(Q33701874)

28 July 2017

title

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

28 July 2017

Rolf C Gaillard

series ordinal

2

1 reference

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

published in

1 reference

28 July 2017

volume

34

1 reference

28 July 2017

issue

4

1 reference

28 July 2017

page(s)

547-555

1 reference

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

28 July 2017

cites work

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