Search Results - "Isoda, Kenichi"

Mislocalization of syntaxin‐1 and impaired neurite growth observed in a human iPSC model for STXBP1‐related epileptic encephalopathy by Yamashita, Satoshi, Chiyonobu, Tomohiro, Yoshida, Michiko, Maeda, Hiroshi, Zuiki, Masashi, Kidowaki, Satoshi, Isoda, Kenichi, Morimoto, Masafumi, Kato, Mitsuhiro, Saitsu, Hirotomo, Matsumoto, Naomichi, Nakahata, Tatsutoshi, Saito, Megumu K., Hosoi, Hajime

“…Summary Syntaxin‐binding protein 1 (STXBP1) is essential for synaptic vesicle exocytosis. Mutations of its encoding gene, STXBP1, are among the most frequent…”
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Leigh-like syndrome with progressive cerebellar atrophy caused by novel HIBCH variants by Taura, Yoshihiro, Tozawa, Takenori, Isoda, Kenichi, Hirai, Satori, Chiyonobu, Tomohiro, Yano, Naoko, Hayashi, Takahiro, Yoshida, Takeshi, Iehara, Tomoko

“…Pathogenic variants in the HIBCH gene cause HIBCH deficiency, leading to mitochondrial disorders associated with valine metabolism. Patients typically present…”
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Persistent release of IL-1s from skin is associated with systemic cardio-vascular disease, emaciation and systemic amyloidosis: the potential of anti-IL-1 therapy for systemic inflammatory diseases by Yamanaka, Keiichi, Nakanishi, Takehisa, Saito, Hiromitsu, Maruyama, Junko, Isoda, Kenichi, Yokochi, Ayumu, Imanaka-Yoshida, Kyoko, Tsuda, Kenshiro, Kakeda, Masato, Okamoto, Ryuji, Fujita, Satoshi, Iwakura, Yoichiro, Suzuki, Noboru, Ito, Masaaki, Maruyama, Kazuo, Gabazza, Esteban C, Yoshida, Toshimichi, Shimaoka, Motomu, Mizutani, Hitoshi

“…The skin is an immune organ that contains innate and acquired immune systems and thus is able to respond to exogenous stimuli producing large amount of…”
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Efficacy of the combined use of a facial cleanser and moisturizers for the care of mild acne patients with sensitive skin by Isoda, Kenichi, Seki, Tsuyoshi, Inoue, Yosuke, Umeda, Koji, Nishizaka, Takahiro, Tanabe, Hisateru, Takagi, Yutaka, Ishida, Koichi, Mizutani, Hitoshi

“…Acne is a common skin disease that involves the seborrheic area of the face and results from the obstruction of hair follicles followed by inflammation…”
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Establishment of isogenic iPSCs from an individual with SCN1A mutation mosaicism as a model for investigating neurocognitive impairment in Dravet syndrome by Maeda, Hiroshi, Chiyonobu, Tomohiro, Yoshida, Michiko, Yamashita, Satoshi, Zuiki, Masashi, Kidowaki, Satoshi, Isoda, Kenichi, Yamakawa, Kazuhiro, Morimoto, Masafumi, Nakahata, Tatsutoshi, Saito, Megumu K, Hosoi, Hajime

“…Dravet syndrome (DS) is a severe childhood epilepsy typically caused by de novo dominant mutations in SCN1A. Although patients with DS frequently have…”
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Novel acoustic evaluation system for scratching behavior in itching dermatitis: Rapid and accurate analysis for nocturnal scratching of atopic dermatitis patients by Noro, Yuichi, Omoto, Youichi, Umeda, Koji, Tanaka, Futa, Shiratsuka, Yousuke, Yamada, Tomomi, Isoda, Kenichi, Matsubara, Kimiko, Yamanaka, Keiichi, Gabazza, Esteban C., Nishikawa, Masakatsu, Mizutani, Hitoshi

