Related references
Note: Only part of the references are listed.Unilateral Adrenalectomy for Primary Bilateral Macronodular Adrenal Hyperplasia: Analysis of 71 Cases
Mohammad Sheikh-Ahmad et al.
EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES (2020)
CuIlin 3 targets the tumor suppressor gene ARMC5 for ubiquitination and degradation
Isadora Pontes Cavalcante et al.
ENDOCRINE-RELATED CANCER (2020)
Genetic alteration of ARMC5 in a patient diagnosed with meningioma and primary macronodular adrenal hyperplasia: a case report
Teruo Jojima et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2020)
ARMC5 Primary Bilateral Macronodular Adrenal Hyperplasia Associated with a Meningioma: A Family Report
M. J. Ferreira et al.
CASE REPORTS IN ENDOCRINOLOGY (2020)
A New Insight into the Surgical Treatment of Primary Macronodular Adrenal Hyperplasia
Fabio Yoshiaki Tanno et al.
JOURNAL OF THE ENDOCRINE SOCIETY (2020)
Long-Term Outcome of Primary Bilateral Macronodular Adrenocortical Hyperplasia After Unilateral Adrenalectomy
Andrea Osswald et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2019)
Outcomes of Adrenal Venous Sampling in Patients with Bilateral Adrenal Masses and ACTH-Independent Cushing's Syndrome
Runa Acharya et al.
WORLD JOURNAL OF SURGERY (2019)
Adrenal venous sampling in patients with ACTH-independent hypercortisolism
Eleni Papakokkinou et al.
ENDOCRINE (2019)
Characteristics of Adrenal Masses in Familial Adenomatous Polyposis
Jonah S. Shiroky et al.
DISEASES OF THE COLON & RECTUM (2018)
The role of ARMC5 in human cell cultures from nodules of primary macronodular adrenocortical hyperplasia (PMAH)
Isadora P. Cavalcante et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (2018)
Age-dependent effects of Armc5 haploinsufficiency on adrenocortical function
A. Berthon et al.
HUMAN MOLECULAR GENETICS (2017)
Resetting the Abnormal Circadian Cortisol Rhythm in Adrenal Incidentaloma Patients With Mild Autonomous Cortisol Secretion
Miguel Debono et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2017)
A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype
N. M. Albiger et al.
ENDOCRINE (2017)
Imaging for the diagnosis of malignancy in incidentally discovered adrenal masses: a systematic review and meta-analysis
Jacqueline Dinnes et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2016)
Management of adrenal incidentalomas: European Society of Endocrinology Clinical Practice Guideline in collaboration with the European Network for the Study of Adrenal Tumors
Martin Fassnacht et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2016)
An analysis of different therapeutic options in patients with Cushing's syndrome due to bilateral macronodular adrenal hyperplasia: a single-centre experience
N. M. Albiger et al.
CLINICAL ENDOCRINOLOGY (2015)
The ARMC5 gene shows extensive genetic variance in primary macronodular adrenocortical hyperplasia
Ricardo Correa et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2015)
Unilateral Adrenalectomy as a First-Line Treatment of Cushing's Syndrome in Patients With Primary Bilateral Macronodular Adrenal Hyperplasia
Emmanuelle Debillon et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2015)
ARMC5 Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences
Stephanie Espiard et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2015)
Molecular and Clinical Evidence for an ARMC5 Tumor Syndrome: Concurrent Inactivating Germline and Somatic Mutations Are Associated With Both Primary Macronodular Adrenal Hyperplasia and Meningioma
Ulf Elbelt et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2015)
Bilateral adrenal incidentalomas differ from unilateral adrenal incidentalomas in subclinical cortisol hypersecretion but not in potential clinical implications
Evangeline Vassilatou et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2014)
Abnormal Sensitivity to Glucagon and Related Peptides in Primary Adrenal Cushing's Syndrome
