Can subunit-specific phenotypes guide surveillance imaging decisions in asymptomaticSDHmutation carriers?-Reference-Cited by-同舟云学术

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Can subunit-specific phenotypes guide surveillance imaging decisions in asymptomaticSDHmutation carriers?

Published:2018-11-28 Issue:1 Volume:90 Page:31-46
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Tufton Nicola¹²^ORCID,Sahdev Anju³,Drake William M.¹²,Akker Scott A.¹²

Affiliation:

1. Department of Endocrinology; St Bartholomew’s Hospital, Barts Health NHS Trust; London UK

2. Centre for Endocrinology, Barts and the London School of Medicine and Dentistry; Queen Mary University of London; London UK

3. Department of Radiology; St Bartholomew’s Hospital, Barts Health NHS Trust; London UK

Funder

The Medical College of Saint Bartholomew’s Hospital Trust

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cen.13877/fullpdf

Reference132 articles.

1. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma;Baysal;Science,2000

2. Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma;Gimm;Cancer Res,2000

3. Germline SDHD mutation in familial phaeochromocytoma;Astuti;Lancet,2001

4. Mutations in SDHC cause autosomal dominant paraganglioma, type 3;Niemann;Nat Genet,2000

5. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma;Astuti;Am J Hum Genet,2001

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1. Overview of recent guidelines and consensus statements on initial screening and management of phaeochromocytoma and paraganglioma in SDHx pathogenic variant carriers and patients;Best Practice & Research Clinical Endocrinology & Metabolism;2024-09

2. Genetic and Molecular Biomarkers in Aggressive Pheochromocytomas and Paragangliomas;International Journal of Molecular Sciences;2024-06-28

3. Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement;Nature Reviews Endocrinology;2023-12-14

4. Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants;The Lancet Diabetes & Endocrinology;2023-05

5. Distortion in transmission of pathogenic SDHB- and SDHD-mutated alleles from parent to offspring;Endocrine-Related Cancer;2023-02-14

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