(Q34581403)

3 August 2017

Genetic analyses of apparently sporadic pheochromocytomas: the Rotterdam experience (English)

1 reference

3 August 2017

1 reference

E Korpershoek

1

1 reference

3 August 2017

F H Van Nederveen

2

1 reference

3 August 2017

H Dannenberg

3

1 reference

3 August 2017

B J Petri

4

1 reference

3 August 2017

P Komminoth

5

1 reference

3 August 2017

A Perren

6

1 reference

3 August 2017

J W Lenders

7

1 reference

3 August 2017

A A Verhofstad

8

1 reference

3 August 2017

W W De Herder

9

1 reference

3 August 2017

R R De Krijger

10

1 reference

3 August 2017

W N M Dinjens

11

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 August 2006

1 reference

Annals of the New York Academy of Sciences

3 August 2017

1 reference

3 August 2017

1073

1 reference

3 August 2017

1

1 reference

28 June 2019

page(s)

138-148

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

3 August 2017

1 reference

The pressure rises: update on the genetics of phaeochromocytoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

How many pathways to pheochromocytoma?

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

Multiple endocrine neoplasia type 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

Multiple endocrine neoplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

Role of VHL gene mutation in human cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

On the association of succinate dehydrogenase mutations with hereditary paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

SDHC mutations in hereditary paraganglioma/pheochromocytoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

Germline mutations in the vhl gene in patients presenting with phaeochromocytomas.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

Clinical characteristics of pheochromocytoma patients with germline mutations in SDHD.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

Genetic and epigenetic profile of sporadic pheochromocytomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

Germ-line mutations in nonsyndromic pheochromocytoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1353.014

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/10.1196%2FANNALS.1353.014

21 January 2018

Identifiers

DOI

10.1196/ANNALS.1353.014

1 reference

3 August 2017

1 reference