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Page last updated: 2024-08-17

histidine and Familial Hypokalemic Periodic Paralysis

histidine has been researched along with Familial Hypokalemic Periodic Paralysis in 6 studies

Research

Studies (6)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (16.67)	18.2507
2000's	4 (66.67)	29.6817
2010's	1 (16.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Cannon, SC; Mi, W; Wu, F	1
Cheah, JS; Lui, KF; Ng, WY; Thai, AC	1
Adjagba, M; Adjien, C; Avode, DG; Darboux, RB; Funalot, B; Hilbert, P; Houinato, D; Laleye, A; Sternberg, D; Vallat, JM	1
Bulman, DE; Ebers, GC; Hahn, AF; Nicolle, MW; Scoggan, KA; Tollar, LL; van Oene, MD	1
Adachi, Y; Kumada, H; Kusumi, M; Nakashima, K	1
Hang, C; Jurkat-Rott, K; Kuzmenkin, A; Lehmann-Horn, F; Lerche, H; Mitrovic, N; Muncan, V	1

Other Studies

6 other study(ies) available for histidine and Familial Hypokalemic Periodic Paralysis

Article	Year
Beneficial effects of bumetanide in a CaV1.1-R528H mouse model of hypokalaemic periodic paralysis. Brain : a journal of neurology, 2013, Volume: 136, Issue:Pt 12 Topics: Acetazolamide; Animals; Arginine; Bumetanide; Calcium Channels, L-Type; Carbonic Anhydrase Inhibitors; Disease Models, Animal; Evoked Potentials, Motor; Furosemide; Glucose; Histidine; Hypokalemic Periodic Paralysis; In Vitro Techniques; Isometric Contraction; Male; Mice; Mice, Transgenic; Muscle, Skeletal; Mutation; Sodium Potassium Chloride Symporter Inhibitors	2013
Absence of ion channels CACN1AS and SCN4A mutations in thyrotoxic hypokalemic periodic paralysis. Thyroid : official journal of the American Thyroid Association, 2004, Volume: 14, Issue:3 Topics: Adult; Arginine; Calcium Channels; Calcium Channels, L-Type; Case-Control Studies; Female; Glycine; Histidine; Humans; Hyperthyroidism; Hypokalemic Periodic Paralysis; Male; Middle Aged; Mutation; NAV1.4 Voltage-Gated Sodium Channel; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Polymorphism, Single-Stranded Conformational; Sodium Channels; Thyrotoxicosis	2004
Hypokalaemic periodic paralysis due to the CACNA1S R1239H mutation in a large African family. Neuromuscular disorders : NMD, 2007, Volume: 17, Issue:5 Topics: Adolescent; Adult; Africa; Arginine; Calcium Channels; DNA Mutational Analysis; Family Health; Female; Histidine; Humans; Hypokalemic Periodic Paralysis; Male; Microscopy, Electron, Transmission; Middle Aged; Muscle, Skeletal; Mutation	2007
A novel sodium channel mutation in a family with hypokalemic periodic paralysis. Neurology, 1999, Dec-10, Volume: 53, Issue:9 Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Arginine; Electromyography; Histidine; Humans; Hypokalemic Periodic Paralysis; Male; Molecular Sequence Data; NAV1.4 Voltage-Gated Sodium Channel; Pedigree; Phenotype; Polymorphism, Single-Stranded Conformational; Sodium Channels	1999
Muscle weakness in a Japanese family of Arg1239His mutation hypokalemic periodic paralysis. Psychiatry and clinical neurosciences, 2001, Volume: 55, Issue:5 Topics: Adult; Amino Acid Substitution; Arginine; Calcium Channels; Calcium Channels, L-Type; Child; Codon; Female; Histidine; Humans; Hypokalemic Periodic Paralysis; Male; Muscle Weakness; Pedigree; Point Mutation	2001
Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalaemic periodic paralysis type II. Brain : a journal of neurology, 2002, Volume: 125, Issue:Pt 4 Topics: Arginine; Cells, Cultured; Glycine; Histidine; Humans; Hydrogen-Ion Concentration; Hypokalemic Periodic Paralysis; Membrane Potentials; Muscle, Skeletal; Mutation; NAV1.4 Voltage-Gated Sodium Channel; Potassium; Sodium Channels	2002