| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Dimitri Renard, Laurent Collombier, Giovanni Castelnovo, Genevieve Fourcade, Charles Debrigode, Pierre Labaug. Radiation therapy-related ataxia associated with FDG-PET cerebellar hypometabolism. Acta neurologica Belgica. vol 110. issue 1. 2010-06-22. PMID:20514935. |
radiation therapy-related ataxia associated with fdg-pet cerebellar hypometabolism. |
2010-06-22 |
2023-08-12 |
Not clear |
| John E Greenlee, Susan A Clawson, Kenneth E Hill, Christopher B Dechet, Noel G Carlso. Antineuronal autoantibodies in paraneoplastic cerebellar degeneration associated with adenocarcinoma of the prostate. Journal of the neurological sciences. vol 291. issue 1-2. 2010-06-17. PMID:20089262. |
here we report a 68year old man who developed progressive ataxia in the setting of stage d2 adenocarcinoma of the prostate and whose mri showed cerebellar atrophy. |
2010-06-17 |
2023-08-12 |
Not clear |
| Taiji Tsunemi, Kinya Ishikawa, Kei Tsukui, Takuro Sumi, Ken Kitamura, Hidehiro Mizusaw. The effect of 3,4-diaminopyridine on the patients with hereditary pure cerebellar ataxia. Journal of the neurological sciences. vol 292. issue 1-2. 2010-06-14. PMID:20181362. |
dbn frequently presents with other cerebellar symptoms such as postural imbalance or ataxia. |
2010-06-14 |
2023-08-12 |
Not clear |
| Sun Shin Yi, In Koo Hwang, Jae Hoon Shin, Sung Hee Baek, Yeo Sung Yoon, Je Kyung Seon. Neuronal differentiation and developmental characteristics in the dentate gyrus of staggerer mutant mice. BMB reports. vol 43. issue 2. 2010-05-20. PMID:20193131. |
homozygous staggerer (rora(sg/sg)) mice showed a severe ataxia caused by cerebellum degeneration. |
2010-05-20 |
2023-08-12 |
mouse |
| Emma M Perkins, Yvonne L Clarkson, Nancy Sabatier, David M Longhurst, Christopher P Millward, Jennifer Jack, Junko Toraiwa, Mitsunori Watanabe, Jeffrey D Rothstein, Alastair R Lyndon, David J A Wyllie, Mayank B Dutia, Mandy Jackso. Loss of beta-III spectrin leads to Purkinje cell dysfunction recapitulating the behavior and neuropathology of spinocerebellar ataxia type 5 in humans. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 30. issue 14. 2010-04-26. PMID:20371805. |
how these mutations give rise to progressive ataxia and what the precise role beta-iii spectrin plays in normal cerebellar physiology are unknown. |
2010-04-26 |
2023-08-12 |
mouse |
| Elizabeth M Wells, Zarir P Khademian, Karin S Walsh, Gilbert Vezina, Richard Sposto, Robert F Keating, Roger J Packe. Postoperative cerebellar mutism syndrome following treatment of medulloblastoma: neuroradiographic features and origin. Journal of neurosurgery. Pediatrics. vol 5. issue 4. 2010-04-22. PMID:20367335. |
the origin and long-term outcome of cerebellar mutism syndrome (cms), a postoperative syndrome of diminished speech, hypotonia, and ataxia that affects approximately 25% of patients with medulloblastoma, is poorly elucidated. |
2010-04-22 |
2023-08-12 |
Not clear |
| Michel Mittelbronn, Jens Schittenhelm, Gellert Bakos, Rob A de Vos, Manfred Wehrmann, Richard Meyermann, Katrin Bür. CD8(+)/perforin/granzyme B(+) effector cells infiltrating cerebellum and inferior olives in gluten ataxia. Neuropathology : official journal of the Japanese Society of Neuropathology. vol 30. issue 1. 2010-04-21. PMID:19622110. |
cd8(+)/perforin/granzyme b(+) effector cells infiltrating cerebellum and inferior olives in gluten ataxia. |
2010-04-21 |
2023-08-12 |
Not clear |
| Michel Mittelbronn, Jens Schittenhelm, Gellert Bakos, Rob A de Vos, Manfred Wehrmann, Richard Meyermann, Katrin Bür. CD8(+)/perforin/granzyme B(+) effector cells infiltrating cerebellum and inferior olives in gluten ataxia. Neuropathology : official journal of the Japanese Society of Neuropathology. vol 30. issue 1. 2010-04-21. PMID:19622110. |
these cd8(+) cytotoxic t and nk cells are likely to act as effector cells responsible for neuronal cell death in patients with gluten sensitivity and neurological disease and might therefore at least partly be responsible for cerebellar symptoms in gluten ataxia. |
2010-04-21 |
2023-08-12 |
Not clear |
| Neeraj Kuma. Pearls: myelopathy. Seminars in neurology. vol 30. issue 1. 2010-04-20. PMID:20127580. |
three hereditary myelopathy phenotypes are recognized: predominantly cerebellar (e.g., friedreich's ataxia), predominantly motor (e.g., hereditary spastic paraparesis), and a leukodystrophy phenotype (e.g., adrenomyeloneuropathy). |
2010-04-20 |
2023-08-12 |
Not clear |
| Li-Min Liou, Yuh-Cherng Guo, Chiou-Lian Lai, Chin-Ling Tsai, Gim-Thean Kho. Isolated ataxia after pure left insular cortex infarction. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 31. issue 1. 2010-04-13. PMID:19806312. |
we present a case of pure left insular cortex infarction with isolated truncal ataxia and demonstrate a crucial relationship between the left insular cortex and the cerebellar system. |
2010-04-13 |
