(Q21261505)

17 August 2022

Frederik J Hes

1

Frederik J

Hes

2 references

ORCID Public Data File 2021

17 August 2022

6

Bert A

Bonsing

Bert A Bonsing

1 reference

17 August 2022

8

Hans

Morreau

Hans Morreau

1 reference

17 August 2022

9

Johannes A

Romijn

Johannes A Romijn

1 reference

17 August 2022

Marjan M Weiss

2

Marjan M

Weiss

1 reference

17 August 2022

Sanne A Woortman

3

Sanne A

Woortman

1 reference

17 August 2022

Patrick A van Bunderen

5

Patrick A

van Bunderen

1 reference

17 August 2022

Marcel P M Stokkel

7

Marcel PM

Stokkel

1 reference

17 August 2022

Jeroen C Jansen

10

Jeroen C

Jansen

1 reference

17 August 2022

Annette H J T Vriends

11

Annette HJT

Vriends

1 reference

17 August 2022

Jean-Pierre L Bayley

12

Jean-Pierre L

Bayley

1 reference

17 August 2022

Eleonora P M Corssmit

13

Eleonora PM

Corssmit

1 reference

Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma

17 August 2022

language of work or name

English

0 references

publication date

2010

0 references

published in

BMC Medical Genetics

0 references

volume

11

0 references

issue

1

0 references

page(s)

92

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891715

The genetics of paragangliomas: a review

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891715

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891715

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

19 March 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891715

19 March 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891715

Penetrance and clinical consequences of a gross SDHB deletion in a large family

6 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891715

The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891715

Paragangliomas: clinical overview

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891715

K40E: a novel succinate dehydrogenase (SDH)B mutation causing familial phaeochromocytoma and paraganglioma.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891715

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891715

Pheochromocytomas and extra-adrenal paragangliomas detected by screening in patients with SDHD-associated head-and-neck paragangliomas.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2891715

Familial malignant catecholamine-secreting paraganglioma with prolonged survival associated with mutation in the succinate dehydrogenase B gene

27 September 2017

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-92

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-92

Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-92

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-92

Molecular characterisation of a common SDHB deletion in paraganglioma patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-11-92

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

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20540712

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Malignant paragangliomas associated with mutations in the succinate dehydrogenase D gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20540712

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-11-92

0 references