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Results 21 - 40 of 526  for All Library Resources

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21
Clinical Characteristics of Coronary-to-Pulmonary Artery Fistula in Patients with Pulmonary Atresia and Ventricular Septal Defect
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Article
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Clinical Characteristics of Coronary-to-Pulmonary Artery Fistula in Patients with Pulmonary Atresia and Ventricular Septal Defect

Journal of cardiovascular development and disease, 2023-01, Vol.10 (1), p.17 [Peer Reviewed Journal]

COPYRIGHT 2023 MDPI AG ;2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2023 by the authors. 2023 ;ISSN: 2308-3425 ;EISSN: 2308-3425 ;DOI: 10.3390/jcdd10010017 ;PMID: 36661912

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22
Association Between Maternal Factors in Early Pregnancy and Congenital Heart Defects in Offspring: The Japan Environment and Children's Study
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Article
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Association Between Maternal Factors in Early Pregnancy and Congenital Heart Defects in Offspring: The Japan Environment and Children's Study

Journal of the American Heart Association, 2023-09, Vol.12 (17), p.e029268-e029268 [Peer Reviewed Journal]

2023 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. ;ISSN: 2047-9980 ;EISSN: 2047-9980 ;DOI: 10.1161/JAHA.122.029268 ;PMID: 37642029

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23
A case of Timothy syndrome with adrenal medullary dystrophy
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Article
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A case of Timothy syndrome with adrenal medullary dystrophy

Pathology international, 2016-10, Vol.66 (10), p.587-592 [Peer Reviewed Journal]

2016 The Authors Pathology International published by Japanese Society of Pathology and John Wiley & Sons Australia, Ltd ;2016 The Authors Pathology International published by Japanese Society of Pathology and John Wiley & Sons Australia, Ltd. ;2016 Japanese Society of Pathology and John Wiley & Sons Australia, Ltd ;ISSN: 1320-5463 ;EISSN: 1440-1827 ;DOI: 10.1111/pin.12456 ;PMID: 27593853

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24
Variable severity of cardiovascular phenotypes in patients with an early-onset form of Marfan syndrome harboring FBN1 mutations in exons 24–32
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Article
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Variable severity of cardiovascular phenotypes in patients with an early-onset form of Marfan syndrome harboring FBN1 mutations in exons 24–32

Heart and vessels, 2016-10, Vol.31 (10), p.1717-1723 [Peer Reviewed Journal]

Springer Japan 2016 ;ISSN: 0910-8327 ;EISSN: 1615-2573 ;DOI: 10.1007/s00380-016-0793-2 ;PMID: 26796135 ;CODEN: HEVEEO

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25
Gene knock-outs of inositol 1,4,5-trisphosphate receptors types 1 and 2 result in perturbation of cardiogenesis
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Article
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Gene knock-outs of inositol 1,4,5-trisphosphate receptors types 1 and 2 result in perturbation of cardiogenesis

PloS one, 2010-09, Vol.5 (9), p.e12500 [Peer Reviewed Journal]

COPYRIGHT 2010 Public Library of Science ;COPYRIGHT 2010 Public Library of Science ;2010 Uchida et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Uchida et al. 2010 ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0012500 ;PMID: 20824138

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26
Analysis of Coronary Arterial Aneurysm Regression in Patients With Kawasaki Disease by Aneurysm Severity: Factors Associated With Regression
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Article
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Analysis of Coronary Arterial Aneurysm Regression in Patients With Kawasaki Disease by Aneurysm Severity: Factors Associated With Regression

Journal of the American Heart Association, 2023-02, Vol.12 (3), p.e022417-e022417 [Peer Reviewed Journal]

2023 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. ;ISSN: 2047-9980 ;EISSN: 2047-9980 ;DOI: 10.1161/JAHA.121.022417 ;PMID: 36718857

