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1
COVID-19 in Adults With Congenital Heart Disease
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COVID-19 in Adults With Congenital Heart Disease

Journal of the American College of Cardiology, 2021-04, Vol.77 (13), p.1644-1655 [Peer Reviewed Journal]

Copyright © 2021 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;COPYRIGHT 2021 Elsevier B.V. ;2021 by the American College of Cardiology Foundation. Published by Elsevier. 2021 American College of Cardiology Foundation ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2021.02.023 ;PMID: 33795039

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2
Estimating the effect size of the 15Q11.2 BP1–BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice
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Estimating the effect size of the 15Q11.2 BP1–BP2 deletion and its contribution to neurodevelopmental symptoms: recommendations for practice

Journal of medical genetics, 2019-10, Vol.56 (10), p.701-710 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2019 Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Distributed under a Creative Commons Attribution 4.0 International License ;Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2019 ;ISSN: 0022-2593 ;ISSN: 1468-6244 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2018-105879 ;PMID: 31451536

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3
Unplanned hospital readmissions following congenital heart diseases surgery. Prevalence and predictors
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Unplanned hospital readmissions following congenital heart diseases surgery. Prevalence and predictors

Saudi medical journal, 2019-08, Vol.40 (8), p.802-809 [Peer Reviewed Journal]

COPYRIGHT 2019 Saudi Medical Journal ;Copyright: © Saudi Medical Journal 2019 ;ISSN: 0379-5284 ;EISSN: 1658-3175 ;DOI: 10.15537/smj.2019.8.24405 ;PMID: 31423517

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4
The spectrum of congenital heart diseases in down syndrome. A retrospective study from Northwest Saudi Arabia
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The spectrum of congenital heart diseases in down syndrome. A retrospective study from Northwest Saudi Arabia

Saudi medical journal, 2016-07, Vol.37 (7), p.767-772 [Peer Reviewed Journal]

COPYRIGHT 2016 Saudi Medical Journal ;Copyright: © Saudi Medical Journal 2016 ;ISSN: 0379-5284 ;EISSN: 1658-3175 ;DOI: 10.15537/smj.2016.7.14536 ;PMID: 27381537

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5
CHARGE syndrome: an update
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CHARGE syndrome: an update

European journal of human genetics : EJHG, 2007-04, Vol.15 (4), p.389-399 [Peer Reviewed Journal]

2007 INIST-CNRS ;Copyright Nature Publishing Group Apr 2007 ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/sj.ejhg.5201778 ;PMID: 17299439

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6
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands

Nature genetics, 2017-11, Vol.49 (11), p.1593-1601 [Peer Reviewed Journal]

COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Nov 2017 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3970 ;PMID: 28991257

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7
Investigation of infant deaths associated with critical congenital heart diseases; 2018-2021, Türkiye
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Investigation of infant deaths associated with critical congenital heart diseases; 2018-2021, Türkiye

BMC public health, 2024-02, Vol.24 (1), p.441-441 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;2024. 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) 2024 ;ISSN: 1471-2458 ;EISSN: 1471-2458 ;DOI: 10.1186/s12889-024-17966-4 ;PMID: 38347475

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8
Genomic analyses implicate noncoding de novo variants in congenital heart disease
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Genomic analyses implicate noncoding de novo variants in congenital heart disease

Nature 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: 32601476

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9
Prognostic value of the model for end-stage liver disease excluding INR score (MELD-XI) in patients with adult congenital heart disease
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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 disease

PloS 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: 31743362

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10
Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors
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Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors

Nature 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: NGENEC

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11
Fully‑automated deep‑learning segmentation of pediatric cardiovascular magnetic resonance of patients with complex congenital heart diseases
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Fully‑automated deep‑learning segmentation of pediatric cardiovascular magnetic resonance of patients with complex congenital heart diseases

Journal of cardiovascular magnetic resonance, 2020-11, Vol.22 (1), p.80-80, Article 80 [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/s12968-020-00678-0 ;PMID: 33256762

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12
The impact of congenital heart diseases on the quality of life of patients and their families in Saudi Arabia. Biological, psychological, and social dimensions
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The impact of congenital heart diseases on the quality of life of patients and their families in Saudi Arabia. Biological, psychological, and social dimensions

Saudi medical journal, 2016-04, Vol.37 (4), p.392-402 [Peer Reviewed Journal]

COPYRIGHT 2016 Saudi Medical Journal ;Copyright: © Saudi Medical Journal 2016 ;ISSN: 0379-5284 ;EISSN: 1658-3175 ;DOI: 10.15537/smj.2016.4.13626 ;PMID: 27052282

