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Items: 1 to 50 of 97

1.

[Proposal to young pediatric neurologists--thinking about the future by reflecting the past (discussion)].

Kurokawa T, Takashima S, Mitsudome A, Yasumoto S, Yamashita Y.

No To Hattatsu. 2014 May;46(3):169-78. Japanese. No abstract available.

PMID:
24902334
2.

Magnetic resonance imaging volumetry and clinical analysis of epilepsy patients with unilateral hippocampal abnormality.

Matsufuji M, Utsunomiya H, Inoue T, Yasumoto S, Takashima S, Mitsudome A.

Pediatr Int. 2012 Feb;54(1):19-26. doi: 10.1111/j.1442-200X.2011.03444.x.

PMID:
21810153
3.

Diagnosing nocturnal frontal lobe epilepsy: a case study of two children.

Tomonoh Y, Yasumoto S, Ihara Y, Fujita T, Nakamura N, Ninomiya S, Kodama R, Ideguchi H, Inoue T, Mitsudome A, Hirose S.

Seizure. 2011 Sep;20(7):583-5. doi: 10.1016/j.seizure.2011.03.004. Epub 2011 Apr 21.

4.

Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan.

Torisu H, Kira R, Ishizaki Y, Sanefuji M, Yamaguchi Y, Yasumoto S, Murakami Y, Shimono M, Nagamitsu S, Masuzaki M, Amamoto M, Kondo R, Uozumi T, Aibe M, Gondo K, Hanai T, Hirose S, Matsuishi T, Shirahata A, Mitsudome A, Hara T.

Brain Dev. 2010 Jun;32(6):454-62. doi: 10.1016/j.braindev.2009.10.006. Epub 2009 Nov 25.

PMID:
19942388
5.

Rats harboring S284L Chrna4 mutation show attenuation of synaptic and extrasynaptic GABAergic transmission and exhibit the nocturnal frontal lobe epilepsy phenotype.

Zhu G, Okada M, Yoshida S, Ueno S, Mori F, Takahara T, Saito R, Miura Y, Kishi A, Tomiyama M, Sato A, Kojima T, Fukuma G, Wakabayashi K, Hase K, Ohno H, Kijima H, Takano Y, Mitsudome A, Kaneko S, Hirose S.

J Neurosci. 2008 Nov 19;28(47):12465-76. doi: 10.1523/JNEUROSCI.2961-08.2008.

6.

A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions.

Ishii A, Fukuma G, Uehara A, Miyajima T, Makita Y, Hamachi A, Yasukochi M, Inoue T, Yasumoto S, Okada M, Kaneko S, Mitsudome A, Hirose S.

Brain Dev. 2009 Jan;31(1):27-33. doi: 10.1016/j.braindev.2008.05.010. Epub 2008 Jul 21.

PMID:
18640800
7.

Developmental changes in KCNQ2 and KCNQ3 expression in human brain: possible contribution to the age-dependent etiology of benign familial neonatal convulsions.

Kanaumi T, Takashima S, Iwasaki H, Itoh M, Mitsudome A, Hirose S.

Brain Dev. 2008 May;30(5):362-9. doi: 10.1016/j.braindev.2007.11.003. Epub 2007 Dec 31.

PMID:
18166285
8.

Different perceptual sensitivities for Chernoff's face between children and adults.

Tsurusawa R, Goto Y, Mitsudome A, Nakashima T, Tobimatsu S.

Neurosci Res. 2008 Feb;60(2):176-83. Epub 2007 Nov 6.

PMID:
18082280
9.

[Sympathetic skin response in patients with severe motor and intellectual disabilities].

Ogawa A, Hamamoto K, Hirose S, Fujikawa M, Mitsudome A.

No To Hattatsu. 2007 Sep;39(5):347-50. Japanese.

PMID:
17879607
10.

Molecular characterization of water-selective AQP (EbAQP4) in hagfish: insight into ancestral origin of AQP4.

Nishimoto G, Sasaki G, Yaoita E, Nameta M, Li H, Furuse K, Fujinaka H, Yoshida Y, Mitsudome A, Yamamoto T.

Am J Physiol Regul Integr Comp Physiol. 2007 Jan;292(1):R644-51. Epub 2006 Sep 21.

11.
12.

An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.

Kanaumi T, Hirose S, Goto Y, Naitou E, Mitsudome A.

Pediatr Neurol. 2006 Mar;34(3):235-8.

PMID:
16504796
13.

Clinicopathologic correlation of C1q nephropathy in children.

Fukuma Y, Hisano S, Segawa Y, Niimi K, Tsuru N, Kaku Y, Hatae K, Kiyoshi Y, Mitsudome A, Iwasaki H.

Am J Kidney Dis. 2006 Mar;47(3):412-8.

PMID:
16490619
14.

Biliary atresia associated with jejunal atresia and a review of the literature in Japan.

Asabe K, Yukitake K, Mori T, Mitsudome A, Shirakusa T.

