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Acta Neurologica Scandinavica|October 1, 1980
Thyroid function in multiple sclerosisW R Kiessling, K W Pflughaupt, I Haubitz, et al.Deutsche Medizinische Wochenschrift (1946)|December 21, 1979
[Treatment of myasthenia gravis with plasmapheresis (author's transl)]P Reuther, D Wiebecke, G Hertel, et al.Muscle & Nerve|September 1, 1985
In vivo P-NMR spectroscopy: muscle energy exchange in paramyotonia patientsF Lehmann-Horn, D Höpfel, R Rüdel, et al.Journal of Neurology|March 1, 1992
Neurological long-term follow-up in left atrial myxoma: are late complications frequent or rare?H Reichmann, R Romberg-Hahnloser, E Hofmann, et al.Muscle & Nerve|November 1, 1989
Adynamia episodica hereditaria: what causes the weakness?K Ricker, L M Camacho, P Grafe, et al.Neurosurgery|November 1, 1992
Continuous-pressure controlled, external ventricular drainage for treatment of acute hydrocephalus--evaluation of risk factorsU Bogdahn, W Lau, W Hassel, et al.Muscle & Nerve|May 1, 1987
Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pHF Lehmann-Horn, G Küther, K Ricker, et al.Muscle & Nerve|September 1, 1981
Membrane defects in paramyotonia congenita with and without myotonia in a warm environmentF Lehmann-Horn, R Rüdel, R Dengler, et al.American Journal of Human Genetics|December 1, 1995
Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotoniaC Meyer-Kleine, K Steinmeyer, K Ricker, et al.Muscle & Nerve|August 1, 1991
Altered Na+ channel activity and reduced Cl- conductance cause hyperexcitability in recessive generalized myotonia (Becker)C Franke, P A Iaizzo, H Hatt, et al.Pageof 10