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1                                 Myotonia and paramyotonia congenita (PC) are rare neuromuscular disor
2                                              Paramyotonia congenita (PC) is a human hereditary diseas
3                                              Paramyotonia congenita (PC) is a human hereditary disord
4 peripheral neuronal sodium channel Nav1.7, a paramyotonia congenita (PMC) mutation in the human skele
5  mutations found in patients with hereditary paramyotonia congenita (T1313M on the III-IV linker and
6 nvolvement in other muscle disorders such as paramyotonia congenita and hyperkalemic periodic paralys
7 II decrements of >20% were 100% specific for paramyotonia congenita and myotonia congenita, respectiv
8 function could well explain the onset of the paramyotonia congenita in this family and emphasize the
9                                              Paramyotonia congenita is a temperature-sensitive skelet
10  a new genetic mutation in a family with the paramyotonia congenita phenotype.
11 ndings have implications for drug therapy of paramyotonia congenita, and also provide an insight into
12 g hyperkalemic periodic paralysis (HyperPP), paramyotonia congenita, and potassium-aggravated myotoni
13            Hyperkalaemic periodic paralysis, paramyotonia congenita, and potassium-aggravated myotoni
14 milies with hyperkalemic periodic paralysis, paramyotonia congenita, and the potassium-aggravated myo
15 thmias but is also found to be effective for paramyotonia congenita, potassium-aggravated myotonia, l
16 utation exhibited symptoms characteristic of paramyotonia congenita--a condition usually thought to b
17 like discharges may be seen in patients with paramyotonia congenita.
18 activation, might be a contributing cause of paramyotonia congenita.
19 d sodium channel deactivation contributes to paramyotonia congenita.
20  including the human cold-sensitive disorder paramyotonia congenita.