Search Results - "Miyazaki, Shuji"

Conjugate Addition Reaction of Indole to Protected 2-Amino-1-nitroethenes Mediated by Silica Gel by Murai, Kenichi, Fujioka, Hiromichi, Miyazaki, Shuji

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Discovery and structure-activity relationship of imidazolinylindole derivatives as kallikrein 7 inhibitors by Murafuji, Hidenobu, Muto, Tsuyoshi, Goto, Megumi, Imajo, Seiichi, Sugawara, Hajime, Oyama, Yoshiaki, Minamitsuji, Yutaka, Miyazaki, Shuji, Murai, Kenichi, Fujioka, Hiromichi

“…[Display omitted] •Novel imidazolinylindole derivatives as KLK7 inhibitor are disclosed, and their SAR is discussed.•The position of substituent on the…”
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Epilepsy in severe motor and intellectual disabilities syndrome (SMIDS)—A clinical and electroencephalographic study of epileptic syndromes by Matsumoto, Akiko, Miyazaki, Shuji, Hayakawa, Chiemi, Komori, Taku, Nakamura, Miho

“…Summary The subjects were 106 SMIDS with epilepsy. They were classified into four epileptic syndromes: (1) SE-MISF (34.0%), (2) SGE (25.5%), (3) SLRE (20.7%),…”
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Williams syndrome and deficiency in visuospatial recognition by Nakamura, Miho, Watanabe, Kazuyoshi, Matsumoto, Akiko, Yamanaka, Tsutomu, Kumagai, Toshiyuki, Miyazaki, Shuji, Matsushima, Masaki, Mita, Katsumi

“…This study aimed to assess the visuospatial abilities of five children with Williams syndrome (four males aged 9 years 3 months, 7 years 11 months, 8 years 1…”
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Reactivity of the ester group attached isoxazoline, benzisoxazole, and isoxazole: a facial preparation of 3-acyl-substituted these heterocycles by Murai, Kenichi, Miyazaki, Shuji, Fujioka, Hiromichi

“…A facile preparation of 3-acyl-substituted isoxazolines, benzisoxazoles, and isoxazoles from the corresponding 3-carboxylate esters is described. The process,…”
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Flow characteristics of a coal-oil-water mixture prepared by disintegration of de-ashed coal agglomerates by Takase, Hitoshi, Miyazaki, Shuji

“…The flow characteristics of a coal-oil-water mixture (COW) were investigated. COW was prepared by disintegrating de-ashed coal agglomerates that had been…”
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Tracheostomy for home-care patients with severe motor and intellectual disabilities by Miura, Kiyokuni, Suzuki, Yoshiko, Kumagai, Toshiyuki, Hayakawa, Chiemi, Matsumoto, Akiko, Miyazaki, Shuji, Mizuno, Seiji

“…We discuss here the indication and complications of tracheostomy performed in 57 home-care pateints with severe motor and intellectual disabilities (SMID)…”
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Clinical symptoms of the Rett syndrome patients with MECP2 gene abnormalities by Miura, Kiyokuni, Kumagai, Toshiyuki, Suzuki, Yoshiko, Ohki, Takashi, Matsumoto, Akiko, Miyazaki, Shuji, Hayakawa, Chiemi, Sonta, Shin-ichi, Yamada, Yasukazu, Wakamatsu, Nobuaki

“…Mutations in a gene on the X-chromosome encoding methyl-CpG-binding protein 2 (MECP2) cause Rett syndrome. We examined clinical symptoms of 27 patients with…”
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Central nervous system involvements in Duchenne/Becker muscular dystrophy by Kumagai, T, Miura, K, Ohki, T, Matsumoto, A, Miyazaki, S, Nakamura, M, Ochi, N, Takahashi, O

“…Duchenne/Becker muscular dystrophy (DMD/BMD) are the most common inherited muscular diseases caused by mutations in the dystrophin gene. The identification of…”
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Observation of HCl- and HF-treated GaAs surfaces by measuring contact angles of water droplets by MATSUSHITA, K, MIYAZAKI, S, OKUYAMA, S, KUMAGAI, Y

“…A GaAs surface chemically treated with hydrochloric acid (HCl) or hydrofluoric acid (HF) has been characterized by measurements of the contact angle between…”
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Prognostic factors for epileptic seizures in severe motor and intellectual disabilities syndrome (SMIDS)—A clinical and electroencephalographic study by Matsumoto, Akiko, Miyazaki, Shuji, Hayakawa, Chiemi, Komori, Taku, Nakamura, Miho, Oshio, Atsushi

