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Archives of Neurology
|
November 1, 1994
Myotonia fluctuans. A third type of muscle sodium channel disease
K Ricker, R T Moxley, R Heine, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 1, 1980
Successuful treatment of paramyotonia congenita (Eulenburg): muscle stiffness and weakness prevented by tocainide
K Ricker, A Haass, R Rüdel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 7, 1998
Hereditary neuromyotonia: a mouse model associated with deficiency or increased gene dosage of the PMP22 gene
K V Toyka, J Zielasek, K Ricker, et al.
Muscle & Nerve
|
September 1, 1985
In vivo P-NMR spectroscopy: muscle energy exchange in paramyotonia patients
F Lehmann-Horn, D Höpfel, R Rüdel, et al.
Muscle & Nerve
|
November 1, 1989
Adynamia episodica hereditaria: what causes the weakness?
K Ricker, L M Camacho, P Grafe, et al.
Archives of Neurology
|
September 1, 1986
Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration
H Reichmann, R Rohkamm, M Zeviani, et al.
Journal of Neurology
|
February 1, 1990
Borrelia burgdorferi myelitis presenting as a partial stiff man syndrome
R Martin, H M Meinck, W Schulte-Mattler, et al.
Muscle & Nerve
|
May 1, 1987
Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH
F Lehmann-Horn, G Küther, K Ricker, et al.
Endokrinologie
|
October 1, 1981
[T3, T4, TSH and circulating antithyroglobulin antibodies in myasthenia gravis]
W R Kiessling, K W Pflughaupt, I Haubitz, et al.
Muscle & Nerve
|
September 1, 1981
Membrane defects in paramyotonia congenita with and without myotonia in a warm environment
F Lehmann-Horn, R Rüdel, R Dengler, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 101) with videos related to
Sort By:
Page
of 11
Archives of Neurology
|
November 1, 1994
Myotonia fluctuans. A third type of muscle sodium channel disease
K Ricker, R T Moxley, R Heine, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 1, 1980
Successuful treatment of paramyotonia congenita (Eulenburg): muscle stiffness and weakness prevented by tocainide
K Ricker, A Haass, R Rüdel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 7, 1998
Hereditary neuromyotonia: a mouse model associated with deficiency or increased gene dosage of the PMP22 gene
K V Toyka, J Zielasek, K Ricker, et al.
Muscle & Nerve
|
September 1, 1985
In vivo P-NMR spectroscopy: muscle energy exchange in paramyotonia patients
F Lehmann-Horn, D Höpfel, R Rüdel, et al.
Muscle & Nerve
|
November 1, 1989
Adynamia episodica hereditaria: what causes the weakness?
K Ricker, L M Camacho, P Grafe, et al.
Archives of Neurology
|
September 1, 1986
Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration
H Reichmann, R Rohkamm, M Zeviani, et al.
Journal of Neurology
|
February 1, 1990
Borrelia burgdorferi myelitis presenting as a partial stiff man syndrome
R Martin, H M Meinck, W Schulte-Mattler, et al.
Muscle & Nerve
|
May 1, 1987
Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH
F Lehmann-Horn, G Küther, K Ricker, et al.
Endokrinologie
|
October 1, 1981
[T3, T4, TSH and circulating antithyroglobulin antibodies in myasthenia gravis]
W R Kiessling, K W Pflughaupt, I Haubitz, et al.
Muscle & Nerve
|
September 1, 1981
Membrane defects in paramyotonia congenita with and without myotonia in a warm environment
F Lehmann-Horn, R Rüdel, R Dengler, et al.
Page
of 11