Richardson AL - Search Results

1

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. Among authors: richardson al. Cancer Res. 2000 Dec 15;60(24):7048-51. Cancer Res. 2000. PMID: 11156410

2

Germline and somatic mutations in an oncogene: RET mutations in inherited medullary thyroid carcinoma.

Marsh DJ, Andrew SD, Eng C, Learoyd DL, Capes AG, Pojer R, Richardson AL, Houghton C, Mulligan LM, Ponder BA, Robinson BG. Marsh DJ, et al. Among authors: richardson al. Cancer Res. 1996 Mar 15;56(6):1241-3. Cancer Res. 1996. PMID: 8640806

3

Genetic testing for familial cancer. Consequences of RET proto-oncogene mutation analysis in multiple endocrine neoplasia, type 2.

Learoyd DL, Marsh DJ, Richardson AL, Twigg SM, Delbridge L, Robinson BG. Learoyd DL, et al. Among authors: richardson al. Arch Surg. 1997 Sep;132(9):1022-5. doi: 10.1001/archsurg.1997.01430330088015. Arch Surg. 1997. PMID: 9301617

4

Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13.

Dwight T, Twigg S, Delbridge L, Wong FK, Farnebo F, Richardson AL, Nelson A, Zedenius J, Philips J, Larsson C, Teh BT, Robinson B. Dwight T, et al. Among authors: richardson al. Clin Endocrinol (Oxf). 2000 Jul;53(1):85-92. doi: 10.1046/j.1365-2265.2000.01010.x. Clin Endocrinol (Oxf). 2000. PMID: 10931084

5

Genetic analysis of lithium-associated parathyroid tumors.

Dwight T, Kytölä S, Teh BT, Theodosopoulos G, Richardson AL, Philips J, Twigg S, Delbridge L, Marsh DJ, Nelson AE, Larsson C, Robinson BG. Dwight T, et al. Among authors: richardson al. Eur J Endocrinol. 2002 May;146(5):619-27. doi: 10.1530/eje.0.1460619. Eur J Endocrinol. 2002. PMID: 11980616

6

A rapid screening method for the detection of mutations in the RET proto-oncogene in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma families.

Marsh DJ, Robinson BG, Andrew S, Richardson AL, Pojer R, Schnitzler M, Mulligan LM, Hyland VJ. Marsh DJ, et al. Among authors: richardson al. Genomics. 1994 Sep 15;23(2):477-9. doi: 10.1006/geno.1994.1526. Genomics. 1994. PMID: 7835899

7

Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinoma.

Marsh DJ, Learoyd DL, Andrew SD, Krishnan L, Pojer R, Richardson AL, Delbridge L, Eng C, Robinson BG. Marsh DJ, et al. Among authors: richardson al. Clin Endocrinol (Oxf). 1996 Mar;44(3):249-57. doi: 10.1046/j.1365-2265.1996.681503.x. Clin Endocrinol (Oxf). 1996. PMID: 8729519

8

MEN type 2a presenting as an intra-abdominal emergency.

Evans JP, Bambach CP, Andrew S, Dwight T, Richardson AL, Robinson BG, Delbridge L. Evans JP, et al. Among authors: richardson al. Aust N Z J Surg. 1997 Nov;67(11):824-6. doi: 10.1111/j.1445-2197.1997.tb04599.x. Aust N Z J Surg. 1997. PMID: 9397010 No abstract available.

9

Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutation.

Marsh DJ, Dahia PL, Coulon V, Zheng Z, Dorion-Bonnet F, Call KM, Little R, Lin AY, Eeles RA, Goldstein AM, Hodgson SV, Richardson AL, Robinson BG, Weber HC, Longy M, Eng C. Marsh DJ, et al. Among authors: richardson al. Genes Chromosomes Cancer. 1998 Jan;21(1):61-9. doi: 10.1002/(sici)1098-2264(199801)21:1<61::aid-gcc8>3.0.co;2-6. Genes Chromosomes Cancer. 1998. PMID: 9443042

10

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: richardson al. Neoplasia. 2001 May-Jun;3(3):236-44. doi: 10.1038/sj.neo.7900154. Neoplasia. 2001. PMID: 11494117 Free PMC article.

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