arginine and Hypokalemia

arginine has been researched along with Hypokalemia in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19905 (50.00)18.7374
1990's3 (30.00)18.2507
2000's1 (10.00)29.6817
2010's1 (10.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bachrach, BE; Gajula, S; Hurt, DE; Kino, T; Lescher, R; Nader, N; Pittman, A1
KELLEY, JW; MULMED, EI; NIENHUIS, LI1
Hur, JK; Kim, JB; Lee, KY1
Ibayashi, H; Kato, K; Miyata, Y; Motomatsu, T; Oda, K1
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
Alvestrand, A; Bergström, J; Fürst, P; Hultman, E; Sahlin, K; Vinnars, E; Widström, A1
Zweig, JI1
Rampini, S1

Reviews

2 review(s) available for arginine and Hypokalemia

ArticleYear
HEPATIC COMA; TREATMENT EMPHASIZING MERIT OF PERITONEAL DIALYSIS.
    American journal of surgery, 1963, Volume: 106

    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.
    Clinical chemistry, 1973, Volume: 19, Issue:9

    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

Other Studies

8 other study(ies) available for arginine and Hypokalemia

ArticleYear
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.
    The Journal of clinical endocrinology and metabolism, 2010, Volume: 95, Issue:5

    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).
    Journal of Korean medical science, 2005, Volume: 20, Issue:1

    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].
    Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, 1982, May-10, Volume: 71, Issue:5

    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.
    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
Influence of severe potassium depletion and subsequent repletion with potassium on muscle electrolytes, metabolites and amino acids in man.
    Clinical science and molecular medicine, 1976, Volume: 51, Issue:6

    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].
    Schweizerische medizinische Wochenschrift, 1967, Sep-09, Volume: 97, Issue:36

    Topics: Alkalosis; Ammonium Chloride; Arginine; Chlorine; Deficiency Diseases; Gastric Juice; Humans; Hydrochloric Acid; Hypokalemia; Potassium; Sodium Chloride

1967