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1 |
Material Type: Article
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Genomic analyses implicate noncoding de novo variants in congenital heart diseaseNature genetics, 2020-08, Vol.52 (8), p.769-777 [Peer Reviewed Journal]COPYRIGHT 2020 Nature Publishing Group ;Copyright Nature Publishing Group Aug 2020 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-020-0652-z ;PMID: 32601476Full text available |
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Prognostic value of the model for end-stage liver disease excluding INR score (MELD-XI) in patients with adult congenital heart diseasePloS one, 2019-11, Vol.14 (11), p.e0225403-e0225403 [Peer Reviewed Journal]COPYRIGHT 2019 Public Library of Science ;COPYRIGHT 2019 Public Library of Science ;2019 Konno 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. ;2019 Konno et al 2019 Konno et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0225403 ;PMID: 31743362Full text available |
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Material Type: Article
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Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumorsNature genetics, 2009-11, Vol.41 (11), p.1247-1252 [Peer Reviewed Journal]2009 INIST-CNRS ;COPYRIGHT 2009 Nature Publishing Group ;Copyright Nature Publishing Group Nov 2009 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.470 ;PMID: 19855393 ;CODEN: NGENECFull text available |
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4 |
Material Type: Article
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Prevalence of Mental Illness in Adolescents and Adults With Congenital Heart Disease from the Colorado Congenital Heart Defect Surveillance SystemThe American journal of cardiology, 2019-08, Vol.124 (4), p.618-626 [Peer Reviewed Journal]2019 Elsevier Inc. ;Copyright © 2019 Elsevier Inc. All rights reserved. ;2019. Elsevier Inc. ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2019.05.023 ;PMID: 31303246Full text available |
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5 |
Material Type: Article
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Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart diseaseClinical genetics, 2010-12, Vol.78 (6), p.533-540 [Peer Reviewed Journal]2010 John Wiley & Sons A/S ;2015 INIST-CNRS ;2010 John Wiley & Sons A/S. ;ISSN: 0009-9163 ;EISSN: 1399-0004 ;DOI: 10.1111/j.1399-0004.2010.01422.x ;PMID: 20456451 ;CODEN: CLGNAYFull text available |
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6 |
Material Type: Article
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Ex vivo cardiovascular magnetic resonance diffusion weighted imaging in congenital heart disease, an insight into the microstructures of tetralogy of Fallot, biventricular and univentricular systemic right ventricleJournal of cardiovascular magnetic resonance, 2020-09, Vol.22 (1), p.69-69, Article 69 [Peer Reviewed Journal]COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1532-429X ;ISSN: 1097-6647 ;EISSN: 1532-429X ;DOI: 10.1186/s12968-020-00662-8 ;PMID: 32951605Full text available |
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7 |
Material Type: Article
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4D flow cardiovascular magnetic resonance for monitoring of aortic valve repair in bicuspid aortic valve diseaseJournal of cardiovascular magnetic resonance, 2020-04, Vol.22 (1), p.29-29, Article 29 [Peer Reviewed Journal]COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1532-429X ;ISSN: 1097-6647 ;EISSN: 1532-429X ;DOI: 10.1186/s12968-020-00608-0 ;PMID: 32354361Full text available |
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8 |
Material Type: Article
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NGS-based expanded carrier screening for genetic disorders in North Indian population reveals unexpected results - a pilot studyBMC medical genetics, 2020-11, Vol.21 (1), p.216-216, Article 216 [Peer Reviewed Journal]COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2020 ;ISSN: 1471-2350 ;EISSN: 1471-2350 ;DOI: 10.1186/s12881-020-01153-4 ;PMID: 33138774Full text available |
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9 |
Material Type: Article
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Prevalence of congenital amusiaEuropean journal of human genetics : EJHG, 2017-05, Vol.25 (5), p.625-630 [Peer Reviewed Journal]Copyright Nature Publishing Group May 2017 ;Copyright © 2017 Macmillan Publishers Limited, part of Springer Nature. 2017 Macmillan Publishers Limited, part of Springer Nature. ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2017.15 ;PMID: 28224991Full text available |
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10 |
Material Type: Article
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Orthotopic Heart Transplantation for Congenital Heart Disease with Dextrocardia: A Single-Center Clinic ExperienceBioMed research international, 2020, Vol.2020, p.3487635-9 [Peer Reviewed Journal]Copyright © 2020 Guohua Wang et al. ;COPYRIGHT 2020 Hindawi Limited ;Copyright © 2020 Guohua Wang et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0 ;Copyright © 2020 Guohua Wang et al. 2020 ;ISSN: 2314-6133 ;EISSN: 2314-6141 ;DOI: 10.1155/2020/3487635 ;PMID: 32596301Full text available |
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11 |
