Primary pigmented nodular adrenocortical disease and Cushing's syndrome (Q37062040)

18 August 2017

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title

Primary pigmented nodular adrenocortical disease and Cushing's syndrome (English)

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primary pigmented nodular adrenocortical disease

18 August 2017

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author

Constantine A Stratakis

series ordinal

2

object named as

Constantine Stratakis

1 reference

18 August 2017

Anelia Horvath

1

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18 August 2017

1 November 2007

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Arquivos Brasileiros de Endocrinologia e Metabologia

18 August 2017

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18 August 2017

51

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18 August 2017

1238-1244

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18 August 2017

8

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

18 August 2017

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

Primary pigmented nodular adrenocortical disease: reevaluation of a patient with carney complex 27 years after unilateral adrenalectomy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

Periodic Cushing syndrome in a short boy: usefulness of the ovine corticotropin releasing hormone test.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

The complex of myxomas, spotty pigmentation, and endocrine overactivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

Mucocutaneous lentigines, cardiomucocutaneous myxomas, and multiple blue nevi: the "LAMB" syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

A syndrome of various cutaneous pigmented lesions, myxoid neurofibromata and atrial myxoma: the NAME syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

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/10.1590%2FS0004-27302007000800009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

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/10.1590%2FS0004-27302007000800009

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/10.1590%2FS0004-27302007000800009

Minireview: PRKAR1A: normal and abnormal functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

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/10.1590%2FS0004-27302007000800009

PRKAR1A Mutations and protein kinase A interactions with other signaling pathways in the adrenal cortex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

AKAPs: from structure to function

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

Cloning and mitochondrial localization of full-length D-AKAP2, a protein kinase A anchoring protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

Molecular mechanisms controlling the localisation of protein kinase A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit (PRKAR1A) in patients with the "complex of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas" (Carney complex)

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

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/10.1590%2FS0004-27302007000800009

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

3',5'-cyclic nucleotide phosphodiesterase 11A: localization in human tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

Expression of PDE11A in normal and malignant human tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

Overview of PDEs and their regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

Cyclic AMP-dependent signaling aberrations in macronodular adrenal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-27302007000800009

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/10.1590%2FS0004-27302007000800009

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/10.1590%2FS0004-27302007000800009

10.1590/S0004-27302007000800009

21 January 2018

Identifiers

DOI

1 reference

18 August 2017

1 reference

PubMed ID

18209861