1                                              Paramyotonia congenita (PC) is a human hereditary diseas

2                                              Paramyotonia congenita (PC) is a human hereditary disord

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

8                                              Paramyotonia congenita is a temperature-sensitive skelet

9  a new genetic mutation in a family with the paramyotonia congenita phenotype.

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

12            Hyperkalaemic periodic paralysis, 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

16 like discharges may be seen in patients with paramyotonia congenita.

17 activation, might be a contributing cause of paramyotonia congenita.

18 d sodium channel deactivation contributes to paramyotonia congenita.

19  including the human cold-sensitive disorder paramyotonia congenita.