histidine has been researched along with Familial Periodic Paralysis in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 2 (66.67) | 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 |
|---|---|
| RUBENSTEIN, M; WOLFF, SM | 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 |
| Hofmann, F; Klugbauer, N; Lehmann-Horn, F; Lerche, H; Melzer, W | 1 |
3 other study(ies) available for histidine and Familial Periodic Paralysis
| Article | Year |
|---|---|
AMINO ACID EXCRETION IN FAMILIAL MEDITERRANEAN FEVER.
Topics: Amino Acids; Chromatography; Familial Mediterranean Fever; Histidine; Humans; Kidney; Paralyses, Familial Periodic; Renal Aminoacidurias | 1964 |
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 |
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 |