(Q35947217)

English

Prevalence of germline mutations in patients with pheochromocytoma or abdominal paraganglioma and sporadic presentation: a population-based study in Western Sweden

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scholarly article

1 reference

Europe PubMed Central

11 August 2017

Prevalence of germline mutations in patients with pheochromocytoma or abdominal paraganglioma and sporadic presentation: a population-based study in Western Sweden (English)

1 reference

Europe PubMed Central

11 August 2017

0 references

phaeochromocytoma

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

object named as

Andreas Muth

1

0 references

author name string

Frida Abel

2

1 reference

Europe PubMed Central

11 August 2017

Svante Jansson

3

1 reference

Europe PubMed Central

11 August 2017

Ola Nilsson

4

1 reference

Europe PubMed Central

11 August 2017

Håkan Ahlman

5

1 reference

Europe PubMed Central

11 August 2017

Bo Wängberg

6

1 reference

Europe PubMed Central

11 August 2017

publication date

1 June 2012

1 reference

Europe PubMed Central

11 August 2017

World Journal of Surgery

1 reference

Europe PubMed Central

11 August 2017

36

1 reference

Europe PubMed Central

11 August 2017

6

1 reference

Europe PubMed Central

11 August 2017

1389-1394

1 reference

Europe PubMed Central

11 August 2017

https://scigraph.springernature.com/pub.10.1007/s00268-012-1430-6

0 references

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=3348434

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=3348434

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=3348434

2 October 2017

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=3348434

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=3348434

2 October 2017

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=3348434

2 October 2017

The completeness of the Swedish Cancer Register: a sample survey for year 1998.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348434

2 October 2017

Methylation of the p16INK4A promoter is associated with malignant behavior in abdominal extra-adrenal paragangliomas but not pheochromocytomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348434

2 October 2017

The kinesin KIF1Bbeta acts downstream from EglN3 to induce apoptosis and is a potential 1p36 tumor suppressor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348434

2 October 2017

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=3348434

2 October 2017

Genetic analyses of apparently sporadic pheochromocytomas: the Rotterdam experience

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348434

2 October 2017

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=3348434

2 October 2017

The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348434

2 October 2017

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348434

2 October 2017

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=3348434

2 October 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348434

24 September 2018

Semi-automated unidirectional sequence analysis for mutation detection in a clinical diagnostic setting.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348434

24 September 2018

Denaturing high performance liquid chromatography detection of SDHB, SDHD, and VHL germline mutations in pheochromocytoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348434

24 September 2018

PHD2 mutation and congenital erythrocytosis with paraganglioma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348434

24 September 2018

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3348434

24 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=3348434

24 September 2018

Characteristics of pheochromocytoma in a 4- to 20-year-old population

1 reference

https://pubmed.ncbi.nlm.nih.gov/22270996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Validation of the multiplex ligation-dependent probe amplification (MLPA) technique for the determination of HER2 gene amplification in breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/22270996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00268-012-1430-6

1 reference

Europe PubMed Central

11 August 2017

1 reference

Europe PubMed Central

11 August 2017

1 reference

Europe PubMed Central

11 August 2017

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