Clinical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropin-independent macronodular adrenal hyperplasia compared with other adrenocortical tumors (Q37315688)

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scientific article published on 09 June 2009

Language	Label	Description	Also known as
English	Clinical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropin-independent macronodular adrenal hyperplasia compared with other adrenocortical tumors	scientific article published on 09 June 2009

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scholarly article

1 reference

Europe PubMed Central

19 August 2017

Clinical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropin-independent macronodular adrenal hyperplasia compared with other adrenocortical tumors (English)

1 reference

Europe PubMed Central

19 August 2017

1 reference

based on heuristic

inferred from title

adrenal hyperplasia

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based on heuristic

inferred from title

Constantine A Stratakis

10

object named as

Constantine A Stratakis

1 reference

Europe PubMed Central

19 August 2017

Isabelle Bourdeau

3

object named as

Isabelle Bourdeau

1 reference

Europe PubMed Central

19 August 2017

9

object named as

André Lacroix

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Europe PubMed Central

19 August 2017

author name string

Hui-Pin Hsiao

1

1 reference

Europe PubMed Central

19 August 2017

Lawrence S Kirschner

2

1 reference

Europe PubMed Central

19 August 2017

Margaret F Keil

4

1 reference

Europe PubMed Central

19 August 2017

Sosipatros A Boikos

5

1 reference

Europe PubMed Central

19 August 2017

Somya Verma

6

1 reference

Europe PubMed Central

19 August 2017

Audrey J Robinson-White

7

1 reference

Europe PubMed Central

19 August 2017

Maria Nesterova

8

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Europe PubMed Central

19 August 2017

language of work or name

0 references

publication date

9 June 2009

1 reference

Europe PubMed Central

19 August 2017

The Journal of Clinical Endocrinology and Metabolism

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Europe PubMed Central

19 August 2017

94

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Europe PubMed Central

19 August 2017

8

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Europe PubMed Central

19 August 2017

2930-2937

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Europe PubMed Central

19 August 2017

New genes and/or molecular pathways associated with adrenal hyperplasias and related adrenocortical tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2730864

6 September 2017

Operative management of Cushing syndrome secondary to micronodular adrenal hyperplasia

1 reference

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Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene

1 reference

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6 September 2017

Diagnostic tests for children who are referred for the investigation of Cushing syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2730864

6 September 2017

Familial adrenocorticotropin-independent macronodular adrenal hyperplasia with aberrant serotonin and vasopressin adrenal receptors

1 reference

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6 September 2017

Adrenal hyperplasia and adenomas are associated with inhibition of phosphodiesterase 11A in carriers of PDE11A sequence variants that are frequent in the population

1 reference

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6 September 2017

A genome-wide scan identifies mutations in the gene encoding phosphodiesterase 11A4 (PDE11A) in individuals with adrenocortical hyperplasia

1 reference

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6 September 2017

Clinical and subclinical ACTH-independent macronodular adrenal hyperplasia and aberrant hormone receptors

1 reference

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Hereditary leiomyomatosis associated with bilateral, massive, macronodular adrenocortical disease and atypical cushing syndrome: a clinical and molecular genetic investigation

1 reference

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6 September 2017

Clinical and molecular genetic studies of bilateral adrenal hyperplasias

1 reference

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6 September 2017

Cushing's syndrome variants secondary to aberrant hormone receptors

1 reference

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6 September 2017

Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysio

1 reference

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6 September 2017

Cyclic AMP-dependent signaling aberrations in macronodular adrenal disease

1 reference

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6 September 2017

Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation

1 reference

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6 September 2017

ACTH-independent massive bilateral adrenal disease (AIMBAD): a subtype of Cushing's syndrome with major diagnostic and therapeutic implications

1 reference

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Evidence for a role of vasopressin in the control of aldosterone secretion in primary aldosteronism: in vitro and in vivo studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2730864

26 June 2018

Clinical and genetic analysis of primary bilateral adrenal diseases (micro- and macronodular disease) leading to Cushing syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2730864

26 June 2018

Aberrant interleukin-1 receptors in a cortisol-secreting adrenal adenoma causing Cushing's syndrome.

