Page last updated: 2024-08-21

amiloride and Familial Hypokalemic Periodic Paralysis

amiloride has been researched along with Familial Hypokalemic Periodic Paralysis in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Kil, TH; Kim, JB	1

Other Studies

1 other study(ies) available for amiloride and Familial Hypokalemic Periodic Paralysis

Article	Year
Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2010, Volume: 14, Issue:3 Topics: Adolescent; Amiloride; Amino Acid Substitution; Arginine; Calcium Channels; Calcium Channels, L-Type; Cold Temperature; DNA Mutational Analysis; Genotype; Glycine; Humans; Hypokalemic Periodic Paralysis; Male; Mutation; Potassium; Respiratory Insufficiency; Spironolactone	2010

Article

Year

Severe respiratory phenotype caused by a de novo Arg528Gly mutation in the CACNA1S gene in a patient with hypokalemic periodic paralysis.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 2010, Volume: 14, Issue:3

Topics: Adolescent; Amiloride; Amino Acid Substitution; Arginine; Calcium Channels; Calcium Channels, L-Type; Cold Temperature; DNA Mutational Analysis; Genotype; Glycine; Humans; Hypokalemic Periodic Paralysis; Male; Mutation; Potassium; Respiratory Insufficiency; Spironolactone

2010