Lin L - Search Results

1

Vascular Network Inside the Heart　- Collateral Flow on Color Doppler Echo in a Child With Anomalous Left Coronary Artery From the Pulmonary Artery (ALCAPA).

Lin L, Murakami T, Shiono J, Horigome H. Lin L, et al. Circ J. 2018 Sep 25;82(10):2680-2681. doi: 10.1253/circj.CJ-18-0075. Epub 2018 Apr 6. Circ J. 2018. PMID: 29628455 Free article. No abstract available.

2

Drug-induced QT-interval prolongation and recurrent torsade de pointes in a child with heterotaxy syndrome and KCNE1 D85N polymorphism.

Lin L, Horigome H, Nishigami N, Ohno S, Horie M, Sumazaki R. Lin L, et al. J Electrocardiol. 2012 Nov-Dec;45(6):770-3. doi: 10.1016/j.jelectrocard.2012.07.013. Epub 2012 Sep 20. J Electrocardiol. 2012. PMID: 22999324

3

Nontraditional placement of an implantable cardioverter-defibrillator in a heterotaxy patient after the completion of total cavopulmonary connection.

Tsukada T, Hiramatsu Y, Kanemoto S, Lin L, Takahashi-Igari M, Horigome H, Matsushita S, Sakakibara Y. Tsukada T, et al. Among authors: lin l. J Artif Organs. 2013 Dec;16(4):495-7. doi: 10.1007/s10047-013-0714-4. Epub 2013 Jun 1. J Artif Organs. 2013. PMID: 23728474

4

Significant associations between hemostatic/fibrinolytic systems and accumulation of cardiovascular risk factors in Japanese elementary schoolchildren.

Lin L, Horigome H, Kato Y, Kikuchi T, Nakahara S, Sumazaki R. Lin L, et al. Blood Coagul Fibrinolysis. 2015 Jan;26(1):75-80. doi: 10.1097/MBC.0000000000000187. Blood Coagul Fibrinolysis. 2015. PMID: 25185676

5

Prenatal Diagnosis of Atrioventricular Block and QT Interval Prolongation by Fetal Magnetocardiography in a Fetus with Trisomy 18 and SCN5A R1193Q Variant.

Lin L, Takahashi-Igari M, Kato Y, Nozaki Y, Obata M, Hamada H, Horigome H. Lin L, et al. Case Rep Pediatr. 2017;2017:6570465. doi: 10.1155/2017/6570465. Epub 2017 May 30. Case Rep Pediatr. 2017. PMID: 28638671 Free PMC article.

6

Persistent QT Prolongation in a Child with Gitelman Syndrome and SCN5A H558R Polymorphism.

Tsukakoshi T, Lin L, Murakami T, Shiono J, Izumi I, Horigome H. Tsukakoshi T, et al. Among authors: lin l. Int Heart J. 2018 Nov 28;59(6):1466-1468. doi: 10.1536/ihj.17-686. Epub 2018 Oct 10. Int Heart J. 2018. PMID: 30305584 Free article.

7

Prenatal diagnosis of congenital absence of aortic valve associated with restrictive foramen ovale: Hemodynamic features and clinical outcome.

Murakami T, Lin L, Ishiodori T, Takeuchi S, Shiono J, Horigome H. Murakami T, et al. Among authors: lin l. J Clin Ultrasound. 2019 Feb;47(2):104-106. doi: 10.1002/jcu.22636. Epub 2018 Oct 14. J Clin Ultrasound. 2019. PMID: 30318622

8

Mexiletine infusion challenge test for neonatal long QT syndrome with 2:1 atrioventricular block.

Okuwaki H, Kato Y, Lin L, Nozaki Y, Takahashi-Igari M, Horigome H. Okuwaki H, et al. Among authors: lin l. J Arrhythm. 2019 Jun 17;35(4):685-688. doi: 10.1002/joa3.12209. eCollection 2019 Aug. J Arrhythm. 2019. PMID: 31410243 Free PMC article.

9

Novel ELN mutation in a Japanese family with a severe form of supravalvular aortic stenosis.

Sugiyama K, Horigome H, Lin L, Murakami T, Shiono J, Yamashiro Y, Matsuura H, Yoda H, Yanagisawa H. Sugiyama K, et al. Among authors: lin l. Mol Genet Genomic Med. 2019 Nov;7(11):e986. doi: 10.1002/mgg3.986. Epub 2019 Sep 27. Mol Genet Genomic Med. 2019. PMID: 31560829 Free PMC article.

10

Multivariate analysis of TU wave complex on electrocardiogram in Andersen-Tawil syndrome with KCNJ2 mutations.

Horigome H, Ishikawa Y, Kokubun N, Yoshinaga M, Sumitomo N, Lin L, Kato Y, Tanabe-Kameda Y, Ohno S, Nagashima M, Horie M. Horigome H, et al. Among authors: lin l. Ann Noninvasive Electrocardiol. 2020 May;25(3):e12721. doi: 10.1111/anec.12721. Epub 2019 Nov 14. Ann Noninvasive Electrocardiol. 2020. PMID: 31724784 Free PMC article.

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