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21
Identification of a Divergent Lineage Porcine Pestivirus in Nursing Piglets with Congenital Tremors and Reproduction of Disease following Experimental Inoculation
Identification of a Divergent Lineage Porcine Pestivirus in Nursing Piglets with Congenital Tremors and Reproduction of Disease following Experimental Inoculation
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Identification of a Divergent Lineage Porcine Pestivirus in Nursing Piglets with Congenital Tremors and Reproduction of Disease following Experimental Inoculation

PloS one, 2016-02, Vol.11 (2), p.e0150104-e0150104 [Peer Reviewed Journal]

COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;2016 Arruda 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 Arruda et al 2016 Arruda et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0150104 ;PMID: 26909691

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22
Investigation of infant deaths associated with critical congenital heart diseases; 2018-2021, Türkiye
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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23
Genomic analyses implicate noncoding de novo variants in congenital heart disease
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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24
Counseling for Prenatal Congenital Heart Disease-Recommendations Based on Empirical Assessment of Counseling Success
Counseling for Prenatal Congenital Heart Disease-Recommendations Based on Empirical Assessment of Counseling Success
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Counseling for Prenatal Congenital Heart Disease-Recommendations Based on Empirical Assessment of Counseling Success

Frontiers in pediatrics, 2020-02, Vol.8, p.26-26 [Peer Reviewed Journal]

Copyright © 2020 Kovacevic, Simmelbauer, Starystach, Elsässer, Müller, Bär and Gorenflo. ;COPYRIGHT 2020 Frontiers Research Foundation ;Copyright © 2020 Kovacevic, Simmelbauer, Starystach, Elsässer, Müller, Bär and Gorenflo. 2020 Kovacevic, Simmelbauer, Starystach, Elsässer, Müller, Bär and Gorenflo ;ISSN: 2296-2360 ;EISSN: 2296-2360 ;DOI: 10.3389/fped.2020.00026 ;PMID: 32175290

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25
Prognostic value of the model for end-stage liver disease excluding INR score (MELD-XI) in patients with adult congenital heart disease
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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26
Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management: A Scientific Statement From the American Heart Association
Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management: A Scientific Statement From the American Heart Association
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Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management: A Scientific Statement From the American Heart Association

Circulation (New York, N.Y.), 2012-08, Vol.126 (9), p.1143-1172 [Peer Reviewed Journal]

2015 INIST-CNRS ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIR.0b013e318265ee8a ;PMID: 22851541 ;CODEN: CIRCAZ

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27
Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors
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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28
The impact of congenital heart diseases on the quality of life of patients and their families in Saudi Arabia. Biological, psychological, and social dimensions
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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29
Fully‑automated deep‑learning segmentation of pediatric cardiovascular magnetic resonance of patients with complex congenital heart diseases
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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30
Short-Term Impact of Cardiac Intervention on the Nutritional Status of Malnourished Children with Congenital Heart Disease - A Report from a Developing African Country, Ethiopia
Short-Term Impact of Cardiac Intervention on the Nutritional Status of Malnourished Children with Congenital Heart Disease - A Report from a Developing African Country, Ethiopia
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Short-Term Impact of Cardiac Intervention on the Nutritional Status of Malnourished Children with Congenital Heart Disease - A Report from a Developing African Country, Ethiopia

Pediatric health, medicine and therapeutics, 2023-12, Vol.14, p.465-475 [Peer Reviewed Journal]

2023 Tesfaye and Tsega. ;COPYRIGHT 2023 Dove Medical Press Limited ;2023 Tesfaye and Tsega. 2023 Tesfaye and Tsega. ;ISSN: 1179-9927 ;EISSN: 1179-9927 ;DOI: 10.2147/PHMT.S431164 ;PMID: 38089853

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31
Model‐informed bridging of rivaroxaban doses for thromboprophylaxis in pediatric patients aged 9 years and older with congenital heart disease
Model‐informed bridging of rivaroxaban doses for thromboprophylaxis in pediatric patients aged 9 years and older with congenital heart disease
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Model‐informed bridging of rivaroxaban doses for thromboprophylaxis in pediatric patients aged 9 years and older with congenital heart disease

CPT: pharmacometrics and systems pharmacology, 2022-08, Vol.11 (8), p.1111-1121 [Peer Reviewed Journal]

2022 Bayer AG. published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics. ;2022. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 2163-8306 ;EISSN: 2163-8306 ;DOI: 10.1002/psp4.12830 ;PMID: 35665486

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32
Three‐dimensional printing in congenital heart disease: A systematic review
Three‐dimensional printing in congenital heart disease: A systematic review
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Three‐dimensional printing in congenital heart disease: A systematic review

