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1
Unintended pregnancy-related factors and the occurrence of offspring congenital heart disease: a multi-site case-control study in China
Unintended pregnancy-related factors and the occurrence of offspring congenital heart disease: a multi-site case-control study in China
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Unintended pregnancy-related factors and the occurrence of offspring congenital heart disease: a multi-site case-control study in China

The European journal of contraception & reproductive health care, 2021-05, Vol.26 (3), p.221-226 [Peer Reviewed Journal]

2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2021 ;ISSN: 1362-5187 ;EISSN: 1473-0782 ;DOI: 10.1080/13625187.2020.1862081

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2
DNA methylation abnormalities in congenital heart disease
DNA methylation abnormalities in congenital heart disease
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DNA methylation abnormalities in congenital heart disease

Epigenetics, 2015, Vol.10 (2), p.167-177 [Peer Reviewed Journal]

2015 The Author(s). Published with license by Taylor & Francis Group, LLC © Clara Serra-Juhé, Ivon Cuscó, Aïda Homs, Raquel Flores, Núria Torán, and Luis A Pérez-Jurado 2015 ;info:eu-repo/semantics/openAccess © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC. /nThis is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by-nc/3.0/ ;2015 The Author(s). Published with license by Taylor & Francis Group, LLC © Clara Serra-Juhé, Ivon Cuscó, Aïda Homs, Raquel Flores, Núria Torán, and Luis A Pérez-Jurado 2015 The Author(s) ;ISSN: 1559-2294 ;EISSN: 1559-2308 ;DOI: 10.1080/15592294.2014.998536 ;PMID: 25587870

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3
Heart failure in congenital heart disease: management options and clinical challenges
Heart failure in congenital heart disease: management options and clinical challenges
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Heart failure in congenital heart disease: management options and clinical challenges

Expert review of cardiovascular therapy, 2020-08, Vol.18 (8), p.503-516 [Peer Reviewed Journal]

2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2020 ;ISSN: 1477-9072 ;EISSN: 1744-8344 ;DOI: 10.1080/14779072.2020.1797488

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4
Liver disease secondary to congenital heart disease in children
Liver disease secondary to congenital heart disease in children
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Liver disease secondary to congenital heart disease in children

Expert review of gastroenterology & hepatology, 2019-07, Vol.13 (7), p.651-666 [Peer Reviewed Journal]

2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2019 ;ISSN: 1747-4124 ;EISSN: 1747-4132 ;DOI: 10.1080/17474124.2019.1621746

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5
Outcome of transcatheter atrial septal defect closure in a nationwide cohort
Outcome of transcatheter atrial septal defect closure in a nationwide cohort
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Outcome of transcatheter atrial septal defect closure in a nationwide cohort

Annals of medicine (Helsinki), 2023-12, Vol.55 (1), p.615-623 [Peer Reviewed Journal]

2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 2023 ;2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 2023 The Author(s) ;ISSN: 0785-3890 ;EISSN: 1365-2060 ;DOI: 10.1080/07853890.2023.2178669 ;PMID: 36786506

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6
Predictors of pulmonary hypertension among children with atrial septal defects (ASD)
Predictors of pulmonary hypertension among children with atrial septal defects (ASD)
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Predictors of pulmonary hypertension among children with atrial septal defects (ASD)

Libyan journal of medicine, 2022-12, Vol.17 (1), p.2007603-2007603 [Peer Reviewed Journal]

2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2021 ;2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This work is licensed under the Creative Commons Attribution – Non-Commercial License 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. ;2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2021 The Author(s) ;ISSN: 1993-2820 ;EISSN: 1819-6357 ;DOI: 10.1080/19932820.2021.2007603 ;PMID: 34813403

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7
DNA methylation abnormalities in congenital heart disease
DNA methylation abnormalities in congenital heart disease
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DNA methylation abnormalities in congenital heart disease

2015 The Author(s). Published with license by Taylor & Francis Group, LLC. /nThis is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by-nc/3.0/ info:eu-repo/semantics/openAccess ;ISSN: 1559-2294 ;EISSN: 1559-2308 ;DOI: 10.1080/15592294.2014.998536

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8
Cholestasis In Infants With Down Syndrome Is Not Due To Extrahepatic Biliary Atresia: A Ten-Year Single Egyptian Centre Experience
Cholestasis In Infants With Down Syndrome Is Not Due To Extrahepatic Biliary Atresia: A Ten-Year Single Egyptian Centre Experience
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Cholestasis In Infants With Down Syndrome Is Not Due To Extrahepatic Biliary Atresia: A Ten-Year Single Egyptian Centre Experience

