Related references
Note: Only part of the references are listed.Atrial fibrillation as presenting sign of primary aldosteronism: results of the Prospective Appraisal on the Prevalence of Primary Aldosteronism in Hypertensive (PAPPHY) Study
Teresa M. Seccia et al.
JOURNAL OF HYPERTENSION (2020)
The Unrecognized Prevalence of Primary Aldosteronism A Cross-sectional Study
Jenifer M. Brown et al.
ANNALS OF INTERNAL MEDICINE (2020)
Five Reasons for the Failure to Diagnose Aldosterone Excess in Hypertension
George P. Piaditis et al.
HORMONE AND METABOLIC RESEARCH (2020)
Genetic and Genomic Mechanisms of Primary Aldosteronism
Fabio L. Fernandes-Rosa et al.
TRENDS IN MOLECULAR MEDICINE (2020)
The 2020 Italian Society of Arterial Hypertension (SIIA) practical guidelines for the management of primary aldosteronism
Gian Paolo Rossi et al.
INTERNATIONAL JOURNAL CARDIOLOGY HYPERTENSION (2020)
Genetic Characteristics of Aldosterone-Producing Adenomas in Blacks
Kazutaka Nanba et al.
HYPERTENSION (2019)
RNA Sequencing Provides Novel Insights into the Transcriptome of Aldosterone Producing Adenomas
Samuel Backman et al.
SCIENTIFIC REPORTS (2019)
A somatic mutation in CLCN2 identified in a sporadic aldosterone-producing adenoma
Ravi Kumar Dutta et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2019)
Macrolides for KCNJ5-mutated aldosterone-producing adenoma (MAPA): design of a study for personalized diagnosis of primary aldosteronism
Giuseppe Maiolino et al.
BLOOD PRESSURE (2018)
The expanding genetic horizon of primary aldosteronism
Silvia Monticone et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2018)
CLCN2 chloride channel mutations in familial hyperaldosteronism type II
Ute I. Scholl et al.
NATURE GENETICS (2018)
A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism
Fabio L. Fernandes-Rosa et al.
NATURE GENETICS (2018)
Endocrine and haemodynamic changes in resistant hypertension, and blood pressure responses to spironolactone or amiloride: the PATHWAY-2 mechanisms substudies
Bryan Williams et al.
LANCET DIABETES & ENDOCRINOLOGY (2018)
Current pattern of primary aldosteronism diagnosis Delayed and complicated
Yin Yu Lim et al.
AUSTRALIAN JOURNAL OF GENERAL PRACTICE (2018)
New gain-of-function mutation shows CACNA1D as recurrently mutated gene in autism spectrum disorders and epilepsy
Alexandra Pinggera et al.
HUMAN MOLECULAR GENETICS (2017)
Aldosterone-Producing Adenomas Histopathology-Genotype Correlation and Identification of a Novel CACNA1D Mutation
Geok Chin Tan et al.
HYPERTENSION (2017)
Prevalence and Clinical Manifestations of Primary Aldosteronism Encountered in Primary Care Practice
Silvia Monticone et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2017)
A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotonia
S. E. Flanagan et al.
PEDIATRIC DIABETES (2017)
Characteristics of Japanese aldosterone-producing adenomas with KCNJ5 mutations
Takashi Okamura et al.
ENDOCRINE JOURNAL (2017)
Genotype-Specific Steroid Profiles Associated With Aldosterone-Producing Adenomas
Tracy Ann Williams et al.
HYPERTENSION (2016)
Functional characterization of two novel germline mutations of the KCNJ5 gene in hypertensive patients without primary aldosteronism but with ACTH-dependent aldosterone hypersecretion
Amalia Sertedaki et al.
CLINICAL ENDOCRINOLOGY (2016)
Cellular Pathophysiology of an Adrenal Adenoma-Associated Mutant of the Plasma Membrane Ca2+-ATPase ATP2B3
Philipp Tauber et al.
ENDOCRINOLOGY (2016)
Clinical and Steroidogenic Characteristics of Aldosterone-Producing Adenomas With ATPase or CACNA1D Gene Mutations
Takumi Kitamoto et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2016)
PRKACA Somatic Mutations Are Rare Findings in Aldosterone-Producing Adenomas
Yara Rhayem et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2016)
The Management of Primary Aldosteronism: Case Detection, Diagnosis, and Treatment: An Endocrine Society Clinical Practice Guideline
John W. Funder et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2016)
Activating mutations in CTNNB1 in aldosterone producing adenomas
Tobias Akerstrom et al.
SCIENTIFIC REPORTS (2016)
CACNA1H Mutations Are Associated With Different Forms of Primary Aldosteronism
Georgios Daniil et al.
