Downregulation of long thymic stromal lymphopoietin (TSLP) variant using antisense oligonucleotide von Pramono, Zacharias A.D, Oh, Glenda G.K, Wee, Dave K.B, Tang, Mark B.Y

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Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia von Numata, Sanae, Teye, Kwesi, Krol, Rafal P, Karashima, Tadashi, Fukuda, Shunpei, Matsuda, Mitsuhiro, Ishii, Norito, Furumura, Minao, Ohata, Chika, Saminathan, Sasi D, Ariffin, Roziana, Pramono, Zacharias A D, Leong, Kin Fon, Hamada, Takahiro, Hashimoto, Takashi

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Mutation and pathogenic study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia von Numata, Sanae, Teye, Kwesi, Krol, Rafal P, Karashima, Tadashi, Fukuda, Shunpei, Matsuda, Mitsuhiro, Ishii, Norito, Furumura, Minao, Ohata, Chika, Saminathan, Sasi D, Ariffin, Roziana, Pramono, Zacharias A.D, Leong, Kin Fon, Hamada, Takahiro, Hashimoto, Takashi

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Corrigendum to ‘Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia’ [Journal of Dermatological Science 78 (201... von Numata, Sanae, Teye, Kwesi, Krol, Rafal P, Karashima, Tadashi, Fukuda, Shunpei, Matsuda, Mitsuhiro, Ishii, Norito, Furumura, Minao, Ohata, Chika, Saminathan, Sasi D, Ariffin, Roziana, Pramono, Zacharias A.D, Leong, Kin Fon, Hamada, Takahiro, Hashimoto, Takashi

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Identification and elucidation of miRNA's role in atopic dermatitis von Pramono, Zacharias A.D, Mo, Xuejun, Gan, Emily Y, Lane, Ellen B, Common, John E, Sundaram, Gopinath, Sampath, Prabha, Tang, Mark B.Y

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Characterization of a novel S13F desmin mutation associated with desmin myopathy and heart block in a Chinese family von Pica, Emmanuel C, Kathirvel, Paramasivam, Pramono, Zacharias A.D, Lai, Poh-San, Yee, Woon-Chee

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Identification of novel homozygous SLURP1 mutation in a Javanese family with Mal de Meleda von Radiono, Sunardi, Pramono, Zacharias A. D., Oh, Glenda G. K., Surana, Uttam, Widiyani, Syahfori, Danarti, Retno

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Ferrochelatase gene mutation in Singapore and a novel frame‐shift mutation in an Asian boy with erythropoietic protoporphyria von Alagappan, Uma, Pramono, Zacharias A. D., Chong, Wei‐Sheng

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Complementary role of a polymerase chain reaction test in the diagnosis of onychomycosis von Chandran, Nisha Suyien, Pan, Jiun-Yit, Pramono, Zacharias AD, Tan, Hiok-Hee, Seow, Chew-Swee

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Acroangiodermatitis of Mali in protein C deficiency due to a novel PROC gene mutation von Wei-Min Tan, Aaron, Lee, Joyce Siong-See, Pramono, Zacharias A D, Chong, Wei-Sheng

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A novel transthyretin mutation V32A in a Chinese man with late-onset amyloid polyneuropathy von Pica, Emmanuel C., Pramono, Zacharias Ad, Verma, Kamal K., San, Lai Poh, Chee, Yee Woon

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