Compounds > arginine

arginine and Familial Periodic Paralysis

arginine has been researched along with Familial Periodic Paralysis in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's3 (60.00)18.2507
2000's0 (0.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Heo, TH; Kim, JB; Kim, MH; Kim, SJ; Song, YW1
Garnacho de Vega, A; Rey, C; Romero González, R1
Bady, B; Elbaz, A; Jurkat-Rott, K; Lapie, P; Links, TP; Monnier, N; Ophoff, RA; Piussan, C; Vale-Santos, J; Vila, A1
Boerman, RH; Elbaz, A; Isles, DE; Links, TP; Ophoff, RA; Sandkuijl, LA; Vale-Santos, JE; van Deutekom, JC; van Eijk, R; Wintzen, AR1
Hofmann, F; Klugbauer, N; Lehmann-Horn, F; Lerche, H; Melzer, W1

Other Studies

5 other study(ies) available for arginine and Familial Periodic Paralysis

ArticleYear
Normokalemic periodic paralysis is not a distinct disease.
    Muscle & nerve, 2012, Volume: 46, Issue:6

    Topics: Adolescent; Arginine; DNA Mutational Analysis; Electrocardiography; Family Health; Female; Glycine; Humans; Male; Mutation; NAV1.4 Voltage-Gated Sodium Channel; Paralyses, Familial Periodic

2012
[Potassium metabolism disorders (II)].
    Medicina clinica, 1981, Jan-10, Volume: 76, Issue:1

    Topics: Addison Disease; Aldosterone; Arginine; Biological Transport; Diuretics; Hematologic Diseases; Humans; Hyperkalemia; Kidney Diseases; Mineralocorticoids; Paralyses, Familial Periodic; Potassium; Succinylcholine

1981
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families.
    American journal of human genetics, 1995, Volume: 56, Issue:2

    Topics: Arginine; Calcium Channels; Calcium Channels, L-Type; Female; Founder Effect; Genotype; Haplotypes; Humans; Male; Muscle Proteins; Mutation; Paralyses, Familial Periodic; Pedigree; Phenotype; Sex Characteristics; White People

1995
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
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