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Results: 1-9 |
Results: 9
Mitochondrial tubulopathy: the many faces of mitochondrial disorders
Authors: Lee, YS Yap, HK Barshop, BA Lee, YS Rajalingam, S Loke, KY
Citation: Ys. Lee et al., Mitochondrial tubulopathy: the many faces of mitochondrial disorders, PED NEPHROL, 16(9), 2001, pp. 710-712
IGFs and IGF-binding proteins in short children with steroid-dependent nephrotic syndrome on chronic glucocorticoids: changes with 1 year exogenous GH
Authors: Zhou, X Loke, KY Pillai, CC How, HK Yap, HK Lee, KO
Citation: X. Zhou et al., IGFs and IGF-binding proteins in short children with steroid-dependent nephrotic syndrome on chronic glucocorticoids: changes with 1 year exogenous GH, EUR J ENDOC, 144(3), 2001, pp. 237-243
Cyclic pamidronate infusion improves bone mineralisation and reduces fracture incidence in osteogenesis imperfecta
Authors: Lee, YS Low, SL Lim, LA Loke, KY
Citation: Ys. Lee et al., Cyclic pamidronate infusion improves bone mineralisation and reduces fracture incidence in osteogenesis imperfecta, EUR J PED, 160(11), 2001, pp. 641-644
Prevalence of ICA and GAD antibodies at initial presentation of type 1 diabetes mellitus in Singapore children
Authors: Lee, YS Ng, WY Thai, AC Lui, KF Loke, KY
Citation: Ys. Lee et al., Prevalence of ICA and GAD antibodies at initial presentation of type 1 diabetes mellitus in Singapore children, J PED END M, 14(6), 2001, pp. 767-772
Molecular analysis of CYP-21 mutations for congenital adrenal hyperplasia in Singapore
Authors: Loke, KY Lee, YS Lee, WWR Poh, LKS
Citation: Ky. Loke et al., Molecular analysis of CYP-21 mutations for congenital adrenal hyperplasia in Singapore, HORMONE RES, 55(4), 2001, pp. 179-184
Type II Gaucher disease: Compound heterozygote with RecNcil and L444P mutations
Authors: Lee, YS Poh, LKS Ida, H Loke, KY
Citation: Ys. Lee et al., Type II Gaucher disease: Compound heterozygote with RecNcil and L444P mutations, J TROP PEDI, 47(2), 2001, pp. 115-117
Prepubertal diagnosis of X-linked congenital adrenal hypoplasia presentingafter infancy
Authors: Loke, KY Larry, KSP Lee, YS Peter, M Drop, SLS
Citation: Ky. Loke et al., Prepubertal diagnosis of X-linked congenital adrenal hypoplasia presentingafter infancy, EUR J PED, 159(9), 2000, pp. 671-675
An atypical kindred with X-linked adrenal hypoplasia congenita, normal puberty, and normal Dax-1 promoter and coding sequence
Authors: Loke, KY Poh, KSL Walker, AP Tan, JAMA Tay, AHN
Citation: Ky. Loke et al., An atypical kindred with X-linked adrenal hypoplasia congenita, normal puberty, and normal Dax-1 promoter and coding sequence, J PED END M, 13(1), 2000, pp. 29-36
A novel parathyroid hormone (PTH)/PTH-related peptide receptor mutation inJansen's metaphyseal chondrodysplasia
Authors: Schipani, E Langman, C Hunzelman, J Le Merrer, M Loke, KY Dillon, MJ Silve, C Juppner, H
Citation: E. Schipani et al., A novel parathyroid hormone (PTH)/PTH-related peptide receptor mutation inJansen's metaphyseal chondrodysplasia, J CLIN END, 84(9), 1999, pp. 3052-3057
Risultati: 1-9 |