EBIOMEDICINE (2016)
ARMC5 mutation analysis in patients with primary aldosteronism and bilateral adrenal lesions
P. Mulatero et al.
JOURNAL OF HUMAN HYPERTENSION (2016)
Novel somatic mutations in primary hyperaldosteronism are related to the clinical, radiological and pathological phenotype
Ute I. Scholl et al.
CLINICAL ENDOCRINOLOGY (2015)
Novel somatic mutations and distinct molecular signature in aldosterone-producing adenomas
Tobias Akerstrom et al.
ENDOCRINE-RELATED CANCER (2015)
Stress-induced Aldosterone Hyper-Secretion in a Substantial Subset of Patients With Essential Hypertension
Athina Markou et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2015)
A Meta-Analysis of Somatic KCNJ5 K+ Channel Mutations In 1636 Patients With an Aldosterone-Producing Adenoma
Livia Lenzini et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2015)
Primary Aldosteronism and ARMC5 Variants
Mihail Zilbermint et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2015)
Understanding primary aldosteronism: impact of next generation sequencing and expression profiling
Silvia Monticone et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (2015)
Immunohistochemical, genetic and clinical characterization of sporadic aldosterone-producing adenomas
Silvia Monticone et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (2015)
Prevalence and clinical correlates of somatic mutation in aldosterone producing adenoma-Taiwanese population
Vin-Cent Wu et al.
SCIENTIFIC REPORTS (2015)
Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism
Ute I. Scholl et al.
ELIFE (2015)
A review of the prevalence of primary aldosteronism in pre-hypertension and hypertension
George Piaditis et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2015)
Discordant Genotype-Phenotype Correlation in Familial Hyperaldosteronism Type III with KCNJ5 Gene Mutation: A Patient Report and Review of the Literature
Masanori Adachi et al.
HORMONE RESEARCH IN PAEDIATRICS (2014)
Somatic ATP1A1, ATP2B3, and KCNJ5 Mutations in Aldosterone-Producing Adenomas
Tracy Ann Williams et al.
HYPERTENSION (2014)
Adrenal Nodularity and Somatic Mutations in Primary Aldosteronism: One Node Is the Culprit?
T. Dekkers et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2014)
Hyperaldosteronism as a Common Cause of Resistant Hypertension
David A. Calhoun
ANNUAL REVIEW OF MEDICINE, VOL 64 (2013)
Evidence of Primary Aldosteronism in a Predominantly Female Cohort of Normotensive Individuals: A Very High Odds Ratio for Progression into Arterial Hypertension
Athina Markou et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2013)
Outcome after surgery for primary hyperaldosteronism may depend on KCNJ5 tumor mutation status: a population-based study from Western Norway
Thomas Arnesen et al.
LANGENBECKS ARCHIVES OF SURGERY (2013)
Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension
Elena A. B. Azizan et al.
NATURE GENETICS (2013)
Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism
Ute I. Scholl et al.
NATURE GENETICS (2013)
Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension
Felix Beuschlein et al.
NATURE GENETICS (2013)
Prevalence, Clinical, and Molecular Correlates of KCNJ5 Mutations in Primary Aldosteronism
Sheerazed Boulkroun et al.
HYPERTENSION (2012)
A Novel Point Mutation in the KCNJ5 Gene Causing Primary Hyperaldosteronism and Early-Onset Autosomal Dominant Hypertension
Evangelia Charmandari et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)
Comprehensive Re-Sequencing of Adrenal Aldosterone Producing Lesions Reveal Three Somatic Mutations near the KCNJ5 Potassium Channel Selectivity Filter
Tobias Akerstrom et al.
PLOS ONE (2012)
High prevalence of autonomous aldosterone secretion among patients with essential hypertension
Aggeliki Gouli et al.
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION (2011)
Prevalence and Characteristics of Familial Hyperaldosteronism The PATOGEN Study (Primary Aldosteronism in TOrino-GENetic forms)
Paolo Mulatero et al.
HYPERTENSION (2011)
K+ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension
Murim Choi et al.
SCIENCE (2011)
A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism
David S. Geller et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2008)
A prospective study of the prevalence of primary aldosteronism in 1,125 hypertensive patients
Gian Paolo Rossi et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2006)
Aldosteronism and hypertension
David A. Calhoun
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2006)
Evidence for an increased rate of cardiovascular events in patients with primary aldosteronism
P Milliez et al.
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY (2005)
Global burden of hypertension: analysis of worldwide data
PM Kearney et al.
LANCET (2005)
Selected major risk factors and global and regional burden of disease
M Ezzati et al.
LANCET (2002)
A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)
AR Lafferty et al.
JOURNAL OF MEDICAL GENETICS (2000)
Share Paper
