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1
Probable congenital SARS-CoV-2 infection in a neonate born to a woman with active SARS-CoV-2 infection
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Probable congenital SARS-CoV-2 infection in a neonate born to a woman with active SARS-CoV-2 infection

Canadian Medical Association journal (CMAJ), 2020-06, Vol.192 (24), p.E647-E650 [Peer Reviewed Journal]

COPYRIGHT 2020 Joule Inc. ;Copyright Joule Inc Jun 15, 2020 ;2020 Joule Inc. or its licensors 2020 ;ISSN: 0820-3946 ;EISSN: 1488-2329 ;DOI: 10.1503/cmaj.200821 ;PMID: 32409520

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2
Rapid development of a DNA vaccine for Zika virus
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Rapid development of a DNA vaccine for Zika virus

Science (American Association for the Advancement of Science), 2016-10, Vol.354 (6309), p.237-240 [Peer Reviewed Journal]

Copyright © 2016 American Association for the Advancement of Science ;Copyright © 2016, American Association for the Advancement of Science. ;Copyright © 2016, American Association for the Advancement of Science ;ISSN: 0036-8075 ;EISSN: 1095-9203 ;DOI: 10.1126/science.aai9137 ;PMID: 27708058 ;CODEN: SCIEAS

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3
Maternal diabetes during pregnancy and early onset of cardiovascular disease in offspring: population based cohort study with 40 years of follow-up
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Maternal diabetes during pregnancy and early onset of cardiovascular disease in offspring: population based cohort study with 40 years of follow-up

BMJ (Online), 2019-12, Vol.367, p.l6398-l6398 [Peer Reviewed Journal]

Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to ;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. ;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 2019 BMJ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2019 BMJ ;ISSN: 1756-1833 ;ISSN: 0959-8138 ;EISSN: 1756-1833 ;DOI: 10.1136/bmj.l6398 ;PMID: 31801789

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4
Meiotic spindle assembly and chromosome segregation in oocytes
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Article
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Meiotic spindle assembly and chromosome segregation in oocytes

The Journal of cell biology, 2016-12, Vol.215 (5), p.611-619 [Peer Reviewed Journal]

2016 Bennabi et al. ;Distributed under a Creative Commons Attribution 4.0 International License ;2016 Bennabi et al. 2016 ;ISSN: 0021-9525 ;EISSN: 1540-8140 ;DOI: 10.1083/jcb.201607062 ;PMID: 27879467 ;CODEN: JCLBA3

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5
Variation in Prenatal Diagnosis of Congenital Heart Disease in Infants
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Article
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Variation in Prenatal Diagnosis of Congenital Heart Disease in Infants

Pediatrics (Evanston), 2015-08, Vol.136 (2), p.e378-e385 [Peer Reviewed Journal]

Copyright © 2015 by the American Academy of Pediatrics. ;Copyright American Academy of Pediatrics Aug 2015 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2014-3783 ;PMID: 26216324 ;CODEN: PEDIAU

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6
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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7
Temporal trends in survival among infants with critical congenital heart defects
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Article
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Temporal trends in survival among infants with critical congenital heart defects

Pediatrics (Evanston), 2013-05, Vol.131 (5), p.e1502-e1508 [Peer Reviewed Journal]

Copyright American Academy of Pediatrics May 2013 ;Copyright © 2013 by the American Academy of Pediatrics 2013 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2012-3435 ;PMID: 23610203 ;CODEN: PEDIAU

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8
A Targeted Approach for Congenital Cytomegalovirus Screening Within Newborn Hearing Screening
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Article
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A Targeted Approach for Congenital Cytomegalovirus Screening Within Newborn Hearing Screening

Pediatrics (Evanston), 2017-02, Vol.139 (2), p.1-1 [Peer Reviewed Journal]

Copyright © 2017 by the American Academy of Pediatrics. ;Copyright American Academy of Pediatrics Feb 2017 ;Copyright © 2017 by the American Academy of Pediatrics 2017 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2016-2128 ;PMID: 28049114 ;CODEN: PEDIAU

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9
Spontaneous Closure of Patent Ductus Arteriosus in Infants ≤1500 g
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Article
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Spontaneous Closure of Patent Ductus Arteriosus in Infants ≤1500 g

Pediatrics (Evanston), 2017-08, Vol.140 (2) [Peer Reviewed Journal]

Copyright © 2017 by the American Academy of Pediatrics. ;Copyright American Academy of Pediatrics Aug 2017 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2016-4258 ;PMID: 28701390

Digital Resources/Online E-Resources

10
Understanding the gut–kidney axis in nephrolithiasis: an analysis of the gut microbiota composition and functionality of stone formers
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Article
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Understanding the gut–kidney axis in nephrolithiasis: an analysis of the gut microbiota composition and functionality of stone formers