Asian J Surg. 2005 Apr;28(2):154-7. Review.

15.

Genetics of idiopathic epilepsies.

Hirose S, Mitsudome A, Okada M, Kaneko S; Epilepsy Genetic Study Group, Japan.

Epilepsia. 2005;46 Suppl 1:38-43. Review.

16.

[A case of parietal lobe epilepsy with ictal laughter].

Tsurusawa R, Ohfu M, Masuzaki M, Inoue T, Yasumoto S, Mitsudome A.

No To Hattatsu. 2005 Jan;37(1):60-4. Japanese.

PMID:
15675361
17.

Severe myoclonic epilepsy in infancy: clinical analysis and relation to SCN1A mutations in a Japanese cohort.

Oguni H, Hayashi K, Osawa M, Awaya Y, Fukuyama Y, Fukuma G, Hirose S, Mitsudome A, Kaneko S.

Adv Neurol. 2005;95:103-17. Review. No abstract available.

PMID:
15508916
18.

Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity.

Kanai K, Hirose S, Oguni H, Fukuma G, Shirasaka Y, Miyajima T, Wada K, Iwasa H, Yasumoto S, Matsuo M, Ito M, Mitsudome A, Kaneko S.

Neurology. 2004 Jul 27;63(2):329-34. Review.

PMID:
15277629
19.

[Rolandic epilepsy: neurophysiological aspects].

Mitsudome A.

No To Hattatsu. 2004 Mar;36(2):97-105. Review. Japanese.

PMID:
15031982
20.

Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB).

Fukuma G, Oguni H, Shirasaka Y, Watanabe K, Miyajima T, Yasumoto S, Ohfu M, Inoue T, Watanachai A, Kira R, Matsuo M, Muranaka H, Sofue F, Zhang B, Kaneko S, Mitsudome A, Hirose S.

Epilepsia. 2004 Feb;45(2):140-8.

21.

F-waves in neonates: increased spinal anterior horn motor neuron excitability.

Yasumoto S, Mitsudome A.

Brain Dev. 2004 Jan;26(1):8-11.

PMID:
14729407
22.

Favorable seizure outcome in Kabuki make-up syndrome associated with epilepsy.

Ogawa A, Yasumoto S, Tomoda Y, Ohfu M, Mitsudome A, Kuroki Y.

J Child Neurol. 2003 Aug;18(8):549-51.

PMID:
13677581
23.

Effect of aging on autonomic function in individuals with severe motor and intellectual disabilities.

Hamamoto K, Ogawa A, Mitsudome A.

Brain Dev. 2003 Aug;25(5):326-9.

PMID:
12850511
24.

The genetics of febrile seizures and related epilepsy syndromes.

Hirose S, Mohney RP, Okada M, Kaneko S, Mitsudome A.

Brain Dev. 2003 Aug;25(5):304-12. Review.

PMID:
12850508
25.

X-linked mental retardation and epilepsy: pathogenetic significance of ARX mutations.

Hirose S, Mitsudome A.

Brain Dev. 2003 Apr;25(3):161-5. Review.

PMID:
12689693
26.

Essential roles of perforin in antigen-specific cytotoxicity mediated by human CD4+ T lymphocytes: analysis using the combination of hereditary perforin-deficient effector cells and Fas-deficient target cells.

Yanai F, Ishii E, Kojima K, Hasegawa A, Azuma T, Hirose S, Suga N, Mitsudome A, Zaitsu M, Ishida Y, Shirakata Y, Sayama K, Hashimoto K, Yasukawa M.

J Immunol. 2003 Feb 15;170(4):2205-13.

27.

[Familial temporal lobe epilepsy].

Mitsudome A.

Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):364-6. Review. Japanese. No abstract available.

PMID:
12483902
28.

[Temporal lobe epilepsy].

Mitsudome A.

Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):37-41. Review. Japanese. No abstract available.

PMID:
12483823
29.

Effect of growth hormone on high plasma levels of glucagon-like peptide-1 (GLP-1) in hypophysectomized rats.

Tateishi K, Kitayama N, Ishikawa H, Mitsudome A, Hirose S.

Exp Clin Endocrinol Diabetes. 2002 Oct;110(7):361-3.

PMID:
12397536
30.

Molecular genetics of human familial epilepsy syndromes.

Hirose S, Okada M, Kaneko S, Mitsudome A.

Epilepsia. 2002;43 Suppl 9:21-5.

31.

Establishment and characterization of a novel human desmoplastic small round cell tumor cell line, JN-DSRCT-1.

Nishio J, Iwasaki H, Ishiguro M, Ohjimi Y, Fujita C, Yanai F, Nibu K, Mitsudome A, Kaneko Y, Kikuchi M.

Lab Invest. 2002 Sep;82(9):1175-82.

PMID:
12218078
32.

Genetic abnormalities underlying familial epilepsy syndromes.

Hirose S, Okada M, Yamakawa K, Sugawara T, Fukuma G, Ito M, Kaneko S, Mitsudome A.

