(Q36090002)

English

Pheochromocytoma/Paraganglioma: Review of perioperative management of blood pressure and update on genetic mutations associated with pheochromocytoma

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Pheochromocytoma/Paraganglioma: Review of perioperative management of blood pressure and update on genetic mutations associated with pheochromocytoma (English)

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

phaeochromocytoma

1 reference

based on heuristic

inferred from title

Robert Z Orlowski

2

object named as

Robert Orlowski

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

3

object named as

Debbie Cohen

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

author name string

Lauren Fishbein

1

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

publication date

15 March 2013

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Journal of Clinical Hypertension

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

15

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

6

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

428-434

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Risk of malignant paraganglioma in SDHB-mutation and SDHD-mutation carriers: a systematic review and meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Updated and new perspectives on diagnosis, prognosis, and therapy of malignant pheochromocytoma/paraganglioma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Perioperative management of pheochromocytoma/paraganglioma: is there a state of the art?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Long-term postoperative follow-up in patients with apparently benign pheochromocytoma and paraganglioma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Plasma methoxytyramine: a novel biomarker of metastatic pheochromocytoma and paraganglioma in relation to established risk factors of tumour size, location and SDHB mutation status

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

SDHAF2 (PGL2-SDH5) and hereditary head and neck paraganglioma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Clinical risk factors for malignancy and overall survival in patients with pheochromocytomas and sympathetic paragangliomas: primary tumor size and primary tumor location as prognostic indicators.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Comparison of two preoperative medical management strategies for laparoscopic resection of pheochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 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=4581847

2 October 2017

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=4581847

2 October 2017

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=4581847

2 October 2017

Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

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=4581847

2 October 2017

Current progress and future challenges in the biochemical diagnosis and treatment of pheochromocytomas and paragangliomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Biochemical diagnosis of pheochromocytoma: how to distinguish true- from false-positive test results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Prevalence of clinically unsuspected pheochromocytoma. Review of a 50-year autopsy series

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Surgical management of pheochromocytoma with the use of metyrosine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

2 October 2017

Posterior retroperitoneoscopic adrenalectomy is a safe and effective alternative to transabdominal laparoscopic adrenalectomy for pheochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

11 July 2018

Lack of symptoms in patients with histologic evidence of pheochromocytoma: a diagnostic challenge

1 reference

https://api.crossref.org/works/10.1111%2FJCH.12084

21 January 2018

Risk Factors for Hemodynamic Instability during Surgery for Pheochromocytoma

1 reference

https://api.crossref.org/works/10.1111%2FJCH.12084

21 January 2018

1,111 patients with adrenal incidentalomas observed at a single endocrinological center: incidence of chromaffin tumors.

1 reference

https://api.crossref.org/works/10.1111%2FJCH.12084

21 January 2018

The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.

1 reference

https://api.crossref.org/works/10.1111%2FJCH.12084

21 January 2018

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

1 reference

https://api.crossref.org/works/10.1111%2FJCH.12084

21 January 2018

Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sites

1 reference

https://api.crossref.org/works/10.1111%2FJCH.12084

21 January 2018

Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.

1 reference

https://api.crossref.org/works/10.1111%2FJCH.12084

21 January 2018

Genetic testing in pheochromocytoma or functional paraganglioma

1 reference

https://api.crossref.org/works/10.1111%2FJCH.12084

21 January 2018

Imaging work-up for screening of paraganglioma and pheochromocytoma in SDHx mutation carriers: a multicenter prospective study from the PGL.EVA Investigators.

1 reference

https://api.crossref.org/works/10.1111%2FJCH.12084

21 January 2018

Efficacy and safety of doxazosin for perioperative management of patients with pheochromocytoma

1 reference

https://api.crossref.org/works/10.1111%2FJCH.12084

21 January 2018

Malignant pheochromocytoma and paraganglioma: a population level analysis of long-term survival over two decades.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

23 September 2018

Alpha blockade in preoperative preparation of patients with pheochromocytomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4581847

23 September 2018

Chromogranin A, a member of neuroendocrine secretory proteins as a selective marker for laboratory diagnosis of pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/23730992

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paraganglioma syndrome: SDHB, SDHC, and SDHD mutations in head and neck paragangliomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/23730992

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Surgical management of organ-contained unilateral pheochromocytoma: comparative outcomes of laparoscopic and conventional open surgical procedures in a large single-institution series

1 reference

https://pubmed.ncbi.nlm.nih.gov/23730992

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Observer variation in the application of the Pheochromocytoma of the Adrenal Gland Scaled Score

1 reference

https://pubmed.ncbi.nlm.nih.gov/23730992

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pheochromocytoma of the Adrenal gland Scaled Score (PASS) to separate benign from malignant neoplasms: a clinicopathologic and immunophenotypic study of 100 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/23730992

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metyrosine and pheochromocytoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/23730992

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/JCH.12084

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q36090002&oldid=1998000645"