Titlebook: Neuroacanthocytosis Syndromes II; Ruth H. Walker,Shinji Saiki,Adrian Danek Book 2008 Springer-Verlag Berlin Heidelberg 2008 Neurorehabilit

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An Update on the Hardie Neuroacanthocytosis Series rare disorder. During the past 15 years, there have been many advances in our understanding of the neuroacanthocytosis syndrome, including the identification of several different molecular causes. We have revisited the original Queen Square series in an attempt to correlate the clinical picture and

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Huntington’s Disease-Like 2ike HD, HDL2 is characterized by mid-life onset, abnormalities of voluntary and involuntary movement, psychiatric syndromes, and dementia, with a relentless progress to death. The disease is rare, and thus far has only been detected in individuals of African ancestry. Striatal and cortical atrophy i

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The Function of Choreinas three other members: VPS13B, VPS13C and VPS13D. These proteins are similar to Vps13p, a yeast protein shown to be involved in intra-cellular trafficking of a number of transmembrane proteins. Chorein and its homologous human proteins lack domains or motifs of known function. This, together with t

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Questions of Cell Shapeis knowledge to the possible pathophysiology underlying the neuroacanthocytosis syndromes. Curvature of animal cell membranes can be induced by a series of different mechanisms: by insertion or deletion of phospholipid from inner or outer leaflet; by contraction or expansion of the underlying cytosk

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