scholarly article | Q13442814 |
P2093 | author name string | K Jurkat-Rott | |
S Servidei | |||
D C Camerino | |||
D Tricarico | |||
P Tonali | |||
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Dihydropyridine receptor mutations cause hypokalemic periodic paralysis | Q28243593 | ||
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Normal insulin release during sustained hyperglycaemia in hypokalaemic periodic paralysis: role of the potassium channel opener pinacidil in impaired muscle strength | Q71832047 | ||
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families | Q72017458 | ||
Cytoplasmic acidosis induces multiple conductance states in ATP-sensitive potassium channels of cardiac myocytes | Q72239336 | ||
Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis | Q73299439 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | adenosine triphosphate | Q80863 |
hypokalemic periodic paralysis | Q622828 | ||
P304 | page(s) | 675-682 | |
P577 | publication date | 1999-03-01 | |
P1433 | published in | Journal of Clinical Investigation | Q3186904 |
P1476 | title | Impairment of skeletal muscle adenosine triphosphate-sensitive K+ channels in patients with hypokalemic periodic paralysis | |
P478 | volume | 103 |
Q36498120 | A calcium channel mutant mouse model of hypokalemic periodic paralysis |
Q40024967 | A patient suffering from hypokalemic periodic paralysis is deficient in skeletal muscle ATP-sensitive K channels |
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