis, Christel Dussert, Yves Agid, Peter Bauer, Christoph Globas, Ullrich Wüllner, Alexis Brice, Olaf Riess, Giovanni Stevani. New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14. Annals of neurology. vol 58. issue 5. 2006-03-14. PMID:16193476. |
autosomal dominant cerebellar ataxias (adca) are a heterogeneous group of neurological disorders. |
2006-03-14 |
2023-08-12 |
Not clear |
| M F Waters, D Fee, K P Figueroa, D Nolte, U Müller, J Advincula, H Coon, V G Evidente, S M Puls. An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus? Neurology. vol 65. issue 7. 2006-03-09. PMID:16135769. |
clinical characterization of a three-generation filipino family segregating a dominant ataxia revealed cerebellar signs and symptoms. |
2006-03-09 |
2023-08-12 |
Not clear |
| Tomoka Nakamura, Motoko Honda, Satoko Kimura, Mitsuo Tanabe, Sen-ichi Oda, Hideki On. Taltirelin improves motor ataxia independently of monoamine levels in rolling mouse nagoya, a model of spinocerebellar atrophy. Biological & pharmaceutical bulletin. vol 28. issue 12. 2006-03-09. PMID:16327158. |
to examine the relationship between motor ataxia and monoamine levels in the central nervous system, the contents and concentrations of noradrenaline (na), dopamine (da) and serotonin (5-ht) in the cerebellum, brain stem and spinal cord were measured in rolling mouse nagoya (rmn), a murine model of spinocerebellar atrophy. |
2006-03-09 |
2023-08-12 |
mouse |
| Tomoka Nakamura, Motoko Honda, Satoko Kimura, Mitsuo Tanabe, Sen-ichi Oda, Hideki On. Taltirelin improves motor ataxia independently of monoamine levels in rolling mouse nagoya, a model of spinocerebellar atrophy. Biological & pharmaceutical bulletin. vol 28. issue 12. 2006-03-09. PMID:16327158. |
repeated administration of tartilerin hydrate, an analog of thyrotropin-releasing hormone, improved the ataxia of rmn, and elicited no obvious changes in either monoamine content or concentration of cerebellum, brain stem and spinal cord. |
2006-03-09 |
2023-08-12 |
mouse |
| Wojciech Kozubsk. [Basilar-type migraine: pathophysiology, symptoms and signs, and treatment]. Neurologia i neurochirurgia polska. vol 39. issue 4 Suppl 1. 2006-03-08. PMID:16419573. |
the diagnosis of btm is based on the finding of two migraine attacks accompanied by a specific aura, with dysarthria, vertigo, tinnitus, impaired hearing, double vision, visual aura elements, ataxia of a cerebellar type, loss of consciousness, and bilateral paresthesias. |
2006-03-08 |
2023-08-12 |
Not clear |
| Isabelle Le Ber, Alexis Brice, Alexandra Dür. New autosomal recessive cerebellar ataxias with oculomotor apraxia. Current neurology and neuroscience reports. vol 5. issue 5. 2006-01-20. PMID:16131425. |
new autosomal recessive cerebellar ataxias with oculomotor apraxia. |
2006-01-20 |
2023-08-12 |
Not clear |
| Isabelle Le Ber, Alexis Brice, Alexandra Dür. New autosomal recessive cerebellar ataxias with oculomotor apraxia. Current neurology and neuroscience reports. vol 5. issue 5. 2006-01-20. PMID:16131425. |
autosomal recessive cerebellar ataxias (arcas) are a phenotypically and genetically heterogeneous group of diseases. |
2006-01-20 |
2023-08-12 |
Not clear |
| Isabelle Le Ber, Alexis Brice, Alexandra Dür. New autosomal recessive cerebellar ataxias with oculomotor apraxia. Current neurology and neuroscience reports. vol 5. issue 5. 2006-01-20. PMID:16131425. |
recently, the genes for two new autosomal recessive cerebellar ataxias with oculomotor apraxia, aoa1 and aoa2, were identified. |
2006-01-20 |
2023-08-12 |
Not clear |
| Nobue K Iwata, Yoshikazu Ugaw. The effects of cerebellar stimulation on the motor cortical excitability in neurological disorders: a review. Cerebellum (London, England). vol 4. issue 4. 2006-01-18. PMID:16321876. |
we applied this method to patients with ataxia and showed that the inhibitory effect was only absent in patients with a lesion at cerebellar efferent pathways or dentatothalamocortical pathway. |
2006-01-18 |
2023-08-12 |
Not clear |
| C Espinós-Armero, P González-Cabo, F Palau-Martíne. [Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology]. Revista de neurologia. vol 41. issue 7. 2006-01-12. PMID:16193447. |
[autosomal recessive cerebellar ataxias. |
2006-01-12 |
2023-08-12 |
Not clear |
| C Espinós-Armero, P González-Cabo, F Palau-Martíne. [Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology]. Revista de neurologia. vol 41. issue 7. 2006-01-12. PMID:16193447. |
autosomal recessive cerebellar ataxias (arca) are a heterogeneous group of rare neurological disorders involving both central and peripheral nervous system, and in some case other systems and organs. |
2006-01-12 |
2023-08-12 |
Not clear |
| Caterina Mariotti, Roberto Fancellu, Stefano Di Donat. An overview of the patient with ataxia. Journal of neurology. vol 252. issue 5. 2006-01-09. PMID:15895274. |
pure cerebellar symptoms are rarely observed, while the clinical picture of both genetic and sporadic ataxia syndromes is sometimes complicated by the presence of extracerebellar neurological or multisystem extraneural pathology. |
2006-01-09 |
2023-08-12 |
Not clear |
| LaKeisha M Applegate, Elan D Loui. Essential tremor: mild olfactory dysfunction in a cerebellar disorder. Parkinsonism & related disorders. vol 11. issue 6. 2005-11-30. PMID:16102998. |
olfactory dysfunction has been reported to occur in patients with cerebellar disorders, including degenerative ataxias and essential tremor (et). |
2005-11-30 |
2023-08-12 |
Not clear |
| A M R Taylor, P J Byr. Molecular pathology of ataxia telangiectasia. Journal of clinical pathology. vol 58. issue 10. 2005-11-15. PMID:16189143. |
ataxia telangiectasia (a-t) is one of a group of autosomal recessive cerebellar ataxias. |
2005-11-15 |
2023-08-12 |
Not clear |
| Sreenath S Andrali, Pia März, Sabire Ozca. Ataxin-10 interacts with O-GlcNAc transferase OGT in pancreatic beta cells. Biochemical and biophysical research communications. vol 337. issue 1. 2005-11-14. PMID:16182253. |
mutations in the sca10 gene cause progressive cerebellar ataxias and seizures. |
2005-11-14 |
2023-08-12 |
mouse |