Takeshita E - Search Results

1

Muscle impairment in MRI affect variability in treatment response to nusinersen in patients with spinal muscular atrophy type 2 and 3: A retrospective cohort study.

Shimizu-Motohashi Y, Chiba E, Mizuno K, Yajima H, Ishiyama A, Takeshita E, Sato N, Oba M, Sasaki M, Ito S, Komaki H. Shimizu-Motohashi Y, et al. Among authors: takeshita e. Brain Dev. 2023 Mar;45(3):161-170. doi: 10.1016/j.braindev.2022.11.002. Epub 2022 Nov 29. Brain Dev. 2023. PMID: 36460551 Free article.

2

Late-onset mental deterioration and fluctuating dystonia in a female patient with a truncating MECP2 mutation.

Takeshita E, Saito Y, Nakagawa E, Komaki H, Sugai K, Sasaki M, Nezu A, Kitamura J, Itoh M, Sawano Y, Goto Y. Takeshita E, et al. J Neurol Sci. 2011 Sep 15;308(1-2):168-72. doi: 10.1016/j.jns.2011.06.008. Epub 2011 Jun 30. J Neurol Sci. 2011. PMID: 21722922

3

Effect of corpus callosotomy on attention deficit and behavioral problems in pediatric patients with intractable epilepsy.

Yonekawa T, Nakagawa E, Takeshita E, Inoue Y, Inagaki M, Kaga M, Sugai K, Sasaki M, Kaido T, Takahashi A, Otsuki T. Yonekawa T, et al. Among authors: takeshita e. Epilepsy Behav. 2011 Dec;22(4):697-704. doi: 10.1016/j.yebeh.2011.08.027. Epub 2011 Oct 5. Epilepsy Behav. 2011. PMID: 21978470

4

Novel AGTR2 missense mutation in a Japanese boy with severe mental retardation, pervasive developmental disorder, and epilepsy.

Takeshita E, Nakagawa E, Nakatani K, Sasaki M, Goto Y. Takeshita E, et al. Brain Dev. 2012 Oct;34(9):776-9. doi: 10.1016/j.braindev.2011.12.010. Epub 2012 Jan 24. Brain Dev. 2012. PMID: 22269148

5

Hypophosphatemia is a common complication in severely disabled individuals with neurological disorders and is caused by infection, refeeding and Fanconi syndrome.

Saito Y, Aoki Y, Takeshita E, Saito T, Sugai K, Komaki H, Nakagawa E, Ishiyama A, Takanoha S, Wada S, Sasaki M. Saito Y, et al. Among authors: takeshita e. Brain Dev. 2014 Nov;36(10):878-83. doi: 10.1016/j.braindev.2013.12.001. Epub 2013 Dec 18. Brain Dev. 2014. PMID: 24360095

6

Episodic tremors representing cortical myoclonus are characteristic in Angelman syndrome due to UBE3A mutations.

Goto M, Saito Y, Honda R, Saito T, Sugai K, Matsuda Y, Miyatake C, Takeshita E, Ishiyama A, Komaki H, Nakagawa E, Sasaki M, Uto C, Kikuchi K, Motoki T, Saitoh S. Goto M, et al. Among authors: takeshita e. Brain Dev. 2015 Feb;37(2):216-22. doi: 10.1016/j.braindev.2014.04.005. Epub 2014 May 3. Brain Dev. 2015. PMID: 24796722

7

A family of distal arthrogryposis type 5 due to a novel PIEZO2 mutation.

Okubo M, Fujita A, Saito Y, Komaki H, Ishiyama A, Takeshita E, Kojima E, Koichihara R, Saito T, Nakagawa E, Sugai K, Yamazaki H, Kusaka K, Tanaka H, Miyake N, Matsumoto N, Sasaki M. Okubo M, et al. Among authors: takeshita e. Am J Med Genet A. 2015 May;167A(5):1100-6. doi: 10.1002/ajmg.a.36881. Epub 2015 Feb 25. Am J Med Genet A. 2015. PMID: 25712306

8

Treatable renal failure found in non-ambulatory Duchenne muscular dystrophy patients.

Motoki T, Shimizu-Motohashi Y, Komaki H, Mori-Yoshimura M, Oya Y, Takeshita E, Ishiyama A, Saito T, Nakagawa E, Sugai K, Murata M, Sasaki M. Motoki T, et al. Among authors: takeshita e. Neuromuscul Disord. 2015 Oct;25(10):754-7. doi: 10.1016/j.nmd.2015.07.006. Epub 2015 Jul 29. Neuromuscul Disord. 2015. PMID: 26298609

9

The long-term health impact and potential predictors of cardiopulmonary arrest in patients with childhood-onset psychomotor impairments.

Kubota K, Shimizu-Motohashi Y, Saito T, Akatsuka S, Takeshita E, Ishiyama A, Komaki H, Nakagawa E, Sugai K, Sasaki M. Kubota K, et al. Among authors: takeshita e. Brain Dev. 2016 Apr;38(4):392-8. doi: 10.1016/j.braindev.2015.10.005. Epub 2015 Oct 21. Brain Dev. 2016. PMID: 26482602

10

Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan.

Goto M, Komaki H, Takeshita E, Abe Y, Ishiyama A, Sugai K, Sasaki M, Goto Y, Nonaka I. Goto M, et al. Among authors: takeshita e. Brain Dev. 2016 Oct;38(9):785-91. doi: 10.1016/j.braindev.2016.04.001. Epub 2016 Apr 21. Brain Dev. 2016. PMID: 27112384

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