Clinical and experimental gastroenterology, 2019-10, Vol.12, p.401-408 [Peer Reviewed Journal]

2019 Kotb et al. ;COPYRIGHT 2019 Dove Medical Press Limited ;COPYRIGHT 2019 Dove Medical Press Limited ;2019. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2019 Kotb et al. 2019 Kotb et al. ;ISSN: 1178-7023 ;EISSN: 1178-7023 ;DOI: 10.2147/CEG.S216189 ;PMID: 31695469

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9
Detection of Novel Pathogenic Variants in Two Families with Recurrent Fetal Congenital Heart Defects
Detection of Novel Pathogenic Variants in Two Families with Recurrent Fetal Congenital Heart Defects
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Detection of Novel Pathogenic Variants in Two Families with Recurrent Fetal Congenital Heart Defects

Pharmacogenomics and personalized medicine, 2023-01, Vol.16, p.173-181 [Peer Reviewed Journal]

2023 Cai et al. ;2023. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2023 Cai et al. 2023 Cai et al. ;ISSN: 1178-7066 ;EISSN: 1178-7066 ;DOI: 10.2147/PGPM.S394120 ;PMID: 36923242

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10
Polymorphisms in gene UGT1A1 modify the association of prenatal exposure to polycyclic aromatic hydrocarbons with congenital heart diseases risk
Polymorphisms in gene UGT1A1 modify the association of prenatal exposure to polycyclic aromatic hydrocarbons with congenital heart diseases risk
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Polymorphisms in gene UGT1A1 modify the association of prenatal exposure to polycyclic aromatic hydrocarbons with congenital heart diseases risk

The journal of maternal-fetal & neonatal medicine, 2023-12, Vol.36 (1) [Peer Reviewed Journal]

2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 2023 ;ISSN: 1476-7058 ;EISSN: 1476-4954 ;DOI: 10.1080/14767058.2023.2183743

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11
Epidemiology and the prognosis of healthcare-associated infective endocarditis in China: the significance of non-nosocomial acquisition
Epidemiology and the prognosis of healthcare-associated infective endocarditis in China: the significance of non-nosocomial acquisition
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Epidemiology and the prognosis of healthcare-associated infective endocarditis in China: the significance of non-nosocomial acquisition

Emerging microbes & infections, 2015-07, Vol.4 (1), p.1-6 [Peer Reviewed Journal]

2015 The Author(s) 2015 ;Copyright Nature Publishing Group Jul 2015 ;2015 The Author(s). This work is licensed under the Creative Commons Attribution – Non-Commercial – No Derivatives License https://creativecommons.org/licenses/by-nc-nd/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Copyright © 2015 Shanghai Shangyixun Cultural Communication Co., Ltd 2015 Shanghai Shangyixun Cultural Communication Co., Ltd ;ISSN: 2222-1751 ;EISSN: 2222-1751 ;DOI: 10.1038/emi.2015.38 ;PMID: 26251828

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12
Perinatal outcome in children born after assisted reproductive technologies
Perinatal outcome in children born after assisted reproductive technologies
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Perinatal outcome in children born after assisted reproductive technologies

Upsala journal of medical sciences, 2020-04, Vol.125 (2), p.158-166 [Peer Reviewed Journal]

2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2020 ;2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This work is licensed under the Creative Commons Attribution License 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. ;2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2020 The Author(s) ;ISSN: 0300-9734 ;EISSN: 2000-1967 ;DOI: 10.1080/03009734.2020.1726534 ;PMID: 32124667

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13
Pediatric ventricular assist devices: current challenges and future prospects
Pediatric ventricular assist devices: current challenges and future prospects
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Pediatric ventricular assist devices: current challenges and future prospects

Vascular health and risk management, 2017-01, Vol.13, p.177-185 [Peer Reviewed Journal]

COPYRIGHT 2017 Dove Medical Press Limited ;COPYRIGHT 2017 Dove Medical Press Limited ;2017. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2017 Burki and Adachi. This work is published and licensed by Dove Medical Press Limited 2017 ;ISSN: 1178-2048 ;ISSN: 1176-6344 ;EISSN: 1178-2048 ;DOI: 10.2147/VHRM.S82379 ;PMID: 28546755

