| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Laura Guerrini, Giacomo Belli, Lorenzo Mazzoni, Silvia Foresti, Andrea Ginestroni, Riccardo Della Nave, Stefano Diciotti, Mario Mascalch. Impact of cerebrospinal fluid contamination on brain metabolites evaluation with 1H-MR spectroscopy: a single voxel study of the cerebellar vermis in patients with degenerative ataxias. Journal of magnetic resonance imaging : JMRI. vol 30. issue 1. 2009-08-19. PMID:19557841. |
impact of cerebrospinal fluid contamination on brain metabolites evaluation with 1h-mr spectroscopy: a single voxel study of the cerebellar vermis in patients with degenerative ataxias. |
2009-08-19 |
2023-08-12 |
human |
| Laura Guerrini, Giacomo Belli, Lorenzo Mazzoni, Silvia Foresti, Andrea Ginestroni, Riccardo Della Nave, Stefano Diciotti, Mario Mascalch. Impact of cerebrospinal fluid contamination on brain metabolites evaluation with 1H-MR spectroscopy: a single voxel study of the cerebellar vermis in patients with degenerative ataxias. Journal of magnetic resonance imaging : JMRI. vol 30. issue 1. 2009-08-19. PMID:19557841. |
to investigate the impact of cerebrospinal fluid (csf) contamination on metabolite evaluation in the superior cerebellar vermis with single-voxel (1)h-mrs in normal subjects and patients with degenerative ataxias. |
2009-08-19 |
2023-08-12 |
human |
| Joanna C Jen, Robert W Balo. Familial episodic ataxia: a model for migrainous vertigo. Annals of the New York Academy of Sciences. vol 1164. 2009-08-18. PMID:19645908. |
mutations in two neuronal ion-channel genes kcna1 and cacna1a abundantly expressed in the cerebellum account for the majority of the identified cases of episodic ataxia. |
2009-08-18 |
2023-08-12 |
Not clear |
| Mahyar Janahmadi, Iran Goudarzi, Mohammad Reza Kaffashian, Gila Behzadi, Yaqub Fathollahi, Sohrab Hajizade. Co-treatment with riluzole, a neuroprotective drug, ameliorates the 3-acetylpyridine-induced neurotoxicity in cerebellar Purkinje neurones of rats: behavioural and electrophysiological evidence. Neurotoxicology. vol 30. issue 3. 2009-08-04. PMID:19442824. |
ataxia is a clinical manifestation of disturbance in coordinated motor activity, which may be caused by cerebellar impairment. |
2009-08-04 |
2023-08-12 |
rat |
| Stefan Mark Rueckriegel, Friederike Blankenburg, Günter Henze, Herrmann Baqué, Pablo Hernáiz Drieve. Loss of fine motor function correlates with ataxia and decline of cognition in cerebellar tumor survivors. Pediatric blood & cancer. vol 53. issue 3. 2009-07-31. PMID:19484752. |
loss of fine motor function correlates with ataxia and decline of cognition in cerebellar tumor survivors. |
2009-07-31 |
2023-08-12 |
Not clear |
| Georgia Mandolesi, Eleonora Autuori, Roberta Cesa, Federica Premoselli, Paolo Cesare, Piergiorgio Strat. GluRdelta2 expression in the mature cerebellum of hotfoot mice promotes parallel fiber synaptogenesis and axonal competition. PloS one. vol 4. issue 4. 2009-07-30. PMID:19370152. |
the glurdelta2-null mice, such as knockout and hotfoot have profoundly altered cerebellar circuitry, which causes ataxia and impaired motor learning. |
2009-07-30 |
2023-08-12 |
mouse |
| Shyamal H Mehta, John C Morgan, Kapil D Seth. Paraneoplastic movement disorders. Current neurology and neuroscience reports. vol 9. issue 4. 2009-07-29. PMID:19515280. |
among the various "classic" and other npss, this review focuses on paraneoplastic movement disorders, including ataxia due to cerebellar degeneration, stiff-person syndrome, opsoclonus-myoclonus syndrome, chorea, parkinsonism, and tremor. |
2009-07-29 |
2023-08-12 |
Not clear |
| S J Sriranjini, Pramod Kumar Pal, K V Devidas, Selva Ganpath. Improvement of balance in progressive degenerative cerebellar ataxias after Ayurvedic therapy: a preliminary report. Neurology India. vol 57. issue 2. 2009-07-23. PMID:19439847. |
improvement of balance in progressive degenerative cerebellar ataxias after ayurvedic therapy: a preliminary report. |
2009-07-23 |
2023-08-12 |
Not clear |
| S J Sriranjini, Pramod Kumar Pal, K V Devidas, Selva Ganpath. Improvement of balance in progressive degenerative cerebellar ataxias after Ayurvedic therapy: a preliminary report. Neurology India. vol 57. issue 2. 2009-07-23. PMID:19439847. |
the treatment options for improving the balance in degenerative cerebellar ataxias are very few. |
2009-07-23 |
2023-08-12 |
Not clear |
| Ryuichi Furukawa, Ryuji Sakakibara, Nobuo Hosoe, Masahiko Kishi, Emina Ogawa, Yasuo Suzuk. Ataxia and middle cerebellar peduncle lesions in hepatic encephalopathy. Neuroradiology. vol 51. issue 4. 2009-07-22. PMID:19259655. |
ataxia and middle cerebellar peduncle lesions in hepatic encephalopathy. |
2009-07-22 |
2023-08-12 |
Not clear |
| Seval Türkmen, Gao Guo, Masoud Garshasbi, Katrin Hoffmann, Amjad J Alshalah, Claudia Mischung, Andreas Kuss, Nicholas Humphrey, Stefan Mundlos, Peter N Robinso. CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait. PLoS genetics. vol 5. issue 5. 2009-07-13. PMID:19461874. |
