Rafi'ee K - Search Results

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A novel NSDHL variant in CHILD syndrome with gastrointestinal manifestations and localized skin involvement.

Tan EC, Chia SY, Rafi'ee K, Lee SX, Kwek ABE, Tan SH, Ng VWL, Wei H, Koo S, Koh AL, Koh MJ. Tan EC, et al. Among authors: rafi ee k. Mol Genet Genomic Med. 2022 Jan;10(1):e1848. doi: 10.1002/mgg3.1848. Epub 2021 Dec 26. Mol Genet Genomic Med. 2022. PMID: 34957706 Free PMC article.

Palmoplantar keratoderma, oral involvement, and homozygous CTSC mutation in two brothers from Cambodia.

Wei H, Wee LWY, Born B, Seang S, Koh MJA, Yee R, Lin G, Rafi'ee K, Mey S, Tan EC. Wei H, et al. Among authors: rafi ee k. Am J Med Genet A. 2020 Feb;182(2):296-302. doi: 10.1002/ajmg.a.61447. Epub 2019 Dec 17. Am J Med Genet A. 2020. PMID: 31846207

CARD14-associated papulosquamous eruption (CAPE) in a toddler responding to treatment with acitretin.

Wong GHZ, Chia SY, Wei H, Rafi'ee K, Koh MJA, Tan EC. Wong GHZ, et al. Among authors: rafi ee k. Pediatr Dermatol. 2021 Jul;38(4):970-972. doi: 10.1111/pde.14638. Epub 2021 Jun 2. Pediatr Dermatol. 2021. PMID: 34075616

Phenotype and genotype correlation of inherited epidermolysis bullosa in Indonesia.

Arline Diana I, Tan EC, Gondokaryono SP, Koh MJ, Dwiyana RF, Rahardja JI, Yogya Y, Rafi'ee K, Suwarsa O. Arline Diana I, et al. Among authors: rafi ee k. Australas J Dermatol. 2023 Nov;64(4):e327-e332. doi: 10.1111/ajd.14121. Epub 2023 Jul 14. Australas J Dermatol. 2023. PMID: 37452458

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