Pseudohypoaldosteronism

Known as: Pseudohypoaldosteronism [Disease/Finding], Pseudohypoaldosteronisms 
A heterogeneous group of disorders characterized by renal electrolyte transport dysfunctions. Congenital forms are rare autosomal disorders… (More)
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
Hypertension affects one billion people and is a principal reversible risk factor for cardiovascular disease… (More)
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Highly Cited
2007
Highly Cited
2007
WNK1 and WNK4 mutations have been reported to cause pseudohypoaldosteronism type II (PHAII), an autosomal-dominant disorder… (More)
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Highly Cited
2002
Highly Cited
2002
Mutations in WNK kinases cause pseudohypoaldosteronism type II (PHA II) and may represent a novel signaling pathway regulating… (More)
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Highly Cited
2001
Highly Cited
2001
Hypertension is a major public health problem of largely unknown cause. Here, we identify two genes causing… (More)
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Highly Cited
1998
Highly Cited
1998
Pseudohypoaldosteronism type I (PHA1) is characterized by neonatal renal salt wasting with dehydration, hypotension… (More)
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Highly Cited
1998
Highly Cited
1998
Genetic evidence supports a critical role for the epithelial sodium channel (ENaC) in both clearance of fetal lung liquid at… (More)
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Highly Cited
1997
Highly Cited
1997
Pseudohypoaldosteronism type 1 (PHA-1) is an inherited disease characterized by severe neonatal salt-wasting and caused by… (More)
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Highly Cited
1997
Highly Cited
1997
Essential hypertension is a common multifactorial trait. The molecular basis of a number of rare diseases that alter blood… (More)
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Highly Cited
1996
Highly Cited
1996
Autosomal recessive pseudohypoaldosteronism type I is a rare life-threatening disease characterized by severe neonatal salt… (More)
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Highly Cited
1996
Highly Cited
1996
Pseudohypoaldosteronism type 1 (PHA1, OMIM 264350) is an uncommon inherited disorder characterized by salt-wasting and end-organ… (More)
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