Gut, 2018-12, Vol.67 (12), p.2097-2106 [Peer Reviewed Journal]

Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;2018 Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;ISSN: 0017-5749 ;EISSN: 1468-3288 ;DOI: 10.1136/gutjnl-2017-315734 ;PMID: 29705728

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11
Maternal-fetal transmission and adverse perinatal outcomes in pregnant women infected with Zika virus: prospective cohort study in French Guiana
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Article
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Maternal-fetal transmission and adverse perinatal outcomes in pregnant women infected with Zika virus: prospective cohort study in French Guiana

BMJ, 2018-10, Vol.363, p.k4431-k4431 [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. ;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 2018 BMJ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Attribution - NonCommercial ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to 2018 BMJ ;ISSN: 0959-8138 ;EISSN: 1756-1833 ;EISSN: 1468-5833 ;DOI: 10.1136/bmj.k4431 ;PMID: 30381296

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12
Psychiatric Disorders in Adolescents With Single Ventricle Congenital Heart Disease
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Article
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Psychiatric Disorders in Adolescents With Single Ventricle Congenital Heart Disease

Pediatrics (Evanston), 2017-03, Vol.139 (3), p.1 [Peer Reviewed Journal]

Copyright © 2017 by the American Academy of Pediatrics. ;Copyright American Academy of Pediatrics Mar 2017 ;Copyright © 2017 by the American Academy of Pediatrics 2017 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2016-2241 ;PMID: 28148729 ;CODEN: PEDIAU

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13
Management and investigation of neonatal encephalopathy: 2017 update
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Article
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Management and investigation of neonatal encephalopathy: 2017 update

Archives of disease in childhood. Fetal and neonatal edition, 2017-07, Vol.102 (4), p.F346-F358 [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://www.bmj.com/company/products-services/rights-and-licensing ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/. ;Copyright: 2017 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing ;Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ 2017 ;ISSN: 1359-2998 ;EISSN: 1468-2052 ;DOI: 10.1136/archdischild-2015-309639 ;PMID: 28389438

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14
Strategies for implementing screening for critical congenital heart disease
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Article
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Strategies for implementing screening for critical congenital heart disease

Pediatrics (Evanston), 2011-11, Vol.128 (5), p.e1259-e1267 [Peer Reviewed Journal]

Copyright American Academy of Pediatrics Nov 2011 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2011-1317 ;PMID: 21987707 ;CODEN: PEDIAU

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15
Neurogenetic fetal akinesia and arthrogryposis: genetics, expanding genotype-phenotypes and functional genomics
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Article
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Neurogenetic fetal akinesia and arthrogryposis: genetics, expanding genotype-phenotypes and functional genomics

Journal of medical genetics, 2021-09, Vol.58 (9), p.609-618 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2020-106901 ;PMID: 33060286

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16
Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms
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Article
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Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms

Gut, 2019-05, Vol.68 (5), p.854-865 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;2019 Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0017-5749 ;ISSN: 1468-3288 ;EISSN: 1468-3288 ;DOI: 10.1136/gutjnl-2018-317619 ;PMID: 30661054

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17
Risks and outcomes associated with primary intraocular lens implantation in children under 2 years of age: the IoLunder2 cohort study
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Article
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Risks and outcomes associated with primary intraocular lens implantation in children under 2 years of age: the IoLunder2 cohort study

British journal of ophthalmology, 2015-11, Vol.99 (11), p.1471-1476 [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://www.bmj.com/company/products-services/rights-and-licensing ;Copyright: 2015 Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing ;ISSN: 0007-1161 ;EISSN: 1468-2079 ;DOI: 10.1136/bjophthalmol-2014-306394 ;PMID: 25947553 ;CODEN: BJOPAL

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18
Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data
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Article
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Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data

Archives of disease in childhood. Fetal and neonatal edition, 2018-01, Vol.103 (1), p.F22-F28 [Peer Reviewed Journal]

Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;2018 Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. 2018 ;ISSN: 1359-2998 ;EISSN: 1468-2052 ;DOI: 10.1136/archdischild-2016-311845 ;PMID: 28667189

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19
Rising national prevalence of life-limiting conditions in children in England
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Article
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Rising national prevalence of life-limiting conditions in children in England

Pediatrics (Evanston), 2012-04, Vol.129 (4), p.e923-e929 [Peer Reviewed Journal]

Copyright American Academy of Pediatrics Apr 2012 ;ISSN: 0031-4005 ;EISSN: 1098-4275 ;DOI: 10.1542/peds.2011-2846 ;PMID: 22412035 ;CODEN: PEDIAU

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20
Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)
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Article
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Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)

Journal of medical genetics, 2022-09, Vol.59 (9), p.865-877 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2022 Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2022 ;ISSN: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmedgenet-2020-107623 ;PMID: 34815299

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