Pseudohypoaldosteronism: Response to long-term treatment with indomethacin

Author:

Bommen M,Brook C G D

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference6 articles.

1. Dillon M J, Leonard J V, Buckler J M, et al. Pseudohypoaldosteronism. Arch Dis Child 1980; 55: 427-34.

2. Congenital pseudohypoaldosteronism: case report and review;Rampini, S.; Furrer, J.; P, Keller H.; Bucher, H.; Zachmann, M.;Helv Paediatr Acta,1978

3. Pseudohypoaldosteronism: multiple target organ unresponsiveness to mineralocorticoid hormones;E, Oberfield S.; S, Levine L.; M, Carey R.; R, Bejar; I, New M.;J Clin Endocrinol Metab,1979

4. Tubular Na, K-ATPase deficiency, the cause of the congenital renal salt-losing syndrome;R, Bierich J.; U, Schmidt;Eur JPediatr,1976

5. Renal prostaglandins and the regulation of blood pressure and sodium and water homeostasis;B, Lee J.; V, Patak R.; K, Mookerjee B.;AmJ Med,1976

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1. Clinical characteristics and treatment requirements of children with autosomal recessive pseudohypoaldosteronism;European Journal of Endocrinology;2021-05

2. Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene;Endocrinology, Diabetes & Metabolism Case Reports;2016-01-01

3. Pseudohypoaldosteronism type 1: clinical features and management in infancy;Endocrinology, Diabetes & Metabolism Case Reports;2013-08-01

4. Infantile variant of Bartter syndrome and sensorineural deafness: A new autosomal recessive disorder;American Journal of Medical Genetics;1995-12-04

5. Glucocorticoid and mineralocorticoid resistance;Journal of Endocrinological Investigation;1995-07

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