Journal of medical radiation sciences, 2018-09, Vol.65 (3), p.226-236 [Peer Reviewed Journal]

2018 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Australian Society of Medical Imaging and Radiation Therapy and New Zealand Institute of Medical Radiation Technology. ;2018 The Authors. Journal of Medical Radiation Sciences published by John Wiley & Sons Australia, Ltd on behalf of Australian Society of Medical Imaging and Radiation Therapy and New Zealand Institute of Medical Radiation Technology. ;2018 Journal of Medical Radiation Sciences published by John Wiley & Sons Australia, Ltd on behalf of Australian Society of Medical Imaging and Radiation Therapy and New Zealand Institute of Medical Radiation Technology ;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. ;ISSN: 2051-3895 ;EISSN: 2051-3909 ;DOI: 10.1002/jmrs.268 ;PMID: 29453808

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33
X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood
X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood
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X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood

European journal of endocrinology, 2019-06, Vol.180 (6), p.397-406 [Peer Reviewed Journal]

2019 European Society of Endocrinology ;Copyright BioScientifica Ltd. Jun 2019 ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0804-4643 ;EISSN: 1479-683X ;DOI: 10.1530/EJE-18-0878 ;PMID: 30991358

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34
Biallelic DNAH9 mutations are identified in Chinese patients with defective left–right patterning and cilia-related complex congenital heart disease
Biallelic DNAH9 mutations are identified in Chinese patients with defective left–right patterning and cilia-related complex congenital heart disease
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Biallelic DNAH9 mutations are identified in Chinese patients with defective left–right patterning and cilia-related complex congenital heart disease

Human genetics, 2022-08, Vol.141 (8), p.1339-1353 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022 ;2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. ;COPYRIGHT 2022 Springer ;The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022. ;ISSN: 0340-6717 ;EISSN: 1432-1203 ;DOI: 10.1007/s00439-021-02426-5 ;PMID: 35050399

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35
Contribution of congenital heart disease to neuropsychiatric outcome in school-age children with 22q11.2 deletion syndrome
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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36
Nutritional status of congenital heart disease (CHD) patients: Burden and determinant of malnutrition at university of Nigeria teaching hospital Ituku - Ozalla, Enugu
Nutritional status of congenital heart disease (CHD) patients: Burden and determinant of malnutrition at university of Nigeria teaching hospital Ituku - Ozalla, Enugu
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Nutritional status of congenital heart disease (CHD) patients: Burden and determinant of malnutrition at university of Nigeria teaching hospital Ituku - Ozalla, Enugu

Pakistan journal of medical sciences, 2015-10, Vol.31 (5), p.1140-1145 [Peer Reviewed Journal]

COPYRIGHT 2015 Knowledge Bylanes ;COPYRIGHT 2015 Knowledge Bylanes ;Copyright AsiaNet Pakistan (Pvt) Ltd. Sep/Oct 2015 ;Copyright: © Pakistan Journal of Medical Sciences 2015 ;ISSN: 1682-024X ;EISSN: 1681-715X ;DOI: 10.12669/pjms.315.6837 ;PMID: 26649002

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37
Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide
Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide
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Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide

Journal of the American College of Cardiology, 2017-02, Vol.69 (7), p.859-870 [Peer Reviewed Journal]

Copyright © 2017 American College of Cardiology Foundation. All rights reserved. ;Copyright Elsevier Limited Feb 21, 2017 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.11.060 ;PMID: 28209227

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38
Asymmetrical dimethylarginine--more sensitive than NT-proBNP to diagnose heart failure in adults with congenital heart disease
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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39
Congenital heart disease and thyroid dysfunction in Down syndrome reported at Children`s Hospital, Lahore, Pakistan
Congenital heart disease and thyroid dysfunction in Down syndrome reported at Children`s Hospital, Lahore, Pakistan
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Congenital heart disease and thyroid dysfunction in Down syndrome reported at Children`s Hospital, Lahore, Pakistan

Turkish journal of pediatrics, 2019, Vol.61 (6), p.915-924 [Peer Reviewed Journal]

Copyright Hacettepe University Faculty of Medicine Nov/Dec 2019 ;ISSN: 0041-4301 ;DOI: 10.24953/turkjped.2019.06.013 ;PMID: 32134586

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40
Genetic syndromes associated with congenital heart disease
Genetic syndromes associated with congenital heart disease
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Genetic syndromes associated with congenital heart disease

Heart (British Cardiac Society), 2023-12, p.heartjnl-2023-323126 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;2023 Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2023-323126

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