1 reference

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26 June 2018

Variable expression of the V1 vasopressin receptor modulates the phenotypic response of steroid-secreting adrenocortical tumors.

1 reference

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26 June 2018

A single midnight serum cortisol measurement distinguishes Cushing's syndrome from pseudo-Cushing states.

1 reference

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26 June 2018

Problems in endocrinologic imaging

1 reference

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26 June 2018

Urinary free cortisol values in normal children and adolescents.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2730864

26 June 2018

Food-dependent Cushing's syndrome mediated by aberrant adrenal sensitivity to gastric inhibitory polypeptide

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2730864

26 June 2018

Gastric inhibitory polypeptide-dependent cortisol hypersecretion--a new cause of Cushing's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2730864

26 June 2018

17q22-24 chromosomal losses and alterations of protein kinase a subunit expression and activity in adrenocorticotropin-independent macronodular adrenal hyperplasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2730864

2 September 2018

Comprehensive study of urinary cortisol metabolites in hyperthyroid and hypothyroid patients

1 reference

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Ectopic expression of vasopressin V1b and V2 receptors in the adrenal glands of familial ACTH-independent macronodular adrenal hyperplasia

1 reference

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In vivo and in vitro screening for illegitimate receptors in adrenocorticotropin-independent macronodular adrenal hyperplasia causing Cushing's syndrome: identification of two cases of gonadotropin/gastric inhibitory polypeptide-dependent hypercorti

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Cyclical Cushing syndrome presenting in infancy: an early form of primary pigmented nodular adrenocortical disease, or a new entity?

1 reference

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2 September 2018

Vasopressin responsiveness of subclinical Cushing's syndrome due to ACTH-independent macronodular adrenocortical hyperplasia

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Molecular and functional analysis of PRKAR1A and its locus (17q22-24) in sporadic adrenocortical tumors: 17q losses, somatic mutations, and protein kinase A expression and activity.

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Tests of pituitary-adrenal suppressibility in the diagnosis of Cushing's syndrome.

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Primary pigmented nodular adrenocortical disease: paradoxical responses of cortisol secretion to dexamethasone occur in vitro and are associated with increased expression of the glucocorticoid receptor

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Cushing's syndrome secondary to adrenocorticotropin-independent macronodular adrenocortical hyperplasia due to activating mutations of GNAS1 gene

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Inherited adrenocorticotropin-independent macronodular adrenal hyperplasia with abnormal cortisol secretion by vasopressin and catecholamines: detection of the aberrant hormone receptors on adrenal gland

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Aberrant membrane hormone receptors in incidentally discovered bilateral macronodular adrenal hyperplasia with subclinical Cushing's syndrome

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Are ectopic or abnormal membrane hormone receptors frequently present in adrenal Cushing's syndrome?

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Propranolol Therapy for Ectopic β-Adrenergic Receptors in Adrenal Cushing's Syndrome

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Clinical evaluation of urinary cortisol determinations by competetive protein-binding radioassay

1 reference

https://pubmed.ncbi.nlm.nih.gov/19509103

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based on heuristic

inferred from PubMed ID database lookup

Lysine vasopressin stimulation of cortisol secretion in patients with adrenocorticotropin-independent macronodular adrenal hyperplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/19509103

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19509103

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Food-dependent Cushing's syndrome: possible involvement of leptin in cortisol hypersecretion

1 reference

https://pubmed.ncbi.nlm.nih.gov/19509103

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based on heuristic

inferred from PubMed ID database lookup

Leuprolide acetate therapy in luteinizing hormone--dependent Cushing's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19509103

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based on heuristic

inferred from PubMed ID database lookup

Adrenocorticotropin-independent macronodular adrenal hyperplasia: an uncommon cause of primary adrenal hypercortisolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19509103

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1210/JC.2009-0516

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

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