(Q42576314)

3 November 2017

Adrenal medullary hyperplasia is a precursor lesion for pheochromocytoma in MEN2 syndrome (English)

1 reference

3 November 2017

1 reference

7

Wouter W de Herder

1 reference

3 November 2017

1

Esther Korpershoek

1 reference

3 November 2017

8

Ronald R de Krijger

1 reference

3 November 2017

9

Winand N M Dinjens

1 reference

3 November 2017

Bart-Jeroen Petri

2

1 reference

3 November 2017

Edward Post

3

1 reference

3 November 2017

Casper H J van Eijck

4

1 reference

3 November 2017

Rogier A Oldenburg

5

1 reference

3 November 2017

Eric J T Belt

6

1 reference

3 November 2017

23 October 2014

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3 November 2017

1 reference

3 November 2017

16

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3 November 2017

10

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3 November 2017

868-873

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Protocol for the examination of specimens from patients with pheochromocytomas and extra-adrenal paragangliomas

3 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Precursor lesions of endocrine system neoplasms

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemia

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

SDHA is a tumor suppressor gene causing paraganglioma

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Precursor lesions of the adrenal gland

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Estimated risk of pheochromocytoma recurrence after adrenal-sparing surgery in patients with multiple endocrine neoplasia type 2A.

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

RET proto-oncogene: a review and update of genotype-phenotype correlations in hereditary medullary thyroid cancer and associated endocrine tumors

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Losses of chromosomes 1p and 3q are early genetic events in the development of sporadic pheochromocytomas

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

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

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Sporadic unilateral adrenomedullary hyperplasia with hypertension cured by adrenalectomy

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Bilateral adrenal medullary hyperplasia: a clinicopathological entity

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas

28 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Long-term outcomes of surgical treatment for hereditary pheochromocytoma

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

PHD2 mutation and congenital erythrocytosis with paraganglioma.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

A germline mutation of the KIF1B beta gene on 1p36 in a family with neural and nonneural tumors

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4212248

Duplication of the mutant RET allele in trisomy 10 or loss of the wild-type allele in multiple endocrine neoplasia type 2-associated pheochromocytomas

16 August 2018

1 reference

12 December 2020

Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p

1 reference

12 December 2020

Multiple endocrine neoplasia type 2

1 reference

12 December 2020

Bilateral adrenal medullary hyperplasia in multiple endocrine neoplasia, type 2: the precursor of bilateral pheochromocytoma

1 reference

12 December 2020

Adrenomedullary hyperplasia and phaeochromocytoma. DNA cytophotometric findings in 47 cases

1 reference

12 December 2020

Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1-0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p

1 reference

12 December 2020

Array-comparative genomic hybridization in sporadic benign pheochromocytomas

1 reference

12 December 2020

Bilateral adrenal medullary hyperplasia associated with an SDHB mutation

1 reference

12 December 2020

10.1016/J.NEO.2014.09.002

Identifiers

DOI

1 reference

3 November 2017

1 reference

3 November 2017

PubMed publication ID

25379023

1 reference