Brain Dev. 2002 Jun;24(4):211-22. Review.

PMID:
12015163
33.

Mutation (Ser284Leu) of neuronal nicotinic acetylcholine receptor alpha 4 subunit associated with frontal lobe epilepsy causes faster desensitization of the rat receptor expressed in oocytes.

Matsushima N, Hirose S, Iwata H, Fukuma G, Yonetani M, Nagayama C, Hamanaka W, Matsunaka Y, Ito M, Kaneko S, Mitsudome A, Sugiyama H.

Epilepsy Res. 2002 Feb;48(3):181-6.

PMID:
11904236
34.

Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A.

Ito M, Nagafuji H, Okazawa H, Yamakawa K, Sugawara T, Mazaki-Miyazaki E, Hirose S, Fukuma G, Mitsudome A, Wada K, Kaneko S.

Epilepsy Res. 2002 Jan;48(1-2):15-23.

PMID:
11823106
35.

Postoperative speech development based on cleft types in children with cleft palate.

Nakajima T, Mitsudome A, Yosikawa A.

Pediatr Int. 2001 Dec;43(6):666-72.

PMID:
11737746
36.

A case of hemiplegic migraine in childhood: transient unilateral hyperperfusion revealed by perfusion MR imaging and MR angiography.

Masuzaki M, Utsunomiya H, Yasumoto S, Mitsudome A.

AJNR Am J Neuroradiol. 2001 Oct;22(9):1795-7.

37.

Nav1.1 mutations cause febrile seizures associated with afebrile partial seizures.

Sugawara T, Mazaki-Miyazaki E, Ito M, Nagafuji H, Fukuma G, Mitsudome A, Wada K, Kaneko S, Hirose S, Yamakawa K.

Neurology. 2001 Aug 28;57(4):703-5.

PMID:
11524484
38.

[Interleukin-6 in the cerebrospinal fluid of two patients with herpes zoster meningitis].

Ohfu M, Masuzaki M, Inoue S, Inoue T, Yasumoto S, Ogawa A, Tomoda Y, Tsuru N, Mitsudome A.

No To Hattatsu. 2001 May;33(3):270-5. Japanese.

PMID:
11391972
39.

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.

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.

Proc Natl Acad Sci U S A. 2001 May 22;98(11):6384-9. Erratum in: Proc Natl Acad Sci U S A 2001 Aug 28;98(18):10515.

40.

A novel SSCP variant (c.828G>A) within the M2 domain of the human neuronal nicotinic acetylcholine receptor alpha 4 subunit gene, CHRNA4.

Akiyoshi H, Iwata H, Fukuma G, Yonetani M, Wada K, Kaneko S, Mitsudome A, Hirose S.

Hum Mutat. 2000 Nov;16(5):450. No abstract available.

PMID:
11058920
41.

Are some idiopathic epilepsies disorders of ion channels?: A working hypothesis.

Hirose S, Okada M, Kaneko S, Mitsudome A.

Epilepsy Res. 2000 Oct;41(3):191-204. Review.

PMID:
10962210
42.

Late-onset type II glutaric aciduria with massive pericardial effusion associated with severe fatty liver.

Hirose S, Hamamoto K, Yoshida I, Inokuchi T, Kogo T, Mitsudome A.

Acta Paediatr. 2000 Jul;89(7):887-8. No abstract available.

PMID:
10943977
43.

A novel mutation of KCNQ3 (c.925T-->C) in a Japanese family with benign familial neonatal convulsions.

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.

Ann Neurol. 2000 Jun;47(6):822-6.

PMID:
10852552
44.

Electroclinical picture of autosomal dominant nocturnal frontal lobe epilepsy in a Japanese family.

Ito M, Kobayashi K, Fujii T, Okuno T, Hirose S, Iwata H, Mitsudome A, Kaneko S.

Epilepsia. 2000 Jan;41(1):52-8. Review.

45.

A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy.

Hirose S, Iwata H, Akiyoshi H, Kobayashi K, Ito M, Wada K, Kaneko S, Mitsudome A.

Neurology. 1999 Nov 10;53(8):1749-53.

PMID:
10563623
46.

Application of rapid random stimulation (RRS) to visual evoked potentials in children.

Fujikawa M, Ohfu M, Fujikawa S, Chen TT, Mitsudome A.

Brain Dev. 1999 Oct;21(7):474-7.

PMID:
10522525
47.
48.

Chromatic sensitive epilepsy: a variant of photosensitive epilepsy.

Tobimatsu S, Zhang YM, Tomoda Y, Mitsudome A, Kato M.

Ann Neurol. 1999 Jun;45(6):790-3.

PMID:
10360772
49.
50.

Development of the temporal lobe in infants and children: analysis by MR-based volumetry.

Utsunomiya H, Takano K, Okazaki M, Mitsudome A.

AJNR Am J Neuroradiol. 1999 Apr;20(4):717-23.

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