Ponder BA - Search Results

1

Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease.

Ritter MM, Frilling A, Crossey PA, Höppner W, Maher ER, Mulligan L, Ponder BA, Engelhardt D. Ritter MM, et al. Among authors: ponder ba. J Clin Endocrinol Metab. 1996 Mar;81(3):1035-7. doi: 10.1210/jcem.81.3.8772572. J Clin Endocrinol Metab. 1996. PMID: 8772572

2

Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II.

Neumann HP, Eng C, Mulligan LM, Glavac D, Zäuner I, Ponder BA, Crossey PA, Maher ER, Brauch H. Neumann HP, et al. Among authors: ponder ba. JAMA. 1995 Oct 11;274(14):1149-51. JAMA. 1995. PMID: 7563486

3

Genetic basis of endocrine disease: multiple endocrine neoplasia type 2.

Mulligan LM, Ponder BA. Mulligan LM, et al. Among authors: ponder ba. J Clin Endocrinol Metab. 1995 Jul;80(7):1989-95. doi: 10.1210/jcem.80.7.7608246. J Clin Endocrinol Metab. 1995. PMID: 7608246 Review. No abstract available.

4

Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma.

Eng C, Mulligan LM, Smith DP, Healey CS, Frilling A, Raue F, Neumann HP, Ponder MA, Ponder BA. Eng C, et al. Among authors: ponder ba, ponder ma. Clin Endocrinol (Oxf). 1995 Jul;43(1):123-7. doi: 10.1111/j.1365-2265.1995.tb01903.x. Clin Endocrinol (Oxf). 1995. PMID: 7641404

5

Presymptomatic screening for medullary thyroid carcinoma in patients with multiple endocrine neoplasia type 2A.

Frilling A, Röher HD, Ponder BA. Frilling A, et al. Among authors: ponder ba. World J Surg. 1994 Jul-Aug;18(4):577-81; discussion 581-2. doi: 10.1007/BF00353769. World J Surg. 1994. PMID: 7725747

6

Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma.

Crossey PA, Eng C, Ginalska-Malinowska M, Lennard TW, Wheeler DC, Ponder BA, Maher ER. Crossey PA, et al. Among authors: ponder ba. J Med Genet. 1995 Nov;32(11):885-6. doi: 10.1136/jmg.32.11.885. J Med Genet. 1995. PMID: 8592333 Free PMC article.

7

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: ponder ba. J Clin Endocrinol Metab. 1997 Sep;82(9):3025-8. doi: 10.1210/jcem.82.9.4197. J Clin Endocrinol Metab. 1997. PMID: 9284737

8

Mapping of von Hippel-Lindau disease to chromosome 3p confirmed by genetic linkage analysis.

Maher ER, Bentley E, Yates JR, Barton D, Jennings A, Fellows IW, Ponder MA, Ponder BA, Benjamin C, Harris R, et al. Maher ER, et al. Among authors: ponder ba, ponder ma. J Neurol Sci. 1990 Dec;100(1-2):27-30. doi: 10.1016/0022-510x(90)90008-b. J Neurol Sci. 1990. PMID: 1982450

9

Mutation of the RET proto-oncogene is correlated with RET immunostaining in subpopulations of cells in sporadic medullary thyroid carcinoma.

Eng C, Thomas GA, Neuberg DS, Mulligan LM, Healey CS, Houghton C, Frilling A, Raue F, Williams ED, Ponder BA. Eng C, et al. Among authors: ponder ba. J Clin Endocrinol Metab. 1998 Dec;83(12):4310-3. doi: 10.1210/jcem.83.12.5345. J Clin Endocrinol Metab. 1998. PMID: 9851769

10

Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2.

Mulligan LM, Gardner E, Smith BA, Mathew CG, Ponder BA. Mulligan LM, et al. Among authors: ponder ba. Genes Chromosomes Cancer. 1993 Mar;6(3):166-77. doi: 10.1002/gcc.2870060307. Genes Chromosomes Cancer. 1993. PMID: 7682102

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