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Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia.
Numata S, Teye K, Krol RP, Karashima T, Fukuda S, Matsuda M, Ishii N, Furumura M, Ohata C, Saminathan SD, Ariffin R, Pramono ZA, Leong KF, Hamada T, Hashimoto T. Numata S, et al. Among authors: ariffin r. J Dermatol Sci. 2015 Apr;78(1):82-5. doi: 10.1016/j.jdermsci.2015.02.006. Epub 2015 Feb 19. J Dermatol Sci. 2015. PMID: 25766764 No abstract available.
MECP2 mutations in Malaysian Rett syndrome patients.
Fong CB, Thong MK, Sam CK, Mohamed Noor MN, Ariffin R. Fong CB, et al. Among authors: ariffin r. Singapore Med J. 2009 May;50(5):529-33. Singapore Med J. 2009. PMID: 19495527 Free article.
Guidelines on retention of pathology records and materials (Version 2/2022).
Wong YP, Abu Backer FM, Tan GC, Looi LM, Mat Salleh MJ, A Subramaniam PA, Rahimi R, Ariffin R, Razali RH, Siew SF, Cheong SK, C Thambiah S, Md Hanapiah S, Kumariah T, Tang YL, Zainol Rashid Z. Wong YP, et al. Among authors: ariffin r. Malays J Pathol. 2022 Aug;44(2):165-176. Malays J Pathol. 2022. PMID: 36043580 Free article.
Outcomes of Patients with EGFR-Mutant Advanced NSCLC in a Developing Country in Southeast Asia.
How SH, Liam CK, Zainal Abidin MA, Hasbullah HH, Tho LM, Ho GF, Muhamad Nor I, Pang YK, Ho KF, Thiagarajan M, Ariffin R, Samsudin A, Omar A, Tan SN, Ong CK, Soon SY, Poh ME. How SH, et al. Among authors: ariffin r. Cancer Manag Res. 2022 Jun 16;14:1995-2005. doi: 10.2147/CMAR.S364713. eCollection 2022. Cancer Manag Res. 2022. PMID: 35733510 Free PMC article.
13 results