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1
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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2
Epidemiology of valvular heart disease in a Swedish nationwide hospital-based register study
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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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3
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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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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4
The developmental biology of genetic Notch disorders
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The developmental biology of genetic Notch disorders

Development (Cambridge), 2017-05, Vol.144 (10), p.1743-1763 [Peer Reviewed Journal]

2017. Published by The Company of Biologists Ltd. ;Copyright The Company of Biologists Ltd May 15, 2017 ;ISSN: 0950-1991 ;ISSN: 1477-9129 ;EISSN: 1477-9129 ;DOI: 10.1242/dev.148007 ;PMID: 28512196

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5
Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment
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Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment

American journal of clinical dermatology, 2018-02, Vol.19 (1), p.51-66 [Peer Reviewed Journal]

The Author(s) 2017 ;Copyright Springer Science & Business Media Feb 2018 ;ISSN: 1175-0561 ;ISSN: 1179-1888 ;EISSN: 1179-1888 ;DOI: 10.1007/s40257-017-0313-x ;PMID: 28815464

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6
Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms
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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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7
Neonatal Screening in Europe Revisited: An ISNS Perspective on the Current State and Developments Since 2010
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Neonatal Screening in Europe Revisited: An ISNS Perspective on the Current State and Developments Since 2010

International journal of neonatal screening, 2021-03, Vol.7 (1), p.15 [Peer Reviewed Journal]

2021 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 (http://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. ;Distributed under a Creative Commons Attribution 4.0 International License ;2021 by the authors. 2021 ;ISSN: 2409-515X ;EISSN: 2409-515X ;DOI: 10.3390/ijns7010015 ;PMID: 33808002

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8
Five and 10 minute Apgar scores and risks of cerebral palsy and epilepsy: population based cohort study in Sweden
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Five and 10 minute Apgar scores and risks of cerebral palsy and epilepsy: population based cohort study in Sweden

BMJ (Online), 2018-02, Vol.360, p.k207-k207 [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. ;Copyright: 2018 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 2018 BMJ ;ISSN: 0959-8138 ;ISSN: 1756-1833 ;EISSN: 1756-1833 ;DOI: 10.1136/bmj.k207 ;PMID: 29437691

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9
Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness
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Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness

Nature medicine, 2013-03, Vol.19 (3), p.345-350 [Peer Reviewed Journal]

COPYRIGHT 2013 Nature Publishing Group ;COPYRIGHT 2013 Nature Publishing Group ;Copyright Nature Publishing Group Mar 2013 ;ISSN: 1078-8956 ;ISSN: 1546-170X ;EISSN: 1546-170X ;DOI: 10.1038/nm.3106 ;PMID: 23380860

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10
Diagnostic and predictive value of Doppler ultrasound for evaluation of the brain circulation in preterm infants: a systematic review
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Diagnostic and predictive value of Doppler ultrasound for evaluation of the brain circulation in preterm infants: a systematic review

Pediatric research, 2020-03, Vol.87 (Suppl 1), p.50-58 [Peer Reviewed Journal]

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 ;ISSN: 1530-0447 ;EISSN: 1530-0447 ;DOI: 10.1038/s41390-020-0777-x ;PMID: 32218536

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11
Runs of homozygosity implicate autozygosity as a schizophrenia risk factor
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Article
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Runs of homozygosity implicate autozygosity as a schizophrenia risk factor

PLoS genetics, 2012-04, Vol.8 (4), p.e1002656-e1002656 [Peer Reviewed Journal]

COPYRIGHT 2012 Public Library of Science ;2012 Keller et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Keller MC, Simonson MA, Ripke S, Neale BM, Gejman PV, et al. (2012) Runs of Homozygosity Implicate Autozygosity as a Schizophrenia Risk Factor. PLoS Genet 8(4): e1002656. doi:10.1371/journal.pgen.1002656 ;Keller et al. 2012 ;ISSN: 1553-7404 ;ISSN: 1553-7390 ;EISSN: 1553-7404 ;DOI: 10.1371/journal.pgen.1002656 ;PMID: 22511889

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12
Constitutive activation of WASp in X-linked neutropenia renders neutrophils hyperactive
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Article
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Constitutive activation of WASp in X-linked neutropenia renders neutrophils hyperactive

The Journal of clinical investigation, 2018-09, Vol.128 (9), p.4115-4131 [Peer Reviewed Journal]

COPYRIGHT 2018 American Society for Clinical Investigation ;COPYRIGHT 2018 American Society for Clinical Investigation ;Copyright American Society for Clinical Investigation Sep 2018 ;Copyright © 2018, American Society for Clinical Investigation 2018 American Society for Clinical Investigation ;ISSN: 0021-9738 ;ISSN: 1558-8238 ;EISSN: 1558-8238 ;DOI: 10.1172/jci64772 ;PMID: 30124469

