(Q35190348)

English

Measurements of plasma methoxytyramine, normetanephrine, and metanephrine as discriminators of different hereditary forms of pheochromocytoma

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Measurements of plasma methoxytyramine, normetanephrine, and metanephrine as discriminators of different hereditary forms of pheochromocytoma (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

phaeochromocytoma

1 reference

based on heuristic

inferred from title

12

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Karel Pacak

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Europe PubMed Central

PubMed publication ID

7 August 2017

Stefan R. Bornstein

7

object named as

Stefan R Bornstein

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Graeme Eisenhofer

1

object named as

Graeme Eisenhofer

1 reference

Europe PubMed Central

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7 August 2017

Jacques W M Lenders

2

object named as

Jacques W M Lenders

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Lorenz C Hofbauer

6

object named as

Lorenz C Hofbauer

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

author name string

Henri Timmers

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Massimo Mannelli

4

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Stefan K Grebe

5

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Oliver Tiebel

8

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Karen Adams

9

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Gennady Bratslavsky

10

1 reference

Europe PubMed Central

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7 August 2017

W Marston Linehan

11

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Europe PubMed Central

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7 August 2017

language of work or name

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publication date

24 January 2011

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Europe PubMed Central

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7 August 2017

Clinical Chemistry

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Europe PubMed Central

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7 August 2017

57

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7 August 2017

3

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7 August 2017

411-420

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

SDHA is a tumor suppressor gene causing paraganglioma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Immunohistochemistry for SDHB triages genetic testing of SDHB, SDHC, and SDHD in paraganglioma-pheochromocytoma syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Germline mutations in TMEM127 confer susceptibility to pheochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Simultaneous liquid-chromatographic determination of plasma catecholamines and metabolites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

The approach to the patient with paraganglioma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Genetics of pheochromocytoma and paraganglioma in Spanish patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Pheochromocytoma: recommendations for clinical practice from the First International Symposium. October 2005.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Genetic testing in pheochromocytoma- and paraganglioma-associated syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Genetic testing in pheochromocytoma: increasing importance for clinical decision making

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Phaeochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Pheochromocytoma: the expanding genetic differential diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Biochemical diagnosis of pheochromocytoma: which test is best?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Plasma metanephrines are markers of pheochromocytoma produced by catechol-O-methyltransferase within tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Simultaneous liquid-chromatographic determination of 3,4-dihydroxyphenylglycol, catecholamines, and 3,4-dihydroxyphenylalanine in plasma, and their responses to inhibition of monoamine oxidase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

13 July 2018

Pilot quality assurance programme for plasma metanephrines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

27 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

27 September 2018

Genetic testing in pheochromocytoma or functional paraganglioma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

27 September 2018

Pheochromocytoma catecholamine phenotypes and prediction of tumor size and location by use of plasma free metanephrines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

27 September 2018

Biochemical and clinical manifestations of dopamine-producing paragangliomas: utility of plasma methoxytyramine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

27 September 2018

Pheochromocytomas in von Hippel-Lindau syndrome and multiple endocrine neoplasia type 2 display distinct biochemical and clinical phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164998

27 September 2018

Genetic mutation screening in an italian cohort of nonsyndromic pheochromocytoma/paraganglioma patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/21262951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical presentations, biochemical phenotypes, and genotype-phenotype correlations in patients with succinate dehydrogenase subunit B-associated pheochromocytomas and paragangliomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/21262951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of metanephrines in plasma by liquid chromatography with electrochemical detection

1 reference

https://pubmed.ncbi.nlm.nih.gov/21262951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von Hippel-Lindau disease and multiple endocrine neoplasia type 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/21262951

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1373/CLINCHEM.2010.153320

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

ResearchGate publication ID

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