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27
Etiology and Morphogenesis of Congenital Heart Disease : From Gene Function and Cellular interaction To Morphology
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Book
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Etiology and Morphogenesis of Congenital Heart Disease : From Gene Function and Cellular interaction To Morphology

https://creativecommons.org/licenses/by-nc/4.0/legalcode ;ISBN: 9783662488454 ;ISBN: 3662488450 ;ISBN: 9784431546276 ;ISBN: 4431546278 ;EISBN: 9784431546283 ;EISBN: 4431546286 ;DOI: 10.1007/978-4-431-54628-3 ;OCLC: OCN: 953026830 ;OCLC: 953026830 ;OCLC: 1048185765

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28
Genome-Wide Association Study of Absolute QRS Voltage Identifies Common Variants of TBX3 as Genetic Determinants of Left Ventricular Mass in a Healthy Japanese Population
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Article
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Genome-Wide Association Study of Absolute QRS Voltage Identifies Common Variants of TBX3 as Genetic Determinants of Left Ventricular Mass in a Healthy Japanese Population

PloS one, 2016-05, Vol.11 (5), p.e0155550-e0155550 [Peer Reviewed Journal]

COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;2016 Sano et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2016 Sano et al 2016 Sano et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0155550 ;PMID: 27195777

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29
Pharmacokinetics of drugs for pediatric pulmonary hypertension
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Article
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Pharmacokinetics of drugs for pediatric pulmonary hypertension

Pediatrics international, 2016-11, Vol.58 (11), p.1112-1117 [Peer Reviewed Journal]

2016 Japan Pediatric Society ;2016 Japan Pediatric Society. ;Copyright © 2016 Japan Pediatric Society ;ISSN: 1328-8067 ;EISSN: 1442-200X ;DOI: 10.1111/ped.12997 ;PMID: 27038140

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30
The 22q11.2 deletion syndrome
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Article
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The 22q11.2 deletion syndrome

The Keio Journal of Medicine, 2002, Vol.51(2), pp.77-88 [Peer Reviewed Journal]

by The Keio Journal of Medicine ;ISSN: 0022-9717 ;EISSN: 1880-1293 ;DOI: 10.2302/kjm.51.77 ;PMID: 12125909

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31
A genetic and developmental biological approach for a family with complex congenital heart diseases-evidence of digenic inheritance
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Article
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A genetic and developmental biological approach for a family with complex congenital heart diseases-evidence of digenic inheritance

Frontiers in cardiovascular medicine, 2023-04, Vol.10, p.1135141-1135141 [Peer Reviewed Journal]

2023 Yoshida, Uchida, Kodo, Ishizaki-Asami, Maeda, Katsumata, Yuasa, Fukuda, Kosaki, Watanabe, Nakagawa and Yamagishi. ;2023 Yoshida, Uchida, Kodo, Ishizaki-Asami, Maeda, Katsumata, Yuasa, Fukuda, Kosaki, Watanabe, Nakagawa and Yamagishi. 2023 Yoshida, Uchida, Kodo, Ishizaki-Asami, Maeda, Katsumata, Yuasa, Fukuda, Kosaki, Watanabe, Nakagawa and Yamagishi ;ISSN: 2297-055X ;EISSN: 2297-055X ;DOI: 10.3389/fcvm.2023.1135141 ;PMID: 37180804

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32
Prevalence and Correlates of Physiological Valvular Regurgitation in Healthy Subjects: A Color Doppler Echocardiographic Study in the Current Era
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Article
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Prevalence and Correlates of Physiological Valvular Regurgitation in Healthy Subjects: A Color Doppler Echocardiographic Study in the Current Era

Circulation Journal, 2011, Vol.75(11), pp.2699-2704 [Peer Reviewed Journal]

2011 THE JAPANESE CIRCULATION SOCIETY ;ISSN: 1346-9843 ;EISSN: 1347-4820 ;DOI: 10.1253/circj.CJ-11-0277

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33
Cardiac Neural Crest
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Article
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Cardiac Neural Crest

Cold Spring Harbor perspectives in biology, 2021-01, Vol.13 (1), p.a036715 [Peer Reviewed Journal]

Copyright © 2021 Cold Spring Harbor Laboratory Press; all rights reserved. ;Copyright Cold Spring Harbor Laboratory Press Jan 2021 ;2021 ;ISSN: 1943-0264 ;EISSN: 1943-0264 ;DOI: 10.1101/cshperspect.a036715 ;PMID: 32071091

