Showing 1 - 20 results of 172 for search '"kabuki"', query time: 0.18s Refine Results
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    KABUKI by , PRAEDIVA TRIPUTRA SUSETIONO, , Wiwik Retno H., S. S., M.Hum

    Published 2014
    “…The author interested to take kabuki as a theme because kabuki have stages, performances, costumes, techniques and roles that different and unique from the other theater arts. …”
    Thesis
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    KABUKI SYNDROME by Doina Maria Ioan, Andrei Zamfirescu

    Published 2008-06-01
    Subjects: “…kabuki syndrome (ks)…”
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    Article
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    KABUKI SYNDROME AND EPILEPSY by Marina Zhitomirskaya, Galina Treskina, Nina Dengina, Galina Odinstova

    Published 2022-07-01
    Subjects: “…kabuki syndrome…”
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    Article
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    Aspects of the Kabuki theater of Japan [videorecording] /

    Published [198
    Subjects: “…Kabuki…”
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    Kabuki syndrome: clinical and molecular characteristics by Chong-Kun Cheon, Jung Min Ko

    Published 2015-09-01
    Subjects: “…Kabuki syndrome…”
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    Article
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    Anesthetic care of a child with Kabuki syndrome by I. Elmitwalli, R. Banoub, R. Heng, J. D. Tobias

    Published 2023-01-01
    Subjects: “…kabuki syndrome…”
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    Article
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    Anatomical and functional abnormalities on MRI in kabuki syndrome by Jennifer Boisgontier, Jean Marc Tacchella, Hervé Lemaître, Natacha Lehman, Ana Saitovitch, Vincent Gatinois, Guilaine Boursier, Elodie Sanchez, Elza Rechtman, Ludovic Fillon, Stanislas Lyonnet, Kim-Hanh Le Quang Sang, Genevieve Baujat, Marlene Rio, Odile Boute, Laurence Faivre, Elise Schaefer, Damien Sanlaville, Monica Zilbovicius, David Grévent, David Geneviève, Nathalie Boddaert

    Published 2019-01-01
    “…Kabuki syndrome (KS) is a rare congenital disorder (1/32000 births) characterized by distinctive facial features, intellectual disability, short stature, and dermatoglyphic and skeletal abnormalities. …”
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    Article
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    Primary immunodeficiency in a patient with Kabuki syndrome by I. S. Dolgopolov, L. Yu. Grivtsova, O. K. Ustinova, M. Yu. Rykov

    Published 2023-01-01
    “…Kabuki syndrome is a well-known disease characterized by postnatal growth failure, dysmorphic facial features, skeletal abnormalities, and mental retardation associated with one of the pathogenic mutations in the KMT2D or KDM6A genes. …”
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    Article
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