K Jurkat-Rott

A calcium channel mutation causing hypokalemic periodic paralysis

K Jurkat-Rott, Frank Lehmann‐Horn, Alexis Elbaz et al. · Human Molecular Genetics · 1994 · 314 citations

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31–32 in three European families

B. Fontaine, J. Vale-Santos, K Jurkat-Rott et al. · Nature Genetics · 1994 · 234 citations

Health Sciences, Cytogenetics, European Families +8

Familial cramp due to potassium-aggravated myotonia

Richard W. Orrell, K Jurkat-Rott, F. Lehmann‐Horn et al. · Journal of Neurology Neurosurgery & Psychiatry · 1998 · 35 citations · Full text

Electrolyte Disorder, Muscle Function, Periodic Paralysis +17

Altered calcium currents in human hypokalemic periodic paralysis myotubes expressing mutant L-type calcium channels.

F. Lehmann‐Horn, I. Sipos, K Jurkat-Rott et al. · PubMed · 1995 · 19 citations

Muscle Function, Genetics, Cellular Physiology +24