| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Dervila Glynn, Cheney J Drew, Kerstin Reim, Nils Brose, A Jennifer Morto. Profound ataxia in complexin I knockout mice masks a complex phenotype that includes exploratory and habituation deficits. Human molecular genetics. vol 14. issue 16. 2005-10-20. PMID:16000319. |
cplx1-/- mice develop a strong ataxia in the absence of cerebellar degeneration. |
2005-10-20 |
2023-08-12 |
mouse |
| Stefanie Richter, Albena Dimitrova, Matthias Maschke, Elke Gizewski, Andreas Beck, Volker Aurich, Dagmar Timman. Degree of cerebellar ataxia correlates with three-dimensional mri-based cerebellar volume in pure cerebellar degeneration. European neurology. vol 54. issue 1. 2005-10-14. PMID:16088175. |
total icars score significantly inversely correlated with the cerebellar volume (r = -0.805, p < 0.0001), correlations between icars subscores and cerebellar volume were significant for upper and lower limb ataxia, ataxia of posture and gait, and dysarthria, but not for the oculomotor subscore. |
2005-10-14 |
2023-08-12 |
Not clear |
| H Harno, S Heikkinen, M A Kaunisto, M Kallela, A-M Häkkinen, M Wessman, M Färkkilä, N Lundbo. Decreased cerebellar total creatine in episodic ataxia type 2: a 1H MRS study. Neurology. vol 64. issue 3. 2005-09-19. PMID:15699392. |
decreased cerebellar total creatine in episodic ataxia type 2: a 1h mrs study. |
2005-09-19 |
2023-08-12 |
human |
| H Harno, S Heikkinen, M A Kaunisto, M Kallela, A-M Häkkinen, M Wessman, M Färkkilä, N Lundbo. Decreased cerebellar total creatine in episodic ataxia type 2: a 1H MRS study. Neurology. vol 64. issue 3. 2005-09-19. PMID:15699392. |
episodic ataxia type 2 (ea2) affects mainly the cerebellum via mutations in the cacna1a gene. |
2005-09-19 |
2023-08-12 |
human |
| Ullrich Wüllner, Michael Reimold, Michael Abele, Katrin Bürk, Martina Minnerop, Bernd-Michael Dohmen, Hans-Juergen Machulla, Roland Bares, Thomas Klockgethe. Dopamine transporter positron emission tomography in spinocerebellar ataxias type 1, 2, 3, and 6. Archives of neurology. vol 62. issue 8. 2005-09-08. PMID:16087769. |
the spinocerebellar ataxias (scas) are a genetically heterogeneous group of autosomal dominant ataxias: some mutations, including sca1, sca2, and sca3, are multisystemic disorders characterized by a variety of noncerebellar symptoms while others, like sca6, give rise to a pure cerebellar syndrome. |
2005-09-08 |
2023-08-12 |
Not clear |
| Bart P C van de Warrenburg, Janneke A G Steijns, Marten Munneke, Berry P H Kremer, Bastiaan R Bloe. Falls in degenerative cerebellar ataxias. Movement disorders : official journal of the Movement Disorder Society. vol 20. issue 4. 2005-08-25. PMID:15645525. |
falls in degenerative cerebellar ataxias. |
2005-08-25 |
2023-08-12 |
Not clear |
| Bart P C van de Warrenburg, Janneke A G Steijns, Marten Munneke, Berry P H Kremer, Bastiaan R Bloe. Falls in degenerative cerebellar ataxias. Movement disorders : official journal of the Movement Disorder Society. vol 20. issue 4. 2005-08-25. PMID:15645525. |
we retrospectively and prospectively assessed the frequency and characteristics of falls in patients with degenerative cerebellar ataxias. |
2005-08-25 |
2023-08-12 |
Not clear |
| Bart P C van de Warrenburg, Janneke A G Steijns, Marten Munneke, Berry P H Kremer, Bastiaan R Bloe. Falls in degenerative cerebellar ataxias. Movement disorders : official journal of the Movement Disorder Society. vol 20. issue 4. 2005-08-25. PMID:15645525. |
the results show that falls occur very frequently in patients with degenerative cerebellar ataxias and that these falls are serious and often lead to injuries or a fear of falling. |
2005-08-25 |
2023-08-12 |
Not clear |
| Beau M Ances, Roberta Vitaliani, Robert A Taylor, David S Liebeskind, Alfredo Voloschin, David J Houghton, Steven L Galetta, Marc Dichter, Abass Alavi, Myrna R Rosenfeld, Josep Dalma. Treatment-responsive limbic encephalitis identified by neuropil antibodies: MRI and PET correlates. Brain : a journal of neurology. vol 128. issue Pt 8. 2005-08-16. PMID:15888538. |
in one patient, fdg hyperactivity in the brainstem that was normal on mri correlated with central hypoventilation; in another case, hyperactivity in the cerebellum anticipated ataxia. |
2005-08-16 |
2023-08-12 |
Not clear |
