Skip to search formSkip to main contentSkip to account menu

Hypokalemic alkalosis

Known as: ALKALOSIS HYPOKALEMIC 
National Institutes of Health

Related topics

Related topics

4 relations
Acid-Base EquilibriumBartter DiseaseGitelman Syndrome

Broader (1)

Alkalosis

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Family with primary periodic paralysis and a mutation in MCM3AP, a gene implicated in mRNA transport
Introduction: Primary periodic paralyses (PPs) are rare genetic neuromuscular disorders commonly caused by mutations in genes… 
2014
2014
A case of Andersen–Tawil syndrome presenting periodic paralysis exacerbated by acetazolamide
Review
1998
Review
1998
Ion transporter mutations in Gitelman's and Bartter's syndromes
The application of modern techniques in molecular genetics to classic diseases in clinical nephrology is highlighted by the… 
1998
1998
Ion transporter and channel mutations in Bartter's and Gitelman's syndromes of inherited hypokalemic alkalosis
The use of modern molecular genetics techniques in defining the pathogenesis of classic diseases in clinical nephrology is… 
1994
1994
Administration of vancomycin for treatment of ascending bacterial cholangiohepatitis in a cat.
A 12-year-old neutered male domestic shorthair cat, being treated with methimazole for hyperthyroidism, developed chronic… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)