Solid tumors associated with multiple endocrine neoplasias (Q34213017)

31 July 2017

title

Solid tumors associated with multiple endocrine neoplasias (English)

1 reference

31 July 2017

author

Constantine A Stratakis

series ordinal

2

object named as

Constantine A Stratakis

1 reference

31 July 2017

1

Madson Q Almeida

1 reference

31 July 2017

publication date

1 November 2010

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Cancer Genetics and Cytogenetics

31 July 2017

published in

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31 July 2017

volume

203

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31 July 2017

issue

1

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31 July 2017

page(s)

30-36

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Clinical and genetic aspects of neurofibromatosis 1.

31 July 2017

cites work

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28 July 2018

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28 July 2018

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Carney complex and lentiginosis

28 July 2018

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Mutations in regulatory subunit type 1A of cyclic adenosine 5'-monophosphate-dependent protein kinase (PRKAR1A): phenotype analysis in 353 patients and 80 different genotypes

28 July 2018

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Modes of resistance to anti-angiogenic therapy

28 July 2018

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Genetic screening for pheochromocytoma: should SDHC gene analysis be included?

28 July 2018

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28 July 2018

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Carney complex: the first 20 years

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans

28 July 2018

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High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing

28 July 2018

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

28 July 2018

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Von Hippel-Lindau disease and endocrine tumour susceptibility

28 July 2018

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Familial multiple endocrine neoplasia: the first 100 years

28 July 2018

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Dysfunction of the RET receptor in human cancer

28 July 2018

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Multiple endocrine adenomas; report of 8 cases in which the parathyroids, pituitary and pancreatic islets were involved.

28 July 2018

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Germ-line mutations in nonsyndromic pheochromocytoma

28 July 2018

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Guidelines for diagnosis and therapy of MEN type 1 and type 2.

28 July 2018

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

The GDNF/RET signaling pathway and human diseases

28 July 2018

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Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Identification of tyrosine residues that are essential for transforming activity of the ret proto-oncogene with MEN2A or MEN2B mutation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Identification of the von Hippel-Lindau disease tumor suppressor gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Low frequency of germline mutations in the RET proto‐oncogene in patients with apparently sporadic medullary thyroid carcinoma

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Characterization of RET proto-oncogene 3' splicing variants and polyadenylation sites: a novel C-terminus for RET

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

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

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Von Recklinghausen neurofibromatosis

28 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

The complex of myxomas, spotty pigmentation, and endocrine overactivity

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Familial multiple endocrine neoplasia type I: a new look at pathophysiology

28 July 2018

1 reference

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Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

28 July 2018

1 reference

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Tyrosine kinase inhibitors and the thyroid.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Carney triad: a syndrome featuring paraganglionic, adrenocortical, and possibly other endocrine tumors

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Heterogeneity of skin manifestations in patients with Carney complex.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

RET oncogene in MEN2, MEN2B, MTC and other forms of thyroid cancer

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Familial gastrointestinal stromal tumors and germ-line mutations.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Genetics of carney triad: recurrent losses at chromosome 1 but lack of germline mutations in genes associated with paragangliomas and gastrointestinal stromal tumors.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Hypoxia-inducible factors: central regulators of the tumor phenotype

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Hypodense nodularity on computed tomography: novel imaging and pathology of micronodular adrenocortical hyperplasia associated with myelolipomatous changes.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Genetic and histologic studies of somatomammotropic pituitary tumors in patients with the "complex of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex).

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Prolactin secretion abnormalities in patients with the "syndrome of spotty skin pigmentation, myxomas, endocrine overactivity and schwannomas" (Carney complex).

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Carney complex: The complex of myxomas, spotty pigmentation, endocrine overactivity, and schwannomas

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2957471

Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma

28 October 2018

1 reference

12 December 2020

Study of a kindred with pheochromocytoma, medullary thyroid carcinoma, hyperparathyroidism and Cushing's disease: multiple endocrine neoplasia, type 2

1 reference

12 December 2020

Multiple endocrine neoplasia type 2

1 reference

12 December 2020

Gastrinomas in the duodenums of patients with multiple endocrine neoplasia type 1 and the Zollinger-Ellison syndrome

1 reference

12 December 2020

Pheochromocytoma; its relationship to the neurocutaneous syndromes

1 reference

12 December 2020

Von Hippel-Lindau Disease

1 reference

12 December 2020

Prospective endoscopic ultrasonographic evaluation of the frequency of nonfunctioning pancreaticoduodenal endocrine tumors in patients with multiple endocrine neoplasia type 1

1 reference

12 December 2020

Clinical and genetic characteristics of patients with neurofibromatosis type 1 and pheochromocytoma

1 reference

12 December 2020

Clinicopathologic studies of thymic carcinoids in multiple endocrine neoplasia type 1

1 reference

12 December 2020

Multiple endocrine neoplasia type 1 in patients with recognized pituitary tumours of different types

1 reference

12 December 2020

10.1016/J.CANCERGENCYTO.2010.09.006

Identifiers

DOI

1 reference

31 July 2017

1 reference

31 July 2017

1 reference