Fujita T - Search Results

1

Early onset and focal spike discharges as indicators of poor prognosis for myoclonic-astatic epilepsy.

Inoue T, Ihara Y, Tomonoh Y, Nakamura N, Ninomiya S, Fujita T, Ideguchi H, Yasumoto S, Zhang B, Hirose S. Inoue T, et al. Among authors: fujita t. Brain Dev. 2014 Aug;36(7):613-9. doi: 10.1016/j.braindev.2013.08.009. Epub 2013 Sep 19. Brain Dev. 2014. PMID: 24055341

2

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. Tomonoh Y, et al. Among authors: fujita t. Seizure. 2011 Sep;20(7):583-5. doi: 10.1016/j.seizure.2011.03.004. Epub 2011 Apr 21. Seizure. 2011. PMID: 21511499 Free article.

3

Reduced PLP1 expression in induced pluripotent stem cells derived from a Pelizaeus-Merzbacher disease patient with a partial PLP1 duplication.

Shimojima K, Inoue T, Imai Y, Arai Y, Komoike Y, Sugawara M, Fujita T, Ideguchi H, Yasumoto S, Kanno H, Hirose S, Yamamoto T. Shimojima K, et al. Among authors: fujita t. J Hum Genet. 2012 Sep;57(9):580-6. doi: 10.1038/jhg.2012.71. Epub 2012 Jun 14. J Hum Genet. 2012. PMID: 22695888

4

Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis.

Ishii A, Yasumoto S, Ihara Y, Inoue T, Fujita T, Nakamura N, Ohfu M, Yamashita Y, Takatsuka H, Taga T, Miyata R, Ito M, Tsuchiya H, Matsuoka T, Kitao T, Murakami K, Lee WT, Kaneko S, Hirose S. Ishii A, et al. Among authors: fujita t. Brain Dev. 2013 Jun;35(6):524-30. doi: 10.1016/j.braindev.2012.09.006. Epub 2012 Oct 13. Brain Dev. 2013. PMID: 23073245

5

[A clinical course of patient with Aicardi-Goutieres syndrome due to SAMHD1 gene abnormality].

Watanabe E, Onozawa K, Fujita T, Tomonoh Y, Ihara Y, Yasumoto S, Nishikomori R, Heike T, Hirose S. Watanabe E, et al. Among authors: fujita t. No To Hattatsu. 2017 Jan;49(1):51-2. No To Hattatsu. 2017. PMID: 30011156 Japanese. No abstract available.

6

Recurrent autonomic and sensory neuropathy in a patient with anti-ganglionic acetylcholine receptor antibodies.

Watanabe E, Fujita T, Shimono M, Koike H, Yasumoto S, Hirose S. Watanabe E, et al. Among authors: fujita t. eNeurologicalSci. 2018 Aug 23;12:36-38. doi: 10.1016/j.ensci.2018.08.001. eCollection 2018 Sep. eNeurologicalSci. 2018. PMID: 30211328 Free PMC article.

7

Different types of suppression-burst patterns in patients with epilepsy of infancy with migrating focal seizures (EIMFS).

Yoshitomi S, Takahashi Y, Imai K, Koshimizu E, Miyatake S, Nakashima M, Saitsu H, Matsumoto N, Kato M, Fujita T, Ishii A, Hirose S, Inoue Y. Yoshitomi S, et al. Among authors: fujita t. Seizure. 2019 Feb;65:118-123. doi: 10.1016/j.seizure.2019.01.009. Epub 2019 Jan 18. Seizure. 2019. PMID: 30684875 Free article.

8

Quinidine therapy and therapeutic drug monitoring in four patients with KCNT1 mutations.

Yoshitomi S, Takahashi Y, Yamaguchi T, Oboshi T, Horino A, Ikeda H, Imai K, Okanishi T, Nakashima M, Saitsu H, Matsumoto N, Yoshimoto J, Fujita T, Ishii A, Hirose S, Inoue Y. Yoshitomi S, et al. Among authors: fujita t. Epileptic Disord. 2019 Feb 1;21(1):48-54. doi: 10.1684/epd.2019.1026. Epileptic Disord. 2019. PMID: 30782581

9

Coffin-Siris syndrome with bilateral macular dysplasia caused by a novel exonic deletion in ARID1B.

Fujita T, Ihara Y, Hayashi H, Ishii A, Ideguchi H, Inoue T, Imaizumi T, Yamamoto T, Hirose S. Fujita T, et al. Congenit Anom (Kyoto). 2020 Nov;60(6):189-193. doi: 10.1111/cga.12383. Epub 2020 Jul 30. Congenit Anom (Kyoto). 2020. PMID: 32618029

10

Three-Year Longitudinal Motor Function and Disability Level of Acute Flaccid Myelitis.

Chong PF, Kira R, Torisu H, Yasumoto S, Okumura A, Mori H, Tanaka-Taya K; AFM Study Group. Chong PF, et al. Pediatr Neurol. 2021 Mar;116:14-19. doi: 10.1016/j.pediatrneurol.2020.11.019. Epub 2020 Dec 3. Pediatr Neurol. 2021. PMID: 33388543

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