Clinicoradiological manifestations of paraganglioma syndromes associated with succinyl dehydrogenase enzyme mutation. (Q35675637)

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23 January 2020

title

Clinicoradiological manifestations of paraganglioma syndromes associated with succinyl dehydrogenase enzyme mutation (English)

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23 January 2020

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6

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23 January 2020

author name string

Brendan Barber

1

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23 January 2020

Mark Ingram

2

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23 January 2020

Sameer Khan

3

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23 January 2020

Gul Bano

4

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23 January 2020

Shirley Hodgson

5

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23 January 2020

publication date

22 April 2011

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23 January 2020

published in

Insights into imaging

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23 January 2020

volume

2

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23 January 2020

issue

4

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23 January 2020

page(s)

431-438

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Clinical aspects of SDHx-related pheochromocytoma and paraganglioma

23 January 2020

cites work

1 reference

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Pheochromocytoma: current approaches and future directions

27 July 2018

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The genetics of paragangliomas: a review

27 July 2018

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Pheochromocytoma: recommendations for clinical practice from the First International Symposium. October 2005.

27 July 2018

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Hereditary paraganglioma/pheochromocytoma and inherited succinate dehydrogenase deficiency

27 July 2018

1 reference

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3259346

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

27 July 2018

1 reference

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

27 July 2018

1 reference

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Genomic imprinting in hereditary glomus tumours: evidence for new genetic theory

27 July 2018

1 reference

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Extraadrenal retroperitoneal paraganglioma: clinical, pathologic, and CT findings

27 July 2018

1 reference

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A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

27 July 2018

1 reference

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

27 July 2018

1 reference

https://api.crossref.org/works/10.1007/S13244-011-0096-1

CT and MR imaging of unusual locations of extra-adrenal paragangliomas (pheochromocytomas).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S13244-011-0096-1

Imaging and management of head and neck paragangliomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S13244-011-0096-1

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S13244-011-0096-1

Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA)

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S13244-011-0096-1

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

21 January 2018

1 reference

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Editorial: paraganglioma--all in the family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S13244-011-0096-1

MR imaging and MIBG scintigraphy of pheochromocytomas and extraadrenal functioning paragangliomas

21 January 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Color Doppler imaging of paragangliomas in the neck

1 reference

12 December 2020

Carotid body tumors at high altitudes: Quito, Ecuador, 1987

1 reference

12 December 2020

Extraadrenal paragangliomas of the body: imaging features

1 reference

12 December 2020

MR imaging of paragangliomas

1 reference

12 December 2020

10.1007/S13244-011-0096-1

Identifiers

DOI

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23 January 2020

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23 January 2020

PubMed publication ID

22347965

1 reference

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