(Q37081807)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267044%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

title

An unusual succinate dehydrogenase gene mutation C in a case of laryngeal paraganglioma (English)

1 reference

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2 January 2020

0 references

1

1 reference

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2 January 2020

author name string

P Raynaud

2

1 reference

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2 January 2020

I Raingeard

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267044%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

C Muyshondt

4

1 reference

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2 January 2020

Q Gardiner

5

1 reference

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2 January 2020

B Guerrier

6

1 reference

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2 January 2020

P Pujol

7

1 reference

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2 January 2020

I Coupier

8

1 reference

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2 January 2020

publication date

11 February 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18267044%20AND%20SRC:MED&resulttype=core&format=json

Journal of Laryngology and Otology

2 January 2020

published in

1 reference

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2 January 2020

volume

123

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2 January 2020

issue

1

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2 January 2020

page(s)

141-144

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Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene

2 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001570

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001570

Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001570

Prevalence of sporadic medullary thyroid carcinoma: the importance of routine measurement of serum calcitonin in the diagnostic evaluation of thyroid nodules

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001570

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001570

Neuroendocrine neoplasms of the larynx: advances in identification, understanding, and management

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001570

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001570

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0022215107001570

10.1017/S0022215107001570

21 January 2018

Identifiers

DOI

1 reference

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2 January 2020

1 reference