| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| M Anhei. [Autosomal recessive cerebellar ataxias]. Revue neurologique. vol 167. issue 5. 2011-11-03. PMID:21087783. |
autosomal recessive cerebellar ataxias (arca) are heterogeneous and complex inherited neurodegenerative diseases that may affect the cerebellum and/or the spinocerebellar tract, the posterior column of the spinal cord and the peripheral nerves. |
2011-11-03 |
2023-08-12 |
Not clear |
| Carlo Colosim. Nonmotor presentations of multiple system atrophy. Nature reviews. Neurology. vol 7. issue 5. 2011-09-26. PMID:21343894. |
multiple system atrophy (msa) is a neurodegenerative disease characterized clinically by a combination of parkinsonian, cerebellar, autonomic and pyramidal features. |
2011-09-26 |
2023-08-12 |
Not clear |
| Andrew King, Satomi Maekawa, Istvan Bodi, Claire Troakes, Safa Al-Sarra. Ubiquitinated, p62 immunopositive cerebellar cortical neuronal inclusions are evident across the spectrum of TDP-43 proteinopathies but are only rarely additionally immunopositive for phosphorylation-dependent TDP-43. Neuropathology : official journal of the Japanese Society of Neuropathology. vol 31. issue 3. 2011-09-22. PMID:21118398. |
we examined p62 immunohistochemistry on cerebellar sections from 43 tdp-43 proteinopathies (including cases of ftld-tdp, ftld-mnd/als and mnd/als) together with 72 cases of other neurodegenerative diseases, seven controls and three other disease conditions. |
2011-09-22 |
2023-08-12 |
Not clear |
| Sachin Patil, Deebika Balu, Joseph Melrose, Christina Cha. Brain region-specificity of palmitic acid-induced abnormalities associated with Alzheimer's disease. BMC research notes. vol 1. 2011-07-14. PMID:18710535. |
alzheimer's disease (ad) is a progressive, neurodegenerative disease mostly affecting the basal forebrain, cortex and hippocampus whereas the cerebellum is relatively spared. |
2011-07-14 |
2023-08-12 |
Not clear |
| Yangho Kim, Kyoung Sook Jeong, Yong-Hun Yun, Myoung-Soon O. Occupational neurologic disorders in Korea. Journal of clinical neurology (Seoul, Korea). vol 6. issue 2. 2011-07-14. PMID:20607045. |
vascular encephalopathy, parkinsonism, chronic toxic encephalopathy, cerebellar dysfunction, peripheral neuropathy, and neurodegenerative diseases are common presentations of occupational neurotoxic syndromes in korea. |
2011-07-14 |
2023-08-12 |
Not clear |
| Slaven Erceg, Mohammad Ronaghi, Ivan Zipancic, Sergio Lainez, Mireia Gárcia Roselló, Chen Xiong, Victoria Moreno-Manzano, Fernando Javier Rodríguez-Jiménez, Rosa Planells, Manuel Alvarez-Dolado, Shom Shanker Bhattacharya, Miodrag Stojkovi. Efficient differentiation of human embryonic stem cells into functional cerebellar-like cells. Stem cells and development. vol 19. issue 11. 2011-04-11. PMID:20521974. |
our findings demonstrate that the universal mechanisms involved in the development of cerebellum can be efficiently recapitulated in vitro, which enables the design of new strategies for cell replacement therapy, to study early human development and pathogenesis of neurodegenerative diseases. |
2011-04-11 |
2023-08-12 |
mouse |
| Martina Minnerop, Eileen Lüders, Karsten Specht, Jürgen Ruhlmann, Nicole Schimke, Paul M Thompson, Yi Y Chou, Arthur W Toga, Michael Abele, Ullrich Wüllner, Thomas Klockgethe. Callosal tissue loss in multiple system atrophy--a one-year follow-up study. Movement disorders : official journal of the Movement Disorder Society. vol 25. issue 15. 2011-02-25. PMID:20623690. |
