Familial micronodular adrenocortical disease, Cushing syndrome, and mutations of the gene encoding phosphodiesterase 11A4 (PDE11A). (Q33701874)

28 July 2017

Familial micronodular adrenocortical disease, Cushing syndrome, and mutations of the gene encoding phosphodiesterase 11A4 (PDE11A). (English)

1 reference

28 July 2017

3

Jérôme Bertherat

0 references

Constantine A Stratakis

series ordinal

4

object named as

Constantine A Stratakis

1 reference

28 July 2017

J Aidan Carney

1

1 reference

PubMed ID

20351491

28 July 2017

Rolf C Gaillard

series ordinal

2

1 reference

PubMed ID

20351491

28 July 2017

language of work or name

English

0 references

publication date

1 April 2010

1 reference

The American Journal of Surgical Pathology

28 July 2017

1 reference

28 July 2017

34

1 reference

28 July 2017

547-555

1 reference

28 July 2017

4

1 reference

Mutations and polymorphisms in the gene encoding regulatory subunit type 1-alpha of protein kinase A (PRKAR1A): an update

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

Abnormalities of cAMP signaling are present in adrenocortical lesions associated with ACTH-independent Cushing syndrome despite the absence of mutations in known genes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

The ectopic adrenocorticotropin syndrome: clinical features, diagnosis, management, and long-term follow-up.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complex.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

The complex of myxomas, spotty pigmentation, and endocrine overactivity

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

Mutation in PDE8B, a cyclic AMP-specific phosphodiesterase in adrenal hyperplasia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

The basophil adenomas of the pituitary body and their clinical manifestations (pituitary basophilism). 1932.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

Bilateral primary pigmented nodular adrenocortical disease. Rare cause of the Cushing syndrome.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4042182

Severe osteopenia in young adults associated with Cushing's syndrome due to micronodular adrenal disease

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20351491

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Use of adrenal biopsy in diagnosing adrenoleukomyeloneuropathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20351491

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Primary adrenocortical nodular dysplasia with Cushing's syndrome and cardiac myxomas. A peculiar familial disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20351491

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1097/PAS.0B013E3181D31F49

1 reference

28 July 2017

1 reference

28 July 2017

1 reference

PubMed ID

20351491