Robinson BG - Search Results

1

The molecular genetics of endocrine tumours.

Learoyd DL, Twigg SM, Zedenius JV, Robinson BG. Learoyd DL, et al. Among authors: robinson bg. J Pediatr Endocrinol Metab. 1998 Mar-Apr;11(2):195-228. doi: 10.1515/jpem.1998.11.2.195. J Pediatr Endocrinol Metab. 1998. PMID: 9642636 Review.

2

Genotype-phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium.

Mulligan LM, Marsh DJ, Robinson BG, Schuffenecker I, Zedenius J, Lips CJ, Gagel RF, Takai SI, Noll WW, Fink M, et al. Mulligan LM, et al. Among authors: robinson bg. J Intern Med. 1995 Oct;238(4):343-6. doi: 10.1111/j.1365-2796.1995.tb01208.x. J Intern Med. 1995. PMID: 7595170

3

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: robinson bg. Genomics. 1994 Sep 15;23(2):477-9. doi: 10.1006/geno.1994.1526. Genomics. 1994. PMID: 7835899

4

Medullary thyroid carcinoma: recent advances and management update.

Marsh DJ, Learoyd DL, Robinson BG. Marsh DJ, et al. Among authors: robinson bg. Thyroid. 1995 Oct;5(5):407-24. doi: 10.1089/thy.1995.5.407. Thyroid. 1995. PMID: 8563482 Review.

5

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: robinson bg. Cancer Res. 1996 Mar 15;56(6):1241-3. Cancer Res. 1996. PMID: 8640806

6

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: robinson bg. Clin Endocrinol (Oxf). 1996 Mar;44(3):249-57. doi: 10.1046/j.1365-2265.1996.681503.x. Clin Endocrinol (Oxf). 1996. PMID: 8729519

7

The identification of false positive responses to the pentagastrin stimulation test in RET mutation negative members of MEN 2A families.

Marsh DJ, McDowall D, Hyland VJ, Andrew SD, Schnitzler M, Gaskin EL, Nevell DF, Diamond T, Delbridge L, Clifton-Bligh P, Robinson BG. Marsh DJ, et al. Among authors: robinson bg. Clin Endocrinol (Oxf). 1996 Feb;44(2):213-20. doi: 10.1046/j.1365-2265.1996.505292.x. Clin Endocrinol (Oxf). 1996. PMID: 8849577

8

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.

Eng C, Clayton D, Schuffenecker I, Lenoir G, Cote G, Gagel RF, van Amstel HK, Lips CJ, Nishisho I, Takai SI, Marsh DJ, Robinson BG, Frank-Raue K, Raue F, Xue F, Noll WW, Romei C, Pacini F, Fink M, Niederle B, Zedenius J, Nordenskjöld M, Komminoth P, Hendy GN, Mulligan LM, et al. Eng C, et al. Among authors: robinson bg. JAMA. 1996 Nov 20;276(19):1575-9. JAMA. 1996. PMID: 8918855

9

Technetium-99m-sestamibi scanning in recurrent medullary thyroid carcinoma.

Learoyd DL, Roach PJ, Briggs GM, Delbridge LW, Wilmshurst EG, Robinson BG. Learoyd DL, et al. Among authors: robinson bg. J Nucl Med. 1997 Feb;38(2):227-30. J Nucl Med. 1997. PMID: 9025742 Free article.

10

Mutation analysis of glial cell line-derived neurotrophic factor, a ligand for an RET/coreceptor complex, in multiple endocrine neoplasia type 2 and sporadic neuroendocrine tumors.

Marsh DJ, Zheng Z, Arnold A, Andrew SD, Learoyd D, Frilling A, Komminoth P, Neumann HP, Ponder BA, Rollins BJ, Shapiro GI, Robinson BG, Mulligan LM, Eng C. Marsh DJ, et al. Among authors: robinson bg. J Clin Endocrinol Metab. 1997 Sep;82(9):3025-8. doi: 10.1210/jcem.82.9.4197. J Clin Endocrinol Metab. 1997. PMID: 9284737

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