Sai Yee Chuah

Summary

Affiliation: National Skin Centre
Country: Singapore

Publications

  1. ncbi request reprint Recurrent and persistent pityriasis rosea: an atypical case presentation
    Sai Yee Chuah
    Department of Dermatology, National Skin Centre, 1 Mandalay Road, Singapore 308205
    Singapore Med J 55:e4-6. 2014
  2. doi request reprint Photopatch testing in Asians: a 5-year experience in Singapore
    Sai Yee Chuah
    Department of Dermatology, National Skin Centre, Singapore
    Photodermatol Photoimmunol Photomed 29:116-20. 2013
  3. doi request reprint Genetic study in a Singaporean patient with erythropoietic protoporphyria
    Sai Yee Chuah
    Department of Dermatology, National Skin Centre, Singapore
    Photodermatol Photoimmunol Photomed 28:269-71. 2012

Collaborators

Detail Information

Publications3

  1. ncbi request reprint Recurrent and persistent pityriasis rosea: an atypical case presentation
    Sai Yee Chuah
    Department of Dermatology, National Skin Centre, 1 Mandalay Road, Singapore 308205
    Singapore Med J 55:e4-6. 2014
    ..However, reports of multiple recurrences, with prolonged duration of each episode and very short remissions in between, have not been made. To the best of our knowledge, this is the first report of such unique presentation. ..
  2. doi request reprint Photopatch testing in Asians: a 5-year experience in Singapore
    Sai Yee Chuah
    Department of Dermatology, National Skin Centre, Singapore
    Photodermatol Photoimmunol Photomed 29:116-20. 2013
    ..Photopatch testing is important for diagnosing photoallergic contact dermatitis. We aimed to evaluate the use of photopatch test at the National Skin Centre, Singapore...
  3. doi request reprint Genetic study in a Singaporean patient with erythropoietic protoporphyria
    Sai Yee Chuah
    Department of Dermatology, National Skin Centre, Singapore
    Photodermatol Photoimmunol Photomed 28:269-71. 2012
    ..This normally requires the co-inheritance of a common hypomorphic FECH allele and a deleterious FECH mutation. Here, we report the first Singaporean Chinese patient with EPP characterized at the molecular level...