Results 151 to 160 of about 7,221 (188)
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Hypokalemic Familial Periodic Paralysis.

Annals of Internal Medicine, 1963
Excerpt A kindred in which 7 males and 2 females exhibit hypokalemic periodic paralysis has been intensively studied by chemical analyses of skeletal muscle, serial measurements of body composition...
P. J. Talso   +3 more
openaire   +1 more source

Hypokalemic Periodic Paralysis: Narrative Review

Current Pediatrics
Hypokalemic periodic paralysis is a rare genetic pathology characterized by spontaneous muscle weakness up to paralysis along with hypokalemia. The disease development is associated with changes in the CACNA1S, SCN4A, KCNJ2, and KCNJ18 genes regulating ...
A. Ivanov, N. Ershova, T. Kulichenko
semanticscholar   +1 more source

Hypokalemic Familial Periodic Paralysis

Anesthesiology, 1983
B, Melnick   +3 more
openaire   +2 more sources

Hypokalemic periodic paralysis

Journal of the Neurological Sciences, 1978
D. de Grandis   +3 more
openaire   +3 more sources

Hypokalemic periodic paralysis

Neurology, 1993
Ilkka M. Kantola, Leo T. Tarssanen
openaire   +2 more sources

Hypokalemic Periodic Paralysis

JAMA, 1966
E L, Howes   +3 more
openaire   +3 more sources

Prevalence and risk factors of low vitamin D levels in children and adolescents with familial hypokalemic periodic paralysis

European Journal of Pediatrics, 2023
J. Min   +5 more
semanticscholar   +1 more source

[Thyrotoxic hypokalemic periodic paralysis].

Harefuah, 1990
A 50-year-old man with thyrotoxicosis complained of recurrent bouts of weakness. On admission all his voluntary muscles were paralyzed except for those of the face, and hypokalemia was found. Thyrotoxic, hypokalemic periodic paralysis is very rare among Caucasians. This is the first case to be reported from Israel.
openaire   +1 more source

Hypokalemic Periodic Paralysis

2009
Dieter Metze   +199 more
openaire   +2 more sources

Hypokalemic periodic paralysis

Journal of the Neurological Sciences, 1974
V. Ionasescu   +4 more
openaire   +1 more source

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