Hemiconvulsion-Hemiplegia-Epilepsy Syndrome Associated With CACNA1A S218L Mutation von Yamazaki, Sawako, MD, Ikeno, Kanju, MD, Abe, Tokinari, MD, Tohyama, Jun, MD, Adachi, Yoshiki, MD

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A 16q12.2q21 deletion identified in a patient with developmental delay, epilepsy, short stature, and distinctive features von Yamamoto, Toshiyuki, Shimojima, Keiko, Yamazaki, Sawako, Ikeno, Kanju, Tohyama, Jun

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Angelman Syndrome Caused by Chromosomal Rearrangements: A Case Report of 46,XX,+der(13)t(13;15)(q14.1;q12)mat,-15 with an Atypical Phenotype and Review of the Literature von Niida, Yo, Sato, Hitoshi, Ozaki, Mamoru, Itoh, Masatsune, Ikeno, Kanju, Takase, Etsuko

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The Lurcher mutation reveals Ca2+ permeability and PKC modification of the GluRδ channels von Ikeno, Kanju, Yamakura, Tomohiro, Yamazaki, Maya, Sakimura, Kenji

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The Lurcher mutation reveals Ca 2+ permeability and PKC modification of the GluRδ channels von Ikeno, Kanju, Yamakura, Tomohiro, Yamazaki, Maya, Sakimura, Kenji

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Hyponatremia in Kawasaki disease von Watanabe, Toru, Abe, Yuki, Sato, Seiichi, Uehara, Yumiko, Ikeno, Kanju, Abe, Tokinari

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Sterile pyuria in patients with Kawasaki disease originates from both the urethra and the kidney von Watanabe, Toru, Abe, Yuki, Sato, Seiichi, Uehara, Yumiko, Ikeno, Kanju, Abe, Tokinari

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Differential palmitoylation of two mouse glutamate receptor interacting protein 1 forms with different N-terminal sequences von Yamazaki, Maya, Fukaya, Masahiro, Abe, Manabu, Ikeno, Kanju, Kakizaki, Toshikazu, Watanabe, Masahiko, Sakimura, Kenji

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A 16q12.2q21 deletion identified in a patient with developmental delay, epilepsy, short stature, and distinctive features von Yamamoto, Toshiyuki, Shimojima, Keiko, Yamazaki, Sawako, Ikeno, Kanju, Tohyama, Jun

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A 16q12.2q21 deletion identified in a patient with developmental delay, epilepsy, short stature, and distinctive features von Yamamoto, Toshiyuki, Shimojima, Keiko, Yamazaki, Sawako, Ikeno, Kanju, Tohyama, Jun

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