Kunio Ohta
Overview
Explore the profile of Kunio Ohta including associated specialties, affiliations and a list of published articles.
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Articles
30
Citations
201
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Recent Articles
1.
Nakamura T, Iwasaki H, Miyazawa H, Mizutomi S, Imi Y, Ohta K, et al.
Front Pediatr
. 2024 Aug;
12:1338130.
PMID: 39210981
Background: Dexmedetomidine (DEX) is a highly selective alpha 2 receptor agonist that has the advantage of causing less respiratory depression than other sedative agents. We evaluated the add-on effects of...
2.
Hara S, Ohta K, Aono D, Tamai T, Kurachi M, Sugimori K, et al.
Adv Health Sci Educ Theory Pract
. 2023 Oct;
29(3):949-965.
PMID: 37851159
Objective structured clinical examination (OSCE) is widely used to assess medical students' clinical skills. Virtual OSCEs were used in place of in-person OSCEs during the COVID-19 pandemic; however, their reliability...
3.
Usuda K, Hayashi K, Nakajima T, Kurata Y, Cui S, Kusayama T, et al.
Europace
. 2023 Jun;
25(6).
PMID: 37386841
Aims: Patients with particular mutations of type-2 long QT syndrome (LQT2) are at an increased risk for malignant arrhythmia during fever. This study aimed to determine the mechanism by which...
4.
Cui S, Hayashi K, Kobayashi I, Hosomichi K, Nomura A, Teramoto R, et al.
J Mol Cell Cardiol
. 2023 Mar;
177:50-61.
PMID: 36898499
Genetic testing for inherited arrhythmias and discriminating pathogenic or benign variants from variants of unknown significance (VUS) is essential for gene-based medicine. KCNQ1 is a causative gene of type 1...
5.
Nishida K, Ikawa Y, Nakamura T, Ohta K, Wada T
Pediatr Int
. 2022 Aug;
64(1):e15250.
PMID: 35998152
No abstract available.
6.
Hakui H, Kioka H, Miyashita Y, Nishimura S, Matsuoka K, Kato H, et al.
Sci Transl Med
. 2022 Jan;
14(628):eabf3274.
PMID: 35044787
Dilated cardiomyopathy (DCM) is a major cause of heart failure, characterized by ventricular dilatation and systolic dysfunction. Familial DCM is reportedly caused by mutations in more than 50 genes, requiring...
7.
Yoshinaga M, Horigome H, Ayusawa M, Yasuda K, Kogaki S, Doi S, et al.
Circ J
. 2021 Oct;
86(1):118-127.
PMID: 34615813
Background: The usefulness of electrocardiographic (ECG) voltage criteria for diagnosing hypertrophic cardiomyopathy (HCM) in pediatric patients is poorly defined. Methods and results: ECGs at the 1st grade (mean [±SD] age...
8.
Hirono K, Miyao N, Yoshinaga M, Nishihara E, Yasuda K, Tateno S, et al.
Heart Vessels
. 2020 Mar;
35(7):985-995.
PMID: 32161993
Left ventricular noncompaction (LVNC) is a hereditary cardiomyopathy and is associated with high morbidity and mortality. However, the role and significance of school screening for LVNC have not been fully...
9.
Sumitomo N, Baba R, Doi S, Higaki T, Horigome H, Ichida F, et al.
Circ J
. 2018 Aug;
82(9):2385-2444.
PMID: 30101812
No abstract available.
10.
Hayashi K, Konno T, Fujino N, Itoh H, Fujii Y, Imi-Hashida Y, et al.
JACC Clin Electrophysiol
. 2018 May;
2(3):279-287.
PMID: 29766885
Objectives: In this study, we scored patients with long QT syndrome (LQTS) according to the different Schwartz diagnostic criteria from 1993, 2006, and 2011, and to examine the validation of...