Trump D - Search Results

1

Loss of heterozygosity studies at the retinoblastoma and breast cancer susceptibility (BRCA2) loci in pituitary, parathyroid, pancreatic and carcinoid tumours.

Pearce SH, Trump D, Wooding C, Sheppard MN, Clayton RN, Thakker RV. Pearce SH, et al. Among authors: trump d. Clin Endocrinol (Oxf). 1996 Aug;45(2):195-200. doi: 10.1046/j.1365-2265.1996.d01-1561.x. Clin Endocrinol (Oxf). 1996. PMID: 8881452

2

Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH.

Trump D, Whyte MP, Wooding C, Pang JT, Pearce SH, Kocher DB, Thakker RV. Trump D, et al. Hum Genet. 1995 Aug;96(2):183-7. doi: 10.1007/BF00207376. Hum Genet. 1995. PMID: 7635467

3

G-protein-coupled receptors in endocrine disease.

Pearce SH, Trump D. Pearce SH, et al. Among authors: trump d. QJM. 1995 Jan;88(1):3-8. QJM. 1995. PMID: 7894986 Review. No abstract available.

4

Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1.

Trump D, Pilia G, Dixon PH, Wooding C, Thakrar R, Leigh SE, Nagaraja R, Whyte MP, Schlessinger D, Thakker RV. Trump D, et al. Hum Genet. 1996 Jan;97(1):60-8. doi: 10.1007/BF00218834. Hum Genet. 1996. PMID: 8557262

5

Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism.

Pearce SH, Trump D, Wooding C, Besser GM, Chew SL, Grant DB, Heath DA, Hughes IA, Paterson CR, Whyte MP, et al. Pearce SH, et al. Among authors: trump d. J Clin Invest. 1995 Dec;96(6):2683-92. doi: 10.1172/JCI118335. J Clin Invest. 1995. PMID: 8675635 Free PMC article.

6

Clinical studies of multiple endocrine neoplasia type 1 (MEN1).

Trump D, Farren B, Wooding C, Pang JT, Besser GM, Buchanan KD, Edwards CR, Heath DA, Jackson CE, Jansen S, Lips K, Monson JP, O'Halloran D, Sampson J, Shalet SM, Wheeler MH, Zink A, Thakker RV. Trump D, et al. QJM. 1996 Sep;89(9):653-69. doi: 10.1093/qjmed/89.9.653. QJM. 1996. PMID: 8917740

7

Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneity.

Gertner JM, Whyte MP, Dixon PH, Pang JT, Trump D, Pearce SH, Wooding C, Thakker RV. Gertner JM, et al. Among authors: trump d. J Bone Miner Res. 1997 Aug;12(8):1204-9. doi: 10.1359/jbmr.1997.12.8.1204. J Bone Miner Res. 1997. PMID: 9258750 Free article.

8

Mutational analysis of PHEX gene in X-linked hypophosphatemia.

Dixon PH, Christie PT, Wooding C, Trump D, Grieff M, Holm I, Gertner JM, Schmidtke J, Shah B, Shaw N, Smith C, Tau C, Schlessinger D, Whyte MP, Thakker RV. Dixon PH, et al. Among authors: trump d. J Clin Endocrinol Metab. 1998 Oct;83(10):3615-23. doi: 10.1210/jcem.83.10.5180. J Clin Endocrinol Metab. 1998. PMID: 9768674

9

Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27.

Trump D, Dixon PH, Mumm S, Wooding C, Davies KE, Schlessinger D, Whyte MP, Thakker RV. Trump D, et al. J Med Genet. 1998 Nov;35(11):905-9. doi: 10.1136/jmg.35.11.905. J Med Genet. 1998. PMID: 9832036 Free PMC article.

10

Perrault syndrome: further evidence for genetic heterogeneity.

Jenkinson EM, Clayton-Smith J, Mehta S, Bennett C, Reardon W, Green A, Pearce SH, De Michele G, Conway GS, Cilliers D, Moreton N, Davis JR, Trump D, Newman WG. Jenkinson EM, et al. Among authors: trump d. J Neurol. 2012 May;259(5):974-6. doi: 10.1007/s00415-011-6285-5. Epub 2011 Oct 27. J Neurol. 2012. PMID: 22037954 No abstract available.

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