All Relations between cerebellum and Ataxia

Publication Sentence Publish Date Extraction Date Species
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
Mustafa Akcakus, Tamer Gunes, Sefer Kumandas, Selim Kurtoglu, Abdulhakim Cosku. Joubert syndrome: Report of a neonatal case. Paediatrics & child health. vol 8. issue 8. 2011-07-14. PMID:20019935. it is a syndrome with a variable phenotype: partial or complete absence of the cerebellar vermis is seen in all patients, while other cardinal findings include episodic tachypnea and apnea in the neonatal period, jerky eye movements, hypotonia, severe mental handicap, developmental delay, ataxia and impaired equilibrium. 2011-07-14 2023-08-12 Not clear
Sanjeev Rajakulendran, Stephanie Schorge, Dimitri M Kullmann, Michael G Hann. Dysfunction of the Ca(V)2.1 calcium channel in cerebellar ataxias. F1000 biology reports. vol 2. 2011-07-14. PMID:20948794. dysfunction of the ca(v)2.1 calcium channel in cerebellar ataxias. 2011-07-14 2023-08-12 human
Michael Gliem, Dimitris Panayotopoulos, Peter Feindt, Sebastian Heikaus, Markus C Fleisch, Rüdiger J Seit. Cerebellar degeneration as presenting symptom of recurrent endometrial stromal sarcoma with sex-cord elements. Case reports in neurology. vol 3. issue 1. 2011-07-14. PMID:21490714. we report a 66-year-old woman with slowly progressive ataxia due to cerebellar atrophy. 2011-07-14 2023-08-12 Not clear
Elizabeth M McNeill, Mariana Klöckner-Bormann, Elizabeth C Roesler, Lynn E Talton, Dieder Moechars, Margaret Clagett-Dam. Nav2 hypomorphic mutant mice are ataxic and exhibit abnormalities in cerebellar development. Developmental biology. vol 353. issue 2. 2011-07-01. PMID:21419114. herein we show that hypomorphic mutant mice lacking the full-length nav2 transcript exhibit ataxia and defects in cerebellar development. 2011-07-01 2023-08-12 mouse
D Marmolino, M Mant. Past, present and future therapeutics for cerebellar ataxias. Current neuropharmacology. vol 8. issue 1. 2011-06-14. PMID:20808545. past, present and future therapeutics for cerebellar ataxias. 2011-06-14 2023-08-12 Not clear
D Marmolino, M Mant. Past, present and future therapeutics for cerebellar ataxias. Current neuropharmacology. vol 8. issue 1. 2011-06-14. PMID:20808545. cerebellar ataxias are a group of disabling neurological disorders. 2011-06-14 2023-08-12 Not clear
D Marmolino, M Mant. Past, present and future therapeutics for cerebellar ataxias. Current neuropharmacology. vol 8. issue 1. 2011-06-14. PMID:20808545. cerebellar ataxias are heterogeneous both at the phenotypic and genotypic point of view. 2011-06-14 2023-08-12 Not clear
Taisuke Miyazaki, Masahiko Watanab. Development of an anatomical technique for visualizing the mode of climbing fiber innervation in Purkinje cells and its application to mutant mice lacking GluRδ2 and Ca(v)2.1. Anatomical science international. vol 86. issue 1. 2011-06-07. PMID:21153457. since then, we have applied this method to various kinds of gene-manipulated mice manifesting ataxia and other cerebellar phenotypes. 2011-06-07 2023-08-12 mouse
Hamed Akhlaghi, Louise Corben, Nellie Georgiou-Karistianis, John Bradshaw, Elsdon Storey, Martin B Delatycki, Gary F Ega. Superior cerebellar peduncle atrophy in Friedreich's ataxia correlates with disease symptoms. Cerebellum (London, England). vol 10. issue 1. 2011-05-27. PMID:21107777. superior cerebellar peduncle atrophy in friedreich's ataxia correlates with disease symptoms. 2011-05-27 2023-08-12 Not clear
Kazunori Nanri, Makoto Shibuya, Takeshi Taguchi, Akira Hasegawa, Nobuyuki Tanak. Selective loss of Purkinje cells in a patient with anti-gliadin-antibody-positive autoimmune cerebellar ataxia. Diagnostic pathology. vol 6. 2011-05-19. PMID:21294863. from these findings, we diagnosed this case as autoimmune cerebellar atrophy associated with gluten ataxia. 2011-05-19 2023-08-12 Not clear