our findings underline the importance of itp-mediated signaling in cerebellar function and provide suggestive evidence that congenital ataxia paired with cerebral dysfunction may, together with unknown contextual factors during development, predispose to quadrupedal gait in humans. |
2009-07-13 |
2023-08-12 |
mouse |
| Koby Baranes, Dorit Raz-Prag, Anat Nitzan, Ronit Galron, Ruth Ashery-Padan, Ygal Rotenstreich, Yaniv Assaf, Yosef Shiloh, Zhao-Qi Wang, Ari Barzilai, Arieh S Solomo. Conditional inactivation of the NBS1 gene in the mouse central nervous system leads to neurodegeneration and disorganization of the visual system. Experimental neurology. vol 218. issue 1. 2009-07-07. PMID:19345213. |
conditional disruption of the murine ortholog of the human nbs1, nbs1, in the cns of mice was previously reported to cause microcephaly, severe cerebellar atrophy and ataxia. |
2009-07-07 |
2023-08-12 |
mouse |
| Yosr Bouhlal, Mourad Zouari, Mounir Kefi, Christiane Ben Hamida, Fayçal Hentati, Rim Amour. Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family. Journal of neurogenetics. vol 22. issue 2. 2009-06-19. PMID:18569450. |
autosomal recessive cerebellar ataxias are a group of clinically and genetically heterogeneous neurodegenerative disorders. |
2009-06-19 |
2023-08-12 |
Not clear |
| Jacques Penderi. The wobbly cat. Diagnostic and therapeutic approach to generalised ataxia. Journal of feline medicine and surgery. vol 11. issue 5. 2009-06-16. PMID:19389635. |
the causes can be subdivided into three forms on the basis of the neuroanatomical diagnosis: cerebellar, vestibular and sensory (spinal or general proprioceptive) ataxia. |
2009-06-16 |
2023-08-12 |
cat |
| Esther B E Becker, Peter L Oliver, Maike D Glitsch, Gareth T Banks, Francesca Achilli, Andrea Hardy, Patrick M Nolan, Elizabeth M C Fisher, Kay E Davie. A point mutation in TRPC3 causes abnormal Purkinje cell development and cerebellar ataxia in moonwalker mice. Proceedings of the National Academy of Sciences of the United States of America. vol 106. issue 16. 2009-05-29. PMID:19351902. |
the hereditary ataxias are a complex group of neurological disorders characterized by the degeneration of the cerebellum and its associated connections. |
2009-05-29 |
2023-08-12 |
mouse |
| Yuka Watanabe, Masaaki Odaka, Koichi Hirat. [Case of Leber's hereditary optic neuropathy with mitochondrial DNA 11778 mutation exhibiting cerebellar ataxia, dilated cardiomyopathy and peripheral neuropathy]. Brain and nerve = Shinkei kenkyu no shinpo. vol 61. issue 3. 2009-05-20. PMID:19301602. |
a neurological examination detected horizontal nystagmus, bradylalia, and truncal and bilateral limb ataxia of the cerebellar type. |
2009-05-20 |
2023-08-12 |
Not clear |
| D Timmann, B Brandauer, J Hermsdörfer, W Ilg, J Konczak, M Gerwig, E R Gizewski, B Schoc. Lesion-symptom mapping of the human cerebellum. Cerebellum (London, England). vol 7. issue 4. 2009-05-18. PMID:18949530. |
one example are correlations with clinical data which are in good accordance with the known functional compartmentalisation of the cerebellum in three sagittal zones: in patients with cerebellar cortical degeneration ataxia of stance and gait was correlated with atrophy of the medial (and intermediate) cerebellum, oculomotor disorders with the medial, dysarthria with the intermediate and limb ataxia with atrophy of the intermediate and lateral cerebellum. |
2009-05-18 |
2023-08-12 |
human |
| Maja Steinli. Cerebellar disorders in childhood: cognitive problems. Cerebellum (London, England). vol 7. issue 4. 2009-05-18. PMID:19057977. |
in ataxia teleangiectasia, a neurodegenerative disorder affecting primarily the cerebellar cortex, a reduced verbal intelligence quotient and problems of judgment of duration are a hint of the importance of the cerebellum in cognition. |
2009-05-18 |
2023-08-12 |
Not clear |
| Shoji Tsuji, Osamu Onodera, Jun Goto, Masatoyo Nishizaw. Sporadic ataxias in Japan--a population-based epidemiological study. Cerebellum (London, England). vol 7. issue 2. 2009-05-15. PMID:18418674. |
the natural history analysis conducted on the basis of international cooperative ataxia rating scale (icars) showed that only 33% of patients with opca were able to walk at least with one stick 4-5 years after the onset of opca, which is much less than that of patients with cortical cerebellar atrophy (cca). |
2009-05-15 |
2023-08-12 |
Not clear |
| Susanne Döhlinger, Till-Karsten Hauser, Johannes Borkert, Andreas R Luft, Jörg B Schul. Magnetic resonance imaging in spinocerebellar ataxias. Cerebellum (London, England). vol 7. issue 2. 2009-05-15. PMID:18418677. |
we will review recent results and how these methods are currently used to (i) separate sporadic and dominantly inherited forms of cerebellar ataxias; (ii) identify specific sca genotypes; (iii) correlate patho-anatomical changes with sca disease symptoms or severity; and (iv) visualize and estimate the rate of progression in sca. |
2009-05-15 |
2023-08-12 |
Not clear |