| Daniela Pietrobo. Function and dysfunction of synaptic calcium channels: insights from mouse models. Current opinion in neurobiology. vol 15. issue 3. 2005-08-09. PMID:15922581. |
the different disorders probably arise from disruption of neurotransmission in specific brain regions: the cortex in the case of migraine, the thalamus in the case of absence epilepsy and the cerebellum in the case of ataxia. |
2005-08-09 |
2023-08-12 |
mouse |
| Naoki Saj. [Small cerebellar vermis infarction with isolated truncal ataxia]. No to shinkei = Brain and nerve. vol 57. issue 6. 2005-07-29. PMID:16026050. |
[small cerebellar vermis infarction with isolated truncal ataxia]. |
2005-07-29 |
2023-08-12 |
Not clear |
| J Infante, O Combarros, V Volpini, J Corral, J Llorca, J Bercian. Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis. Acta neurologica Scandinavica. vol 111. issue 6. 2005-07-28. PMID:15876341. |
autosomal dominant cerebellar ataxias in spain: molecular and clinical correlations, prevalence estimation and survival analysis. |
2005-07-28 |
2023-08-12 |
Not clear |
| J Infante, O Combarros, V Volpini, J Corral, J Llorca, J Bercian. Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis. Acta neurologica Scandinavica. vol 111. issue 6. 2005-07-28. PMID:15876341. |
the genetic and clinical profile of autosomal dominant cerebellar ataxias (adca) displays marked geographical and ethnical variability. |
2005-07-28 |
2023-08-12 |
Not clear |
| I D Wilkinson, M Hadjivassiliou, J M Dickson, L Wallis, R A Grünewald, S C Coley, E Widjaja, P D Griffith. Cerebellar abnormalities on proton MR spectroscopy in gluten ataxia. Journal of neurology, neurosurgery, and psychiatry. vol 76. issue 7. 2005-07-19. PMID:15965215. |
cerebellar abnormalities on proton mr spectroscopy in gluten ataxia. |
2005-07-19 |
2023-08-12 |
Not clear |
| I D Wilkinson, M Hadjivassiliou, J M Dickson, L Wallis, R A Grünewald, S C Coley, E Widjaja, P D Griffith. Cerebellar abnormalities on proton MR spectroscopy in gluten ataxia. Journal of neurology, neurosurgery, and psychiatry. vol 76. issue 7. 2005-07-19. PMID:15965215. |
the metabolic status of the cerebellum was investigated in 15 patients with gluten ataxia and 10 controls using proton mr spectroscopy. |
2005-07-19 |
2023-08-12 |
Not clear |
| I D Wilkinson, M Hadjivassiliou, J M Dickson, L Wallis, R A Grünewald, S C Coley, E Widjaja, P D Griffith. Cerebellar abnormalities on proton MR spectroscopy in gluten ataxia. Journal of neurology, neurosurgery, and psychiatry. vol 76. issue 7. 2005-07-19. PMID:15965215. |
these data support the hypothesis that cerebellar neuronal physiology differs between patients with gluten ataxia and healthy controls. |
2005-07-19 |
2023-08-12 |
Not clear |
| Z Yapici, M Erakso. Non-progressive congenital ataxia with cerebellar hypoplasia in three families. Acta paediatrica (Oslo, Norway : 1992). vol 94. issue 2. 2005-07-15. PMID:15981765. |
non-progressive congenital ataxia with cerebellar hypoplasia in three families. |
2005-07-15 |
2023-08-12 |
Not clear |
| Z Yapici, M Erakso. Non-progressive congenital ataxia with cerebellar hypoplasia in three families. Acta paediatrica (Oslo, Norway : 1992). vol 94. issue 2. 2005-07-15. PMID:15981765. |
non-progressive ataxias with cerebellar hypoplasia are a rarely seen heterogeneous group of hereditary cerebellar ataxias. |
2005-07-15 |
2023-08-12 |
Not clear |
| Pierre-Olivier Frappart, Wei-Min Tong, Ilja Demuth, Ivan Radovanovic, Zdenko Herceg, Adriano Aguzzi, Martin Digweed, Zhao-Qi Wan. An essential function for NBS1 in the prevention of ataxia and cerebellar defects. Nature medicine. vol 11. issue 5. 2005-07-12. PMID:15821748. |
an essential function for nbs1 in the prevention of ataxia and cerebellar defects. |
2005-07-12 |
2023-08-12 |
mouse |
| Pierre-Olivier Frappart, Wei-Min Tong, Ilja Demuth, Ivan Radovanovic, Zdenko Herceg, Adriano Aguzzi, Martin Digweed, Zhao-Qi Wan. An essential function for NBS1 in the prevention of ataxia and cerebellar defects. Nature medicine. vol 11. issue 5. 2005-07-12. PMID:15821748. |
nijmegen breakage syndrome (nbs), ataxia telangiectasia and ataxia telangiectasia-like disorder (atld) show overlapping phenotypes such as growth retardation, microcephaly, cerebellar developmental defects and ataxia. |
2005-07-12 |
2023-08-12 |
mouse |