2023-08-12 |
Not clear |
| Pu Chen, Mingyi Ma, Huifang Shang, Dan Su, Sizhong Zhang, Yuan Yan. [Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. vol 26. issue 6. 2010-04-13. PMID:19953483. |
[copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes]. |
2010-04-13 |
2023-08-12 |
Not clear |
| Pu Chen, Mingyi Ma, Huifang Shang, Dan Su, Sizhong Zhang, Yuan Yan. [Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. vol 26. issue 6. 2010-04-13. PMID:19953483. |
to standardize the experimental procedure of the gene test for autosomal dominant cerebellar ataxias (adca), and provide the basis for quantitative criteria of the dynamic mutation of spinocerebellar ataxia (sca) genes in chinese population. |
2010-04-13 |
2023-08-12 |
Not clear |
| Gülin Oz, Christopher D Nelson, Dee M Koski, Pierre-Gilles Henry, Malgorzata Marjanska, Dinesh K Deelchand, Ryan Shanley, Lynn E Eberly, Harry T Orr, H Brent Clar. Noninvasive detection of presymptomatic and progressive neurodegeneration in a mouse model of spinocerebellar ataxia type 1. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 30. issue 10. 2010-04-09. PMID:20220018. |
cerebellar concentrations of n-acetylaspartate (naa), myo-inositol, and glutamate as measured by magnetic resonance spectroscopy (mrs) correlate with ataxia scores of patients with sca1, indicating their potential as reliable biomarkers of neurodegeneration. |
2010-04-09 |
2023-08-12 |
mouse |
| Carmen Espinós, Francesc Pala. Genetics and pathogenesis of inherited ataxias and spastic paraplegias. Advances in experimental medicine and biology. vol 652. 2010-04-02. PMID:20225032. |
inherited ataxias are clinically characterized by progressive degeneration of cerebellum and spinocerebellar tracts of the spinal cord associated with a variable combination of signs of central and peripheral nervous system. |
2010-04-02 |
2023-08-12 |
Not clear |
| M Anheim, M Fleury, B Monga, V Laugel, D Chaigne, G Rodier, E Ginglinger, C Boulay, S Courtois, N Drouot, M Fritsch, J P Delaunoy, D Stoppa-Lyonnet, C Tranchant, M Koeni. Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management. Neurogenetics. vol 11. issue 1. 2010-03-22. PMID:19440741. |
patients with no identified mutation have more often a pure cerebellar degenerative disease or a spastic ataxia phenotype. |
2010-03-22 |
2023-08-12 |
Not clear |
| Giovanni Airoldi, Andrea Guidarelli, Orazio Cantoni, Chris Panzeri, Chiara Vantaggiato, Sara Bonato, Maria Grazia D'Angelo, Sestina Falcone, Clara De Palma, Alessandra Tonelli, Claudia Crimella, Sara Bondioni, Nereo Bresolin, Emilio Clementi, Maria Teresa Bass. Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxin. Neurogenetics. vol 11. issue 1. 2010-03-22. PMID:19593598. |
ataxia with oculomotor apraxia (aoa) type 2 (aoa2 mim 606002) is a recessive subtype of aoa characterized by cerebellar atrophy, oculomotor apraxia, early loss of reflexes, and peripheral neuropathy. |
2010-03-22 |
2023-08-12 |
Not clear |
| Lihong Zhao, Christine Rosales, Kevin Seburn, David Ron, Susan L Ackerma. Alteration of the unfolded protein response modifies neurodegeneration in a mouse model of Marinesco-Sjögren syndrome. Human molecular genetics. vol 19. issue 1. 2010-03-09. PMID:19801575. |
mutations in the sil1 gene have been associated with marinesco-sjögren syndrome, hallmarks of which include ataxia and cerebellar atrophy. |
2010-03-09 |
2023-08-12 |
mouse |
| Merce Márquez, Lola Pérez, Anna Serafín, Susana Teijeira, Carmen Navarro, Martí Pumarol. Characterisation of Lafora-like bodies and other polyglucosan bodies in two aged dogs with neurological disease. Veterinary journal (London, England : 1997). vol 183. issue 2. 2010-03-03. PMID:19010069. |
in this study, two aged dogs that presented with progressive tremors, ataxia and paraplegia had abundant pgbs throughout the brain, mainly in the hypothalamus and molecular layer of the cerebellum. |
2010-03-03 |
2023-08-12 |
Not clear |
| Edith V Sullivan, Jessica Rose, Adolf Pfefferbau. Physiological and focal cerebellar substrates of abnormal postural sway and tremor in alcoholic women. Biological psychiatry. vol 67. issue 1. 2010-02-25. PMID:19782966. |
whether alcoholic women, whose ataxia can persist with prolonged sobriety, exhibit the same physiological signature of balance instability and relation to cerebellar vermian volume as alcoholic men or can benefit from stabilizing factors is unknown. |
2010-02-25 |
2023-08-12 |
Not clear |
| James K Grant, Natalie C Yin, Annette M Zaytoun, Hena Waseem, Jacqueline A Hobb. Persistent adeno-associated virus 2 and parvovirus B19 sequences in post-mortem human cerebellum. Cerebellum (London, England). vol 8. issue 4. 2010-02-19. PMID:19585179. |
further studies will lead to insights into aav2- and/or b19-cblm interactions including mechanisms of infection, persistence, and possibly neuropathology, including cerebellar hypoplasia and ataxia. |
2010-02-19 |
2023-08-12 |
human |