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3 peripheral neuronal sodium channel Nav1.7, a paramyotonia congenita (PMC) mutation in the human skele
4 mutations found in patients with hereditary paramyotonia congenita (T1313M on the III-IV linker and
5 nvolvement in other muscle disorders such as paramyotonia congenita and hyperkalemic periodic paralys
6 II decrements of >20% were 100% specific for paramyotonia congenita and myotonia congenita, respectiv
7 function could well explain the onset of the paramyotonia congenita in this family and emphasize the
10 ndings have implications for drug therapy of paramyotonia congenita, and also provide an insight into
11 g hyperkalemic periodic paralysis (HyperPP), paramyotonia congenita, and potassium-aggravated myotoni
13 milies with hyperkalemic periodic paralysis, paramyotonia congenita, and the potassium-aggravated myo
14 thmias but is also found to be effective for paramyotonia congenita, potassium-aggravated myotonia, l
15 utation exhibited symptoms characteristic of paramyotonia congenita--a condition usually thought to b
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