histidine has been researched along with Hypokalemia in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 3 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Boerman, RH; Elbaz, A; Isles, DE; Links, TP; Ophoff, RA; Sandkuijl, LA; Vale-Santos, JE; van Deutekom, JC; van Eijk, R; Wintzen, AR | 1 |
Fardella, CE; Homoki, J; Hum, DW; Miller, WL | 1 |
Hofmann, F; Klugbauer, N; Lehmann-Horn, F; Lerche, H; Melzer, W | 1 |
3 other study(ies) available for histidine and Hypokalemia
Article | Year |
---|---|
Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.
Topics: Adolescent; Adult; Age of Onset; Arginine; Base Sequence; Calcium Channels; Calcium Channels, L-Type; Child; Chromosome Mapping; Chromosomes, Human, Pair 1; DNA Primers; Female; Genes, Dominant; Genetic Linkage; Histidine; Humans; Hypokalemia; Male; Molecular Sequence Data; Muscle Proteins; Netherlands; Paralyses, Familial Periodic; Pedigree; Point Mutation; Receptors, Cholinergic | 1995 |
Point mutation of Arg440 to His in cytochrome P450c17 causes severe 17 alpha-hydroxylase deficiency.
Topics: Adolescent; Adrenal Hyperplasia, Congenital; Arginine; Base Sequence; Cell Line; Female; Germany; Histidine; Humans; Hypertension; Hypokalemia; Molecular Sequence Data; Mutagenesis, Site-Directed; Point Mutation; Polymerase Chain Reaction; Steroid 17-alpha-Hydroxylase; Transfection | 1994 |
Expression and functional characterization of the cardiac L-type calcium channel carrying a skeletal muscle DHP-receptor mutation causing hypokalaemic periodic paralysis.
Topics: Animals; Arginine; Barium; Base Sequence; Calcium Channels; Calcium Channels, L-Type; Histidine; Humans; Hydrogen-Ion Concentration; Hypokalemia; Ion Channels; Molecular Sequence Data; Muscle, Skeletal; Mutation; Myocardium; Paralyses, Familial Periodic; Rabbits | 1996 |