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| Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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| 1 |
Material Type: Article
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A "twelve-section ultrasonic screening and diagnosis method" and management system for screening and treating neonatal congenital heart disease at the grassroots level in Tang County, Hebei Province, ChinaBMC pregnancy and childbirth, 2024-05, Vol.24 (1), p.371-371 [Peer Reviewed Journal]2024. The Author(s). ;The Author(s) 2024 ;EISSN: 1471-2393 ;DOI: 10.1186/s12884-024-06569-x ;PMID: 38750445Full text available |
| 2 |
Material Type: Article
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How Will Artificial Intelligence Shape the Future of Decision-Making in Congenital Heart Disease?Journal of clinical medicine, 2024-05, Vol.13 (10), p.2996 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2077-0383 ;EISSN: 2077-0383 ;DOI: 10.3390/jcm13102996 ;PMID: 38792537Full text available |
| 3 |
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Untangling the Complex Associations between Socioeconomic and Demographic Characteristics and Prenatal Detection and Outcomes in Congenital Heart DiseaseJournal of cardiovascular development and disease, 2024-05, Vol.11 (5), p.155 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2308-3425 ;EISSN: 2308-3425 ;DOI: 10.3390/jcdd11050155 ;PMID: 38786977Full text available |
| 4 |
Material Type: Article
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Efficiency of copy number variation sequencing combined with karyotyping in fetuses with congenital heart disease and the following outcomesMolecular cytogenetics, 2024-05, Vol.17 (1), p.12-12 [Peer Reviewed Journal]2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;The Author(s) 2024 ;ISSN: 1755-8166 ;EISSN: 1755-8166 ;DOI: 10.1186/s13039-024-00681-5 ;PMID: 38741090Full text available |
| 5 |
Material Type: Article
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Cost-utility analysis of prenatal diagnosis of congenital cardiac diseases using deep learningCost effectiveness and resource allocation, 2024-05, Vol.22 (1), p.44-44 [Peer Reviewed Journal]2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;The Author(s) 2024 ;ISSN: 1478-7547 ;EISSN: 1478-7547 ;DOI: 10.1186/s12962-024-00550-3 ;PMID: 38773527Full text available |
| 6 |
Material Type: Article
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Hypothyroidism in Patients with Down Syndrome: Prevalence and Association with Congenital Heart DefectsChildren (Basel), 2024-05, Vol.11 (5), p.513 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2227-9067 ;EISSN: 2227-9067 ;DOI: 10.3390/children11050513 ;PMID: 38790508Full text available |
| 7 |
Material Type: Article
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Heart Transplantation Following Fontan Failure: Long-Term Survival AnalysisJournal of clinical medicine, 2024-05, Vol.13 (10), p.2960 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2077-0383 ;EISSN: 2077-0383 ;DOI: 10.3390/jcm13102960 ;PMID: 38792500Full text available |
| 8 |
Material Type: Article
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Molecular Mechanisms of Fetal and Neonatal Lupus: A Narrative Review of an Autoimmune Disease Transferal across the PlacentaInternational journal of molecular sciences, 2024-05, Vol.25 (10), p.5224 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms25105224 ;PMID: 38791261Full text available |
| 9 |
Material Type: Article
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Management of Ebstein Anomaly in the Current Era: The Story of One Fetus and the Collaboration of Many-A Case ReportJournal of cardiovascular development and disease, 2024-05, Vol.11 (5), p.147 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2308-3425 ;EISSN: 2308-3425 ;DOI: 10.3390/jcdd11050147 ;PMID: 38786969Full text available |
| 10 |
Material Type: Article
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Images of Extremely Rare Cantrell PhenomenonDiagnostics (Basel), 2024-05, Vol.14 (10), p.1003 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2075-4418 ;EISSN: 2075-4418 ;DOI: 10.3390/diagnostics14101003 ;PMID: 38786301Full text available |
| 11 |
Material Type: Article
