A 3 V MMIC chip set for 1.9 GHz mobile communication systems von Tanaka, S., Hase, E., Nakajima, A., Sugano, K., Fujioka, T., Imakado, Y., Fujiwara, K., Okamoto, T., Shigeno, Y., Sato, K., Arai, I., Yamane, M., Kusano, C., Sakamoto, K., Nakagawa, J., Koya, M.

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A GaAs MMIC chip set for 1.9 GHz Japanese personal handy phone system von Kamozaki, K., Tanaka, S., Hase, E., Nakajima, A., Fujioka, T., Sugano, K., Imakado, Y., Fujiwara, K., Okamoto, T., Sato, K., Shigeno, Y., Arai, I., Yamane, M., Kondoh, H.

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Expression of angiogenic factors in neurofibromas von Kawachi, Yasuhiro, Xu, Xuezhu, Ichikawa, Eiko, Imakado, Sumihisa, Otsuka, Fujio

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A Japanese case of naevoid basal cell carcinoma syndrome associated with segmental vitiligo von Muramatsu, S., Suga, Y., Mizuno, Y., Hasegawa, T., Komuro, Y., Kubo, Y., Imakado, S., Ogawa, H.

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PDGF‐BB Induces MAP Kinase Phosphorylation and VEGF Expression in Neurofibroma‐Derived Cultured Cells from Patients with Neurofibromatosis 1 von Kotsuji‐Maruyama, Tomoe, Imakado, Sumihisa, Kawachi, Yasuhiro, Otsuka, Fujio

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Eccrine syringofibroadenoma in a patient with a burn scar ulcer von Ichikawa, E., Fujisawa, Y., Tateishi, Y., Imakado, S., Otsuka, F.

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Diagnosis of Epidermolytic Palmoplantar Keratoderma in a Very Early Stage by Gene Analysis von Shimazu, Kiyo, Tsunemi, Yuichiro, Hattori, Naoko, Adachi, Makoto, Imakado, Sumihisa, Saeki, Hidehisa, Komine, Mayumi, Tamaki, Kunihiko

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Hereditary complement (C9) deficiency associated with dermatomyositis von Ichikawa, E., Furuta, J., Kawachi, Y., Imakado, S., Otsuka, F.

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A Keratin 10 Gene Mutation (Arg156Cys) in a Japanese Patient with Bullous Congenital Ichthyosiform Erythroderma von Saeki, Hidehisa, Hattori, Naoko, Mitsui, Hiroshi, Adachi, Makoto, Imakado, Sumihisa, Ishibashi, Yasumasa, Tamaki, Kunihiko

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Lack of progesterone receptor expression in extramammary Paget's disease von Imakado, S, Satomi, H, Ishii, Y, Aiyoshi, Y, Otsuka, F

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Diffuse necrobiosis lipoidica diabeticorum associated with non-insulin dependent diabetes mellitus von IMAKADO, S, SATOMI, H, ISKIKAWA, M, IWATA, M, TSUBOUCHI, Y, OTSUKA, F

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Cutaneous Bronchogenic Cyst of the Chin von Kotsuji-Maruyama, Tomoe, Umebayashi, Yoshihiro, Imakado, Sumihisa, Otsuka, Fujio

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Eccrine syringofibroadenoma in a patient with a burn scar ulcer: ECCRINE SYRINGOFIBROADENOMA IN A BURN von Ichikawa, E., Fujisawa, Y., Tateishi, Y., Imakado, S., Otsuka, F.

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Osteosarcomatous changes in malignant melanoma: immunohistochemical and ultrastructural studies of a case von NAKAGAWA, H, IMAKADO, S, NOGITA, T, ISHIBASHI, Y

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Lisch Nodules and Skin Manifestation in Neurofibromatosis Type 1 von Otsuka, Fujio, Kawashima, Tomoko, Imakado, Sumihisa, Usuki, Yoshie, Hon-mura, Sachiko

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Case report: a patient with a six-month history of fever of unknown origin, followed by various manifestations of the central nervous system, finally diagnosed as having intravascu... von Hagiwara, Kiyofumi, Abe, Yu, Sato, Takeo, Inokuma, Shigeko, Akiyama, Osamu, Suzuki, Kenshi, Sato, Hiroyuki, Imakado, Sumihisa, Takemura, Tamiko

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Absence of Lisch Nodules in Sporadic Neurofibromatosis Type 1 May Reflect Somatic Mosaicism—Reply von Otsuka, Fujio, Kawashima, Tomoko, Imakado, Sumihisa, Usaki, Yoshie, Hon-mura, Sachiko

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A Japanese case of naevoid basal cell carcinoma syndrome associated with segmental vitiligo von Muramatsu, S, Suga, Y, Mizuno, Y, Haseegawa, T, Komuro, Y, Kubo, Y, Imakado, S, Ogawa, H

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Eccrine syringofibroadenoma in a patient with a burn scar ulcer von Ichikawa, E., Fujisawa, Y., Tateishi, Y., Imakado, S., Otsuka, F.

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Hereditary complement (C9) deficiency associated with dermatomyositis von Ichikawa, E., Furuta, J., Kawachi, Y., Imakado, S., Otsuka, F.

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