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Results 1 - 8 of 8 for Familial periodic paralysis
  1. ... An expanding view for the molecular basis of familial periodic paralysis. Neuromuscul Disord. 2002 Aug;12(6):533-43. ... Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic ... muscle weakness: the familial periodic paralyses. J Neurol. 2006 Nov;253(11): ...
  2. ... An expanding view for the molecular basis of familial periodic paralysis. Neuromuscul Disord. 2002 Aug;12(6):533-43. ... K, Lehmann-Horn F. Paroxysmal muscle weakness: the familial periodic paralyses. J ... paralysis: understanding channelopathies. Curr Neurol Neurosci Rep. 2002 Jan; ...
  3. ... J. Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family. J Mol Med (Berl). 2005 Mar;83(3):203-8. doi: 10.1007/s00109-005-0638-4. Epub 2005 Feb 22. Citation on PubMed or Free ... F. Hypokalemic Periodic Paralysis. 2002 Apr 30 [updated 2018 Jul 26]. In: ...
  4. ... different even among affected members of the same family. About 60 percent of affected individuals have all three major features (periodic paralysis, cardiac arrhythmia, and physical abnormalities). Andersen-Tawil syndrome ...
  5. ... books/NBK1338/ Citation on PubMed Weber F. Hyperkalemic Periodic Paralysis. 2003 Jul 18 ... Citation on PubMed
  6. ... a disorder characterized by episodes of muscle weakness (periodic paralysis), changes in heart rhythm (arrhythmia), and physical abnormalities ... potassium ions out of these cells, resulting in periodic paralysis and an irregular heart rhythm. It is not ...
  7. ... component of several other genetic syndromes, including hypokalemic periodic paralysis (a condition that causes episodes of extreme muscle ...
  8. ... in the ears (tinnitus). Seizures, muscle weakness, and paralysis that affect one side of the body (hemiplegia) ... JM, Yamaoka LH, Vance JM, Pericak-Vance MA. Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective ...