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Results: 1-17 |
Results: 17
A case of hemiplegic migraine in childhood: Transient unilateral hyperperfusion revealed by perfusion MR imaging and MR angiography
Authors: Masuzaki, M Utsunomiya, H Yasumoto, S Mitsudome, A
Citation: M. Masuzaki et al., A case of hemiplegic migraine in childhood: Transient unilateral hyperperfusion revealed by perfusion MR imaging and MR angiography, AM J NEUROR, 22(9), 2001, pp. 1795-1797
Na(upsilon)1.1 mutations cause febrile seizures associated with afebrile partial seizures
Authors: Sugawara, T Mazaki-Miyazaki, E Ito, M Nagafuji, H Fukuma, G Mitsudome, A Wada, K Kaneko, S Hirose, S Yamakawa, K
Citation: T. Sugawara et al., Na(upsilon)1.1 mutations cause febrile seizures associated with afebrile partial seizures, NEUROLOGY, 57(4), 2001, pp. 703-705
A missense mutation of the Na+ channel alpha(11) subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction (vol 98, pg 6384, 2001)
Authors: Sugawara, T Tsurubuchi, Y Agarwala, KL Ito, M Fukuma, G Mazaki-Miyazaki, E Nagafuji, H Noda, M Imoto, K Wada, K Mitsudome, A Kaneko, S Montal, M Nagata, K Hirose, S Yamakawa, K
Citation: T. Sugawara et al., A missense mutation of the Na+ channel alpha(11) subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction (vol 98, pg 6384, 2001), P NAS US, 98(18), 2001, pp. 10515-10515
A missense mutation of the Na+ channel alpha(II) subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction
Authors: Sugawara, T Tsurubuchi, Y Agarwala, KL Ito, M Fukuma, G Mazaki-Miyazaki, E Nagafuji, H Noda, M Imoto, K Wada, K Mitsudome, A Kaneko, S Montal, M Nagata, K Hirose, S Yamakawa, K
Citation: T. Sugawara et al., A missense mutation of the Na+ channel alpha(II) subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction, P NAS US, 98(11), 2001, pp. 6384-6389
Are some idiopathic epilepsies disorders of ion channels?: A working hypothesis
Authors: Hirose, S Okada, M Kaneko, S Mitsudome, A
Citation: S. Hirose et al., Are some idiopathic epilepsies disorders of ion channels?: A working hypothesis, EPILEPSY R, 41(3), 2000, pp. 191-204
Late-onset type II glutaric aciduria with massive pericardial effusion associated with severe fatty liver
Authors: Hirose, S Hamamoto, K Yoshida, I Inokuchi, T Kogo, T Mitsudome, A
Citation: S. Hirose et al., Late-onset type II glutaric aciduria with massive pericardial effusion associated with severe fatty liver, ACT PAEDIAT, 89(7), 2000, pp. 887-888
A novel mutation of KCNQ3 (c.925T -> C) in a Japanese family with benign familial neonatal convulsions
Authors: Hirose, S Zenri, F Akiyoshi, H Fukuma, G Iwata, H Inoue, T Yonetani, M Tsutsumi, M Muranaka, H Kurokawa, T Hanai, T Wada, K Kaneko, S Mitsudome, A
Citation: S. Hirose et al., A novel mutation of KCNQ3 (c.925T -> C) in a Japanese family with benign familial neonatal convulsions, ANN NEUROL, 47(6), 2000, pp. 822-826
The pocket monsters episode - Reply
Authors: Tobimatsu, S Zhang, YM Tomoda, T Mitsudome, A Kato, M
Citation: S. Tobimatsu et al., The pocket monsters episode - Reply, ANN NEUROL, 47(2), 2000, pp. 275-276
Electroclinical picture of autosomal dominant nocturnal frontal lobe epilepsy in a Japanese family
Authors: Ito, M Kobayashi, K Fujii, T Okuno, T Hirose, S Iwata, H Mitsudome, A Kaneko, S
Citation: M. Ito et al., Electroclinical picture of autosomal dominant nocturnal frontal lobe epilepsy in a Japanese family, EPILEPSIA, 41(1), 2000, pp. 52-58
Visual evoked potentials in school children: A comparative study of transient and steady-state methods with pattern reversal and flash stimulation
Authors: Tomoda, Y Tobimatsu, S Mitsudome, A
Citation: Y. Tomoda et al., Visual evoked potentials in school children: A comparative study of transient and steady-state methods with pattern reversal and flash stimulation, CLIN NEU, 110(1), 1999, pp. 97-102
Application of rapid random stimulation (RRS) to visual evoked potentials in children
Authors: Fujikawa, M Ohfu, M Fujikawa, S Chen, TT Mitsudome, A
Citation: M. Fujikawa et al., Application of rapid random stimulation (RRS) to visual evoked potentials in children, BRAIN DEVEL, 21(7), 1999, pp. 474-477
Chromatic sensitive epilepsy: A variant of photosensitive epilepsy
Authors: Tobimatsu, S Zhang, YM Tomoda, Y Mitsudome, A Kato, M
Citation: S. Tobimatsu et al., Chromatic sensitive epilepsy: A variant of photosensitive epilepsy, ANN NEUROL, 45(6), 1999, pp. 790-793
A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G -> A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiency (vol 104, pg 36, 1999)
Authors: Kanai, N Yanai, F Hirose, S Nibu, K Izuhara, K Tani, T Kubota, T Mitsudome, A
Citation: N. Kanai et al., A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G -> A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiency (vol 104, pg 36, 1999), HUM GENET, 104(2), 1999, pp. 196-196
A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G -> A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiency
Authors: Kanai, N Yanai, F Hirose, S Nibu, K Izuhara, K Tani, T Kubota, T Mitsudome, A
Citation: N. Kanai et al., A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G -> A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiency, HUM GENET, 104(1), 1999, pp. 36-42
Development of the temporal lobe in infants and children: Analysis by MR-based volumetry
Authors: Utsunomiya, H Takano, K Okazaki, M Mitsudome, A
Citation: H. Utsunomiya et al., Development of the temporal lobe in infants and children: Analysis by MR-based volumetry, AM J NEUROR, 20(4), 1999, pp. 717-723
A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy
Authors: Hirose, S Iwata, H Akiyoshi, H Kobayashi, K Ito, M Wada, K Kaneko, S Mitsudome, A
Citation: S. Hirose et al., A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy, NEUROLOGY, 53(8), 1999, pp. 1749-1753
Hypothalamic hamartoma associated with multiple congenital abnormalities -Two patients and a review of reported cases
Authors: Tsugu, H Fukushima, T Nagashima, T Utsunomiya, H Tomonaga, M Mitsudome, A
Citation: H. Tsugu et al., Hypothalamic hamartoma associated with multiple congenital abnormalities -Two patients and a review of reported cases, PED NEUROS, 29(6), 1998, pp. 290-296
Risultati: 1-17 |