Long-standing "stiff-man" syndrome: a particular form of disseminated inflammatory CNS disease?

Por Meinck, H M, Ricker, K
Publicado em 1987

The stiff-man syndrome: new pathophysiological aspects from abnormal exteroceptive reflexes and the response to clomipramine, clonidine, and tizanidine.

Por Meinck, H M, Ricker, K, Conrad, B
Publicado em 1984

Hereditary neuromyotonia: a mouse model associated with deficiency or increased gene dosage of the PMP22 gene

Por TOYKA, K., ZIELASEK, J., RICKER, K., ADLKOFER, K., SUTER, U.
Publicado em 1997

Successuful treatment of paramyotonia congenita (Eulenburg): muscle stiffness and weakness prevented by tocainide.

Por Ricker, K, Haass, A, Rüdel, R, Böhlen, R, Mertens, H G
Publicado em 1980

Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotonia.

Por Meyer-Kleine, C, Steinmeyer, K, Ricker, K, Jentsch, T J, Koch, M C
Publicado em 1995

Evidence for genetic homogeneity in autosomal recessive generalised myotonia (Becker).

Por Koch, M C, Ricker, K, Otto, M, Wolf, F, Zoll, B, Lorenz, C, Steinmeyer, K, Jentsch, T J
Publicado em 1993

Pertussis toxin-sensitive G proteins influence nitric oxide synthase III activity and protein levels in rat heart.

Por Hare, J M, Kim, B, Flavahan, N A, Ricker, K M, Peng, X, Colman, L, Weiss, R G, Kass, D A
Publicado em 1998

Confirmation of linkage of hyperkalaemic periodic paralysis to chromosome 17.

Por Koch, M C, Ricker, K, Otto, M, Grimm, T, Hoffman, E P, Rüdel, R, Bender, K, Zoll, B, Harper, P S, Lehmann-Horn, F
Publicado em 1991

Molecular genetic and genetic correlations in sodium channelopathies: Lack of founder effect and evidence for a second gene

Por Wang, J., Zhou, J., Todorovic, S. M., Feero, W. G., Barany, F., Conwit, R., Hausmanowa-Petrusewicz, I., Fidzianska, A., Arahata, K., Wessel, H. B., Sillen, A., Marks, H. G., Hartlage, P., Galloway, G., Ricker, K., Lehmann-Horn, F., Hayakawa, H., Hoffman, E. P.
Publicado em 1993