“…Quantitative analysis of itching in patients with itching dermatitis including atopic dermatitis (AD) is indispensable for the evaluation of disease activity…”
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Development of Corpus Callosum in Preterm Infants Is Affected by the Prematurity: In Vivo Assessment of Diffusion Tensor Imaging at Term-Equivalent Age by Hasegawa, Tatsuji, Yamada, Kei, Morimoto, Masafumi, Morioka, Shigemi, Tozawa, Takenori, Isoda, Kenichi, Murakami, Aki, Chiyonobu, Tomohiro, Tokuda, Sachiko, Nishimura, Akira, Nishimura, Tsunehiko, Hosoi, Hajime

“…Callosal injury in preterm infants is a key factor affecting neurodevelopmental outcome. We investigated the characteristics of corpus callosum (CC) in preterm…”
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Effects of chemotherapy on the brain in childhood: diffusion tensor imaging of subtle white matter damage by Morioka, Shigemi, Morimoto, Masafumi, Yamada, Kei, Hasegawa, Tatsuji, Morita, Takashi, Moroto, Masaharu, Isoda, Kenichi, Chiyonobu, Tomohiro, Imamura, Toshihiko, Nishimura, Akira, Morimoto, Akira, Hosoi, Hajime

“…Introduction With reducing mortality in children with hematological malignancies, the survivors' quality of life regarding development of chronic neurological…”
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Emaciation, Congestive Heart Failure, and Systemic Amyloidosis in Severe Recessive Dystrophic Epidermolysis Bullosa: Possible Internal Complications Due to Skin-Derived Inflammatory Cytokines Derived from the Injured Skin by Matsushima, Yoshiaki, Mizutani, Kento, Goto, Hiroyuki, Nakanishi, Takehisa, Kondo, Makoto, Habe, Koji, Isoda, Kenichi, Mizutani, Hitoshi, Yamanaka, Keiichi

“…Inherited epidermolysis bullosa (EB) is a rare genetic skin disorder characterized by epithelial tissue fragility. Recessive dystrophic epidermolysis bullosa…”
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Olopatadine, a non-sedating H1 antihistamine, decreases the nocturnal scratching without affecting sleep quality in atopic dermatitis by Yamanaka, Keiichi, Motomura, Eishi, Noro, Yuichi, Umeda, Koji, Morikawa, Takuya, Umeda-Togami, Kumi, Omoto, Youichi, Isoda, Kenichi, Kondo, Makoto, Tsuda, Kenshiro, Okuda, Masahiro, Gabazza, Esteban C., Mizutani, Hitoshi

“…We have demonstrated for the first time that a second‐generation antihistamine ameliorates nocturnal scratching behavior in atopic dermatitis patients using a…”
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Single step modified ink staining for Tzanck test: Quick detection of herpetic giant cells in Tzanck smear by MIZUTANI, Hitoshi, AKEDA, Tomoko, YAMANAKA, Kei-ichi, ISODA, Kenichi, GABAZZA, Esteban C.

“…Tzanck test has been recently re‐evaluated as a method for the diagnosis of herpes virus infection. Giemsa staining for the Tzanck test is time‐consuming and…”
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Swyer-James Syndrome in a 7-Year-Old Female by Mori, Jun, Kaneda, Daisuke, Fujiki, Atsushi, Isoda, Kenichi, Kotani, Tomoya, Ushijima, Yo

“…Swyer-James syndrome is a rare syndrome that occurs as a result of repeated bronchiolitis and pneumonitis in childhood. Most cases are asymptomatic, and…”
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Effects of stress of postnatal development on corticosterone, serotonin and behavioral changes by Matsui, Fumihiro, Morimoto, Masafumi, Yoshimoto, Kanji, Nakatomi, Yasuhito, Syoji, Hiroto, Nishimura, Akira, Isoda, Kenichi, Tanda, Kouichi, Hosoi, Hajime

