EBE Becker, BL Fogel, S Rajakulendran, A Dulneva… - The Cerebellum, 2011 - Springer ... dysfunction exhibit cerebellarataxia [2, 8]. Collectively, these studies point to an important role of TRPC3 in the pathways leading to cerebellarataxia in mice and humans and suggest TRPC3 as a promising candidate gene for hereditary forms of human cerebellarataxia. ... Related articles - All 4 versions
M Pikkarainen, P Hartikainen, H Soininen… - The Cerebellum, 2011 - Springer ... ataxias (LOCA) were first described more than a decade ago [1, 2]. Harding proposed a classification of these disorders based on clinical and genetic data and introduced the term idiopathic late-onset cerebellarataxia (ILOCA) to denote non-hereditary adult onset ataxias [3, ... Related articles - All 2 versions
J Sato, S Sasaki, N Yamada… - Veterinary Pathology …, 2011 - vet.sagepub.com ... Synaptic neurochemical alteration associated with neuronal degeneration in an inherited cerebellarataxia of Gordon setters. J Neuropathol Exp Neurol. 1984;43:580-591. 12. Montgomery DL, Storts RW. Hereditary striatonigral and cerebello-olivary degeneration of the Kerry ... Related articles - All 2 versions
G Urkasemsin, KE Linder, JS Bell… - Veterinary Pathology …, 2011 - vet.sagepub.com ...Hereditarycerebellar degeneration is a common neurodegene- rative disorder that affects a broad ... in several dog breeds.9 Generally, affected dogs show cerebellar signs characterized by nystagmus, a base-wide stance, hypermetric gait, ataxia, and intention ...
[HTML] from translational-medicine.comWZ Yang, Y Zhang, F Wu… - Journal of …, 2011 - translational-medicine.com ... a subset of subjects. These data suggest a potential treatment using CBMC transplantation for hereditaryataxia and possibly other neurodegenerative conditions involving the spinal cord or cerebellum. Based on the current ... Related articles - Cached - All 4 versions
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