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1
Neurodevelopmental outcome at 5 years of age after general anaesthesia or awake-regional anaesthesia in infancy (GAS): an international, multicentre, randomised, controlled equivalence trial
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Neurodevelopmental outcome at 5 years of age after general anaesthesia or awake-regional anaesthesia in infancy (GAS): an international, multicentre, randomised, controlled equivalence trial

The Lancet (British edition), 2019-02, Vol.393 (10172), p.664-677 [Peer Reviewed Journal]

2019 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license ;Copyright © 2019 Elsevier Ltd. All rights reserved. ;2019. The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(18)32485-1 ;PMID: 30782342

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2
The Major Causes of Death in Children and Adolescents in the United States
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The Major Causes of Death in Children and Adolescents in the United States

The 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: 30575483

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3
Somatic MAP2K1 Mutations Are Associated with Extracranial Arteriovenous Malformation
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Somatic MAP2K1 Mutations Are Associated with Extracranial Arteriovenous Malformation

American 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: 28190454

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4
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 2016
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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 2016

The 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: 28919116

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5
Association Between MRI Exposure During Pregnancy and Fetal and Childhood Outcomes
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Article
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Association Between MRI Exposure During Pregnancy and Fetal and Childhood Outcomes

JAMA : 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: 27599330

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6
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 Study
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Article
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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 Study

JAMA pediatrics, 2019-06, Vol.173 (6), p.e190337 [Peer Reviewed Journal]

ISSN: 2168-6211 ;EISSN: 2168-6211 ;DOI: 10.1001/jamapediatrics.2019.0337 ;PMID: 31034019

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7
Epidemiology of valvular heart disease in a Swedish nationwide hospital-based register study
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Article
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Epidemiology of valvular heart disease in a Swedish nationwide hospital-based register study

Heart (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: 28432156

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8
Caring for individuals with a difference of sex development (DSD): a Consensus Statement
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Article
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Caring for individuals with a difference of sex development (DSD): a Consensus Statement

Nature 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: 29769693

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9
Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome
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Article
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Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome

Journal 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: JMDGAE

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10
Trends in Long-Term Mortality After Congenital Heart Surgery
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Article
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Trends in Long-Term Mortality After Congenital Heart Surgery

Journal 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: 29793633

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11
Genomic and phenotypic delineation of congenital microcephaly
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Article
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Genomic and phenotypic delineation of congenital microcephaly

Genetics in medicine, 2019-03, Vol.21 (3), p.545-552 [Peer Reviewed Journal]

Copyright Nature Publishing Group Mar 2019 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-018-0140-3 ;PMID: 30214071

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12
Mortality from gastrointestinal congenital anomalies at 264 hospitals in 74 low-income, middle-income, and high-income countries: a multicentre, international, prospective cohort study
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Article
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Mortality from gastrointestinal congenital anomalies at 264 hospitals in 74 low-income, middle-income, and high-income countries: a multicentre, international, prospective cohort study

The Lancet (British edition), 2021-07, Vol.398 (10297), p.325-339 [Peer Reviewed Journal]

2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license ;Copyright © 2021 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. ;2021. The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. This work is published under https://creativecommons.org/licenses/by/3.0/ (theLicense”). 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 Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license 2021 ;ISSN: 0140-6736 ;ISSN: 1474-547X ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(21)00767-4 ;PMID: 34270932

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13
TBX6 Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis
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Article
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TBX6 Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis

The New England journal of medicine, 2015-01, Vol.372 (4), p.341-350 [Peer Reviewed Journal]

Copyright © 2015 Massachusetts Medical Society. All rights reserved. ;Copyright © 2015 Massachusetts Medical Society. All rights reserved 2015 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1406829 ;PMID: 25564734

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14
Protein-Losing Enteropathy in Patients With Congenital Heart Disease
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Article
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Protein-Losing Enteropathy in Patients With Congenital Heart Disease

Journal of the American College of Cardiology, 2017-06, Vol.69 (24), p.2929-2937 [Peer Reviewed Journal]

American College of Cardiology Foundation ;2017 American College of Cardiology Foundation ;Copyright © 2017 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Jun 20, 2017 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2017.04.023 ;PMID: 28619193

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15
Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome
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Article
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Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome

American journal of human genetics, 2012-06, Vol.90 (6), p.1108-1115 [Peer Reviewed Journal]

2012 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright © 2012 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Jun 8, 2012 ;2012 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2012 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2012.05.006 ;PMID: 22658544 ;CODEN: AJHGAG

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16
Mutations in NOTCH1 Cause Adams-Oliver Syndrome
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Article
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Mutations in NOTCH1 Cause Adams-Oliver Syndrome

American journal of human genetics, 2014-09, Vol.95 (3), p.275-284 [Peer Reviewed Journal]

2014 The American Society of Human Genetics ;Copyright © 2014 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Sep 4, 2014 ;2014 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2014 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2014.07.011 ;PMID: 25132448

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17
Mutations in WNT1 Cause Different Forms of Bone Fragility
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Article
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Mutations in WNT1 Cause Different Forms of Bone Fragility

American journal of human genetics, 2013-04, Vol.92 (4), p.565-574 [Peer Reviewed Journal]

2013 The American Society of Human Genetics ;Copyright © 2013 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright Cell Press Apr 4, 2013 ;2013 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2013 The American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2013.02.010 ;PMID: 23499309

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18
Aortic Valve Replacement and the Ross Operation in Children and Young Adults
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Article
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Aortic Valve Replacement and the Ross Operation in Children and Young Adults

Journal of the American College of Cardiology, 2016-06, Vol.67 (24), p.2858-2870 [Peer Reviewed Journal]

American College of Cardiology Foundation ;2016 American College of Cardiology Foundation ;Copyright © 2016 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Jun 21, 2016 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2016.04.021 ;PMID: 27311525

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19
The Zika Virus Epidemic in Brazil: From Discovery to Future Implications
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Article
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The Zika Virus Epidemic in Brazil: From Discovery to Future Implications

International journal of environmental research and public health, 2018-01, Vol.15 (1), p.96 [Peer Reviewed Journal]

Copyright MDPI AG 2018 ;cc by (c) Lowe et al., 2018 info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/3.0/es/ ;2018 by the authors. 2018 ;ISSN: 1660-4601 ;ISSN: 1661-7827 ;EISSN: 1660-4601 ;DOI: 10.3390/ijerph15010096 ;PMID: 29315224

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20
A somatic activating NRAS variant associated with kaposiform lymphangiomatosis
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Article
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A somatic activating NRAS variant associated with kaposiform lymphangiomatosis

Genetics in medicine, 2019-07, Vol.21 (7), p.1517-1524 [Peer Reviewed Journal]

2019 The Author(s) ;Copyright Nature Publishing Group Jul 2019 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-018-0390-0 ;PMID: 30542204

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