Search Results - "Shimono, Kuriko Kagitani"

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    Atypical structural connectivity of language networks in autism spectrum disorder: A meta‐analysis of diffusion tensor imaging studies by Li, Min, Wang, Yide, Tachibana, Masaya, Rahman, Shafiur, KagitaniShimono, Kuriko

    Published in Autism research (01-09-2022)
    “…Patients with autism spectrum disorder (ASD) often show pervasive and complex language impairments that are closely associated with aberrant structural…”
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    Everolimus for epilepsy and autism spectrum disorder in tuberous sclerosis complex: EXIST-3 substudy in Japan by Mizuguchi, Masashi, Ikeda, Hiroko, Kagitani-Shimono, Kuriko, Yoshinaga, Harumi, Suzuki, Yasuhiro, Aoki, Makoto, Endo, Masae, Yonemura, Masataka, Kubota, Masaya

    Published in Brain & development (Tokyo. 1979) (01-01-2019)
    “…Epilepsy and autism spectrum disorder (ASD) are the common neurological manifestations of tuberous sclerosis complex (TSC). EXIST-3 study has recently…”
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    Tuberous sclerosis complex: Recent advances in manifestations and therapy by Wataya‐Kaneda, Mari, Uemura, Motohide, Fujita, Kazutoshi, Hirata, Haruhiko, Osuga, Keigo, KagitaniShimono, Kuriko, Nonomura, Norio

    Published in International journal of urology (01-09-2017)
    “…Tuberous sclerosis complex is an autosomal dominant inherited disorder characterized by generalized involvement and variable manifestations with a birth…”
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    Clinical Factors Related to Outcomes in Pediatric Epilepsy Surgery: Insight into Predictors of Poor Surgical Outcome by OSHINO, Satoru, TANI, Naoki, KHOO, Hui Ming, KAGITANI-SHIMONO, Kuriko, NABATAME, Shin, TOMINAGA, Koji, YANAGISAWA, Takufumi, HIRATA, Masayuki, KISHIMA, Haruhiko

    Published in Neurologia Medico-Chirurgica (15-05-2023)
    “…Successful surgery for drug-resistant pediatric epilepsy can facilitate motor and cognitive development and improve quality of life by resolution or reduction…”
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    Nationwide survey of glucose transporter-1 deficiency syndrome (GLUT-1DS) in Japan by Ito, Yasushi, Takahashi, Satoru, Kagitani-Shimono, Kuriko, Natsume, Jun, Yanagihara, Keiko, Fujii, Tatsuya, Oguni, Hirokazu

    Published in Brain & development (Tokyo. 1979) (01-09-2015)
    “…Abstract Objectives We conducted a nationwide survey of glucose transporter type-1 deficiency syndrome (GLUT-1DS) in Japan in order to clarify its incidence as…”
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    Clinicogenetical features of a Japanese patient with giant axonal neuropathy by Akagi, Motohiro, Mohri, Ikuko, Iwatani, Yoshiko, Kagitani-Shimono, Kuriko, Okinaga, Takeshi, Sakai, Norio, Ozono, Keiichi, Taniike, Masako

    Published in Brain & development (Tokyo. 1979) (01-02-2012)
    “…Abstract Giant axonal neuropathy (GAN) is a rare autosomal recessive disorder that affects both the peripheral nerves and central nervous system. Since the…”
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    Lipocalin-type prostaglandin D synthase is up-regulated in oligodendrocytes in lysosomal storage diseases and binds gangliosides by Mohri, Ikuko, Taniike, Masako, Okazaki, Issei, Kagitani-Shimono, Kuriko, Aritake, Kosuke, Kanekiyo, Takahisa, Yagi, Takashi, Takikita, Shoichi, Kim, Hyung-Suk, Urade, Yoshihiro, Suzuki, Kinuko

    Published in Journal of neurochemistry (01-05-2006)
    “…Lipocalin-type prostaglandin (PG) D synthase (L-PGDS) is a dually functional protein, acting both as a PGD₂-synthesizing enzyme and as an extracellular…”
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    Altered white matter connectivity of ventral language networks in autism spectrum disorder: An automated fiber quantification analysis with multi-site datasets by Li, Min, Izumoto, Maya, Wang, Yide, Kato, Yoko, Iwatani, Yoshiko, Hirata, Ikuko, Mizuno, Yoshifumi, Tachibana, Masaya, Mohri, Ikuko, Kagitani-Shimono, Kuriko

