| 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]. |
2011-11-03 |
2023-08-12 |
Not clear |
| 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 |
| C Marelli, C Cazeneuve, A Brice, G Stevanin, A Dür. Autosomal dominant cerebellar ataxias. Revue neurologique. vol 167. issue 5. 2011-11-03. PMID:21546047. |
autosomal dominant cerebellar ataxias. |
2011-11-03 |
2023-08-12 |
Not clear |
| C Marelli, C Cazeneuve, A Brice, G Stevanin, A Dür. Autosomal dominant cerebellar ataxias. Revue neurologique. vol 167. issue 5. 2011-11-03. PMID:21546047. |
cerebellar ataxias with autosomal dominant transmission (adca) are far rarer than sporadic cases of cerebellar ataxia. |
2011-11-03 |
2023-08-12 |
Not clear |
| Yosr Bouhlal, Rim Amouri, Ghada El Euch-Fayeche, Fayçal Hentat. Autosomal recessive spastic ataxia of Charlevoix-Saguenay: an overview. Parkinsonism & related disorders. vol 17. issue 6. 2011-10-24. PMID:21450511. |
autosomal recessive spastic ataxia of charlevoix-saguenay (arsacs) is a distinct form of hereditary early-onset spastic ataxia related to progressive degeneration of the cerebellum and spinal cord. |
2011-10-24 |
2023-08-12 |
Not clear |
| Ginevra Zanni, Enrico S Bertin. X-linked disorders with cerebellar dysgenesis. Orphanet journal of rare diseases. vol 6. 2011-10-18. PMID:21569638. |
the neurological features of xlcd include hypotonia, developmental delay, intellectual disability, ataxia and/or other cerebellar signs. |
2011-10-18 |
2023-08-12 |
Not clear |
| Nathaniel Robb Whaley, Shinsuke Fujioka, Zbigniew K Wszole. Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics. Orphanet journal of rare diseases. vol 6. 2011-10-18. PMID:21619691. |
gait, truncal, and limb ataxia are often the most obvious cerebellar findings though nystagmus, saccadic abnormalities, and dysarthria are usually associated. |
2011-10-18 |
2023-08-12 |
Not clear |
| Slaven Erceg, Victoria Moreno-Manzano, Marcela Garita-Hernandez, Miodrag Stojkovic, Shomi S Bhattachary. Concise review: stem cells for the treatment of cerebellar-related disorders. Stem cells (Dayton, Ohio). vol 29. issue 4. 2011-10-13. PMID:21319272. |
the recent advances in the field of hesc and ips cells, including their capacity for differentiation toward regional specific neural lineages, could open a new era of transplantation in cell-based therapy for cerebellar ataxias. |
2011-10-13 |
2023-08-12 |
human |
| Hiroshi Doi, Kunihiro Yoshida, Takao Yasuda, Mitsunori Fukuda, Yoko Fukuda, Hiroshi Morita, Shu-ichi Ikeda, Rumiko Kato, Yoshinori Tsurusaki, Noriko Miyake, Hirotomo Saitsu, Haruya Sakai, Satoko Miyatake, Masaaki Shiina, Nobuyuki Nukina, Shigeru Koyano, Shoji Tsuji, Yoshiyuki Kuroiwa, Naomichi Matsumot. Exome sequencing reveals a homozygous SYT14 mutation in adult-onset, autosomal-recessive spinocerebellar ataxia with psychomotor retardation. American journal of human genetics. vol 89. issue 2. 2011-10-10. PMID:21835308. |
autosomal-recessive cerebellar ataxias (arcas) are clinically and genetically heterogeneous disorders associated with diverse neurological and nonneurological features that occur before the age of 20. |
2011-10-10 |
2023-08-12 |
mouse |
| John F Anderson, Efrain Siller, José M Barra. The neurodegenerative-disease-related protein sacsin is a molecular chaperone. Journal of molecular biology. vol 411. issue 4. 2011-10-06. PMID:21726565. |
in this study, we assign a novel molecular chaperone activity to the protein sacsin responsible for autosomal recessive spastic ataxia of charlevoix-saguenay, a degenerative disorder of the cerebellum and spinal cord. |
2011-10-06 |
2023-08-12 |
human |
| Ruxandra Bachmann-Gagescu, Fukie Marie Hisama, Amy Lawson Yue. Myhre syndrome with ataxia and cerebellar atrophy. Clinical dysmorphology. vol 20. issue 3. 2011-09-29. PMID:21490502. |
myhre syndrome with ataxia and cerebellar atrophy. |
2011-09-29 |
2023-08-12 |
Not clear |