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13
Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome
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Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2014-03, Vol.165B (2), p.137-147 [Peer Reviewed Journal]

2013 Wiley Periodicals, Inc. ;2013 Wiley Periodicals, Inc. 2013 ;ISSN: 1552-4841 ;EISSN: 1552-485X ;DOI: 10.1002/ajmg.b.32215 ;PMID: 24265253

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14
Asymmetrical dimethylarginine--more sensitive than NT-proBNP to diagnose heart failure in adults with congenital heart disease
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Asymmetrical dimethylarginine--more sensitive than NT-proBNP to diagnose heart failure in adults with congenital heart disease

PloS one, 2012-03, Vol.7 (3), p.e33795-e33795 [Peer Reviewed Journal]

COPYRIGHT 2012 Public Library of Science ;COPYRIGHT 2012 Public Library of Science ;2012 Tutarel 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. ;Tutarel et al. 2012 ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0033795 ;PMID: 22470476

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15
New York Heart Association (NYHA) classification in adults with congenital heart disease: relation to objective measures of exercise and outcome
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New York Heart Association (NYHA) classification in adults with congenital heart disease: relation to objective measures of exercise and outcome

European heart journal. Quality of care & clinical outcomes, 2018-01, Vol.4 (1), p.51-58 [Peer Reviewed Journal]

Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2017. For permissions, please email: journals.permissions@oup.com. 2017 ;Published on behalf of the European Society of Cardiology. All rights reserved. © The Author 2017. For permissions please email: journals.permissions@oup.com. ;COPYRIGHT 2018 Oxford University Press ;Copyright © 2017 European Society of Cardiology ;ISSN: 2058-5225 ;EISSN: 2058-1742 ;DOI: 10.1093/ehjqcco/qcx031 ;PMID: 28950356

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16
Congenital emphysematous lung disease associated with a novel Filamin A mutation. Case report and literature review
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Congenital emphysematous lung disease associated with a novel Filamin A mutation. Case report and literature review

BMC pediatrics, 2019-03, Vol.19 (1), p.86-86, Article 86 [Peer Reviewed Journal]

COPYRIGHT 2019 BioMed Central Ltd. ;COPYRIGHT 2019 BioMed Central Ltd. ;2019. 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). 2019 ;ISSN: 1471-2431 ;EISSN: 1471-2431 ;DOI: 10.1186/s12887-019-1460-4 ;PMID: 30922288

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17
Increased prevalence of inattention-related symptoms in a large cohort of patients with congenital heart disease
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Increased prevalence of inattention-related symptoms in a large cohort of patients with congenital heart disease

European child & adolescent psychiatry, 2021-04, Vol.30 (4), p.647-655 [Peer Reviewed Journal]

Springer-Verlag GmbH Germany, part of Springer Nature 2020 ;COPYRIGHT 2021 Springer ;Springer-Verlag GmbH Germany, part of Springer Nature 2020. ;ISSN: 1018-8827 ;EISSN: 1435-165X ;DOI: 10.1007/s00787-020-01547-y ;PMID: 32394091

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18
Prevalence of Mental Illness in Adolescents and Adults With Congenital Heart Disease from the Colorado Congenital Heart Defect Surveillance System
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Prevalence of Mental Illness in Adolescents and Adults With Congenital Heart Disease from the Colorado Congenital Heart Defect Surveillance System

The 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: 31303246

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19
Mosaic trisomy 22 in a 4‐year‐old boy with congenital heart disease and general hypotrophy: A case report
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Mosaic trisomy 22 in a 4‐year‐old boy with congenital heart disease and general hypotrophy: A case report

Journal of clinical laboratory analysis, 2019-02, Vol.33 (2), p.e22663-n/a [Peer Reviewed Journal]

2018 Wiley Periodicals, Inc. ;Copyright © 2019 Wiley Periodicals, Inc. ;ISSN: 0887-8013 ;EISSN: 1098-2825 ;DOI: 10.1002/jcla.22663 ;PMID: 30259573

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20
Association of congenital heart disease and neurodevelopmental disorders: an observational and Mendelian randomization study
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Association of congenital heart disease and neurodevelopmental disorders: an observational and Mendelian randomization study

Italian journal of pediatrics, 2024-04, Vol.50 (1), p.63-63 [Peer Reviewed Journal]

2024. The Author(s). ;2024. 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) 2024 ;ISSN: 1720-8424 ;EISSN: 1824-7288 ;DOI: 10.1186/s13052-024-01610-3 ;PMID: 38589916

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