    Published in NeuroImage (Orlando, Fla.) (15-08-2024)
    “…•We investigated precise WM changes in ventral language networks of ASD by AFQ.•Children with ASD showed under-connectivity in left ILF and IFOF.•More…”
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    SLC2A1 gene analysis of Japanese patients with glucose transporter 1 deficiency syndrome by Hashimoto, Natsuko, Kagitani-Shimono, Kuriko, Sakai, Norio, Otomo, Takanobu, Tominaga, Koji, Nabatame, Shin, Mogami, Yukiko, Takahashi, Yukitoshi, Imai, Katsumi, Yanagihara, Keiko, Okinaga, Takeshi, Nagai, Toshisaburo, Taniike, Masako, Ozono, Keiichi

    Published in Journal of human genetics (01-12-2011)
    “…Glucose transporter 1 deficiency syndrome (Glut1-DS) is a congenital metabolic disorder characterized by refractory seizures with early infantile onset,…”
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    Examining normative values using the Cambridge neuropsychological test automated battery and developmental traits of executive functions among elementary school-aged children in Japan by Aoki, Sho, Nagatani, Fumiyo, Kagitani-Shimono, Kuriko, Ohno, Yuko, Taniike, Masako, Mohri, Ikuko

    Published in Frontiers in psychology (16-08-2023)
    “…The Cambridge Neuropsychological Test Automated Battery (CANTAB) is a computerized and child-friendly neuropsychological assessment battery that includes…”
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    Epilepsy in Wolf‐Hirschhorn Syndrome (4p‐) by KagitaniShimono, Kuriko, Imai, Katsumi, Otani, Kazumasa, Kamio, Noriko, Okinaga, Takeshi, Toribe, Yasuhisa, Suzuki, Yasuhiro, Ozono, Keiichi

    Published in Epilepsia (Copenhagen) (01-01-2005)
    “…Purpose: We investigated the evolution of epilepsy, seizure types, and effective drugs in Wolf‐Hirschhorn syndrome, which is a malformation syndrome often with…”
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    Clinical evaluation of neuroinflammation in child-onset focal epilepsy: a translocator protein PET study by Kagitani-Shimono, Kuriko, Kato, Hiroki, Kuwayama, Ryoko, Tominaga, Koji, Nabatame, Shin, Kishima, Haruhiko, Hatazawa, Jun, Taniike, Masako

    Published in Journal of neuroinflammation (06-01-2021)
    “…Neuroinflammation is associated with various chronic neurological diseases, including epilepsy; however, neuroimaging approaches for visualizing…”
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    Promising Effect of a New Ketogenic Diet Regimen in Patients with Advanced Cancer by Hagihara, Keisuke, Kajimoto, Katsufumi, Osaga, Satoshi, Nagai, Naoko, Shimosegawa, Eku, Nakata, Hideyuki, Saito, Hitomi, Nakano, Mai, Takeuchi, Mariko, Kanki, Hideaki, Kagitani-Shimono, Kuriko, Kijima, Takashi

    Published in Nutrients (19-05-2020)
    “…A ketogenic diet is expected to be an effective support therapy for patients with cancer, but the degree and duration of carbohydrate restriction are unclear…”
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    Sleep disordered breathing in childhood-onset acid maltase deficiency by Nabatame, Shin, Taniike, Masako, Sakai, Norio, Kato-Nishimura, Kumi, Mohri, Ikuko, Kagitani-Shimono, Kuriko, Okinaga, Takeshi, Tachibana, Naoko, Ozono, Keiichi

    Published in Brain & development (Tokyo. 1979) (01-03-2009)
    “…Abstract Objectives: To clarify the feature of sleep disordered breathing (SDB) associated with childhood-onset acid maltase deficiency (AMD): the progressive…”
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    Abnormal White Matter Microstructure in the Limbic System Is Associated With Tuberous Sclerosis Complex-Associated Neuropsychiatric Disorders by Sato, Akemi, Tominaga, Koji, Iwatani, Yoshiko, Kato, Yoko, Wataya-Kaneda, Mari, Makita, Kai, Nemoto, Kiyotaka, Taniike, Masako, Kagitani-Shimono, Kuriko

    Published in Frontiers in neurology (14-03-2022)
    “…Tuberous sclerosis complex (TSC) is a genetic disease that arises from or abnormalities and induces the overactivation of the mammalian/mechanistic target of…”
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    Extension of microglial activation is associated with epilepsy and cognitive dysfunction in Tuberous sclerosis complex: A TSPO-PET study by Kagitani-Shimono, Kuriko, Kato, Hiroki, Soeda, Fumihiko, Iwatani, Yoshiko, Mukai, Masashi, Ogawa, Katsuhiro, Tominaga, Koji, Nabatame, Shin, Taniike, Masako

    Published in NeuroImage clinical (01-01-2023)
    “…•TSC causes overactivation of the mTOR pathway, which is linked to neuroinflammation.•Most cortical tubers in TSC patients showed microglial…”
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