(Q36018189)

11 August 2017

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title

Clinical and molecular genetic studies of bilateral adrenal hyperplasias (English)

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11 August 2017

Isabelle Bourdeau

1

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11 August 2017

publication date

1 November 2004

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11 August 2017

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11 August 2017

volume

30

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11 August 2017

issue

4

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11 August 2017

page(s)

575-583

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

11 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Cushing's syndrome caused by nodular adrenal hyperplasia in children with McCune-Albright syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

A case of Cushing's syndrome due to ACTH-independent bilateral macronodular hyperplasia associated with excessive secretion of mineralocorticoids

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Adrenocorticotropin-independent bilateral macronodular adrenal hyperplasia: an unusual cause of Cushing's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Virilization in bilateral macronodular adrenal hyperplasia controlled by luteinizing hormone

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the carney complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Mutations of the PRKAR1A gene in Cushing's syndrome due to sporadic primary pigmented nodular adrenocortical disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Cyclic AMP-dependent signaling aberrations in macronodular adrenal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Positional cloning of the gene for multiple endocrine neoplasia-type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Activating mutations of the stimulatory G protein in the McCune-Albright syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Familial ACTH-independent Cushing's syndrome with bilateral macronodular adrenal hyperplasia clinically affecting only female family members

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Catecholamine-dependent hereditary Cushing's syndrome - follow-up after unilateral adrenalectomy

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

In vivo and in vitro effects of AVP and V1a receptor antagonist on Cushing's syndrome due to ACTH-independent bilateral macronodular adrenocortical hyperplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Case of adrenocorticotropic hormone-independent macronodular adrenal hyperplasia with possible adrenal hypersensitivity to angiotensin II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Management approaches to adrenal incidentalomas. A view from Rochester, Minnesota

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Adrenocortical overexpression of gastric inhibitory polypeptide receptor underlies food-dependent Cushing's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Overexpression of serotonin4 receptors in cisapride-responsive adrenocorticotropin-independent bilateral macronodular adrenal hyperplasia causing Cushing's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Gene expression profiles in normal and cancer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Gene array analysis of macronodular adrenal hyperplasia confirms clinical heterogeneity and identifies several candidate genes as molecular mediators

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

WISP genes are members of the connective tissue growth factor family that are up-regulated in wnt-1-transformed cells and aberrantly expressed in human colon tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

The cadherin-catenin adhesion system in signaling and cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Identification of c-MYC as a target of the APC pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

Beta-catenin regulates expression of cyclin D1 in colon carcinoma cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FERC-200043735

21 January 2018

Identifiers

DOI

10.1081/ERC-200043735

1 reference

11 August 2017

1 reference