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13
Major adverse events and atrial tachycardia in Ebstein’s anomaly predicted by cardiovascular magnetic resonance
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Article
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Major adverse events and atrial tachycardia in Ebstein’s anomaly predicted by cardiovascular magnetic resonance

Heart (British Cardiac Society), 2018-01, Vol.104 (1), p.37-44 [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. ;Copyright: 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. ;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: 1355-6037 ;ISSN: 1468-201X ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2017-311274 ;PMID: 28684436

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14
Further delineation of the KAT6B molecular and phenotypic spectrum
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Article
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Further delineation of the KAT6B molecular and phenotypic spectrum

European journal of human genetics : EJHG, 2015-09, Vol.23 (9), p.1165-1170 [Peer Reviewed Journal]

Copyright Nature Publishing Group Sep 2015 ;Distributed under a Creative Commons Attribution 4.0 International License ;Copyright © 2015 Macmillan Publishers Limited 2015 Macmillan Publishers Limited ;ISSN: 1018-4813 ;ISSN: 1476-5438 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2014.248 ;PMID: 25424711

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15
Associations between antinuclear antibody staining patterns and clinical features of systemic lupus erythematosus: analysis of a regional Swedish register
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Associations between antinuclear antibody staining patterns and clinical features of systemic lupus erythematosus: analysis of a regional Swedish register

BMJ open, 2013-01, Vol.3 (10), p.e003608-e003608 [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 2013 This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) 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/3.0/ Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;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 2013 ;ISSN: 2044-6055 ;EISSN: 2044-6055 ;DOI: 10.1136/bmjopen-2013-003608 ;PMID: 24163206

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16
China's community-based strategy of universal preconception care in rural areas at a population level using a novel risk classification system for stratifying couples´ preconception health status
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China's community-based strategy of universal preconception care in rural areas at a population level using a novel risk classification system for stratifying couples´ preconception health status

BMC health services research, 2016-12, Vol.16 (1), p.689-689, Article 689 [Peer Reviewed Journal]

COPYRIGHT 2016 BioMed Central Ltd. ;Copyright BioMed Central 2016 ;info:eu-repo/semantics/openAccess ;The Author(s). 2016 ;ISSN: 1472-6963 ;EISSN: 1472-6963 ;DOI: 10.1186/s12913-016-1930-4 ;PMID: 28031048

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17
Translational balancing questioned: Unaltered glycosylation during disulfiram treatment in mannosyl‐oligosaccharide alpha‐1,2‐mannnosidase‐congenital disorders of glycosylation (MAN1B1‐CDG)
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Article
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Translational balancing questioned: Unaltered glycosylation during disulfiram treatment in mannosyl‐oligosaccharide alpha‐1,2‐mannnosidase‐congenital disorders of glycosylation (MAN1B1‐CDG)

JIMD reports, 2021-07, Vol.60 (1), p.42-55 [Peer Reviewed Journal]

2021 The Authors. published by John Wiley & Sons Ltd on behalf of SSIEM. ;2021 The Authors. JIMD Reports published by John Wiley & Sons Ltd on behalf of SSIEM. ;2021. 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. ;ISSN: 2192-8312 ;ISSN: 2192-8304 ;EISSN: 2192-8312 ;DOI: 10.1002/jmd2.12213 ;PMID: 34258140

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18
Immobilization of Dystrophin and Laminin α2-Chain Deficient Zebrafish Larvae In Vivo Prevents the Development of Muscular Dystrophy
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Article
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Immobilization of Dystrophin and Laminin α2-Chain Deficient Zebrafish Larvae In Vivo Prevents the Development of Muscular Dystrophy

PloS one, 2015-11, Vol.10 (11), p.e0139483-e0139483 [Peer Reviewed Journal]

2015 Li, Arner. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2015 Li, Arner 2015 Li, Arner ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0139483 ;PMID: 26536238

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19
Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association
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Article
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Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association

PloS one, 2014-01, Vol.9 (1), p.e85313 [Peer Reviewed Journal]

COPYRIGHT 2014 Public Library of Science ;COPYRIGHT 2014 Public Library of Science ;2014 Winberg et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2014 Winberg et al 2014 Winberg et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0085313 ;PMID: 24416387

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20
Cause-specific infant mortality in a population-based Swedish study of term and post-term births: the contribution of gestational age and birth weight
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Article
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Cause-specific infant mortality in a population-based Swedish study of term and post-term births: the contribution of gestational age and birth weight

BMJ open, 2012-01, Vol.2 (4), p.e001152 [Peer Reviewed Journal]

2012, 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. ;2012 2012, 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. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2012, 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. 2012 ;ISSN: 2044-6055 ;EISSN: 2044-6055 ;DOI: 10.1136/bmjopen-2012-001152 ;PMID: 22763662

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