Benn DE - Search Results

1

Loss of heterozygosity of 17p13, with possible involvement of ACADVL and ALOX15B, in the pathogenesis of adrenocortical tumors.

Soon PS, Libe R, Benn DE, Gill A, Shaw J, Sywak MS, Groussin L, Bertagna X, Gicquel C, Bertherat J, McDonald KL, Sidhu SB, Robinson BG. Soon PS, et al. Among authors: benn de. Ann Surg. 2008 Jan;247(1):157-64. doi: 10.1097/SLA.0b013e318153ff55. Ann Surg. 2008. PMID: 18156936

2

Peripheral blood mononuclear cells are a reliable internal standard for the flow cytometric DNA analysis of frozen malignant breast biopsies.

Benn DE, Robinson BG. Benn DE, et al. Cytometry. 1996 Jun 15;26(2):161-5. doi: 10.1002/(SICI)1097-0320(19960615)26:2<161::AID-CYTO10>3.0.CO;2-L. Cytometry. 1996. PMID: 8817093 Free article.

3

Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p.

Benn DE, Dwight T, Richardson AL, Delbridge L, Bambach CP, Stowasser M, Gordon RD, Marsh DJ, Robinson BG. Benn DE, et al. Cancer Res. 2000 Dec 15;60(24):7048-51. Cancer Res. 2000. PMID: 11156410

4

Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography.

Marsh DJ, Theodosopoulos G, Howell V, Richardson AL, Benn DE, Proos AL, Eng C, Robinson BG. Marsh DJ, et al. Among authors: benn de. Neoplasia. 2001 May-Jun;3(3):236-44. doi: 10.1038/sj.neo.7900154. Neoplasia. 2001. PMID: 11494117 Free PMC article.

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. Oncogene. 2003 Mar 6;22(9):1358-64. doi: 10.1038/sj.onc.1206300. Oncogene. 2003. PMID: 12618761

6

K40E: a novel succinate dehydrogenase (SDH)B mutation causing familial phaeochromocytoma and paraganglioma.

McDonnell CM, Benn DE, Marsh DJ, Robinson BG, Zacharin MR. McDonnell CM, et al. Among authors: benn de. Clin Endocrinol (Oxf). 2004 Oct;61(4):510-4. doi: 10.1111/j.1365-2265.2004.02122.x. Clin Endocrinol (Oxf). 2004. PMID: 15473885 Review.

7

Phaeochromocytoma: current concepts.

Alderazi Y, Yeh MW, Robinson BG, Benn DE, Sywak MS, Learoyd DL, Delbridge LW, Sidhu SB. Alderazi Y, et al. Among authors: benn de. Med J Aust. 2005 Aug 15;183(4):201-4. doi: 10.5694/j.1326-5377.2005.tb06997.x. Med J Aust. 2005. PMID: 16097921 Review.

8

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

Benn DE, Gimenez-Roqueplo AP, Reilly JR, Bertherat J, Burgess J, Byth K, Croxson M, Dahia PL, Elston M, Gimm O, Henley D, Herman P, Murday V, Niccoli-Sire P, Pasieka JL, Rohmer V, Tucker K, Jeunemaitre X, Marsh DJ, Plouin PF, Robinson BG. Benn DE, et al. J Clin Endocrinol Metab. 2006 Mar;91(3):827-36. doi: 10.1210/jc.2005-1862. Epub 2005 Nov 29. J Clin Endocrinol Metab. 2006. PMID: 16317055

9

Genetic basis of phaeochromocytoma and paraganglioma.

Benn DE, Robinson BG. Benn DE, et al. Best Pract Res Clin Endocrinol Metab. 2006 Sep;20(3):435-50. doi: 10.1016/j.beem.2006.07.005. Best Pract Res Clin Endocrinol Metab. 2006. PMID: 16980204 Review.

10

Genetic testing in pheochromocytoma- and paraganglioma-associated syndromes.

Benn DE, Richardson AL, Marsh DJ, Robinson BG. Benn DE, et 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.

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