| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| W Ilg, A J Bastian, S Boesch, R G Burciu, P Celnik, J Claaßen, K Feil, R Kalla, I Miyai, W Nachbauer, L Schöls, M Strupp, M Synofzik, J Teufel, D Timman. Consensus paper: management of degenerative cerebellar disorders. Cerebellum (London, England). vol 13. issue 2. 2014-09-12. PMID:24222635. |
this is currently available only for a very small subset of cerebellar ataxias with known metabolic dysfunction. |
2014-09-12 |
2023-08-12 |
Not clear |
| W Ilg, A J Bastian, S Boesch, R G Burciu, P Celnik, J Claaßen, K Feil, R Kalla, I Miyai, W Nachbauer, L Schöls, M Strupp, M Synofzik, J Teufel, D Timman. Consensus paper: management of degenerative cerebellar disorders. Cerebellum (London, England). vol 13. issue 2. 2014-09-12. PMID:24222635. |
in this paper, data from recent drug trials in patients with recessive and dominant cerebellar ataxias will be summarized. |
2014-09-12 |
2023-08-12 |
Not clear |
| Ah Young Lee, Sung Ho Jang, Sang Seok Yeo, Ensil Lee, Yun Woo Cho, Su Min So. Changes in a cerebellar peduncle lesion in a patient with Dandy-Walker malformation: A diffusion tensor imaging study. Neural regeneration research. vol 8. issue 5. 2014-09-10. PMID:25206690. |
we report a patient with severe ataxia due to dandy-walker malformation, who showed functional recovery over 10 months corresponding to a change in a cerebellar peduncle lesion. |
2014-09-10 |
2023-08-13 |
human |
| Conceição Bettencourt, Mina Ryten, Paola Forabosco, Stephanie Schorge, Joshua Hersheson, John Hardy, Henry Houlde. Insights from cerebellar transcriptomic analysis into the pathogenesis of ataxia. JAMA neurology. vol 71. issue 7. 2014-09-08. PMID:24862029. |
insights from cerebellar transcriptomic analysis into the pathogenesis of ataxia. |
2014-09-08 |
2023-08-13 |
Not clear |
| Zsuzsanna Soós, Mónika Salamon, Katalin Erdei, Nóra Kaszás, András Folyovich, Anna Szücs, Gábor Barcs, Zsuzsanna Arányi, József Skaliczkis, Károly Vadasdi, Gábor Winkle. LADA type diabetes, celiac diasease, cerebellar ataxia and stiff person syndrome. A rare association of autoimmune disorders. Ideggyogyaszati szemle. vol 67. issue 5-6. 2014-08-29. PMID:25087381. |
a 63-years old woman was diagnosed with epilepsy at the age of 19, and with progressive limb ataxia at the age of 36, which was initially thought to be caused by cerebellar atrophy, later probably by stiff person syndrome. |
2014-08-29 |
2023-08-13 |
Not clear |
| Nasir H Bhanpuri, Allison M Okamura, Amy J Bastia. Predicting and correcting ataxia using a model of cerebellar function. Brain : a journal of neurology. vol 137. issue Pt 7. 2014-08-25. PMID:24812203. |
predicting and correcting ataxia using a model of cerebellar function. |
2014-08-25 |
2023-08-13 |
Not clear |
| Nasir H Bhanpuri, Allison M Okamura, Amy J Bastia. Predicting and correcting ataxia using a model of cerebellar function. Brain : a journal of neurology. vol 137. issue Pt 7. 2014-08-25. PMID:24812203. |
cerebellar damage results in uncoordinated, variable and dysmetric movements known as ataxia. |
2014-08-25 |
2023-08-13 |
Not clear |
| Nasir H Bhanpuri, Allison M Okamura, Amy J Bastia. Predicting and correcting ataxia using a model of cerebellar function. Brain : a journal of neurology. vol 137. issue Pt 7. 2014-08-25. PMID:24812203. |
we hypothesized that cerebellar damage causes a mismatch between the brain's modelled dynamics and the actual body dynamics, resulting in ataxia. |
2014-08-25 |
2023-08-13 |
Not clear |
| Andrea Mignarri, Alessandra Tessa, Maria Alessandra Carluccio, Alessandra Rufa, Eugenia Storti, Giovanni Bonelli, Christian Marcotulli, Filippo Maria Santorelli, Luca Leonardi, Carlo Casali, Antonio Federico, Maria Teresa Dott. Cerebellum and neuropsychiatric disorders: insights from ARSACS. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 35. issue 1. 2014-08-21. PMID:24318559. |
autosomal recessive spastic ataxia of charlevoix-saguenay (arsacs) is a rare neurodegenerative disorder characterized by ataxia, spastic paraparesis, polyneuropathy, and evidence of superior cerebellar vermis atrophy at magnetic resonance imaging (mri). |
2014-08-21 |
2023-08-12 |
Not clear |
| Hadi Kazemi, Erwin-Josef Speckmann, Ali Gorj. Familial hemiplegic migraine and spreading depression. Iranian journal of child neurology. vol 8. issue 3. 2014-08-21. PMID:25143767. |
fhm1 with ataxia is attributable to specific mutations that differ from mutations that cause pure fhm1 and have peculiar consequences on cerebellar cav2.1 currents that lead to profound purkinje cell dysfunction and neuronal loss with atrophy. |
