Search Results - Mazaki-Miyazaki, Emi

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  1. 1
    Mutations of sodium channel α subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic–clonic seizures

    Mutations of sodium channel α subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic–clonic seizures by Fujiwara, Tateki, Sugawara, Takashi, Mazaki‐Miyazaki, Emi, Takahashi, Yukitoshi, Fukushima, Katsuyuki, Watanabe, Masako, Hara, Keita, Morikawa, Tateki, Yagi, Kazuichi, Yamakawa, Kazuhiro, Inoue, Yushi

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  2. 2
    A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures

    A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures by Kimura, Kazue, Sugawara, Takashi, Mazaki-Miyazaki, Emi, Hoshino, Kyoko, Nomura, Yoshiko, Tateno, Akihiko, Hachimori, Kei, Yamakawa, Kazuhiro, Segawa, Masaya

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  3. 3
    A missense mutation of the Na+ channel αII subunit gene Nav1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

    A missense mutation of the Na+ channel αII subunit gene Nav1.2 in a patient with febrile and afebrile seizures causes channel dysfunction by Sugawara, Takashi, Tsurubuchi, Yuji, Agarwala, Kishan Lal, Ito, Masatoshi, Fukuma, Goryu, Mazaki-Miyazaki, Emi, Nagafuji, Hiroshi, Noda, Masaharu, Imoto, Keiji, Wada, Kazumaru, Mitsudome, Akihisa, Kaneko, Sunao, Montal, Mauricio, Nagata, Keiichi, Hirose, Shinichi, Yamakawa, Kazuhiro

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  4. 4
    A family of generalized epilepsy with febrile seizures plus type 2—a new missense mutation of SCN1A found in the pedigree of several patients with complex febrile seizures

    A family of generalized epilepsy with febrile seizures plus type 2—a new missense mutation of SCN1A found in the pedigree of several patients with complex febrile seizures by Nagao, Yoshiro, Mazaki-Miyazaki, Emi, Okamura, Nami, Takagi, Manabu, Igarashi, Takashi, Yamakawa, Kazuhiro

    Published in Epilepsy research
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  5. 5
    Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents

    Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents by Sugawara, Takashi, Tsurubuchi, Yuji, Fujiwara, Tateki, Mazaki-Miyazaki, Emi, Nagata, Keiichi, Montal, Mauricio, Inoue, Yushi, Yamakawa, Kazuhiro

    Published in Epilepsy research
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  6. 6
    A family of generalized epilepsy with febrile seizures plus type 2- : a new missense mutation of SCN1N found in the pedigree of several patients with complex febrile seizures

    A family of generalized epilepsy with febrile seizures plus type 2- : a new missense mutation of SCN1N found in the pedigree of several patients with complex febrile seizures by NAGAO, Yoshiro, MAZAKI-MIYAZAKI, Emi, OKAMURA, Nami, TAKAGI, Manabu, IGARASHI, Takashi, YAMAKAWA, Kazuhiro

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  7. 7
    Mutations of sodium channel a subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures

    Mutations of sodium channel a subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures by FUJIWARA, Tateki, SUGAWARA, Takashi, INOUE, Yushi, MAZAKI-MIYAZAKI, Emi, TAKAHASHI, Yukitoshi, FUKUSHIMA, Katsuyuki, WATANABE, Masako, HARA, Keita, MORIKAWA, Tateki, YAGI, Kazuichi, YAMAKAWA, Kazuhiro

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  8. 8
    Na v1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents

    Na v1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents by Sugawara, Takashi, Tsurubuchi, Yuji, Fujiwara, Tateki, Mazaki-Miyazaki, Emi, Nagata, Keiichi, Montal, Mauricio, Inoue, Yushi, Yamakawa, Kazuhiro

    Published in Epilepsy research
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  9. 9
    Nav 1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents

    Nav 1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents by SUGAWARA, Takashi, TSURUBUCHI, Yuji, FUJIWARA, Tateki, MAZAKI-MIYAZAKI, Emi, NAGATA, Keiichi, MONTAL, Mauricio, INOUE, Yushi, YAMAKAWA, Kazuhiro

    Published in Epilepsy research
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  10. 10
    A Missense Mutation of the Na+Channel αIISubunit Gene Nav1.2 in a Patient with Febrile and Afebrile Seizures Causes Channel Dysfunction

    A Missense Mutation of the Na+Channel αIISubunit Gene Nav1.2 in a Patient with Febrile and Afebrile Seizures Causes Channel Dysfunction by Sugawara, Takashi, Tsurubuchi, Yuji, Agarwala, Kishan Lal, Ito, Masatoshi, Fukuma, Goryu, Mazaki-Miyazaki, Emi, Nagafuji, Hiroshi, Noda, Masaharu, Imoto, Keiji, Wada, Kazumaru, Mitsudome, Akihisa, Kaneko, Sunao, Montal, Mauricio, Nagata, Keiichi, Hirose, Shinichi, Yamakawa, Kazuhiro

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  11. 11
    A missense mutation of the Na + channel α II subunit gene Na v 1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

    A missense mutation of the Na + channel α II subunit gene Na v 1.2 in a patient with febrile and afebrile seizures causes channel dysfunction by Sugawara, Takashi, Tsurubuchi, Yuji, Agarwala, Kishan Lal, Ito, Masatoshi, Fukuma, Goryu, Mazaki-Miyazaki, Emi, Nagafuji, Hiroshi, Noda, Masaharu, Imoto, Keiji, Wada, Kazumaru, Mitsudome, Akihisa, Kaneko, Sunao, Montal, Mauricio, Nagata, Keiichi, Hirose, Shinichi, Yamakawa, Kazuhiro

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