Frank Horn-Lehmann

Oberduerrbacher Str. 6
Wuerzburg, BY 97080, Germany

Last Updated: 09/26/2026

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Found 43 publications

Kir2.2 p.Thr140Met: a genetic susceptibility to sporadic periodic paralysis.

Myotonia permanens with Nav1.4-G1306E displays varied phenotypes during course of life.

23Na MRI and myometry to compare eplerenone vs. glucocorticoid treatment in Duchenne dystrophy.

Successful treatment of periodic paralysis with coenzyme Q10: two case reports.

Eplerenone repolarizes muscle membrane through Na,K-ATPase activation by Tyr10 dephosphorylation.

Showing 1-12 of 43

Last Updated: 09/26/2026