يعرض 1 - 10 نتائج من 214 نتيجة بحث عن '"Yamasaki, Mami"', وقت الاستعلام: 0.98s تنقيح النتائج
  1. 1
    كتاب إلكتروني
    X-Linked Hydrocephalus

    المؤلفون: Yamasaki, MamiAff4, Aff5, Kanemura, YonehiroAff7, Aff6, Di Rocco, Concezio, Section editorAff8, Tamburrini, Gianpiero, Section editorAff9

    المساهمون: Di Rocco, Concezio, editorAff1, Pang, Dachling, editorAff2, Rutka, James T., editorAff3

    المصدر: Textbook of Pediatric Neurosurgery. :521-531

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  2. 2
    كتاب إلكتروني
    Understanding Hydrocephalus: Genetic View

    المؤلفون: Yamasaki, MamiAff2

    المساهمون: Ammar, Ahmed, editorAff1

    المصدر: Hydrocephalus : What do we know? And what do we still not know?. :53-65

    Degree: M.D., Ph.D.

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  3. 3
    دورية أكاديمية
    A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome

    المؤلفون: Hori, Ikumi, Miya, FuyukiAff2, Aff3, Negishi, Yutaka, Hattori, Ayako, Ando, Naoki, Boroevich, Keith A., Okamoto, Nobuhiko, Kato, Mitsuhiro, Tsunoda, TatsuhikoAff2, Aff3, Yamasaki, Mami, Kanemura, YonehiroAff7, Aff8, Kosaki, Kenjiro, Saitoh, ShinjiAff1

    المصدر: Journal of Human Genetics. 63(9):957-963

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  4. 4
    دورية أكاديمية
    Significance of molecular classification of ependymomas: C11orf95-RELA fusion-negative supratentorial ependymomas are a heterogeneous group of tumors

    المؤلفون: Fukuoka, KoheiAff1, Aff2, Kanemura, YonehiroAff3, Aff4, Shofuda, Tomoko, Fukushima, Shintaro, Yamashita, Satoshi, Narushima, Daichi, Kato, Mamoru, Honda-Kitahara, Mai, Ichikawa, Hitoshi, Kohno, Takashi, Sasaki, Atsushi, Hirato, Junko, Hirose, Takanori, Komori, Takashi, Satomi, KaishiAff1, Aff13, Yoshida, Akihiko, Yamasaki, KaiAff1, Aff14, Nakano, YoshikoAff1, Aff14, Takada, Ai, Nakamura, TaishiAff1, Aff15, Takami, HirokazuAff1, Aff16, Matsushita, YukoAff1, Aff17, Suzuki, Tomonari, Nakamura, Hideo, Makino, Keishi, Sonoda, YukihikoAff20, Aff21, Saito, Ryuta, Tominaga, Teiji, Matsusaka, Yasuhiro, Kobayashi, Keiichi, Nagane, Motoo, Furuta, TakuyaAff24, Aff25, Nakada, Mitsutoshi, Narita, Yoshitaka, Hirose, Yuichi, Ohba, Shigeo, Wada, Akira, Shimizu, Katsuyoshi, Kurozumi, Kazuhiko, Date, Isao, Fukai, Junya, Miyairi, Yousuke, Kagawa, Naoki, Kawamura, Atsufumi, Yoshida, Makiko, Nishida, Namiko, Wataya, Takafumi, Yamaoka, Masayoshi, Tsuyuguchi, Naohiro, Uda, Takehiro, Takahashi, Mayu, Nakano, Yoshiteru, Akai, TakuyaAff38, Aff39, Izumoto, Shuichi, Nonaka, Masahiro, Yoshifuji, Kazuhisa, Kodama, YoshinoriAff43, Aff44, Mano, Masayuki, Ozawa, Tatsuya, Ramaswamy, Vijay, Taylor, Michael D.Aff45, Aff46, Ushijima, Toshikazu, Shibui, Soichiro, Yamasaki, Mami, Arai, Hajime, Sakamoto, Hiroaki, Nishikawa, Ryo, Ichimura, KoichiAff1, on behalf of the Japan Pediatric Molecular Neuro-Oncology Group (JPMNG)

