- Fee assured
- Verified this account
Areas of interest
General dermatology including acne, eczema, psoriasis, hair loss and vitiligo; Screening and treatment of skin cancers; Paediatric dermatology; HIV-associated skin diseases; Male genital skin disorders.
Current NHS consultant posts held
St Mary's Hospital
Imperial College Healthcare NHS Trust
Chan I. The role of extracellular matrix protein 1 in human skin. Clin Exp Dermatol 2004; 29: 52-6.
Chan I, Oyama N, Hamada T et al. Rapid diagnosis of lipoid proteinosis using an anti-extracellular matrix protein 1 (ECM1) antibody. J Dermatol Sci 2004; 35: 151-3.
Chan I, Hamada T, Hardman C et al. Progressive osseous heteroplasia resulting from a new mutation on the GNAS1 gene. Clin Exp Dermatol 2004; 29: 77-80.
Oyama N, Chan I, Neill S et al. Development of antigen-specific ELISA for circulating autoantibodies to extracellular matrix protein 1 (ECM1) in lichen sclerosus. J Clin Invest 2004; 113: 1550-9.
Chan I, Calonje E, Whittaker SJ. Cutaneous Waldenström’s macroglobulinaemia. Clin Exp Dermatol 2003; 28: 491-2.
Chan I, El-Zurghany A, Zendah B et al. Molecular basis of lipoid proteinosis in a Libyan family. Clin Exp Dermatol 2003; 28: 545-8.
Oyama N, Chan I, Neill S et al. Autoantibodies to extracellular matrix protein 1 in lichen sclerosus. Lancet 2003; 362: 118-23.
Hamada T, Chan I, Willoughby CE et al. Common mutations in Arg304 of the p63 gene in EEC syndrome: Lack of genotype-phenotype correlation and implications for mutation detection strategies. J Invest Dermatol 2002; 119:1202-3.
Chan I, Oyama N, Neill S et al. Characterization of autoantibodies to extracellular matrix protein 1 (ECM1) in lichen sclerosus. Clin Exp Dermatol 2004; 29: 499-504.
Chan I, Sethuraman G, Sharma VK et al. Molecular basis of lipoid proteinosis in two Indian siblings. J Dermatol 2004; 31: 764-6.
Chan I, Bingewar G, Patil K et al. An Indian child with lipoid proteinosis resulting from a recurrent frameshift mutation (507delT) in the extracellular matrix protein 1 (ECM1) gene. Br J Dermatol 2004; 151: 726-7.
Chan I, Harper JI, Mellerio JE et al. ADULT ectodermal dysplasia syndrome resulting from the missense mutation R298Q in the p63 gene. Clin Exp Dermatol 2004; 29: 669-72.
Reference number 4436429
Post treatment communication
Following treatment of a Bupa member, I will communicate with GPs in line with Department of Health, GMC and appropriate professional bodies guidelines.