Familial hyperaldosteronism type III

Disordered zonal and cellular CYP11B2 enzyme expression in familial hyperaldosteronism type 3

(2017) Celso E. Gomez-Sanchez et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Functional characterization of two novel germline mutations of theKCNJ5gene in hypertensive patients without primary aldosteronism but with ACTH-dependent aldosterone hypersecretion

(2016) Amalia Sertedaki et al.   CLINICAL ENDOCRINOLOGY

A Novel Phenotype of Familial Hyperaldosteronism Type III: Concurrence of Aldosteronism and Cushing's Syndrome

(2016) Anli Tong et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Study Heterogeneity and Estimation of Prevalence of Primary Aldosteronism: A Systematic Review and Meta-Regression Analysis

(2016) Sabine C. Käyser et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

The Management of Primary Aldosteronism: Case Detection, Diagnosis, and Treatment: An Endocrine Society Clinical Practice Guideline

(2016) John W. Funder et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

An Update on Familial Hyperaldosteronism

(2015) H. Korah et al.   HORMONE AND METABOLIC RESEARCH

A Case of Severe Hyperaldosteronism Caused by a De Novo Mutation Affecting a Critical Salt Bridge Kir3.4 Residue

(2015) Silvia Monticone et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Understanding primary aldosteronism: impact of next generation sequencing and expression profiling

(2015) Silvia Monticone et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Pharmacology and Pathophysiology of Mutated KCNJ5 Found in Adrenal Aldosterone-Producing Adenomas

(2014) P. Tauber et al.   ENDOCRINOLOGY

Discordant Genotype-Phenotype Correlation in Familial Hyperaldosteronism Type III with KCNJ5 Gene Mutation: A Patient Report and Review of the Literature

(2014) Masanori Adachi et al.   Hormone Research in Paediatrics

Role for Germline Mutations and a Rare Coding Single Nucleotide Polymorphism Within the KCNJ5 Potassium Channel in a Large Cohort of Sporadic Cases of Primary Aldosteronism

(2014) Meena Murthy et al.   HYPERTENSION

Cardiovascular Complications Associated With Primary Aldosteronism

(2013) Sébastien Savard et al.   HYPERTENSION

Long-Term Cardio- and Cerebrovascular Events in Patients With Primary Aldosteronism

(2013) Paolo Mulatero et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

A Novel Y152C KCNJ5 Mutation Responsible for Familial Hyperaldosteronism Type III

(2013) Silvia Monticone et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism

(2013) Ute I Scholl et al.   NATURE GENETICS

Polyuric-polydipsic syndrome in a pediatric case of non-glucocorticoid remediable familial hyperaldosteronism

(2012) Alessandro Mussa et al.   ENDOCRINE JOURNAL

The Potassium Channel, Kir3.4 Participates in Angiotensin II-Stimulated Aldosterone Production by a Human Adrenocortical Cell Line

(2012) Kenji Oki et al.   ENDOCRINOLOGY

A Novel Point Mutation in theKCNJ5Gene Causing Primary Hyperaldosteronism and Early-Onset Autosomal Dominant Hypertension

(2012) Evangelia Charmandari et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

18-Hydroxycorticosterone, 18-Hydroxycortisol, and 18-Oxocortisol in the Diagnosis of Primary Aldosteronism and Its Subtypes

(2012) Paolo Mulatero et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Effect ofKCNJ5Mutations on Gene Expression in Aldosterone-Producing Adenomas and Adrenocortical Cells

(2012) Silvia Monticone et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Role of KCNJ5 in familial and sporadic primary aldosteronism

(2012) Paolo Mulatero et al.   Nature Reviews Endocrinology

Hypertension with or without adrenal hyperplasia due to different inherited mutations in the potassium channel KCNJ5

(2012) U. I. Scholl et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

KCNJ5 Mutations in European Families With Nonglucocorticoid Remediable Familial Hyperaldosteronism

(2011) Paolo Mulatero et al.   HYPERTENSION

K+ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension

(2011) M. Choi et al.   SCIENCE

Further evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in Italian as well as Australian and South American families

(2009) Norlela Sukor et al.   JOURNAL OF HYPERTENSION

A Novel Form of Human Mendelian Hypertension Featuring Nonglucocorticoid-Remediable Aldosteronism

(2008) David S. Geller et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM