Search Results - Saito‐Nanjo, Yuka

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  1. 1
    Pediatric psoriasis induced by HLA‐B46‐Cw1 haplotype: A retrospective study of psoriasis onset after hematopoietic stem cell transplantation

    Pediatric psoriasis induced by HLA‐B46‐Cw1 haplotype: A retrospective study of psoriasis onset after hematopoietic stem cell transplantation by Terui, Hitoshi, Yamasaki, Kenshi, Hagiwara‐Takita, Akiko, Shimada‐Omori, Ryoko, Tsuchiyama, Kenichiro, Saito‐Nanjo, Yuka, Rikiishi, Takeshi, Sasahara, Yoji, Aiba, Setsuya

    Published in Journal of dermatology
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  2. 2
    Somatic BRAF c.1799T>A p.V600E Mosaicism syndrome characterized by a linear syringocystadenoma papilliferum, anaplastic astrocytoma, and ocular abnormalities

    Somatic BRAF c.1799T>A p.V600E Mosaicism syndrome characterized by a linear syringocystadenoma papilliferum, anaplastic astrocytoma, and ocular abnormalities by Watanabe, Yuko, Shido, Kosuke, Niihori, Tetsuya, Niizuma, Hidetaka, Katata, Yu, Iizuka, Chie, Oba, Daiju, Moriya, Kunihiko, Saito-Nanjo, Yuka, Onuma, Masaei, Rikiishi, Takeshi, Sasahara, Yoji, Watanabe, Mika, Aiba, Setsuya, Saito, Ryuta, Sonoda, Yukihiko, Tominaga, Teiji, Aoki, Yoko, Kure, Shigeo

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  3. 3
    Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome

    Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome by Irie, Masahiro, Niihori, Tetsuya, Nakano, Tomohiro, Suzuki, Tasuku, Katayama, Saori, Moriya, Kunihiko, Niizuma, Hidetaka, Suzuki, Nobu, Saito-Nanjo, Yuka, Onuma, Masaei, Rikiishi, Takeshi, Sato, Atsushi, Hangai, Mayumi, Hiwatari, Mitsuteru, Ikeda, Junji, Tanoshima, Reo, Shiba, Norio, Yuza, Yuki, Yamamoto, Nobuyuki, Hashii, Yoshiko, Kato, Motohiro, Takita, Junko, Maeda, Miho, Aoki, Yoko, Imaizumi, Masue, Sasahara, Yoji

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  4. 4
    Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia

    Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia by Niihori, Tetsuya, Ouchi-Uchiyama, Meri, Sasahara, Yoji, Kaneko, Takashi, Hashii, Yoshiko, Irie, Masahiro, Sato, Atsushi, Saito-Nanjo, Yuka, Funayama, Ryo, Nagashima, Takeshi, Inoue, Shin-ichi, Nakayama, Keiko, Ozono, Keiichi, Kure, Shigeo, Matsubara, Yoichi, Imaizumi, Masue, Aoki, Yoko

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  5. 5
    Phenotypic heterogeneity in individuals with MECOM variants in 2 families

    Phenotypic heterogeneity in individuals with MECOM variants in 2 families by Niihori, Tetsuya, Tanoshima, Reo, Sasahara, Yoji, Sato, Atsushi, Irie, Masahiro, Saito-Nanjo, Yuka, Funayama, Ryo, Shirota, Matsuyuki, Abe, Taiki, Okuyama, Yuko, Ishii, Naoto, Nakayama, Keiko, Kure, Shigeo, Imaizumi, Masue, Aoki, Yoko

    Published in Blood advances
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  6. 6
    Interstitial lung disease in two brothers with novel compound heterozygous ABCA3 mutations

    Interstitial lung disease in two brothers with novel compound heterozygous ABCA3 mutations by Kitazawa, Hiroshi, Moriya, Kunihiko, Niizuma, Hidetaka, Kawano, Kengo, Saito-Nanjo, Yuka, Uchiyama, Toru, Rikiishi, Takeshi, Sasahara, Yoji, Sakamoto, Osamu, Setoguchi, Yasuhiro, Kure, Shigeo

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  7. 7
    Mutations in MECOM, encoding oncoprotein EVI1, cause amegakaryocytic thrombocytopenia with radioulnar synostosis, an inherited bone marrow failure syndrome

    Mutations in MECOM, encoding oncoprotein EVI1, cause amegakaryocytic thrombocytopenia with radioulnar synostosis, an inherited bone marrow failure syndrome by Imaizumi, Masue, Niihori, Tetsuya, Ouchi-Uchiyama, Meri, Sasahara, Yoji, Kaneko, Takashi, Hashii, Yoshiko, Irie, Masahiro, Sato, Atsushi, Saito-Nanjo, Yuka, Funayama, Ryo, Nagashima, Takeshi, Inoue, Shin-ichi, Nakayama, Keiko, Ozono, Keiichi, Kure, Shigeo, Matsubara, Yoichi, Aoki, Yoko

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