(Q45135507)

English

Clinical features, diagnosis, treatment and molecular studies in paediatric Cushing's syndrome due to primary nodular adrenocortical hyperplasia.

scientific article published in November 2004

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15521956%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Clinical features, diagnosis, treatment and molecular studies in paediatric Cushing's syndrome due to primary nodular adrenocortical hyperplasia (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15521956%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

Cushing's syndrome

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based on heuristic

inferred from title

Katharina M Main

4

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4 January 2020

Ashley Grossman

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Grossman AB

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4 January 2020

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Storr HL

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4 January 2020

Martin O. Savage

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Savage MO

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4 January 2020

Adrian J. L. Clark

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Clark AJ

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4 January 2020

author name string

Mitchell H

2

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4 January 2020

Swords FM

3

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4 January 2020

Hindmarsh PC

5

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4 January 2020

Betts PR

6

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4 January 2020

Shaw NJ

7

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4 January 2020

Johnston DI

8

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4 January 2020

Reznek RH

10

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4 January 2020

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publication date

1 November 2004

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4 January 2020

Clinical Endocrinology

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4 January 2020

61

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4 January 2020

5

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4 January 2020

553-559

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4 January 2020

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02124.X

21 January 2018

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

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02124.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02124.X

21 January 2018

Sequence analysis of the PRKAR1A gene in sporadic somatotroph and other pituitary tumours

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02124.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02124.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02124.X

21 January 2018

Cushing's syndrome in children and adolescents. Presentation, diagnosis, and therapy.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02124.X

21 January 2018

The diagnosis and differential diagnosis of Cushing's syndrome and pseudo-Cushing's states

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02124.X

21 January 2018

Clinical and molecular genetics of Carney complex

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02124.X

21 January 2018

Human tumors associated with Carney complex and germline PRKAR1A mutations: a protein kinase A disease!

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02124.X

21 January 2018

Clinical and Molecular Features of the Carney Complex: Diagnostic Criteria and Recommendations for Patient Evaluation

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2265.2004.02124.X

21 January 2018

Identifiers

10.1111/J.1365-2265.2004.02124.X

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15521956%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15521956%20AND%20SRC:MED&resulttype=core&format=json

4 January 2020

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