Detalhe da pesquisa
1.
Assessing the efficacy of saline flush in frequency-domain optical coherence tomography for intracoronary imaging.
Heart Vessels
; 39(4): 310-318, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38062328
2.
Usefulness of serum biopterin as a predictive biomarker for childhood asthma control: A prospective cohort study.
Allergol Int
; 68(1): 96-100, 2019 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-30297096
3.
Different responses to exercise between Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia.
Europace
; 20(10): 1675-1682, 2018 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29309601
4.
Deteriorative Effect of a Combination of Hypertriglyceridemia and Low High-Density Lipoprotein Cholesterolemia on Target Lesion Revascularization after Everolimus-Eluting Stent Implantation.
J Atheroscler Thromb
; 30(12): 1778-1790, 2023 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37100628
5.
Seasonal and circadian distributions of cardiac events in genotyped patients with congenital long QT syndrome.
Circ J
; 76(9): 2112-8, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22785222
6.
Molecular characterization of phenylketonuria and tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Japan.
J Hum Genet
; 56(4): 306-12, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21307867
7.
Clinical and Genetic Characteristics of Patients with Mild Hyperphenylalaninemia Identified by Newborn Screening Program in Japan.
Int J Neonatal Screen
; 7(1)2021 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-33803550
8.
Heart rate-dependent variability of cardiac events in type 2 congenital long-QT syndrome.
Europace
; 12(11): 1623-9, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20880952
9.
Atrioventricular block-induced Torsades de Pointes with clinical and molecular backgrounds similar to congenital long QT syndrome.
Circ J
; 74(12): 2562-71, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20975234
10.
Effect of Glycemic Control During Follow-up on Late Target Lesion Revascularization After Implantation of New-Generation Drug-Eluting Stents in Patients With Diabetesã- A Single-Center Observational Study.
Circ Rep
; 2(9): 479-489, 2020 Aug 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33693273
11.
A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport.
J Cardiol
; 73(5): 343-350, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30591322
12.
Successful Surgery of Right Common Iliac Artery Injury during Lumbar Discectomy with Endovascular Balloon Occlusion of the Aorta Performed by Cardiologists.
Ann Vasc Dis
; 12(1): 60-62, 2019 Mar 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-30931059
13.
Post-intervention minimal stent area as a predictor of target lesion revascularization after everolimus-eluting stent implantation for in-stent restenosis: a single-center observational study.
Coron Artery Dis
; 30(6): 432-439, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30883432
14.
Age- and genotype-specific triggers for life-threatening arrhythmia in the genotyped long QT syndrome.
J Cardiovasc Electrophysiol
; 19(8): 794-9, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18373596
15.
Long QT syndrome with compound mutations is associated with a more severe phenotype: a Japanese multicenter study.
Heart Rhythm
; 7(10): 1411-8, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20541041
16.
A novel KCNH2 mutation as a modifier for short QT interval.
Int J Cardiol
; 137(1): 83-5, 2009 Sep 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-18692916
17.
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndrome.
J Am Coll Cardiol
; 54(9): 812-9, 2009 Aug 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-19695459
18.
Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome.
Circ Arrhythm Electrophysiol
; 2(5): 511-23, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19843919
19.
Hydroxyzine, a first generation H(1)-receptor antagonist, inhibits human ether-a-go-go-related gene (HERG) current and causes syncope in a patient with the HERG mutation.
J Pharmacol Sci
; 108(4): 462-71, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19057127
20.
Mutation site dependent variability of cardiac events in Japanese LQT2 form of congenital long-QT syndrome.
Circ J
; 72(5): 694-9, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18441445