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

scientific article (publication date: 3 July 2003)

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

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Sotirios G Stergiopoulos

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1

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Constantine A Stratakis

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2

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language of work or name

English

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publication date

3 July 2003

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published in

FEBS Letters

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volume

546

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issue

1

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page(s)

59-64

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cites work

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

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

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

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Neurosurgical implications of Carney complex

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Testicular ultrasound in Carney complex: report of three cases

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

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

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

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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

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Regulatory subunit type I-alpha of protein kinase A (PRKAR1A): a tumor-suppressor gene for sporadic thyroid cancer.

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Carney complex: diagnosis and management of the complex of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas

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Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex)

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Ductal adenoma of the breast with tubular features. A probable component of the complex of myxomas, spotty pigmentation, endocrine overactivity, and schwannomas

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Ductal adenoma of the breast and the Carney complex

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Genetic heterogeneity of familial atrial myxoma syndromes (Carney complex)

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Dominant inheritance of the complex of myxomas, spotty pigmentation, and endocrine overactivity

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7 January 2021

The complex of myxomas, spotty pigmentation, and endocrine overactivity

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Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease

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Differences between nonfamilial and familial cardiac myxoma

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Identification of a novel genetic locus for familial cardiac myxomas and Carney complex

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7 January 2021

(Q28182362)

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

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