Loke KY - Search Results

1

A distinctive type of metaphyseal chondrodysplasia with characteristic thickening of the distal ulna and radius: possible metaphyseal chondrodysplasia-Rosenberg.

Lee YS, Elliott AM, Loke KY, Lachman RS. Lee YS, et al. Among authors: loke ky. Am J Med Genet A. 2003 May 15;119A(1):50-6. doi: 10.1002/ajmg.a.20074. Am J Med Genet A. 2003. PMID: 12707959

2

The molecular pathogenesis of obesity: an unfinished jigsaw puzzle.

Lee YS, Loke KY. Lee YS, et al. Among authors: loke ky. Ann Acad Med Singap. 2000 May;29(3):388-95. Ann Acad Med Singap. 2000. PMID: 10976395 Review.

3

Prepubertal diagnosis of X-linked congenital adrenal hypoplasia presenting after infancy.

Loke KY, Larry KS, Lee YS, Peter M, Drop SL. Loke KY, et al. Eur J Pediatr. 2000 Sep;159(9):671-5. doi: 10.1007/pl00008404. Eur J Pediatr. 2000. PMID: 11014466

4

Type II Gaucher disease: compound heterozygote with RecNciI and L444P mutations.

Lee YS, Poh LK, Ida H, Loke KY. Lee YS, et al. Among authors: loke ky. J Trop Pediatr. 2001 Apr;47(2):115-7. doi: 10.1093/tropej/47.2.110-a. J Trop Pediatr. 2001. PMID: 11336129

5

Prevalence of ICA and GAD antibodies at initial presentation of type 1 diabetes mellitus in Singapore children.

Lee YS, Ng WY, Thai AC, Lui KF, Loke KY. Lee YS, et al. Among authors: loke ky. J Pediatr Endocrinol Metab. 2001 Jun;14(6):767-72. doi: 10.1515/jpem.2001.14.6.767. J Pediatr Endocrinol Metab. 2001. PMID: 11453527

6

Mitochondrial tubulopathy: the many faces of mitochondrial disorders.

Lee YS, Yap HK, Barshop BA, Lee YS, Rajalingam S, Loke KY. Lee YS, et al. Among authors: loke ky. Pediatr Nephrol. 2001 Sep;16(9):710-2. doi: 10.1007/s004670100637. Pediatr Nephrol. 2001. PMID: 11511982

7

Molecular analysis of CYP-21 mutations for congenital adrenal hyperplasia in Singapore.

Loke KY, Lee YS, Lee WW, Poh LK. Loke KY, et al. Horm Res. 2001;55(4):179-84. doi: 10.1159/000049992. Horm Res. 2001. PMID: 11598371

8

Cyclic pamidronate infusion improves bone mineralisation and reduces fracture incidence in osteogenesis imperfecta.

Lee YS, Low SL, Lim LA, Loke KY. Lee YS, et al. Among authors: loke ky. Eur J Pediatr. 2001 Nov;160(11):641-4. doi: 10.1007/s004310100844. Eur J Pediatr. 2001. PMID: 11760017 Clinical Trial.

9

An activating mutation of the thyrotropin receptor gene in hereditary non-autoimmune hyperthyroidism.

Lee YS, Poh L, Loke KY. Lee YS, et al. Among authors: loke ky. J Pediatr Endocrinol Metab. 2002 Feb;15(2):211-5. doi: 10.1515/jpem.2002.15.2.211. J Pediatr Endocrinol Metab. 2002. PMID: 11874187

10

A novel melanocortin 3 receptor gene (MC3R) mutation associated with severe obesity.

Lee YS, Poh LK, Loke KY. Lee YS, et al. Among authors: loke ky. J Clin Endocrinol Metab. 2002 Mar;87(3):1423-6. doi: 10.1210/jcem.87.3.8461. J Clin Endocrinol Metab. 2002. PMID: 11889220

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

76 results

Search Page

Filters