Material Type: Article
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Identification of rare de novo epigenetic variations in congenital disordersNature communications, 2018-05, Vol.9 (1), p.2064-11, Article 2064 [Peer Reviewed Journal]2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2018 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-04540-x ;PMID: 29802345Full text available |
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12 |
Material Type: Article
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Imaging of the pulmonary vasculature in congenital heart disease without gadolinium contrast: Intraindividual comparison of a novel Compressed SENSE accelerated 3D modified REACT with 4D contrast-enhanced magnetic resonance angiographyJournal of cardiovascular magnetic resonance, 2020-01, Vol.22 (1), p.8-8, Article 8 [Peer Reviewed Journal]COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s). 2020 ;ISSN: 1532-429X ;ISSN: 1097-6647 ;EISSN: 1532-429X ;DOI: 10.1186/s12968-019-0591-y ;PMID: 31969137Full text available |
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13 |
Material Type: Article
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Modified-Release Hydrocortisone in Congenital Adrenal HyperplasiaThe journal of clinical endocrinology and metabolism, 2021-05, Vol.106 (5), p.e2063-e2077 [Peer Reviewed Journal]The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. 2021 ;The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. ;COPYRIGHT 2021 Oxford University Press ;ISSN: 0021-972X ;ISSN: 1945-7197 ;EISSN: 1945-7197 ;DOI: 10.1210/clinem/dgab051 ;PMID: 33527139Full text available |
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14 |
Material Type: Article
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Expanding the phenotype of CACNA1C mutation disordersMolecular genetics & genomic medicine, 2021-06, Vol.9 (6), p.e1673-n/a [Peer Reviewed Journal]2021 The Authors. published by Wiley Periodicals LLC ;2021 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals LLC. ;2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2324-9269 ;EISSN: 2324-9269 ;DOI: 10.1002/mgg3.1673 ;PMID: 33797204Full text available |
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15 |
Material Type: Article
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Stroke in Adults With Congenital Heart Disease: Incidence, Cumulative Risk, and PredictorsCirculation (New York, N.Y.), 2015-12, Vol.132 (25), p.2385-2394 [Peer Reviewed Journal]2015 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2015 American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.115.011241 ;PMID: 26597113Full text available |
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16 |
Material Type: Article
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Paternal age and offspring congenital heart defects: a national cohort studyPloS one, 2015-03, Vol.10 (3), p.e0121030-e0121030 [Peer Reviewed Journal]COPYRIGHT 2015 Public Library of Science ;COPYRIGHT 2015 Public Library of Science ;2015 Su 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. ;2015 Su et al 2015 Su et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0121030 ;PMID: 25806788Full text available |
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17 |
Material Type: Article
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Modified 16-Dot plication technique for correction of penile curvature: prevention of knot-related complicationsInternational journal of impotence research, 2018-06, Vol.30 (3), p.117-121 [Peer Reviewed Journal]COPYRIGHT 2018 Nature Publishing Group ;COPYRIGHT 2018 Nature Publishing Group ;Copyright Nature Publishing Group Jun 2018 ;ISSN: 0955-9930 ;EISSN: 1476-5489 ;DOI: 10.1038/s41443-018-0018-6 ;PMID: 29736012Full text available |
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Material Type: Article
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Anomalous aortic origin of right coronary artery from left coronary cusp: a management conundrum: a case reportJournal of medical case reports, 2023-05, Vol.17 (1), p.191-191, Article 191 [Peer Reviewed Journal]2023. The Author(s). ;COPYRIGHT 2023 BioMed Central Ltd. ;2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2023 ;ISSN: 1752-1947 ;EISSN: 1752-1947 ;DOI: 10.1186/s13256-023-03921-1 ;PMID: 37161579Full text available |
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Material Type: Article
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High Prevalence of Respiratory Ciliary Dysfunction in Congenital Heart Disease Patients With HeterotaxyCirculation (New York, N.Y.), 2012-05, Vol.125 (18), p.2232-2242 [Peer Reviewed Journal]2015 INIST-CNRS ;2012 American Heart Association, Inc. 2012 ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.111.079780 ;PMID: 22499950 ;CODEN: CIRCAZFull text available |
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Material Type: Article
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Specialized Adult Congenital Heart Disease Care: The Impact of Policy on MortalityCirculation (New York, N.Y.), 2014-05, Vol.129 (18), p.1804-1812 [Peer Reviewed Journal]2014 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2015 INIST-CNRS ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIRCULATIONAHA.113.005817 ;PMID: 24589851 ;CODEN: CIRCAZFull text available |