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Ultrasonic Evaluation of the Achilles Tendon in Patients Treated for Congenital Clubfoot: Comparison between Patients Treated with Plaster Alone, Achilles Tenotomy, and Z-Plasty LengtheningChildren (Basel), 2024-05, Vol.11 (5), p.580 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2227-9067 ;EISSN: 2227-9067 ;DOI: 10.3390/children11050580 ;PMID: 38790575Full text available |
| 12 |
Material Type: Article
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Proposed Screening for Congenital Hyperinsulinism in Newborns: Perspective from a Neonatal-Perinatal Medicine GroupJournal of clinical medicine, 2024-05, Vol.13 (10), p.2953 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2077-0383 ;EISSN: 2077-0383 ;DOI: 10.3390/jcm13102953 ;PMID: 38792494Full text available |
| 13 |
Material Type: Article
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2020 ESC Guidelines for the management of adult congenital heart disease The Task Force for the management of adult congenital heart disease of the European Society of Cardiology (ESC). Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Adult Congenital Heart Disease (ISACHD)EUROPEAN HEART JOURNAL, 2021-02, Vol.42 (6), p.563-645 [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645Full text available |
| 14 |
Material Type: Article
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Postnatal Brain Trajectories and Maternal Intelligence Predict Childhood Outcomes in Complex CHDJournal of clinical medicine, 2024-05, Vol.13 (10), p.2922 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2077-0383 ;EISSN: 2077-0383 ;DOI: 10.3390/jcm13102922 ;PMID: 38792464Full text available |
| 15 |
Material Type: Article
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Recommendations for advance care planning in adults with congenital heart disease: a position paper from the ESC Working Group of Adult Congenital Heart Disease, the Association of Cardiovascular Nursing and Allied Professions (ACNAP), the European Association for Palliative Care (EAPC), and the International Society for Adult Congenital Heart Disease (ISACHD)EUROPEAN HEART JOURNAL, 2020-11, Vol.41 (43), p.4200-4210 [Peer Reviewed Journal]ISSN: 0195-668X ;EISSN: 1522-9645Full text available |
| 16 |
Material Type: Article
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A Pilot Comparative Study between Creatinine- and Cystatin-C-Based Equations to Estimate GFR and Kidney Ultrasound Percentiles in Children with Congenital Anomalies of the Kidney and Urinary TractDiagnostics (Basel), 2024-05, Vol.14 (10), p.994 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2075-4418 ;EISSN: 2075-4418 ;DOI: 10.3390/diagnostics14100994 ;PMID: 38786292Full text available |
| 17 |
Material Type: Article
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The Approach to a Child with Dysmorphic Features: What the Pediatrician Should KnowChildren (Basel), 2024-05, Vol.11 (5), p.578 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2227-9067 ;EISSN: 2227-9067 ;DOI: 10.3390/children11050578 ;PMID: 38790573Full text available |
| 18 |
Material Type: Article
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Sudden Cardiac Death, Post-Mortem Investigation: A Proposing Panel of First Line and Second Line Genetic TestsJournal of personalized medicine, 2024-05, Vol.14 (5), p.544 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 2075-4426 ;EISSN: 2075-4426 ;DOI: 10.3390/jpm14050544 ;PMID: 38793126Full text available |
| 19 |
Material Type: Article
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Assessing Uveitis Risk following Pediatric Down Syndrome Diagnosis: A TriNetX Database StudyMedicina (Kaunas, Lithuania), 2024-05, Vol.60 (5), p.710 [Peer Reviewed Journal]COPYRIGHT 2024 MDPI AG ;2024 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. ;ISSN: 1648-9144 ;ISSN: 1010-660X ;EISSN: 1648-9144 ;DOI: 10.3390/medicina60050710 ;PMID: 38792893Full text available |
| 20 |
Material Type: Article
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Rare Genetic Developmental Disabilities: Mabry Syndrome (MIM 239300) Index Cases and Glycophosphatidylinositol (GPI) DisordersGenes, 2024-05, Vol.15 (5), p.619 [Peer Reviewed Journal]2024 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. ;EISSN: 2073-4425 ;DOI: 10.3390/genes15050619 ;PMID: 38790248Full text available |
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