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14
Association of maternal methionine synthase reductase gene polymorphisms with the risk of congenital heart disease in offspring: a hospital-based case-control study
Association of maternal methionine synthase reductase gene polymorphisms with the risk of congenital heart disease in offspring: a hospital-based case-control study
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Association of maternal methionine synthase reductase gene polymorphisms with the risk of congenital heart disease in offspring: a hospital-based case-control study

The journal of maternal-fetal & neonatal medicine, 2023-12, Vol.36 (1) [Peer Reviewed Journal]

2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 2023 ;ISSN: 1476-7058 ;EISSN: 1476-4954 ;DOI: 10.1080/14767058.2023.2211201

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15
Isolated spontaneous dissection of the celiac trunk in a patient with bicuspid aortic valve
Isolated spontaneous dissection of the celiac trunk in a patient with bicuspid aortic valve
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Isolated spontaneous dissection of the celiac trunk in a patient with bicuspid aortic valve

Vascular health and risk management, 2010-01, Vol.6 (default), p.383-386 [Peer Reviewed Journal]

2010. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2010 Zeina et al, publisher and licensee Dove Medical Press Ltd. ;ISSN: 1178-2048 ;ISSN: 1176-6344 ;EISSN: 1178-2048 ;DOI: 10.2147/vhrm.s9912 ;PMID: 20539840

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16
Free radicals and birth defects
Free radicals and birth defects
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Free radicals and birth defects

The journal of maternal-fetal & neonatal medicine, 2004, Vol.15 (1), p.6-14 [Peer Reviewed Journal]

2004 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2004 ;Copyright CRC Press Jan 2004 ;ISSN: 1476-7058 ;EISSN: 1476-4954 ;DOI: 10.1080/14767050310001650662 ;PMID: 15101606 ;CODEN: JMNMAE

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17
Ectopia cordis: prenatal diagnosis, perinatal outcomes, and postnatal follow-up of an international multicenter cohort case series
Ectopia cordis: prenatal diagnosis, perinatal outcomes, and postnatal follow-up of an international multicenter cohort case series
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Ectopia cordis: prenatal diagnosis, perinatal outcomes, and postnatal follow-up of an international multicenter cohort case series

The journal of maternal-fetal & neonatal medicine, 2023-12, Vol.36 (1) [Peer Reviewed Journal]

2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group 2023 ;ISSN: 1476-7058 ;EISSN: 1476-4954 ;DOI: 10.1080/14767058.2023.2203791

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18
Genetic Susceptibility to Chronic Kidney Disease: Links, Risks and Management
Genetic Susceptibility to Chronic Kidney Disease: Links, Risks and Management
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Genetic Susceptibility to Chronic Kidney Disease: Links, Risks and Management

International journal of nephrology and renovascular disease, 2023-01, Vol.16, p.1-15 [Peer Reviewed Journal]

2023 Sawaf et al. ;COPYRIGHT 2023 Dove Medical Press Limited ;2023. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2023 Sawaf et al. 2023 Sawaf et al. ;ISSN: 1178-7058 ;EISSN: 1178-7058 ;DOI: 10.2147/IJNRD.S363041 ;PMID: 36636322

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19
Atrioventricular valvular anomalies and their role in the etiopathogenesis of cardiorespiratory syndrome in farmed common foxes (Vulpes vulpes)
Atrioventricular valvular anomalies and their role in the etiopathogenesis of cardiorespiratory syndrome in farmed common foxes (Vulpes vulpes)
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Atrioventricular valvular anomalies and their role in the etiopathogenesis of cardiorespiratory syndrome in farmed common foxes (Vulpes vulpes)

The Veterinary quarterly, 2016-01, Vol.36 (1), p.16-21 [Peer Reviewed Journal]

2015 Taylor & Francis 2015 ;ISSN: 0165-2176 ;EISSN: 1875-5941 ;DOI: 10.1080/01652176.2015.1114192 ;PMID: 26609873

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20
MicroRNA profiling of patients with sporadic atrial septal defect
MicroRNA profiling of patients with sporadic atrial septal defect
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MicroRNA profiling of patients with sporadic atrial septal defect

Biotechnology, biotechnological equipment, 2019-01, Vol.33 (1), p.510-519 [Peer Reviewed Journal]

2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2019 ;2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This work is licensed under the Creative Commons Attribution License 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: 1310-2818 ;EISSN: 1314-3530 ;DOI: 10.1080/13102818.2019.1591932

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