Page last updated: 2024-08-17

histidine and Hypokalemia

histidine has been researched along with Hypokalemia in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's3 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Boerman, RH; Elbaz, A; Isles, DE; Links, TP; Ophoff, RA; Sandkuijl, LA; Vale-Santos, JE; van Deutekom, JC; van Eijk, R; Wintzen, AR1
Fardella, CE; Homoki, J; Hum, DW; Miller, WL1
Hofmann, F; Klugbauer, N; Lehmann-Horn, F; Lerche, H; Melzer, W1

Other Studies

3 other study(ies) available for histidine and Hypokalemia

ArticleYear
Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.
    Journal of medical genetics, 1995, Volume: 32, Issue:1

    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.
    The Journal of clinical endocrinology and metabolism, 1994, Volume: 79, Issue:1

    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.
    Pflugers Archiv : European journal of physiology, 1996, Volume: 431, Issue:3

    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