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K Ricker

Showing results (71-80 of 101) with videos related to

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Journal of Neurology|January 1, 1981
Serum myoglobin in primary and secondary skeletal muscle disordersW R Kiessling, K Ricker, K W Pflughaupt, 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.
Neurology|June 1, 1981
Thyroid function and circulating antithyroid antibodies in myasthenia gravisW R Kiessling, K W Pflughaupt, 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.
Journal of Neurology|January 1, 1994
Stiff man syndrome: clinical and laboratory findings in eight patientsH M Meinck, K Ricker, P J Hülser, et al.
Muscle & Nerve|February 1, 1983
Two cases of adynamia episodica hereditaria: in vitro investigation of muscle cell membrane and contraction parametersF Lehmann-Horn, R Rüdel, K Ricker, et al.
Society of General Physiologists Series|January 1, 1995
In vivo sodium channel structure/function studies: consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4J Wang, V Dubowitz, F Lehmann-Horn, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenitaP A Iaizzo, C Franke, H Hatt, et al.
Neurology|October 1, 1994
A rippling muscle disease gene is localized to 1q41: evidence for multiple genesD A Stephan, N R Buist, A B Chittenden, et al.
Human Genetics|January 1, 1991
No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markersK Kausch, C R Müller, T Grimm, et al.
Pageof 11

Showing results (71-80 of 101) with videos related to

Sort By:
Pageof 11
Journal of Neurology|January 1, 1981
Serum myoglobin in primary and secondary skeletal muscle disordersW R Kiessling, K Ricker, K W Pflughaupt, 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.
Neurology|June 1, 1981
Thyroid function and circulating antithyroid antibodies in myasthenia gravisW R Kiessling, K W Pflughaupt, 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.
Journal of Neurology|January 1, 1994
Stiff man syndrome: clinical and laboratory findings in eight patientsH M Meinck, K Ricker, P J Hülser, et al.
Muscle & Nerve|February 1, 1983
Two cases of adynamia episodica hereditaria: in vitro investigation of muscle cell membrane and contraction parametersF Lehmann-Horn, R Rüdel, K Ricker, et al.
Society of General Physiologists Series|January 1, 1995
In vivo sodium channel structure/function studies: consecutive Arg1448 changes to Cys, His, and Pro at the extracellular surface of IVS4J Wang, V Dubowitz, F Lehmann-Horn, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenitaP A Iaizzo, C Franke, H Hatt, et al.
Neurology|October 1, 1994
A rippling muscle disease gene is localized to 1q41: evidence for multiple genesD A Stephan, N R Buist, A B Chittenden, et al.
Human Genetics|January 1, 1991
No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markersK Kausch, C R Müller, T Grimm, et al.
Pageof 11