“…Summary Purpose The purpose of this study is to examine prognostic factors for seizures in 106 epileptic patients with SMIDS. Subjects and methods…”
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Nonsense and Frameshift Mutations in ZFHX1B, Encoding Smad-Interacting Protein 1, Cause a Complex Developmental Disorder with a Great Variety of Clinical Features by Yamada, Kenichiro, Yamada, Yasukazu, Nomura, Noriko, Miura, Kiyokuni, Wakako, Rie, Hayakawa, Chiemi, Matsumoto, Akiko, Kumagai, Toshiyuki, Yoshimura, Ikuko, Miyazaki, Shuji, Kato, Kanefusa, Sonta, Shin-ichi, Ono, Hiroshi, Yamanaka, Tsutomu, Nagaya, Masahiro, Wakamatsu, Nobuaki

“…Mutations in ZFHX1B, encoding Smad-interacting protein 1 (SIP1), have been recently reported to cause a form of Hirschsprung disease (HSCR). Patients with…”
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Neurophysiological evaluation of newborns with congenital hydrocephalus by Watanabe, K, Yamada, H, Hara, K, Miyazaki, S, Nakamura, S

“…EEGs and visual and auditory evoked potentials (VEP and AEP) were studied in 27 newborns with congenital hydrocephalus. Asynchronous sleep patterns were the…”
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Apparent brain atrophy and subdural hematoma following ACTH therapy by Hara, K, Watanabe, K, Miyazaki, S, Hakamada, S, Yamada, H, Nakamura, S

“…A case of subdural hematoma following ACTH-Z therapy for infantile spasms was presented. A female baby of 5 months old showed little clinical evidence of…”
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Williams syndrome and deficiency in visuospatial recognition by Nakamura, Miho, Watanabe, Kazuyoshi, Matsumoto, Akiko, Yamanaka, Tsutomu, Kumagai, Toshiyuki, Miyazaki, Shuji, Matsushima, Masaki, Mita, Katsumi

“…This study aimed to assess the visuospatial abilities of five children with Williams syndrome (four males aged 9 years 3 months, 7 years 11 months, 8 years 1…”
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A Female Case of the Lesch-Nyhan Syndrome by HARA, KIMIKO, KASHIWAMATA, SHIGEO, OGASAWARA, NOBUAKI, OHISHI, HIDETSUNE, NATSUME, REISUKE, YAMANAKA, TSUTOMU, HAKAMADA, SUSUMU, MIYAZAKI, SHUJI, WATANABE, KAZUYOSHI

“…HARA, K., KASHIWAMATA, S., OGASAWARA, N., OHISHI, H., NATSUME, R., YAMANAKA, T., HAKAMADA, S., MIYAZAKI, S. and WATANABE, K. A Female Case of the Lesch-Nyhan…”
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Epilepsy in Angelman syndrome associated with chromosome 15q deletion by Matsumoto, A, Kumagai, T, Miura, K, Miyazaki, S, Hayakawa, C, Yamanaka, T

“…We report eight sporadic cases of typical Angelman syndrome (AS) associated with chromosome 15q12 deletion. Age at first visit was 3-35 months (average 18…”
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Molecular analysis of Japanese patients with Rett syndrome: Identification of five novel mutations and genotype-phenotype correlation by Yamada, Yasukazu, Miura, Kiyokuni, Kumagai, Toshiyuki, Hayakawa, Chiemi, Miyazaki, Shuji, Matsumoto, Akiko, Kurosawa, Kenji, Nomura, Noriko, Taniguchi, Hiroko, Sonta, Shin-Ichi, Yamanaka, Tsutomu, Wakamatsu, Nobuaki

“…Rett syndrome is an X‐linked dominant neurodevelopmental disorder that affects females almost exclusively. The recent identification of mutations of the…”
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Urinary 3-methylhistidine excretion in children with neuromuscular diseases by Kumagai, T, Takeuchi, T, Hara, K, Miyazaki, S, Riko, T, Shionoya, T, Komatsu, K, Mizutani, N, Watanabe, K

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Clinical course of a case of epileptic encephalopathy with marked dysphasia: a neuropsychological and electroencephalographic study by Matsumoto, A, Takeuchi, T, Kumagai, T, Miyazaki, S, Hara, K, Kunishima, N, Watanabe, K

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