Benn DE - Search Results

1

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

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

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.

6

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.

7

A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas.

Dahia PL, Ross KN, Wright ME, Hayashida CY, Santagata S, Barontini M, Kung AL, Sanso G, Powers JF, Tischler AS, Hodin R, Heitritter S, Moore F, Dluhy R, Sosa JA, Ocal IT, Benn DE, Marsh DJ, Robinson BG, Schneider K, Garber J, Arum SM, Korbonits M, Grossman A, Pigny P, Toledo SP, Nosé V, Li C, Stiles CD. Dahia PL, et al. Among authors: benn de. PLoS Genet. 2005 Jul;1(1):72-80. doi: 10.1371/journal.pgen.0010008. Epub 2005 Jul 25. PLoS Genet. 2005. PMID: 16103922 Free PMC article.

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

An apparently sporadic paraganglioma with an SDHB gene germline mutation presenting at age 68 years.

Elston MS, Benn D, Robinson BG, Conaglen JV. Elston MS, et al. Intern Med J. 2006 Feb;36(2):129-31. doi: 10.1111/j.1445-5994.2006.01023.x. Intern Med J. 2006. PMID: 16472267

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

55 results

Search Page