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1
Atrioventricular canal defect is the classic congenital heart disease in Bardet–Biedl syndrome
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Atrioventricular canal defect is the classic congenital heart disease in Bardet–Biedl syndrome

Annals of human genetics, 2021-05, Vol.85 (3-4), p.101-102 [Peer Reviewed Journal]

2021 John Wiley & Sons Ltd/University College London ;COPYRIGHT 2021 Blackwell Publishers Ltd. ;ISSN: 0003-4800 ;EISSN: 1469-1809 ;DOI: 10.1111/ahg.12413 ;PMID: 33433911

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2
Hydrops fetalis in PKD1L1‐related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrum
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Hydrops fetalis in PKD1L1‐related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrum

Annals of human genetics, 2021-05, Vol.85 (3-4), p.138-145 [Peer Reviewed Journal]

2021 John Wiley & Sons Ltd/University College London ;2021 John Wiley & Sons Ltd/University College London. ;COPYRIGHT 2021 Blackwell Publishers Ltd. ;ISSN: 0003-4800 ;EISSN: 1469-1809 ;DOI: 10.1111/ahg.12417 ;PMID: 33655537

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3
The role of FOXP3+ regulatory T cells in human autoimmune and inflammatory diseases
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The role of FOXP3+ regulatory T cells in human autoimmune and inflammatory diseases

Clinical and experimental immunology, 2019-07, Vol.197 (1), p.24-35 [Peer Reviewed Journal]

2019 British Society for Immunology ;2019 British Society for Immunology. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0009-9104 ;EISSN: 1365-2249 ;DOI: 10.1111/cei.13288 ;PMID: 30830965

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4
Maternal fever during preconception and conception is associated with congenital heart diseases in offspring: An updated meta-analysis of observational studies
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Maternal fever during preconception and conception is associated with congenital heart diseases in offspring: An updated meta-analysis of observational studies

Medicine (Baltimore), 2021-03, Vol.100 (9), p.e24899-e24899 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000024899 ;PMID: 33655950

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5
An artificial neural network prediction model of congenital heart disease based on risk factors: A hospital-based case-control study
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An artificial neural network prediction model of congenital heart disease based on risk factors: A hospital-based case-control study

Medicine (Baltimore), 2017-02, Vol.96 (6), p.e6090 [Peer Reviewed Journal]

Copyright © 2017 the Author(s). Published by Wolters Kluwer Health, Inc. 2017 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000006090 ;PMID: 28178169

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6
Diagnostic Value of Fetal Echocardiography for Congenital Heart Disease: A Systematic Review and Meta-Analysis
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Diagnostic Value of Fetal Echocardiography for Congenital Heart Disease: A Systematic Review and Meta-Analysis

Medicine (Baltimore), 2015-10, Vol.94 (42), p.e1759-e1759 [Peer Reviewed Journal]

Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. 2015 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000001759 ;PMID: 26496297

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7
Effect of dexmedetomidine on perioperative hemodynamics and organ protection in children with congenital heart disease: A randomized controlled trial
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Effect of dexmedetomidine on perioperative hemodynamics and organ protection in children with congenital heart disease: A randomized controlled trial

Medicine (Baltimore), 2021-01, Vol.100 (1), p.e23998-e23998 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000023998 ;PMID: 33429762

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8
Comparison of the 1-year survival rate in infants with congenital heart disease diagnosed by prenatal and postnatal ultrasound: A retrospective study
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Comparison of the 1-year survival rate in infants with congenital heart disease diagnosed by prenatal and postnatal ultrasound: A retrospective study

Medicine (Baltimore), 2021-01, Vol.100 (4), p.e23325-e23325 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000023325 ;PMID: 33530157

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9
Application effect of initiation of enteral nutrition at different time periods after surgery in neonates with complex congenital heart disease: A retrospective analysis
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Application effect of initiation of enteral nutrition at different time periods after surgery in neonates with complex congenital heart disease: A retrospective analysis

Medicine (Baltimore), 2021-01, Vol.100 (1), p.e24149-e24149 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000024149 ;PMID: 33429794

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10
Connection of GLI1 variants to congenital heart disease susceptibility: A case-control study
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Connection of GLI1 variants to congenital heart disease susceptibility: A case-control study