2014-08-21 |
2023-08-13 |
mouse |
| Akinori Futamura, Mitsuru Kawamur. [Functional coupling of the frontal and parietal lobes in action]. Brain and nerve = Shinkei kenkyu no shinpo. vol 66. issue 4. 2014-08-15. PMID:24748093. |
parietal ataxia is caused by lesions in the parietal lobe, which are thought to be caused by disconnection between the cerebellum and brodmann area 5 in the parietal lobe. |
2014-08-15 |
2023-08-13 |
Not clear |
| Stefan Kipfer, Simon Jung, Johannes R Lemke, Anna Kipfer-Kauer, Jeremy P Howell, Alain Kaelin-Lang, Thomas Nyffeler, Klemens Gutbrod, Angela Abicht, René M Mür. Novel CACNA1A mutation(s) associated with slow saccade velocities. Journal of neurology. vol 260. issue 12. 2014-08-06. PMID:24046065. |
the de novo frame-shift cacna1a mutation and the unclassified in-frame cacna1a variant were associated with the episodic ataxia type 2 phenotype and reduced mean saccade velocity, which suggests involvement of brainstem or neural pathways connecting brainstem and the cerebellum in this disease. |
2014-08-06 |
2023-08-12 |
Not clear |
| Angela Pyle, Helen Griffin, Jennifer Duff, Shona Bennett, Simon Zwolinski, Tania Smertenko, Patrick Yu-Wai Man, Mauro Santibanez-Koref, Rita Horvath, Patrick F Chinner. Late-onset sacsinopathy diagnosed by exome sequencing and comparative genomic hybridization. Journal of neurogenetics. vol 27. issue 4. 2014-08-06. PMID:24180463. |
the molecular diagnosis of adult-onset autosomal recessive cerebellar ataxias remains challenging because of genetic heterogeneity. |
2014-08-06 |
2023-08-12 |
Not clear |
| Stuart Currie, Nigel Hoggard, Matthew J R Clark, David S Sanders, Iain D Wilkinson, Paul D Griffiths, Marios Hadjivassilio. Alcohol induces sensitization to gluten in genetically susceptible individuals: a case control study. PloS one. vol 8. issue 10. 2014-08-05. PMID:24204900. |
additional or even alternative causes of cerebellar degeneration are often overlooked in suspected cases of alcohol-related ataxia. |
2014-08-05 |
2023-08-12 |
Not clear |
| Christina Votsi, Eleni Zamba-Papanicolaou, Lefkos T Middleton, Marios Pantzaris, Kyproula Christodoulo. A novel GBA2 gene missense mutation in spastic ataxia. Annals of human genetics. vol 78. issue 1. 2014-08-01. PMID:24252062. |
autosomal recessive cerebellar ataxias (arca) encompass a heterogeneous group of rare diseases that affect the cerebellum, the spinocerebellar tract and/or the sensory tracts of the spinal cord. |
2014-08-01 |
2023-08-12 |
human |
| Ellika Schalling, Lena Harteliu. Speech in spinocerebellar ataxia. Brain and language. vol 127. issue 3. 2014-07-28. PMID:24182841. |
spinocerebellar ataxias (scas) are a heterogeneous group of autosomal dominant cerebellar ataxias clinically characterized by progressive ataxia, dysarthria and a range of other concomitant neurological symptoms. |
2014-07-28 |
2023-08-12 |
Not clear |
| Erin Sandford, Margit Burmeiste. Genes and genetic testing in hereditary ataxias. Genes. vol 5. issue 3. 2014-07-24. PMID:25055202. |
ataxia is a neurological cerebellar disorder characterized by loss of coordination during muscle movements affecting walking, vision, and speech. |
2014-07-24 |
2023-08-13 |
Not clear |
| Uta Bultmann, Daniela Pierscianek, Elke R Gizewski, Beate Schoch, Nicole Fritsche, Dagmar Timmann, Matthias Maschke, Markus Fring. Functional recovery and rehabilitation of postural impairment and gait ataxia in patients with acute cerebellar stroke. Gait & posture. vol 39. issue 1. 2014-07-23. PMID:24119775. |
in the acute phase patients showed a mild to severe ataxia with a worse performance in patients with infarction of the superior in comparison to the posterior inferior cerebellar artery. |
2014-07-23 |
2023-08-12 |
Not clear |
| Uta Bultmann, Daniela Pierscianek, Elke R Gizewski, Beate Schoch, Nicole Fritsche, Dagmar Timmann, Matthias Maschke, Markus Fring. Functional recovery and rehabilitation of postural impairment and gait ataxia in patients with acute cerebellar stroke. Gait & posture. vol 39. issue 1. 2014-07-23. PMID:24119775. |
in patients with ataxia of stance, gait and lower limbs lesions were more common in cerebellar lobules iv to vi. |
2014-07-23 |
2023-08-12 |
Not clear |
| Venkatesan Jagadesan, Kannapiran R Thiruvengadam, Rengarajalu Muralidhara. Cerebellar Stroke-manifesting as Mania. Indian journal of psychological medicine. vol 36. issue 3. 2014-07-18. PMID:25035567. |
neurological examination revealed left cerebellar signs like ataxia and slurring of speech. |
2014-07-18 |
2023-08-13 |
Not clear |