E. Louiset et al.
HORMONE AND METABOLIC RESEARCH (2014)
ARMC5 Mutations Are Common in Familial Bilateral Macronodular Adrenal Hyperplasia
Lucia Gagliardi et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2014)
ARMC5 Mutations Are a Frequent Cause of Primary Macronodular Adrenal Hyperplasia
Guilherme Asmar Alencar et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2014)
Macronodular Adrenal Hyperplasia due to Mutations in an Armadillo Repeat Containing 5 (ARMC5) Gene: A Clinical and Genetic Investigation
Fabio R. Faucz et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2014)
Bilateral and unilateral adrenal incidentalomas: biochemical and clinical characteristics
V. Morelli et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2013)
Adrenal Nodular Hyperplasia in Hereditary Leiomyomatosis and Renal Cell Cancer
Brian Shuch et al.
JOURNAL OF UROLOGY (2013)
ARMC5 Mutations in Macronodular Adrenal Hyperplasia with Cushing's Syndrome
Guillaume Assie et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
Intraadrenal Corticotropin in Bilateral Macronodular Adrenal Hyperplasia
Estelle Louiset et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
ACTH-independent macronodular adrenocortical hyperplasia reveals prevalent aberrant in vivo and in vitro responses to hormonal stimuli and coupling of arginine-vasopressin type 1a receptor to 11β-hydroxylase
Johannes Hofland et al.
ORPHANET JOURNAL OF RARE DISEASES (2013)
Adrenal involvement in MEN1. Analysis of 715 cases from the Groupe d'e ' tude des Tumeurs Endocrines database
B. Gatta-Cherifi et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2012)
Phosphodiesterase 11A (PDE11A) Gene Defects in Patients with ACTH-Independent Macronodular Adrenal Hyperplasia (AIMAH): Functional Variants May Contribute to Genetic Susceptibility of Bilateral Adrenal Tumors
Delphine Vezzosi et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)
18F-FDG-PET/CT Imaging of ACTH-Independent Macronodular Adrenocortical Hyperplasia (AIMAH) Demonstrating Increased 18F-FDG Uptake
Guilherme Asmar Alencar et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2011)
Inactivation of the APC Gene Is Constant in Adrenocortical Tumors from Patients with Familial Adenomatous Polyposis but Not Frequent in Sporadic Adrenocortical Cancers
Sebastien Gaujoux et al.
CLINICAL CANCER RESEARCH (2010)
Aberrant cortisol regulations in bilateral macronodular adrenal hyperplasia: a frequent finding in a prospective study of 32 patients with overt or subclinical Cushing's syndrome
Rossella Libe et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2010)
Cushing Syndrome in the McCune-Albright Syndrome
Rebecca J. Brown et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2010)
PET/CT for the Characterization of Adrenal Masses in Patients with Cancer: Qualitative Versus Quantitative Accuracy in 150 Consecutive Patients
Giles W. L. Boland et al.
AMERICAN JOURNAL OF ROENTGENOLOGY (2009)
Phosphodiesterase 11A (PDE11A) and genetic predisposition to adrenocortical tumors
Rossella Libe et al.
CLINICAL CANCER RESEARCH (2008)
The role of unilateral adrenalectomy in ACTH-independent macronodular adrenal hyperplasia (AIMAH)
Maurizio Iacobone et al.
WORLD JOURNAL OF SURGERY (2008)
Expression of vasopressin receptors in ACTH-independent macronodular bilateral adrenal hyperplasia causing Cushing's syndrome: molecular, immunohistochemical and pharmacological correlates
E. Louiset et al.
JOURNAL OF ENDOCRINOLOGY (2008)
Prevalence and natural history of adrenal incidentalomas
L Barzon et al.
EUROPEAN JOURNAL OF ENDOCRINOLOGY (2003)
Cushing's syndrome secondary to adrenocorticotropin-independent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene
MCBV Fragoso et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2003)
Overexpression of serotonin(4) receptors in cisapride-responsive adrenocorticotropin-independent bilateral macronodular adrenal hyperplasia causing Cushing's syndrome
D Cartier et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2003)
Adrenocorticotropin-independent macronodular adrenal hyperplasia: An uncommon cause of primary adrenal hypercortisolism
JL Doppman et al.
RADIOLOGY (2000)
Share Paper