Medicine (Baltimore), 2020-07, Vol.99 (27), p.e19868-e19868 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000019868 ;PMID: 32629623

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11
Associations of maternal diabetes mellitus and adiponectin gene polymorphisms with congenital heart disease in offspring: A case-control study
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Associations of maternal diabetes mellitus and adiponectin gene polymorphisms with congenital heart disease in offspring: A case-control study

Medicine (Baltimore), 2021-03, Vol.100 (9), p.e24672-e24672 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000024672 ;PMID: 33655931

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12
Correlations between ISL1 rs1017 polymorphism and congenital heart disease risk: A PRISMA-compliant meta-analysis
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Correlations between ISL1 rs1017 polymorphism and congenital heart disease risk: A PRISMA-compliant meta-analysis

Medicine (Baltimore), 2020-01, Vol.99 (2), p.e18715-e18715 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000018715 ;PMID: 31914083

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13
Supraglottic foreign body in a woman with Down's syndrome and congenital heart disease: A case report
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Supraglottic foreign body in a woman with Down's syndrome and congenital heart disease: A case report

Medicine (Baltimore), 2021-04, Vol.100 (14), p.e25455-e25455 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000025455 ;PMID: 33832154

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14
The efficacy of bosentan combined with vardenafil in the treatment of postoperative pulmonary hypertension in children with congenital heart disease: A protocol of randomized controlled trial
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The efficacy of bosentan combined with vardenafil in the treatment of postoperative pulmonary hypertension in children with congenital heart disease: A protocol of randomized controlled trial

Medicine (Baltimore), 2021-01, Vol.100 (1), p.e23896-e23896 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000023896 ;PMID: 33429750

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15
Combined effects of AKT serine/threonine kinase 1 polymorphisms and environment on congenital heart disease risk: A case-control study
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Combined effects of AKT serine/threonine kinase 1 polymorphisms and environment on congenital heart disease risk: A case-control study

Medicine (Baltimore), 2020-06, Vol.99 (26), p.e20400-e20400 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020400 ;PMID: 32590727

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16
Associations and interaction effects of maternal smoking and genetic polymorphisms of cytochrome P450 genes with risk of congenital heart disease in offspring: A case-control study
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Associations and interaction effects of maternal smoking and genetic polymorphisms of cytochrome P450 genes with risk of congenital heart disease in offspring: A case-control study

Medicine (Baltimore), 2021-06, Vol.100 (23), p.e26268 [Peer Reviewed Journal]

Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. ;Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. 2021 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000026268 ;PMID: 34115022

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17
Efficacy and safety of valganciclovir in patients with symptomatic congenital cytomegalovirus disease: Study Protocol Clinical Trial (SPIRIT Compliant)
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Efficacy and safety of valganciclovir in patients with symptomatic congenital cytomegalovirus disease: Study Protocol Clinical Trial (SPIRIT Compliant)

Medicine (Baltimore), 2020-04, Vol.99 (17), p.e19765-e19765 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000019765 ;PMID: 32332615

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18
Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome
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Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome

Medicine (Baltimore), 2018-12, Vol.97 (50), p.e13617-e13617 [Peer Reviewed Journal]

Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. 2018 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000013617 ;PMID: 30558042

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19
Congenital heart disease combined with Arrhythmogenic Right Ventricular Cardiomyopathy: A CARE compliant case report and literature review
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Congenital heart disease combined with Arrhythmogenic Right Ventricular Cardiomyopathy: A CARE compliant case report and literature review

Medicine (Baltimore), 2020-06, Vol.99 (25), p.e20279-e20279 [Peer Reviewed Journal]

Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. 2020 ;ISSN: 0025-7974 ;EISSN: 1536-5964 ;DOI: 10.1097/MD.0000000000020279 ;PMID: 32569162

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20
Unveiling Mysteries in Congenital Diseases: A Case Report of Williams-Beuren Syndrome
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Unveiling Mysteries in Congenital Diseases: A Case Report of Williams-Beuren Syndrome

Cardiovascular innovations and applications, 2024-01, Vol.9 (1), p.984 [Peer Reviewed Journal]

ISSN: 2009-8618 ;EISSN: 2009-8782 ;DOI: 10.15212/CVIA.2024.0005

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