Takeda N - Search Results

1

Deep Learning Models for Predicting Left Heart Abnormalities From Single-Lead Electrocardiogram for the Development of Wearable Devices.

Sato M, Kodera S, Setoguchi N, Tanabe K, Kushida S, Kanda J, Saji M, Nanasato M, Maki H, Fujita H, Kato N, Watanabe H, Suzuki M, Takahashi M, Sawada N, Yamasaki M, Sawano S, Katsushika S, Shinohara H, Takeda N, Fujiu K, Daimon M, Akazawa H, Morita H, Komuro I. Sato M, et al. Among authors: takeda n. Circ J. 2023 Dec 25;88(1):146-156. doi: 10.1253/circj.CJ-23-0216. Epub 2023 Nov 14. Circ J. 2023. PMID: 37967949 Free article.

2

Subarachnoid hemorrhage from mycotic aneurysms.

Shimizu T, Takeda N, Takahashi M, Imai Y, Ishizaka N, Hirata Y, Nagai R. Shimizu T, et al. Among authors: takeda n. Intern Med. 2006;45(20):1189-90. doi: 10.2169/internalmedicine.45.6073. Epub 2006 Nov 15. Intern Med. 2006. PMID: 17106169 Free article. No abstract available.

3

Bone marrow-derived cells contribute to vascular inflammation but do not differentiate into smooth muscle cell lineages.

Iwata H, Manabe I, Fujiu K, Yamamoto T, Takeda N, Eguchi K, Furuya A, Kuro-o M, Sata M, Nagai R. Iwata H, et al. Among authors: takeda n. Circulation. 2010 Nov 16;122(20):2048-57. doi: 10.1161/CIRCULATIONAHA.110.965202. Epub 2010 Nov 1. Circulation. 2010. PMID: 21041690

4

Present status of anticoagulation treatment in Japanese patients with atrial fibrillation: a report from the J-RHYTHM Registry.

Atarashi H, Inoue H, Okumura K, Yamashita T, Kumagai N, Origasa H; J-RHYTHM Registry Investigators. Atarashi H, et al. Circ J. 2011;75(6):1328-33. doi: 10.1253/circj.cj-10-1119. Epub 2011 Apr 5. Circ J. 2011. PMID: 21467664 Free article.

5

Pathophysiology and Japanese clinical characteristics in Marfan syndrome.

Fujita D, Takeda N, Imai Y, Inuzuka R, Komuro I, Hirata Y. Fujita D, et al. Among authors: takeda n. Pediatr Int. 2014 Aug;56(4):484-91. doi: 10.1111/ped.12423. Pediatr Int. 2014. PMID: 24931486 Review.

6

Congenital contractural arachnodactyly complicated with aortic dilatation and dissection: Case report and review of literature.

Takeda N, Morita H, Fujita D, Inuzuka R, Taniguchi Y, Imai Y, Hirata Y, Komuro I. Takeda N, et al. Am J Med Genet A. 2015 Oct;167A(10):2382-7. doi: 10.1002/ajmg.a.37162. Epub 2015 May 14. Am J Med Genet A. 2015. PMID: 25975422

7

Congenital Contractural Arachnodactyly without FBN1 or FBN2 Gene Mutations Complicated by Dilated Cardiomyopathy.

Yagi H, Hatano M, Takeda N, Harada S, Suzuki Y, Taniguchi Y, Shintani Y, Morita H, Kanamori N, Aoyama T, Watanabe M, Manabe I, Akazawa H, Kinugawa K, Komuro I. Yagi H, et al. Among authors: takeda n. Intern Med. 2015;54(10):1237-41. doi: 10.2169/internalmedicine.54.4280. Epub 2015 May 15. Intern Med. 2015. PMID: 25986263 Free article.

8

Monitoring β-arrestin recruitment via β-lactamase enzyme fragment complementation: purification of peptide E as a low-affinity ligand for mammalian bombesin receptors.

Ikeda Y, Kumagai H, Okazaki H, Fujishiro M, Motozawa Y, Nomura S, Takeda N, Toko H, Takimoto E, Akazawa H, Morita H, Suzuki J, Yamazaki T, Komuro I, Yanagisawa M. Ikeda Y, et al. Among authors: takeda n. PLoS One. 2015 Jun 1;10(6):e0127445. doi: 10.1371/journal.pone.0127445. eCollection 2015. PLoS One. 2015. PMID: 26030739 Free PMC article.

9

A deletion mutation in myosin heavy chain 11 causing familial thoracic aortic dissection in two Japanese pedigrees.

Imai Y, Morita H, Takeda N, Miya F, Hyodo H, Fujita D, Tajima T, Tsunoda T, Nagai R, Kubo M, Komuro I. Imai Y, et al. Among authors: takeda n. Int J Cardiol. 2015 Sep 15;195:290-2. doi: 10.1016/j.ijcard.2015.05.178. Epub 2015 Jun 3. Int J Cardiol. 2015. PMID: 26056961 No abstract available.

10

A deleterious MYH11 mutation causing familial thoracic aortic dissection.

Takeda N, Morita H, Fujita D, Inuzuka R, Taniguchi Y, Nawata K, Komuro I. Takeda N, et al. Hum Genome Var. 2015 Aug 6;2:15028. doi: 10.1038/hgv.2015.28. eCollection 2015. Hum Genome Var. 2015. PMID: 27081537 Free PMC article.

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