1. Jen, J. and Ptacek, L.J. (2001) Channelopathies. In Scriver, C.R., Beaudet, A.L., Sly, W.S. and Valle, D. (eds), Metabolic and Molecular Bases of Inherited Disease, 8th ed. McGraw-Hill, New York, pp. 5223–5238.
2. Lenz, R. and Ptacek, L.J. (2004) Channelopathies. In Bradley, W.G., Daroff, R.B., Fenichel, G. and Jankovic, J. (eds), Neurology in Clinical Practice, 4th ed. Butterworth-Heinemann, Philadelphia, pp. 1847–1866.
3. Ptacek, L.J. and Fu, Y.H. (2001) Channelopathies: episodic disorders of the nervous system. Epilepsia, 42, 35–43.
4. Fouad, G.T., Servidei, S., Durcan, S., Bertini, E. and Ptacek, L.J. (1996) A gene for familial paroxysmal dyskinesia (FPD1) maps to chromosome 2q. Am. J. Hum. Genet., 59, 135–139.
5. Bennett, L.B., Roach, E.S. and Bowcock, A.M. (2000) A locus for paroxysmal kinesigenic dyskinesia maps to human chromosome 16. Neurology, 54, 125-130.