Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ricker, K.
Right arrow Articles by Böhlen, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ricker, K.
Right arrow Articles by Böhlen, R.
NEUROLOGY 1986;36:682
© 1986 American Academy of Neurology

Adynamia episodica and paralysis periodica paramyotonica

Kenneth Ricker, Reinhard Rohkamm and Reinhard Böhlen

Department of Neurology. University of Würzburg, West Germany.

We studied hyperkalemic attacks in one family with adynamia episodica (AE) and one family with paralysis periodica paramyotonica (PPP). Under exercise, serum potassium increased as in healthy subjects. Thiazide did not affect this increase. Thirty minutes after exercise, a second potassium increase occurred, but could be prevented by thiazide and not by mexiletine. After cooling, muscle relaxation time was normal in AE but increased up to 100 times in PPP; this cooling effect was prevented by mexiletine. Although hyperkalemic attacks are similar in AE and in PPP, the membrane defect in PPP seems more complex.

Address correspondence and reprint requests to Dr. Ricker, Neurologische Universitätsklinik. Josef-Schneider-Strasse 11, D-8700 Würzburg, West Germany.

Supported by Deutsche Gesellschaft Bekämpfung der Muskelkrankheiten e.V.

Accepted for publication September 20, 1985.




This article has been cited by other articles:


Home page
J. Neurol. Neurosurg. PsychiatryHome page
J Kim, Y Hahn, E H Sohn, Y J Lee, J H Yun, J M Kim, and J H Chung
Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica
J. Neurol. Neurosurg. Psychiatry, May 1, 2001; 70(5): 618 - 623.
[Abstract] [Full Text] [PDF]


Home page
Arch NeurolHome page
D. B. Allen
Defective Aldosterone Synthesis Associated With Hyperkalemic Periodic Paralysis
Arch Neurol, March 1, 1993; 50(3): 325 - 328.
[Abstract] [PDF]


Home page
Arch NeurolHome page
K. Ricker, F. Lehmann-Horn, and R. T. Moxley III
Myotonia Fluctuans
Arch Neurol, March 1, 1990; 47(3): 268 - 272.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1986 by AAN Enterprises, Inc.