Search Results - Emori, Aki

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  1. 1
    Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis

    Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis by Yoshida, Shigeo, Yoshida, Ayako, Nakao, Shintaro, Emori, Aki, Nakamura, Takao, Fujisawa, Kimihiko, Kumano, Yuji, Ishibashi, Tatsuro

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  2. 2
    Novel mutation in FZD4 gene in a Japanese pedigree with familial exudative vitreoretinopathy

    Novel mutation in FZD4 gene in a Japanese pedigree with familial exudative vitreoretinopathy by Yoshida, Shigeo, Arita, Ryo-Ichi, Yoshida, Ayako, Tada, Hanayo, Emori, Aki, Noda, Yoshihiro, Nakao, Shintaro, Fujisawa, Kimihiko, Ishibashi, Tatsuro

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    Novel mutation inFZD4gene in a Japanese pedigree with familial exudative vitreoretinopathy

    Novel mutation inFZD4gene in a Japanese pedigree with familial exudative vitreoretinopathy by Yoshida, Shigeo, Arita, Ryo-Ichi, Yoshida, Ayako, Tada, Hanayo, Emori, Aki, Noda, Yoshihiro, Nakao, Shintaro, Fujisawa, Kimihiko, Ishibashi, Tatsuro

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  4. 4
    Ruptured brachial artery aneurysm in a patient with type 1 neurofibromatosis

    Ruptured brachial artery aneurysm in a patient with type 1 neurofibromatosis by Emori, Makoto, MD, Naka, Norifumi, MD, PhD, Takami, Hiroshi, MD, PhD, Tanaka, Taka-Aki, MD, Tomita, Yasuhiko, MD, PhD, Araki, Nobuhito, MD, PhD

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