arginine has been researched along with Hypokalemia in 10 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (50.00) | 18.7374 |
1990's | 3 (30.00) | 18.2507 |
2000's | 1 (10.00) | 29.6817 |
2010's | 1 (10.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bachrach, BE; Gajula, S; Hurt, DE; Kino, T; Lescher, R; Nader, N; Pittman, A | 1 |
KELLEY, JW; MULMED, EI; NIENHUIS, LI | 1 |
Hur, JK; Kim, JB; Lee, KY | 1 |
Ibayashi, H; Kato, K; Miyata, Y; Motomatsu, T; Oda, K | 1 |
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 |
Alvestrand, A; Bergström, J; Fürst, P; Hultman, E; Sahlin, K; Vinnars, E; Widström, A | 1 |
Zweig, JI | 1 |
Rampini, S | 1 |
2 review(s) available for arginine and Hypokalemia
Article | Year |
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HEPATIC COMA; TREATMENT EMPHASIZING MERIT OF PERITONEAL DIALYSIS.
Topics: Adrenal Cortex Hormones; Alkalosis; Ammonium Chloride; Anti-Bacterial Agents; Arginine; Chlorothiazide; Dialysis; Diet; Gastrointestinal Hemorrhage; Hepatic Encephalopathy; Hepatitis; Hepatitis A; Humans; Hypokalemia; Liver Cirrhosis; Narcotics; Perfusion; Peritoneal Dialysis; Peritoneum; Potassium Deficiency; Proteins; Renal Dialysis; Urea | 1963 |
Effects of lysine on ammonia formation, hydrogen ion, and potassium ion balance: a review and an hypothesis.
Topics: Acid-Base Equilibrium; Adolescent; Adult; Ammonia; Animals; Arginine; Biological Transport; Cystinuria; Diabetes Mellitus; Dogs; Dose-Response Relationship, Drug; Electrocardiography; Female; Hepatic Encephalopathy; Humans; Hydrogen; Hydrogen-Ion Concentration; Hypokalemia; In Vitro Techniques; Insulin; Liver Cirrhosis; Liver Diseases; Lysine; Male; Models, Biological; Potassium; Pregnancy; Rats; Urea | 1973 |
8 other study(ies) available for arginine and Hypokalemia
Article | Year |
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A novel point mutation in helix 10 of the human glucocorticoid receptor causes generalized glucocorticoid resistance by disrupting the structure of the ligand-binding domain.
Topics: Amino Acid Substitution; Arginine; Binding Sites; Exons; Female; Glucocorticoids; Glutamine; Humans; Hypoglycemia; Hypokalemia; Infant; Ligands; Point Mutation; Polymorphism, Single Nucleotide; Protein Conformation; Puberty, Precocious; Receptors, Glucocorticoid | 2010 |
A Korean family of hypokalemic periodic paralysis with mutation in a voltage-gated calcium channel (R1239G).
Topics: Acetazolamide; Adolescent; Arginine; Calcium Channels; Calcium Channels, L-Type; Codon; Exons; Family Health; Female; Glycine; Humans; Hypokalemia; Hypokalemic Periodic Paralysis; Korea; Male; Muscle, Skeletal; Mutation; Pedigree; Protein Structure, Tertiary; Sequence Analysis, DNA; Spironolactone | 2005 |
[Transient and marked improvement of paralysis after the intravenous infusion of arginine in a case of hypokalemic periodic paralysis].
Topics: Adult; Arginine; Humans; Hypokalemia; Infusions, Parenteral; Male; Periodicity; Quadriplegia | 1982 |
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 |
Influence of severe potassium depletion and subsequent repletion with potassium on muscle electrolytes, metabolites and amino acids in man.
Topics: Acidosis; Adult; Amino Acids; Animals; Arginine; Creatine Kinase; Electrolytes; Female; Humans; Hypokalemia; Lysine; Muscles; Ornithine; Potassium Chloride; Potassium Deficiency; Rats; Sodium | 1976 |
[Management of hypochloremic metabolic alkalosis in pediatrics. The role of chlorine].
Topics: Alkalosis; Ammonium Chloride; Arginine; Chlorine; Deficiency Diseases; Gastric Juice; Humans; Hydrochloric Acid; Hypokalemia; Potassium; Sodium Chloride | 1967 |