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Hypoaldosteronism
Original Article Clinical Characteristics and Mutation Analysis of Two Chinese Children with 17A-Hydroxylase/17,20-Lyase Deficiency
Congenital Hypoaldosteronism Developmental Delay
Primary Hyperaldosteronism: a Case of Unilateral Adrenal Hyperplasia with Contralateral Incidentaloma Sujit Vakkalanka,1 Andrew Zhao,1 Mohammed Samannodi2
Monogenic Forms of Mineralocorticoid Hypertension: Insights Into the Pathogenesis of ‘Essential’ Hypertension?
Adrenal Insufficiency Immunodeficiency Sy in a Patient Ndrome
Failing Hormones
Glucocorticoid-Remediable Aldosteronism
The First Reported Case of Hyperreninemic Hypoaldosteronism Due to Mucopolysaccharidosis Disorder
Transient Pseudohypoaldosteronism in Childrens Secondary to Urinary
Isolated Hypoaldosteronism: an Overlooked Cause of Hyponatraemia ⁎ I
Pseudohypoaldosteronism Due to Sweat Gland Dysfunction
Addison's Disease Associated with Hypokalemia
Diagnosis and Management of Primary Aldosteronism
Pseudohypoaldosteronism
Adrenal Disorders for the USMLE, Step One
Diagnosis and Management of Pseudohypoaldosteronism Type 1 In
The Greatest Pretender: Challenging Adrenal Insufficiencies
Primary Hyperaldosteronism: Screening, Diagnosis, and Management for the Clinician Eugene T
Top View
The Diagnosis and Staging of Hypocortisolism in Progressing Autoimmune Adrenalitis
The Pathogenetic Spectrum of Bartter's Syndrome Principal Discussant: JAY H
A Short Review of Primary Aldosteronism in a Question and Answer Fashion
The Molecular Biology of Hypertensive Congenital Adrenal Hyperplasia
Mineralocorticoid Dysfunction During Critical Illness
Nephrocalcinosis: a Review of Monogenic Causes and Insights They Provide Into This Heterogeneous Condition
Pseudohypoaldosteronism
Novel Cases of Congenital Hyperreninemic Hypoaldosteronism
Congenital Adrenal Hyperplasia Precision Panel Overview
17Α‑Hydroxylase/17,20‑Lyase Deficiency in Congenital Adrenal Hyperplasia: a Case Report
Table S4. Disease Prevalence
Persistent Severe Hyperkalemia Following Surgical Treatment of Aldosterone‑Producing Adenoma Epo R T
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Hereditary Causes of Primary Aldosteronism and Other Disorders of Apparent Excess Mineralocorticoid Activity
Aldosterone Synthase Deficiency Type II: an Unusual Presentation of the First Greek Case Reported with Confirmed Genetic Analysis
Hyponatremia in Primary Adrenal Insufficiency:An Often Overlooked
JCRPE Ic Sayfalar Link Internete
Salt-Losing Tubulopathies in Children: What’S New, What’S Controversial?
Hyperkalemia and Hyporeninemic Hypoaldosteronism Principal Discussant: RALPH A