Itomi K - Search Results

1

Identification of novel BCL11A variants in patients with epileptic encephalopathy: Expanding the phenotypic spectrum.

Yoshida M, Nakashima M, Okanishi T, Kanai S, Fujimoto A, Itomi K, Morimoto M, Saitsu H, Kato M, Matsumoto N, Chiyonobu T. Yoshida M, et al. Among authors: itomi k. Clin Genet. 2018 Feb;93(2):368-373. doi: 10.1111/cge.13067. Epub 2017 Oct 6. Clin Genet. 2018. PMID: 28589569

2

Successful corpus callosotomy for post-encephalopathic refractory epilepsy in a patient with MECP2 duplication syndrome.

Kanai S, Okanishi T, Fujimoto A, Itamura S, Baba S, Nishimura M, Itomi K, Enoki H. Kanai S, et al. Among authors: itomi k. Brain Dev. 2019 Mar;41(3):296-300. doi: 10.1016/j.braindev.2018.09.008. Epub 2018 Oct 9. Brain Dev. 2019. PMID: 30314874

3

Negishi Y, Aoki Y, Itomi K, Yasuda K, Taniguchi H, Ishida A, Arakawa T, Miyamoto S, Nakashima M, Saitsu H, Saitoh S. Negishi Y, et al. Among authors: itomi k. Brain Dev. 2021 Aug;43(7):804-808. doi: 10.1016/j.braindev.2021.03.004. Epub 2021 Apr 4. Brain Dev. 2021. PMID: 33827760

4

Cerebrovascular diseases in two patients with entire NSD1 deletion.

Itai T, Miyatake S, Hatano T, Hattori N, Ohno A, Aoki Y, Itomi K, Mori H, Saitsu H, Matsumoto N. Itai T, et al. Among authors: itomi k. Hum Genome Var. 2021 May 24;8(1):20. doi: 10.1038/s41439-021-00151-z. Hum Genome Var. 2021. PMID: 34031356 Free PMC article.

5

Effect of levodopa on pathological gait in Dravet syndrome: A randomized crossover trial using three-dimensional gait analysis.

Suzuki T, Natsume J, Ito Y, Ito T, Noritake K, Kinoshita F, Fukasawa T, Tsuji T, Itomi K, Kurahashi H, Kubota K, Okanishi T, Saitoh S, Sugiura H, Watanabe H, Takahashi Y, Kidokoro H. Suzuki T, et al. Among authors: itomi k. Epilepsia. 2024 May;65(5):1304-1313. doi: 10.1111/epi.17888. Epub 2024 Mar 12. Epilepsia. 2024. PMID: 38469885 Clinical Trial.

6

Epileptic spasms preceded by partial seizures with a close temporal association.

Kubota T, Aso K, Negoro T, Okumura A, Natsume J, Takada H, Itomi K, Watanabe K, Yamamoto N. Kubota T, et al. Among authors: itomi k. Epilepsia. 1999 Nov;40(11):1572-9. doi: 10.1111/j.1528-1157.1999.tb02042.x. Epilepsia. 1999. PMID: 10565585 Free article.

7

Microarray and FISH-based genotype-phenotype analysis of 22 Japanese patients with Wolf-Hirschhorn syndrome.

Shimizu K, Wakui K, Kosho T, Okamoto N, Mizuno S, Itomi K, Hattori S, Nishio K, Samura O, Kobayashi Y, Kako Y, Arai T, Tsutomu OI, Kawame H, Narumi Y, Ohashi H, Fukushima Y. Shimizu K, et al. Among authors: itomi k. Am J Med Genet A. 2014 Mar;164A(3):597-609. doi: 10.1002/ajmg.a.36308. Epub 2013 Dec 19. Am J Med Genet A. 2014. PMID: 24357569

8

PET in infancy predicts long-term outcome during adolescence in cryptogenic West syndrome.

Natsume J, Maeda N, Itomi K, Kidokoro H, Ishihara N, Takada H, Okumura A, Kubota T, Miura K, Aso K, Morikawa T, Kato K, Negoro T, Watanabe K. Natsume J, et al. Among authors: itomi k. AJNR Am J Neuroradiol. 2014 Aug;35(8):1580-5. doi: 10.3174/ajnr.A3899. Epub 2014 Mar 27. AJNR Am J Neuroradiol. 2014. PMID: 24676006 Free PMC article.

9

Natural histories of patients with Wolf-Hirschhorn syndrome derived from variable chromosomal abnormalities.

Yamamoto-Shimojima K, Kouwaki M, Kawashima Y, Itomi K, Momosaki K, Ozasa S, Okamoto N, Yokochi K, Yamamoto T. Yamamoto-Shimojima K, et al. Among authors: itomi k. Congenit Anom (Kyoto). 2019 Sep;59(5):169-173. doi: 10.1111/cga.12318. Epub 2018 Nov 15. Congenit Anom (Kyoto). 2019. PMID: 30378700

10

[Subacute encephalitis/encephalopathy with residual cognitive deficit].

Itomi K, Okumura A, Kato T, Fujimoto S, Negoro T, Kuno K, Watanabe K. Itomi K, et al. No To Hattatsu. 2005 Nov;37(6):467-72. No To Hattatsu. 2005. PMID: 16296349 Japanese.

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