| Masatoshi Wakatsuki, Kiyoshi Matsuo, Hiroe Kayatani, Keiichi Fujiwara, Toshiro Yonei, Toshio Sat. [A case of small cell lung cancer that presented with paraneoplastic syndrome]. Nihon Kokyuki Gakkai zasshi = the journal of the Japanese Respiratory Society. vol 49. issue 7. 2011-09-27. PMID:21842689. |
as he also showed ataxia of the left lower extremity, we also diagnosed paraneoplastic cerebellar degeneration. |
2011-09-27 |
2023-08-12 |
Not clear |
| Kwan Young Lee, Jin Seong Kim, Se Hoon Kim, Hyung Seo Park, Young-Gil Jeong, Nam-Seob Lee, Dong Kwan Ki. Altered Purkinje cell responses and calmodulin expression in the spontaneously ataxic mouse, Pogo. The European journal of neuroscience. vol 33. issue 8. 2011-09-16. PMID:21410792. |
ataxia is often associated with altered cerebellar motor control, a process in which purkinje cells (pcs) play a principal role. |
2011-09-16 |
2023-08-12 |
mouse |
| C Zühlke, F Kreuz, K Bür. [Clinical details and genetics of recessive ataxias]. Der Nervenarzt. vol 82. issue 4. 2011-09-02. PMID:20640395. |
autosomal recessive cerebellar ataxias (arca) are a heterogeneous group of rare neurological diseases affecting both the central and the peripheral nervous systems. |
2011-09-02 |
2023-08-12 |
Not clear |
| C Zühlke, F Kreuz, K Bür. [Clinical details and genetics of recessive ataxias]. Der Nervenarzt. vol 82. issue 4. 2011-09-02. PMID:20640395. |
they are characterized by autosomal recessive inheritance, progressive ataxia and degeneration of the cerebellum and spinal cord. |
2011-09-02 |
2023-08-12 |
Not clear |
| Kyoji Tsuda, Eiichi Ishikawa, Atsushi Saito, Kaishi Satomi, Akiko Sakata, Shingo Takano, Yukio Morishita, Masayuki Noguchi, Akira Matsumur. Primary cerebellar pilocytic astrocytoma with anaplastic features in a patient with neurofibromatosis type 1 - case report - . Neurologia medico-chirurgica. vol 51. issue 4. 2011-08-30. PMID:21515958. |
a 70-year-old woman with neurofibromatosis type 1 (nf-1) presented with a primary cerebellar pilocytic astrocytoma (pa) with anaplastic features manifesting as worsening headache and ataxia. |
2011-08-30 |
2023-08-12 |
Not clear |
| Yosr Bouhlal, Douglas M Jennewein, Brent Anderson, Joe Reynoldson, Wiem Maamouri, Fayçal Hentati, Rim Amouri, Carol Lushboug. Computational analysis of a novel SACS gene mutation with BioExtract server. Journal of molecular neuroscience : MN. vol 44. issue 1. 2011-08-05. PMID:21416271. |
autosomal recessive spastic ataxia of charlevoix-saguenay is a distinct form of hereditary early-onset spastic ataxia caused by cerebellum and spinal cord degeneration. |
2011-08-05 |
2023-08-12 |
human |
| M Saeed Da. Sustained antagonism of acute ethanol-induced ataxia following microinfusion of cyclic AMP and cpt-cAMP in the mouse cerebellum. Pharmacology, biochemistry, and behavior. vol 98. issue 3. 2011-07-28. PMID:21192968. |
sustained antagonism of acute ethanol-induced ataxia following microinfusion of cyclic amp and cpt-camp in the mouse cerebellum. |
2011-07-28 |
2023-08-12 |
mouse |
| Lixiang Wang, Masatoshi Nomura, Yutaka Goto, Kimitaka Tanaka, Ryuichi Sakamoto, Ichiro Abe, Shohei Sakamoto, Atsushi Shibata, Patricio L M Enciso, Masahiro Adachi, Keizo Ohnaka, Hisaya Kawate, Ryoichi Takayanag. Smad2 protein disruption in the central nervous system leads to aberrant cerebellar development and early postnatal ataxia in mice. The Journal of biological chemistry. vol 286. issue 21. 2011-07-28. PMID:21464123. |
smad2 protein disruption in the central nervous system leads to aberrant cerebellar development and early postnatal ataxia in mice. |
2011-07-28 |
2023-08-12 |
mouse |
| Hyung Le. Neuro-otological aspects of cerebellar stroke syndrome. Journal of clinical neurology (Seoul, Korea). vol 5. issue 2. 2011-07-14. PMID:19587812. |
the low incidence of vertigo associated with infarction involving the superior cerebellar artery distribution may be a useful way of distinguishing it clinically from pica or aica cerebellar infarction in patients with acute vertigo and limb ataxia. |
2011-07-14 |
2023-08-12 |
Not clear |