multiple system atrophy (msa) is a neurodegenerative disease not only affecting the basal ganglia, brainstem, cerebellum, and intermediolateral cell columns of the spinal cord but also the cerebral cortex. |
2011-02-25 |
2023-08-12 |
Not clear |
| Ron Levy, Andres M Lozano, Anthony E Lang, Jonathan O Dostrovsk. Event-related desynchronization of motor cortical oscillations in patients with multiple system atrophy. Experimental brain research. vol 206. issue 1. 2010-12-28. PMID:20821197. |
multiple system atrophy (msa) is a progressive neurodegenerative disease characterized by parkinsonism (msa-p), cerebellar and autonomic deficits. |
2010-12-28 |
2023-08-12 |
human |
| Antoni Matilla-Dueñas, Ivelisse Sánchez, Marc Corral-Juan, Antoni Dávalos, Ramiro Alvarez, Pilar Latorr. Cellular and molecular pathways triggering neurodegeneration in the spinocerebellar ataxias. Cerebellum (London, England). vol 9. issue 2. 2010-08-12. PMID:19890685. |
the autosomal dominant spinocerebellar ataxias (scas) are a group of progressive neurodegenerative diseases characterised by loss of balance and motor coordination due to the primary dysfunction of the cerebellum. |
2010-08-12 |
2023-08-12 |
Not clear |
| Ryan A Thames, Ian D Robertson, Thomas Flegel, Diana Henke, Dennis P O'Brien, Joan R Coates, Natasha J Olb. Development of a morphometric magnetic resonance image parameter suitable for distinguishing between normal dogs and dogs with cerebellar atrophy. Veterinary radiology & ultrasound : the official journal of the American College of Veterinary Radiology and the International Veterinary Radiology Association. vol 51. issue 3. 2010-06-08. PMID:20469545. |
neurodegenerative diseases affect the cerebellum of numerous dog breeds. |
2010-06-08 |
2023-08-12 |
dog |
| Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, Massimo Plumari, Giorgio Battaglia, Annalisa Pastore, Adele Finardi, Claudia Cagnoli, Filippo Tempia, Marina Frontali, Liana Veneziano, Tiziana Sacco, Enrica Boda, Alessandro Brussino, Florian Bonn, Barbara Castellotti, Silvia Baratta, Caterina Mariotti, Cinzia Gellera, Valentina Fracasso, Stefania Magri, Thomas Langer, Paolo Plevani, Stefano Di Donato, Marco Muzi-Falconi, Franco Taron. Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. Nature genetics. vol 42. issue 4. 2010-04-16. PMID:20208537. |
this work identifies afg3l2 as a novel cause of dominant neurodegenerative disease and indicates a previously unknown role for this component of the mitochondrial protein quality control machinery in protecting the human cerebellum against neurodegeneration. |
2010-04-16 |
2023-08-12 |
human |
| Hristelina Ilieva, Magdalini Polymenidou, Don W Clevelan. Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond. The Journal of cell biology. vol 187. issue 6. 2010-01-15. PMID:19951898. |
damage to a specific set of key partner cells as well as to vulnerable neurons may account for the selective susceptibility of neuronal subtypes in many human neurodegenerative diseases, including huntington's disease (hd), parkinson's disease (pd), prion disease, the spinal cerebellar ataxias (scas), and alzheimer's disease (ad). |
2010-01-15 |
2023-08-12 |
human |
| Kerri M Carlson, J Michael Andresen, Harry T Or. Emerging pathogenic pathways in the spinocerebellar ataxias. Current opinion in genetics & development. vol 19. issue 3. 2009-09-25. PMID:19345087. |
understanding how these genes cause disease will allow a deeper understanding of the cerebellum in particular as well as neurodegenerative disease in general. |
2009-09-25 |
2023-08-12 |
Not clear |