    المصدر: Acta Neuropathologica Communications. 6(1)

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  5. 5
    دورية أكاديمية
    Siblings with optic neuropathy and RTN4IP1 mutation

    المؤلفون: Okamoto, NobuhikoAff1, IDjhg201768_cor1, Miya, FuyukiAff2, Aff3, Hatsukawa, Yoshikazu, Suzuki, Yasuhiro, Kawato, Kazumi, Yamamoto, Yuto, Tsunoda, TatsuhikoAff2, Aff3, Kato, Mitsuhiro, Saitoh, Shinji, Yamasaki, Mami, Kanemura, YonehiroAff9, Aff10, Kosaki, Kenjiro

    المصدر: Journal of Human Genetics. 62(10):927-929

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  6. 6
    دورية أكاديمية
    Drifting algae and fish: Implications of tropical Sargassum invasion due to ocean warming in western Japan

    المؤلفون: Yamasaki, Mami, Aono, Mikina, Ogawa, Naoto, Tanaka, Koichiro, Imoto, Zenji, Nakamura, Yohei

    المصدر: In Estuarine, Coastal and Shelf Science 20 June 2014 147:32-41

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  7. 7
    دورية أكاديمية
    Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate

    المؤلفون: Kato, KojiAff1, Aff2, Miya, FuyukiAff3, Aff4, Hori, Ikumi, Ieda, Daisuke, Ohashi, Kei, Negishi, Yutaka, Hattori, Ayako, Okamoto, Nobuhiko, Kato, Mitsuhiro, Tsunoda, TatsuhikoAff3, Aff4, Yamasaki, Mami, Kanemura, YonehiroAff8, Aff9, Kosaki, Kenjiro, Saitoh, ShinjiAff1

    المصدر: Journal of Human Genetics. 64(7):701-702

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  8. 8
    دورية أكاديمية
    IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis

    المؤلفون: Shigemizu, DaichiAff1, Aff2, Aff3, Aff4, Aff5, Miya, FuyukiAff2, Aff3, Akiyama, Shintaro, Okuda, Shujiro, Boroevich, Keith A, Fujimoto, Akihiro, Nakagawa, Hidewaki, Ozaki, KouichiAff1, Aff3, Niida, Shumpei, Kanemura, YonehiroAff8, Aff9, Okamoto, Nobuhiko, Saitoh, Shinji, Kato, Mitsuhiro, Yamasaki, Mami, Matsunaga, Tatsuo, Mutai, Hideki, Kosaki, Kenjiro, Tsunoda, TatsuhikoAff2, Aff3, Aff4, Aff5

    المصدر: Scientific Reports. 8(1)

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  9. 9
    دورية أكاديمية
    A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate

    المؤلفون: Kato, KojiAff1, Aff2, Miya, FuyukiAff3, Aff4, Hori, Ikumi, Ieda, Daisuke, Ohashi, Kei, Negishi, Yutaka, Hattori, Ayako, Okamoto, Nobuhiko, Kato, Mitsuhiro, Tsunoda, TatsuhikoAff3, Aff4, Yamasaki, Mami, Kanemura, YonehiroAff8, Aff9, Kosaki, Kenjiro, Saitoh, ShinjiAff1, IDjhg201753_cor14

    المصدر: Journal of Human Genetics. 62(9):861-863

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  10. 10
    دورية أكاديمية
    Sudden death in a case of megalencephaly capillary malformation associated with a de novo mutation in AKT3

    المؤلفون: Harada, Atsuko, Miya, Fuyuki, Utsunomiya, Hidetsuna, Kato, Mitsuhiro, Yamanaka, Takumi, Tsunoda, Tatsuhiko, Kosaki, Kenjiro, Kanemura, Yonehiro, Yamasaki, Mami

    المصدر: Child's Nervous System. March 2015 31(3):465-471

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