Honour JW - Search Results

1

Evidence for digenic inheritance in some cases of Antley-Bixler syndrome?

Reardon W, Smith A, Honour JW, Hindmarsh P, Das D, Rumsby G, Nelson I, Malcolm S, Adès L, Sillence D, Kumar D, DeLozier-Blanchet C, McKee S, Kelly T, McKeehan WL, Baraitser M, Winter RM. Reardon W, et al. Among authors: honour jw. J Med Genet. 2000 Jan;37(1):26-32. doi: 10.1136/jmg.37.1.26. J Med Genet. 2000. PMID: 10633130 Free PMC article.

2

Heterogeneity in the gene locus for steroid 21-hydroxylase deficiency.

Rumsby G, Fielder AH, Hague WM, Honour JW. Rumsby G, et al. Among authors: honour jw. J Med Genet. 1988 Sep;25(9):596-9. doi: 10.1136/jmg.25.9.596. J Med Genet. 1988. PMID: 3263505 Free PMC article.

3

In vitro gene amplification for prenatal diagnosis of congenital adrenal hyperplasia.

Rumsby G, Honour JW. Rumsby G, et al. Among authors: honour jw. J Med Genet. 1990 Nov;27(11):676-8. doi: 10.1136/jmg.27.11.676. J Med Genet. 1990. PMID: 2277381 Free PMC article.

4

Letter to the Editor: "Evaluating the Low-Dose ACTH Stimulation Test in Children: Ideal Times for Cortisol Measurement".

Hindmarsh PC, Honour JW. Hindmarsh PC, et al. Among authors: honour jw. J Clin Endocrinol Metab. 2020 Mar 1;105(3):dgaa009. doi: 10.1210/clinem/dgaa009. J Clin Endocrinol Metab. 2020. PMID: 31912152 No abstract available.

5

Management of altered hydrocortisone pharmacokinetics in a boy with congenital adrenal hyperplasia using a continuous subcutaneous hydrocortisone infusion.

Bryan SM, Honour JW, Hindmarsh PC. Bryan SM, et al. Among authors: honour jw. J Clin Endocrinol Metab. 2009 Sep;94(9):3477-80. doi: 10.1210/jc.2009-0630. Epub 2009 Jun 30. J Clin Endocrinol Metab. 2009. PMID: 19567522

6

Would Cortisol Measurements Be a Better Gauge of Hydrocortisone Replacement Therapy? Congenital Adrenal Hyperplasia as an Exemplar.

Hindmarsh PC, Honour JW. Hindmarsh PC, et al. Among authors: honour jw. Int J Endocrinol. 2020 Oct 13;2020:2470956. doi: 10.1155/2020/2470956. eCollection 2020. Int J Endocrinol. 2020. PMID: 33299411 Free PMC article. Review.

7

Combined 17 alpha-hydroxylase/17,20-lyase deficiency caused by heterozygous stop codons in the cytochrome P450 17 alpha-hydroxylase gene.

Rumsby G, Skinner C, Lee HA, Honour JW. Rumsby G, et al. Among authors: honour jw. Clin Endocrinol (Oxf). 1993 Oct;39(4):483-5. doi: 10.1111/j.1365-2265.1993.tb02397.x. Clin Endocrinol (Oxf). 1993. PMID: 8287576

8

Prenatal diagnosis of congenital adrenal hyperplasia by direct detection of mutations in the steroid 21-hydroxylase gene.

Rumsby G, Honour JW, Rodeck C. Rumsby G, et al. Among authors: honour jw. Clin Endocrinol (Oxf). 1993 Apr;38(4):421-5. doi: 10.1111/j.1365-2265.1993.tb00524.x. Clin Endocrinol (Oxf). 1993. PMID: 8319374

9

Problems in diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Honour JW, Rumsby G. Honour JW, et al. J Steroid Biochem Mol Biol. 1993 Apr;45(1-3):69-74. doi: 10.1016/0960-0760(93)90124-f. J Steroid Biochem Mol Biol. 1993. PMID: 8481353 Review.

10

Characterization of polymorphisms at the 11 beta-hydroxylase (CYP11B1) locus.

Skinner CA, Yousaf N, Honour JW, Rumsby G. Skinner CA, et al. Among authors: honour jw. Ann Hum Genet. 1998 Mar;62(Pt 2):181-3. doi: 10.1046/j.1469-1809.1998.6220181.x. Ann Hum Genet. 1998. PMID: 9759478

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

159 results

Search Page

Filters