Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
---|---|---|---|
1 |
Material Type: Article
|
The Major Causes of Death in Children and Adolescents in the United StatesThe New England journal of medicine, 2018-12, Vol.379 (25), p.2468-2475 [Peer Reviewed Journal]Copyright © 2018 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMsr1804754 ;PMID: 30575483Full text available |
|
2 |
Material Type: Article
|
De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomaliesScience (American Association for the Advancement of Science), 2015-12, Vol.350 (6265), p.1262-1266 [Peer Reviewed Journal]Copyright © 2015 American Association for the Advancement of Science ;Copyright © 2015, American Association for the Advancement of Science. ;Copyright © 2015, American Association for the Advancement of Science ;ISSN: 0036-8075 ;EISSN: 1095-9203 ;DOI: 10.1126/science.aac9396 ;PMID: 26785492 ;CODEN: SCIEASDigital Resources/Online E-Resources |
|
3 |
Material Type: Article
|
SyphilisThe Lancet (British edition), 2017-04, Vol.389 (10078), p.1550-1557 [Peer Reviewed Journal]Elsevier Ltd ;2017 Elsevier Ltd ;Copyright © 2017 Elsevier Ltd. All rights reserved. ;Copyright Elsevier Limited Apr 15, 2017 ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(16)32411-4 ;PMID: 27993382Full text available |
|
4 |
Material Type: Article
|
22q11.2 deletion syndromeNature reviews. Disease primers, 2015-11, Vol.1 (1), p.15071-15071, Article 15071 [Peer Reviewed Journal]Macmillan Publishers Limited 2015. ;ISSN: 2056-676X ;EISSN: 2056-676X ;DOI: 10.1038/nrdp.2015.71 ;PMID: 27189754Full text available |
|
5 |
Material Type: Article
|
Somatic MAP2K1 Mutations Are Associated with Extracranial Arteriovenous MalformationAmerican journal of human genetics, 2017-03, Vol.100 (3), p.546-554 [Peer Reviewed Journal]2017 American Society of Human Genetics ;Copyright © 2017 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Mar 2, 2017 ;2017 American Society of Human Genetics. 2017 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2017.01.018 ;PMID: 28190454Full text available |
|
6 |
Material Type: Article
|
Global, regional, and national age-sex specific mortality for 264 causes of death, 1980–2016: a systematic analysis for the Global Burden of Disease Study 2016The Lancet (British edition), 2017-09, Vol.390 (10100), p.1151-1210 [Peer Reviewed Journal]2017 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license ;Copyright © 2017 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved. ;Copyright Elsevier Limited Sep 16, 2017 ;info:eu-repo/semantics/openAccess ;2017 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license 2017 ;ISSN: 0140-6736 ;ISSN: 1474-547X ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(17)32152-9 ;PMID: 28919116Full text available |
|
7 |
Material Type: Article
|
Association Between MRI Exposure During Pregnancy and Fetal and Childhood OutcomesJAMA : the journal of the American Medical Association, 2016-09, Vol.316 (9), p.952 [Peer Reviewed Journal]EISSN: 1538-3598 ;DOI: 10.1001/jama.2016.12126 ;PMID: 27599330Digital Resources/Online E-Resources |
|
8 |
Material Type: Article
|
Neurocognitive factors in sensory restoration of early deafness: a connectome modelLancet neurology, 2016-05, Vol.15 (6), p.610-621 [Peer Reviewed Journal]Elsevier Ltd ;2016 Elsevier Ltd ;Copyright © 2016 Elsevier Ltd. All rights reserved. ;Copyright Elsevier Limited May 2016 ;ISSN: 1474-4422 ;EISSN: 1474-4465 ;DOI: 10.1016/S1474-4422(16)00034-X ;PMID: 26976647 ;CODEN: LANCAOFull text available |
|
9 |
Material Type: Article
|
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probandsNature 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: 28991257Full text available |
|
10 |
Material Type: Article
|
Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital AnomaliesAmerican journal of human genetics, 2010-05, Vol.86 (5), p.749-764 [Peer Reviewed Journal]2010 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright (c) 2010 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright University of Chicago, acting through its Press May 14, 2010 ;2010 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2010 The American Society of Human Genetics ;ISSN: 0002-9297 ;ISSN: 1537-6605 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2010.04.006 ;PMID: 20466091 ;CODEN: AJHGAGFull text available |