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34
GATA transcription factors in congenital heart defects: a commentary on a novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect
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Article
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GATA transcription factors in congenital heart defects: a commentary on a novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect

Journal of human genetics, 2010-10, Vol.55 (10), p.637-638 [Peer Reviewed Journal]

The Japan Society of Human Genetics 2010. ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/jhg.2010.105 ;PMID: 20739941

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35
Exercise prescription using an insertable cardiac monitor in a patient with catecholaminergic polymorphic ventricular tachycardia
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Article
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Exercise prescription using an insertable cardiac monitor in a patient with catecholaminergic polymorphic ventricular tachycardia

HeartRhythm case reports, 2022-01, Vol.8 (1), p.17-21 [Peer Reviewed Journal]

2021 Heart Rhythm Society ;2021 Heart Rhythm Society. Published by Elsevier Inc. 2021 Heart Rhythm Society ;ISSN: 2214-0271 ;EISSN: 2214-0271 ;DOI: 10.1016/j.hrcr.2021.10.004 ;PMID: 35070701

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36
Riociguat in children with pulmonary arterial hypertension: The PATENT–CHILD study
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Article
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Riociguat in children with pulmonary arterial hypertension: The PATENT–CHILD study

Pulmonary circulation, 2022-07, Vol.12 (3), p.e12133-n/a [Peer Reviewed Journal]

2022 The Authors. published by John Wiley & Sons Ltd on behalf of Pulmonary Vascular Research Institute. ;2022. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2045-8940 ;ISSN: 2045-8932 ;EISSN: 2045-8940 ;DOI: 10.1002/pul2.12133

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37
Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesis
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Article
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Bop encodes a muscle-restricted protein containing MYND and SET domains and is essential for cardiac differentiation and morphogenesis

Nature genetics, 2002-05, Vol.31 (1), p.25-32 [Peer Reviewed Journal]

2002 INIST-CNRS ;COPYRIGHT 2002 Nature Publishing Group ;Copyright Nature Publishing Group May 2002 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng866 ;PMID: 11923873 ;CODEN: NGENEC

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38
Modulation of Cardiac Growth and Development by HOP, an Unusual Homeodomain Protein
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Article
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Modulation of Cardiac Growth and Development by HOP, an Unusual Homeodomain Protein

Cell, 2002-09, Vol.110 (6), p.725-735 [Peer Reviewed Journal]

2002 Cell Press ;ISSN: 0092-8674 ;EISSN: 1097-4172 ;DOI: 10.1016/S0092-8674(02)00933-9 ;PMID: 12297046

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39
A Molecular Pathway Revealing a Genetic Basis for Human Cardiac and Craniofacial Defects
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Article
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A Molecular Pathway Revealing a Genetic Basis for Human Cardiac and Craniofacial Defects

Science (American Association for the Advancement of Science), 1999-02, Vol.283 (5405), p.1158-1161 [Peer Reviewed Journal]

Copyright 1999 American Association for the Advancement of Science ;1999 INIST-CNRS ;COPYRIGHT 1999 American Association for the Advancement of Science ;Copyright American Association for the Advancement of Science Feb 19, 1999 ;ISSN: 0036-8075 ;EISSN: 1095-9203 ;DOI: 10.1126/science.283.5405.1158 ;PMID: 10024240 ;CODEN: SCIEAS

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40
Successful radiofrequency catheter ablation of life-threatening atrial tachycardia in an infant with asplenia syndrome
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Article
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Successful radiofrequency catheter ablation of life-threatening atrial tachycardia in an infant with asplenia syndrome

Journal of cardiology cases, 2019-01, Vol.19 (1), p.1-4 [Peer Reviewed Journal]

2018 ;2018 Published by Elsevier Ltd on behalf of Japanese College of Cardiology. 2018 ;ISSN: 1878-5409 ;EISSN: 1878-5409 ;DOI: 10.1016/j.jccase.2018.08.005 ;PMID: 30693048

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