Pseudohypoaldosteronism type 1: clinical features and management in infancy.
about
Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene.Severe hyperkalemia is rescued by low-potassium diet in renal βENaC-deficient mice.Pseudohypoaldosteronism Type 1 (arPHA1) Treated With Sodium Polystyrene Sulfonate Pretreated Milk.Phenotypic variation of autosomal recessive pseudohypoaldosteronism type I: a case in pointPseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes.
P2860
Pseudohypoaldosteronism type 1: clinical features and management in infancy.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
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scientific article published on 30 August 2013
@en
vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
Pseudohypoaldosteronism type 1: clinical features and management in infancy.
@en
Pseudohypoaldosteronism type 1: clinical features and management in infancy.
@nl
type
label
Pseudohypoaldosteronism type 1: clinical features and management in infancy.
@en
Pseudohypoaldosteronism type 1: clinical features and management in infancy.
@nl
prefLabel
Pseudohypoaldosteronism type 1: clinical features and management in infancy.
@en
Pseudohypoaldosteronism type 1: clinical features and management in infancy.
@nl
P2093
P2860
P356
P1476
Pseudohypoaldosteronism type 1: clinical features and management in infancy.
@en
P2093
N P Wright
P2860
P304
P356
10.1530/EDM-13-0010
P50
P577
2013-08-30T00:00:00Z