Search Results - "Hanai, Toshio"

Sodium phenylbutyrate improved the clinical state in an adult patient with arginase 1 deficiency by Matsufuji, Mayumi, Takeshita, Eiko, Nakashima, Masayuki, Watanabe, Yoriko, Fukui, Kaori, Hanai, Toshio, Ishibashi, Hiromi, Takashima, Sachio

“…An adult female patient was diagnosed with arginase 1 deficiency (ARG1-D) at 4 years of age, and had been managed with protein restriction combined with sodium…”
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Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan by Torisu, Hiroyuki, Kira, Ryutaro, Ishizaki, Yoshito, Sanefuji, Masafumi, Yamaguchi, Yui, Yasumoto, Sawa, Murakami, Yoshihiko, Shimono, Masayuki, Nagamitsu, Shinichiro, Masuzaki, Mayumi, Amamoto, Masano, Kondo, Rikako, Uozumi, Tomohiko, Aibe, Miyuki, Gondo, Kenjiro, Hanai, Toshio, Hirose, Sinichi, Matsuishi, Toyojiro, Shirahata, Akira, Mitsudome, Akihisa, Hara, Toshiro

“…Abstract Acute disseminated encephalomyelitis (ADEM) has recently been studied in several countries owing to the development and wide spread use of imaging…”
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Treatment of infantile spasms with zonisamide by Yanai, Shinji, Hanai, Toshio, Narazaki, Osamu

“…We determined the efficacy of and tolerability to zonisamide (ZNS) in newly diagnosed patients with infantile spasms. ZNS, 4–20 mg/kg per day, was introduced…”
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Quality of life in children with epilepsy by Hanai, T

“…To study quality of life in school children with epilepsy, we surveyed families of 443 elementary and junior high school children with epilepsy, as well as…”
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Prognosis of occlusive disease of the circle of Willis (moyamoya disease) in children by Kurokawa, T, Tomita, S, Ueda, K, Narazaki, O, Hanai, T, Hasuo, K, Matsushima, T, Kitamura, K

“…The prognosis of 27 patients with moyamoya disease was studied. The ages at onset ranged from 11 months to 4-11/12 years. Follow-up study was performed within…”
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A case of hereditary motor and sensory neuropathy (HMSN) with excessive myelin outfolding with autosomal recessive inheritance by Ohnishi, A, Narazaki, O, Hanai, T

“…A 3-year-old girl with rare and unique myelin abnormality in the sural nerve is described. Her parents are first cousins. Her clinical features were similar to…”
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A novel mutation of KCNQ3 (c.925T→C) in a Japanese family with benign familial neonatal convulsions by Hirose, Shinichi, Zenri, Fumiko, Akiyoshi, Hidetaka, Fukuma, Goryu, Iwata, Hiromi, Inoue, Takahito, Yonetani, Minako, Tsutsumi, Makoto, Muranaka, Hideki, Kurokawa, Toru, Hanai, Toshio, Wada, Kazumaru, Kaneko, Sunao, Mitsudome, Akihisa

“…At present, only one mutation of KCNQ3, a KCNQ potassium channel gene, has been identified as a cause of benign familial neonatal convulsions type 2 (BFNC2)…”
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Surgical management of intractable epilepsy in patients with ganglioglioma by Morioka, T, Nishio, S, Ishibashi, H, Ikezaki, K, Tokunaga, Y, Hanai, T, Kurokawa, T, Fukui, M

“…Long-standing intractable seizures are common manifestation of cerebral gangliogliomas. There is much controversy regarding the most appropriate surgical…”
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A case of a thalamic tumor with a thalamic hand by Sakamoto, K, Narazaki, O, Hanai, T, Kurokawa, T, Fukui, M

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Sodium phenylbutyrate improved the clinical state in an adult patient with arginase 1 deficiency by Matsufuji, Mayumi, Takeshita, Eiko, Nakashima, Masayuki, Watanabe, Yoriko, Fukui, Kaori, Hanai, Toshio, Ishibashi, Hiromi, Takashima, Sachio

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A novel mutation ofKCNQ3 (c.925T?C) in a Japanese family with benign familial neonatal convulsions by Hirose, Shinichi, Zenri, Fumiko, Akiyoshi, Hidetaka, Fukuma, Goryu, Iwata, Hiromi, Inoue, Takahito, Yonetani, Minako, Tsutsumi, Makoto, Muranaka, Hideki, Kurokawa, Toru, Hanai, Toshio, Wada, Kazumaru, Kaneko, Sunao, Mitsudome, Akihisa

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A case of hereditary motor and sensory neuropathy type III with a decrease in unmyelinated fibers by Narazaki, O, Hanai, T, Sakamoto, K, Ohnishi, A

“…We report a 3-year-old girl with hereditary motor and sensory neuropathy type III with a decrease in unmyelinated fibers. There have been few reports of such…”
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Menkes disease: is vitamin C treatment effective? by Ueki, Y, Narazaki, O, Hanai, T

“…The pathogenesis of Menkes disease seems to be linked to metallothionein which binds to copper trapped within cells in some tissues. The only known therapy for…”
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Mortality and clinical features in cases of death among epileptic children by Kurokawa, T, Fung, K C, Hanai, T, Goya, N

“…At a follow-up study of 385 patients with epilepsy beginning under age 15, 22 (5.7%) had died during the first 10 years after the onset of epilepsy and another…”
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Linear nevus sebaceus syndrome. Report of a case with Lennox-Gastaut syndrome following infantile spasms by Kurokawa, T, Sasaki, K, Hanai, T, Goya, N, Komaki, S

“…We report what we believe to be the first known case of linear nevus sebaceus syndrome with infantile spasms followed by Lennox-Gastaut syndrome. The EEG…”
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