Clinical features and outcomes of epidermolysis bullosa in thai children: A 20-Year review from a Tertiary Care Center

Autor: Niltem Ekamon, Rujimethapass Nootchanard, Sukhneewat Chonnakarn, Limpongsanurak Wanida, Singalavanija Srisupalak

Publikováno v: Archives of Community Medicine and Public Health. 8:140-146

Background: Epidermolysis Bullosa (EB) is a heterogeneous genetic disorder with skin fragility. Only a few cases have been reported in Thailand. This study aims to determine the clinical characteristics, complications, and outcomes of EB stratified b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::98b00b147a9d9ec7271a3a6cadf85366
https://doi.org/10.17352/2455-5479.000190

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SLC39A4 mutation in zinc deficiency patients.

Autor: Limpongsanurak W, Kuptanon C, Singhamatr P, Singalavanija S, Sirisutthisuwan S

Publikováno v: Journal of the Medical Association of Thailand = Chotmaihet thangphaet [J Med Assoc Thai] 2014 Jun; Vol. 97 Suppl 6, pp. S14-9.

Stevens-Johnson syndrome in Thai children: a 29-year study.

Autor: Singalavanija S; Dermatology Unit, Queen Sirikit National Institute of Child Health, College of Medicine, Rangsit University, Bangkok, Thailand. srisupalak@yahoo.com, Limpongsanurak W

Publikováno v: Journal of the Medical Association of Thailand = Chotmaihet thangphaet [J Med Assoc Thai] 2011 Aug; Vol. 94 Suppl 3, pp. S85-90.