|
11 |
Material Type: Article
|
Physical activity modification in youth with congenital heart disease: a comprehensive narrative reviewPediatric research, 2021-05, Vol.89 (7), p.1650-1658 [Peer Reviewed Journal]The Author(s) 2020. 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. ;The Author(s) 2020 ;ISSN: 0031-3998 ;EISSN: 1530-0447 ;DOI: 10.1038/s41390-020-01194-8 ;PMID: 33049756Full text available |
|
12 |
Material Type: Article
|
Diseases, Injuries, and Risk Factors in Child and Adolescent Health, 1990 to 2017: Findings From the Global Burden of Diseases, Injuries, and Risk Factors 2017 StudyJAMA pediatrics, 2019-06, Vol.173 (6), p.e190337 [Peer Reviewed Journal]ISSN: 2168-6211 ;EISSN: 2168-6211 ;DOI: 10.1001/jamapediatrics.2019.0337 ;PMID: 31034019Digital Resources/Online E-Resources |
|
13 |
Material Type: Article
|
Cognitive and Executive Function in Congenital Heart Disease: A Meta-analysisPediatrics (Evanston), 2021-10, Vol.148 (4), p.1 [Peer Reviewed Journal]Copyright © 2021 by the American Academy of Pediatrics. ;Copyright American Academy of Pediatrics Oct 1, 2021 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2021-050875 ;PMID: 34561266Digital Resources/Online E-Resources |
|
14 |
Material Type: Article
|
Epidemiology of valvular heart disease in a Swedish nationwide hospital-based register studyHeart (British Cardiac Society), 2017-11, Vol.103 (21), p.1696-1703 [Peer Reviewed Journal]Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;Copyright: 2017 © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. 2017 ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2016-310894 ;PMID: 28432156Full text available |
|
15 |
Material Type: Article
|
Caring for individuals with a difference of sex development (DSD): a Consensus StatementNature reviews. Endocrinology, 2018-07, Vol.14 (7), p.415-429 [Peer Reviewed Journal]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. ;Macmillan Publishers Ltd., part of Springer Nature 2018 ;ISSN: 1759-5029 ;ISSN: 1759-5037 ;EISSN: 1759-5037 ;DOI: 10.1038/s41574-018-0010-8 ;PMID: 29769693Full text available |
|
16 |
Material Type: Article
|
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndromeJournal of medical genetics, 2014-03, Vol.51 (3), p.152-158 [Peer Reviewed Journal]Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Copyright: 2014 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2013-102113 ;PMID: 24399845 ;CODEN: JMDGAEFull text available |
|
17 |
Material Type: Article
|
Trends in Long-Term Mortality After Congenital Heart SurgeryJournal of the American College of Cardiology, 2018-05, Vol.71 (21), p.2434-2446 [Peer Reviewed Journal]2018 American College of Cardiology Foundation ;Copyright © 2018 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited May 29, 2018 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2018.03.491 ;PMID: 29793633Full text available |
|
18 |
Material Type: Article
|
Mosaic RAS/MAPK variants cause sporadic vascular malformations which respond to targeted therapyThe Journal of clinical investigation, 2018-04, Vol.128 (4), p.1496-1508 [Peer Reviewed Journal]COPYRIGHT 2018 American Society for Clinical Investigation ;COPYRIGHT 2018 American Society for Clinical Investigation ;Copyright American Society for Clinical Investigation Apr 2018 ;Copyright © 2018 Al-Olabi et al. 2018 Al-Olabi et al. ;ISSN: 0021-9738 ;EISSN: 1558-8238 ;DOI: 10.1172/jci98589 ;PMID: 29461977Full text available |
|
19 |
Material Type: Article
|
Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectivenessGenetics in medicine, 2019-01, Vol.21 (1), p.173-180 [Peer Reviewed Journal]2019 The Author(s) ;Copyright Nature Publishing Group Jan 2019 ;American College of Medical Genetics and Genomics 2018. ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-018-0006-8 ;PMID: 29765138Full text available |
|
20 |
Material Type: Article
|
Red Blood Cell Transfusion: 2023 AABB International GuidelinesJAMA : the journal of the American Medical Association, 2023-11, Vol.330 (19), p.1892 [Peer Reviewed Journal]EISSN: 1538-3598 ;DOI: 10.1001/jama.2023.12914 ;PMID: 37824153Digital Resources/Online E-Resources |