(Q55078949)

17 June 2018

case report

0 references

title

Case Report of a Prolactinoma in a Patient With a Novel MAX Mutation and Bilateral Pheochromocytomas. (English)

1 reference

17 June 2018

1 reference

1 reference

Kelly Lauter Roszko

1

1 reference

17 June 2018

Erica Blouch

2

1 reference

17 June 2018

Michael Blake

3

1 reference

17 June 2018

James F Powers

4

1 reference

17 June 2018

Arthur S Tischler

5

1 reference

17 June 2018

Richard Hodin

6

1 reference

17 June 2018

Peter Sadow

7

1 reference

17 June 2018

Elizabeth A Lawson

8

1 reference

17 June 2018

publication date

23 October 2017

1 reference

17 June 2018

Journal of the Endocrine Society

published in

1 reference

17 June 2018

volume

1

1 reference

17 June 2018

issue

11

1 reference

17 June 2018

page(s)

1401-1407

1 reference

17 June 2018

Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International

copyright license

start time

23 October 2017

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Progress in the Diagnosis and Classification of Pituitary Adenomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

15 YEARS OF PARAGANGLIOMA: Imaging and imaging-based treatment of pheochromocytoma and paraganglioma

18 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort

18 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

MAX and MYC: a heritable breakup

18 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

18 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

Genetics of pheochromocytoma and paraganglioma in Spanish patients.

18 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas

18 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

Germ-line mutations in nonsyndromic pheochromocytoma

18 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

Production and secretion of parathyroid hormone-related protein in pheochromocytoma: participation of an alpha-adrenergic mechanism

18 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

Quantitative assessment of the association between L769L and S836S polymorphisms at RET gene and medullary thyroid carcinoma risk.

18 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

MAX mutations status in Swedish patients with pheochromocytoma and paraganglioma tumours.

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

Intronic single nucleotide polymorphisms in the RET protooncogene are associated with a subset of apparently sporadic pheochromocytoma and may modulate age of onset

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

13 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5686672

30 November 2018

Identifiers

DOI

10.1210/JS.2017-00135

1 reference

17 June 2018

release_3dchwewotvfjzf6h3d7jleqjym

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/3dchwewotvfjzf6h3d7jleqjym

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMCID

5686672

1 reference

17 June 2018

PubMed ID

29264463

1 reference

17 June 2018