Takeshita E - Search Results

1

Pediatric necrotizing myopathy associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibodies.

Liang WC, Uruha A, Suzuki S, Murakami N, Takeshita E, Chen WZ, Jong YJ, Endo Y, Komaki H, Fujii T, Kawano Y, Mori-Yoshimura M, Oya Y, Xi J, Zhu W, Zhao C, Watanabe Y, Ikemoto K, Nishikawa A, Hamanaka K, Mitsuhashi S, Suzuki N, Nishino I. Liang WC, et al. Among authors: takeshita e. Rheumatology (Oxford). 2017 Feb;56(2):287-293. doi: 10.1093/rheumatology/kew386. Epub 2016 Nov 6. Rheumatology (Oxford). 2017. PMID: 27818386 Free PMC article.

2

Evaluating the frequency and characteristics of seizures in 142 Japanese patients with Prader-Willi syndrome.

Takeshita E, Murakami N, Sakuta R, Nagai T. Takeshita E, et al. Am J Med Genet A. 2013 Aug;161A(8):2052-5. doi: 10.1002/ajmg.a.36015. Epub 2013 Jul 3. Am J Med Genet A. 2013. PMID: 23824702

3

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

4

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

5

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

6

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

7

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

8

Clinical trial network for the promotion of clinical research for rare diseases in Japan: muscular dystrophy clinical trial network.

Shimizu R, Ogata K, Tamaura A, Kimura E, Ohata M, Takeshita E, Nakamura H, Takeda S, Komaki H. Shimizu R, et al. Among authors: takeshita e. BMC Health Serv Res. 2016 Jul 11;16:241. doi: 10.1186/s12913-016-1477-4. BMC Health Serv Res. 2016. PMID: 27401940 Free PMC article.

9

Duchenne muscular dystrophy in a female with compound heterozygous contiguous exon deletions.

Takeshita E, Minami N, Minami K, Suzuki M, Awashima T, Ishiyama A, Komaki H, Nishino I, Sasaki M. Takeshita E, et al. Neuromuscul Disord. 2017 Jun;27(6):569-573. doi: 10.1016/j.nmd.2017.03.011. Epub 2017 Apr 3. Neuromuscul Disord. 2017. PMID: 28434908

10

Duchenne muscular dystrophy with platypnea-orthodeoxia from Chilaiditi syndrome.

Ogasawara M, Ishiyama A, Sugiura A, Segawa K, Nonaka I, Takeshita E, Shimizu-Motohashi Y, Komaki H, Sasaki M. Ogasawara M, et al. Among authors: takeshita e. Brain Dev. 2018 Apr;40(4):339-342. doi: 10.1016/j.braindev.2017.11.001. Epub 2017 Nov 20. Brain Dev. 2018. PMID: 29157800

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