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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 2 |
2015 | 1 |
2017 | 2 |
2018 | 2 |
2024 | 0 |
Search Results
7 results
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Page 1
Bayesian approach to determining penetrance of pathogenic SDH variants.
J Med Genet. 2018 Nov;55(11):729-734. doi: 10.1136/jmedgenet-2018-105427. Epub 2018 Sep 10.
J Med Genet. 2018.
PMID: 30201732
Free PMC article.
Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.
Andrews KA, Ascher DB, Pires DEV, Barnes DR, Vialard L, Casey RT, Bradshaw N, Adlard J, Aylwin S, Brennan P, Brewer C, Cole T, Cook JA, Davidson R, Donaldson A, Fryer A, Greenhalgh L, Hodgson SV, Irving R, Lalloo F, McConachie M, McConnell VPM, Morrison PJ, Murday V, Park SM, Simpson HL, Snape K, Stewart S, Tomkins SE, Wallis Y, Izatt L, Goudie D, Lindsay RS, Perry CG, Woodward ER, Antoniou AC, Maher ER.
Andrews KA, et al.
J Med Genet. 2018 Jun;55(6):384-394. doi: 10.1136/jmedgenet-2017-105127. Epub 2018 Jan 31.
J Med Genet. 2018.
PMID: 29386252
Free PMC article.
Item in Clipboard
Clinical and Molecular Features of Renal and Pheochromocytoma/Paraganglioma Tumor Association Syndrome (RAPTAS): Case Series and Literature Review.
Casey RT, Warren AY, Martin JE, Challis BG, Rattenberry E, Whitworth J, Andrews KA, Roberts T, Clark GR, West H, Smith PS, Docquier FM, Rodger F, Murray V, Simpson HL, Wallis Y, Giger O, Tran M, Tomkins S, Stewart GD, Park SM, Woodward ER, Maher ER.
Casey RT, et al.
J Clin Endocrinol Metab. 2017 Nov 1;102(11):4013-4022. doi: 10.1210/jc.2017-00562.
J Clin Endocrinol Metab. 2017.
PMID: 28973655
Free PMC article.
Review.
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A case of a metastatic SDHA mutated paraganglioma re-presenting twenty-three years after initial surgery.
Casey RT, Challis BG, Marker A, Pitfield D, Cheow HK, Shaw A, Park SM, Simpson HL, Maher ER.
Casey RT, et al.
Endocr Relat Cancer. 2017 Aug;24(8):L69-L71. doi: 10.1530/ERC-17-0206.
Endocr Relat Cancer. 2017.
PMID: 28729468
Free PMC article.
No abstract available.
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Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis.
Luchetti A, Walsh D, Rodger F, Clark G, Martin T, Irving R, Sanna M, Yao M, Robledo M, Neumann HP, Woodward ER, Latif F, Abbs S, Martin H, Maher ER.
Luchetti A, et al.
Int J Endocrinol. 2015;2015:138573. doi: 10.1155/2015/138573. Epub 2015 Mar 25.
Int J Endocrinol. 2015.
PMID: 25883647
Free PMC article.
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Phaeochromocytoma and paraganglioma: next-generation sequencing and evolving Mendelian syndromes.
Maher ER.
Maher ER.
Clin Med (Lond). 2014 Aug;14(4):440-4. doi: 10.7861/clinmedicine.14-4-440.
Clin Med (Lond). 2014.
PMID: 25099851
Free PMC article.
No abstract available.
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Germline FH mutations presenting with pheochromocytoma.
Clark GR, Sciacovelli M, Gaude E, Walsh DM, Kirby G, Simpson MA, Trembath RC, Berg JN, Woodward ER, Kinning E, Morrison PJ, Frezza C, Maher ER.
Clark GR, et al.
J Clin Endocrinol Metab. 2014 Oct;99(10):E2046-50. doi: 10.1210/jc.2014-1659. Epub 2014 Jul 8.
J Clin Endocrinol Metab. 2014.
PMID: 25004247
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