“…Abstract Stressful events early in life are associated with later psychiatric disorders. We focused on developmental stage and evaluated changes in the…”
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Rare case of disseminated cysticercosis and taeniasis in a Japanese traveler after returning from India by Kobayashi, Ken-ichiro, Nakamura-Uchiyama, Fukumi, Nishiguchi, Takeshi, Isoda, Kenichi, Kokubo, Yasumasa, Ando, Katsuhiko, Katurahara, Masaki, Sako, Yasuhito, Yanagida, Tetsuya, Ito, Akira, Iwabuchi, Sentaro, Ohnishi, Kenji

“…We report disseminated cysticercosis concurrent with taeniasis in a 31-year-old male Japanese, who had visited India three times and stayed for 1 month each…”
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Treatment of cloth with a fabric softener ameliorates skin dryness by ISODA, Kenichi, TAKAGI, Yutaka, KITAHARA, Takashi, SANO, Yutaka, SUGANO, Ikuo, UMEDA-TOGAMI, Kumi, UMEDA, Koji, YAMANAKA, Keiichi, YAMADA, Tomomi, MIZUTANI, Hitoshi

“…Dry skin is a condition characterized by impaired skin barrier function including atopic dermatitis and senile eczemas. Fabric softening chemicals (FSC)…”
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An age-dependent change in serotonin innervation to the forebrain of Mecp2-null mice by Isoda, Kenichi, Matsui, Fumihiro, Hasegawa, Tatsuji, Tozawa, Takenori, Morioka, Shigemi, Chiyonobu, Tomohiro, Nishimura, Akira, Morimoto, Masafumi, Yoshimoto, Kanji, Hosoi, Hajime

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Case Report: Rare Case of Disseminated Cysticercosis and Taeniasis in a Japanese Traveler after Returning from India by Kobayashi, Ken-ichiro, Nakamura-Uchiyama, Fukumi, Nishiguchi, Takeshi, Isoda, Kenichi, Kokubo, Yasumasa, Ando, Katsuhiko, Katurahara, Masaki, Sako, Yasuhito, Yanagida, Tetsuya, Ito, Akira, Iwabuchi, Sentaro, Ohnishi, Kenji

“…We report disseminated cysticercosis concurrent with taeniasis in a 31-year-old male Japanese, who had visited India three times and stayed for 1 month each…”
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Mislocalization of syntaxin‐1 and impaired neurite growth observed in a human iPSC model for STXBP 1 ‐related epileptic encephalopathy by Yamashita, Satoshi, Chiyonobu, Tomohiro, Yoshida, Michiko, Maeda, Hiroshi, Zuiki, Masashi, Kidowaki, Satoshi, Isoda, Kenichi, Morimoto, Masafumi, Kato, Mitsuhiro, Saitsu, Hirotomo, Matsumoto, Naomichi, Nakahata, Tatsutoshi, Saito, Megumu K., Hosoi, Hajime

“…Syntaxin‐binding protein 1 ( STXBP 1) is essential for synaptic vesicle exocytosis. Mutations of its encoding gene, STXBP 1, are among the most frequent…”
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Maintenance Hemodialysis Using Native Arteriovenous Fistula in a Patient with Severe Generalized Recessive Dystrophic Epidermolysis Bullosa by Ito, Takayasu, Ishikawa, Eiji, Matsuo, Hiroshi, Fujimoto, Mika, Murata, Tomohiro, Isoda, Kenichi, Mizutani, Hitoshi, Ito, Masaaki

“…Renal failure and infectious disease are strongly associated with morbidity and mortality in patients with severe generalized recessive dystrophic…”
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Neuro-Sweet disease: report of the first autopsy case by Kokubo, Yasumasa, Kuzuhara, Shigeki, Isoda, Kenichi, Sato, Kenji, Kawada, Norikazu, Narita, Yugo

“…Background: Neuro-Sweet disease is a rare condition of central nervous involvement accompanied by cutaneous Sweet lesions. Neuropathological changes in…”
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