| Tatsuya Yamamoto, Ryuji Sakakibara, Tomoyuki Uchiyama, Zhi Liu, Takashi Ito, Yusuke Awa, Tomonori Yamanishi, Takamichi Hattor. Questionnaire-based assessment of pelvic organ dysfunction in multiple system atrophy. Movement disorders : official journal of the Movement Disorder Society. vol 24. issue 7. 2009-08-19. PMID:19243063. |
multiple system atrophy (msa) is a neurodegenerative disease characterized clinically by any combination of autonomic, cerebellar, and extrapyramidal symptoms. |
2009-08-19 |
2023-08-12 |
Not clear |
| Michael S Salman, Sandra L Marles, Frances A Booth, Marc R Del Bigi. Early-onset neurodegenerative disease of the cerebellum and motor axons. Pediatric neurology. vol 40. issue 5. 2009-08-17. PMID:19380073. |
early-onset neurodegenerative disease of the cerebellum and motor axons. |
2009-08-17 |
2023-08-12 |
Not clear |
| Michael S Salman, Sandra L Marles, Frances A Booth, Marc R Del Bigi. Early-onset neurodegenerative disease of the cerebellum and motor axons. Pediatric neurology. vol 40. issue 5. 2009-08-17. PMID:19380073. |
this clinical entity likely represents a novel neurodegenerative disease of the cerebellum and long motor axons. |
2009-08-17 |
2023-08-12 |
Not clear |
| Ryuji Sakakibara, Tomoyuki Uchiyama, Tomonori Yamanishi, Masahiko Kish. Sphincter EMG as a diagnostic tool in autonomic disorders. Clinical autonomic research : official journal of the Clinical Autonomic Research Society. vol 19. issue 1. 2009-04-30. PMID:18780143. |
multiple system atrophy (msa) is a neurodegenerative disease presenting with a combination of parkinsonian, cerebellar, and autonomic (including cardiovascular, urinary, and anorectal) dysfunction. |
2009-04-30 |
2023-08-12 |
Not clear |
| Kazuhiro Shiba, Takashi Torashima, Hirokazu Hirai, Kazuma Ogawa, Nasima Akhter, Kenichi Nakajima, Seigo Kinuya, Hirofumi Mor. Potential usefulness of D2R reporter gene imaging by IBF as gene therapy monitoring for cerebellar neurodegenerative diseases. Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism. vol 29. issue 2. 2009-02-23. PMID:19002197. |
potential usefulness of d2r reporter gene imaging by ibf as gene therapy monitoring for cerebellar neurodegenerative diseases. |
2009-02-23 |
2023-08-12 |
mouse |
| Daniel Gardner, David H Goldberg, Bernice Grafstein, Adrian Robert, Esther P Gardne. Terminology for neuroscience data discovery: multi-tree syntax and investigator-derived semantics. Neuroinformatics. vol 6. issue 3. 2009-02-19. PMID:18958630. |
semantics enabling nif data discovery were selected at one or more workshops by investigators expert in particular systems (vision, olfaction, behavioral neuroscience, neurodevelopment), brain areas (cerebellum, thalamus, hippocampus), preparations (molluscs, fly), diseases (neurodegenerative disease), or techniques (microscopy, computation and modeling, neurogenetics). |
2009-02-19 |
2023-08-12 |
human |
| Matthew J Trifilo, Manuel Sanchez-Alavez, Laura Solforosi, Joie Bernard-Trifilo, Stefan Kunz, Dorian McGavern, Michael B A Oldston. Scrapie-induced defects in learning and memory of transgenic mice expressing anchorless prion protein are associated with alterations in the gamma aminobutyric acid-ergic pathway. Journal of virology. vol 82. issue 20. 2008-10-14. PMID:18667494. |
we report here that infected gpi(-/-) prp tg mice, although free from progressive neurodegenerative disease of the cerebellum and extrapyramidal and pyramidal systems, nevertheless suffer defects in learning and memory, long-term potentiation, and neuronal excitability. |
2008-10-14 |
2023-08-12 |
mouse |