Richardson AL - Search Results

1

Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma.

Dwight T, Na U, Kim E, Zhu Y, Richardson AL, Robinson BG, Tucker KM, Gill AJ, Benn DE, Clifton-Bligh RJ, Winge DR. Dwight T, et al. Among authors: richardson al. BMC Cancer. 2017 Jul 24;17(1):497. doi: 10.1186/s12885-017-3486-z. BMC Cancer. 2017. PMID: 28738844 Free PMC article.

2

Genetic testing in pheochromocytoma- and paraganglioma-associated syndromes.

Benn DE, Richardson AL, Marsh DJ, Robinson BG. Benn DE, et al. Among authors: richardson al. Ann N Y Acad Sci. 2006 Aug;1073:104-11. doi: 10.1196/annals.1353.011. Ann N Y Acad Sci. 2006. PMID: 17102077 Review.

3

Immunohistochemistry for SDHB triages genetic testing of SDHB, SDHC, and SDHD in paraganglioma-pheochromocytoma syndromes.

Gill AJ, Benn DE, Chou A, Clarkson A, Muljono A, Meyer-Rochow GY, Richardson AL, Sidhu SB, Robinson BG, Clifton-Bligh RJ. Gill AJ, et al. Among authors: richardson al. Hum Pathol. 2010 Jun;41(6):805-14. doi: 10.1016/j.humpath.2009.12.005. Epub 2010 Mar 17. Hum Pathol. 2010. PMID: 20236688

4

Denaturing high performance liquid chromatography detection of SDHB, SDHD, and VHL germline mutations in pheochromocytoma.

Meyer-Rochow GY, Smith JM, Richardson AL, Marsh DJ, Sidhu SB, Robinson BG, Benn DE. Meyer-Rochow GY, et al. Among authors: richardson al. J Surg Res. 2009 Nov;157(1):55-62. doi: 10.1016/j.jss.2008.07.043. Epub 2008 Sep 4. J Surg Res. 2009. PMID: 19215943

5

Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas.

Benn DE, Croxson MS, Tucker K, Bambach CP, Richardson AL, Delbridge L, Pullan PT, Hammond J, Marsh DJ, Robinson BG. Benn DE, et al. Among authors: richardson al. Oncogene. 2003 Mar 6;22(9):1358-64. doi: 10.1038/sj.onc.1206300. Oncogene. 2003. PMID: 12618761

6

Germline SDHC mutation presenting as recurrent SDH deficient GIST and renal carcinoma.

Gill AJ, Lipton L, Taylor J, Benn DE, Richardson AL, Frydenberg M, Shapiro J, Clifton-Bligh RJ, Chow CW, Bogwitz M. Gill AJ, et al. Among authors: richardson al. Pathology. 2013 Dec;45(7):689-91. doi: 10.1097/PAT.0000000000000018. Pathology. 2013. PMID: 24150194 No abstract available.

7

Bayesian approach to determining penetrance of pathogenic SDH variants.

Benn DE, Zhu Y, Andrews KA, Wilding M, Duncan EL, Dwight T, Tothill RW, Burgess J, Crook A, Gill AJ, Hicks RJ, Kim E, Luxford C, Marfan H, Richardson AL, Robinson B, Schlosberg A, Susman R, Tacon L, Trainer A, Tucker K, Maher ER, Field M, Clifton-Bligh RJ. Benn DE, et al. Among authors: richardson al. 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.

8

Rapid mutation screening for HRPT2 and MEN1 mutations associated with familial and sporadic primary hyperparathyroidism.

Howell VM, Cardinal JW, Richardson AL, Gimm O, Robinson BG, Marsh DJ. Howell VM, et al. Among authors: richardson al. J Mol Diagn. 2006 Nov;8(5):559-66. doi: 10.2353/jmoldx.2006.060015. J Mol Diagn. 2006. PMID: 17065424 Free PMC article.

9

Genome-wide copy number imbalances identified in familial and sporadic medullary thyroid carcinoma.

Marsh DJ, Theodosopoulos G, Martin-Schulte K, Richardson AL, Philips J, Röher HD, Delbridge L, Robinson BG. Marsh DJ, et al. Among authors: richardson al. J Clin Endocrinol Metab. 2003 Apr;88(4):1866-72. doi: 10.1210/jc.2002-021155. J Clin Endocrinol Metab. 2003. PMID: 12679485

10

Independent genetic events associated with the development of multiple parathyroid tumors in patients with primary hyperparathyroidism.

Dwight T, Nelson AE, Theodosopoulos G, Richardson AL, Learoyd DL, Philips J, Delbridge L, Zedenius J, Teh BT, Larsson C, Marsh DJ, Robinson BG. Dwight T, et al. Among authors: richardson al. Am J Pathol. 2002 Oct;161(4):1299-306. doi: 10.1016/S0002-9440(10)64406-9. Am J Pathol. 2002. PMID: 12368203 Free PMC article.

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