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Items: 1 to 20 of 34

1.

THE AFTER-POTENTIAL THAT FOLLOWS TRAINS OF IMPULSES IN FROG MUSCLE FIBERS.

FREYGANG WH Jr, GOLDSTEIN DA, HELLAM DC.

J Gen Physiol. 1964 May;47:929-52.

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Two cases of adynamia episodica hereditaria: in vitro investigation of muscle cell membrane and contraction parameters.

Lehmann-Horn F, Rüdel R, Ricker K, Lorković H, Dengler R, Hopf HC.

Muscle Nerve. 1983 Feb;6(2):113-21.

PMID:
6304507
6.
7.

Membrane defects in paramyotonia congenita with and without myotonia in a warm environment.

Lehmann-Horn F, Rüdel R, Dengler R, Lorković H, Haass A, Ricker K.

Muscle Nerve. 1981 Sep-Oct;4(5):396-406.

PMID:
6270549
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11.

Radial spread of contraction in frog muscle fibres.

Adrian RH, Costantin LL, Peachey LD.

J Physiol. 1969 Sep;204(1):231-57.

12.

Reconstruction of the action potential of frog sartorius muscle.

Adrian RH, Peachey LD.

J Physiol. 1973 Nov;235(1):103-31.

14.

On the repetitive discharge in myotonic muscle fibres.

Adrian RH, Bryant SH.

J Physiol. 1974 Jul;240(2):505-15.

15.

Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH.

Lehmann-Horn F, Küther G, Ricker K, Grafe P, Ballanyi K, Rüdel R.

Muscle Nerve. 1987 May;10(4):363-74.

PMID:
3587272
16.
17.

Membrane changes in cells from myotonia patients.

Rüdel R, Lehmann-Horn F.

Physiol Rev. 1985 Apr;65(2):310-56. Review. No abstract available.

PMID:
2580324
18.

Adynamia episodica hereditaria: what causes the weakness?

Ricker K, Camacho LM, Grafe P, Lehmann-Horn F, Rüdel R.

Muscle Nerve. 1989 Nov;12(11):883-91.

PMID:
2558315
19.

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene.

Fontaine B, Khurana TS, Hoffman EP, Bruns GA, Haines JL, Trofatter JA, Hanson MP, Rich J, McFarlane H, Yasek DM, et al.

Science. 1990 Nov 16;250(4983):1000-2.

PMID:
2173143
20.

Schwartz-Jampel syndrome: II. Na+ channel defect causes myotonia.

Lehmann-Horn F, Iaizzo PA, Franke C, Hatt H, Spaans F.

Muscle Nerve. 1990 Jun;13(6):528-35.

PMID:
2164152

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