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1
Tetralogy of Fallot in infants less than one year old in the Valencia Region (Spain)
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Tetralogy of Fallot in infants less than one year old in the Valencia Region (Spain)

European journal of public health, 2019-11, Vol.29 (Supplement_4) [Peer Reviewed Journal]

The Author(s) 2019. Published by Oxford University Press on behalf of the European Public Health Association. All rights reserved. 2019 ;The Author(s) 2019. Published by Oxford University Press on behalf of the European Public Health Association. All rights reserved. ;ISSN: 1101-1262 ;EISSN: 1464-360X ;DOI: 10.1093/eurpub/ckz186.624

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2
The transcription factor GATA4 promotes myocardial regeneration in neonatal mice
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Article
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The transcription factor GATA4 promotes myocardial regeneration in neonatal mice

EMBO molecular medicine, 2017-02, Vol.9 (2), p.265-279 [Peer Reviewed Journal]

2017 The Authors. Published under the terms of the CC BY 4.0 license ;2017 The Authors. Published under the terms of the CC BY 4.0 license. ;ISSN: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.201606602 ;PMID: 28053183

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3
Educational achievement of children with selected major congenital anomalies and associated factors: a Finnish registry-based study
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Article
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Educational achievement of children with selected major congenital anomalies and associated factors: a Finnish registry-based study

European journal of public health, 2023-12, Vol.33 (6), p.1027-1034 [Peer Reviewed Journal]

The Author(s) 2023. Published by Oxford University Press on behalf of the European Public Health Association. 2023 ;The Author(s) 2023. Published by Oxford University Press on behalf of the European Public Health Association. ;COPYRIGHT 2023 Oxford University Press ;ISSN: 1101-1262 ;ISSN: 1464-360X ;EISSN: 1464-360X ;DOI: 10.1093/eurpub/ckad149 ;PMID: 37594898

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4
Proteome profiling of early gestational plasma reveals novel biomarkers of congenital heart disease
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Proteome profiling of early gestational plasma reveals novel biomarkers of congenital heart disease

EMBO molecular medicine, 2023-12, Vol.15 (12), p.e17745-n/a [Peer Reviewed Journal]

2023 The Authors. Published under the terms of the CC BY 4.0 license ;2023 The Authors. Published under the terms of the CC BY 4.0 license. ;2023. 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: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.202317745 ;PMID: 37840432

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5
Looking at a baby's heart through the lens of the mother's blood
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Article
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Looking at a baby's heart through the lens of the mother's blood

EMBO molecular medicine, 2023-12, Vol.15 (12), p.e18680-n/a [Peer Reviewed Journal]

2023 The Authors. Published under the terms of the CC BY 4.0 license ;2023 The Authors. Published under the terms of the CC BY 4.0 license. ;2023. 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: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.202318680 ;PMID: 37840430

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6
TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT
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TECRL, a new life‐threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT

EMBO molecular medicine, 2016-12, Vol.8 (12), p.1390-1408 [Peer Reviewed Journal]

2016 The Authors. Published under the terms of the CC BY 4.0 license ;2016 The Authors. Published under the terms of the CC BY 4.0 license. ;COPYRIGHT 2016 John Wiley & Sons, Inc. ;2016. 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: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.201505719 ;PMID: 27861123

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7
RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis
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RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis

EMBO molecular medicine, 2023-05, Vol.15 (5), p.e17078-n/a [Peer Reviewed Journal]

2023 The Authors. Published under the terms of the CC BY 4.0 license. ;2023. 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: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.202217078 ;PMID: 37066513

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8
The use of cardiac magnetic resonance imaging (CMRI) for adult congenital heart disease patients: qualitative comparative review
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The use of cardiac magnetic resonance imaging (CMRI) for adult congenital heart disease patients: qualitative comparative review

Clinical medicine (London, England), 2020-03, Vol.20 (2), p.s6-s7 [Peer Reviewed Journal]

2020 © 2020 THE AUTHORS. Published by Elsevier Limited on behalf of the Royal College of Physicians. ;Copyright Royal College of Physicians Mar 2020 ;Royal College of Physicians 2020. All rights reserved. 2020 ;ISSN: 1470-2118 ;EISSN: 1473-4893 ;DOI: 10.7861/clinmed.20-2-s6 ;PMID: 32409337

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9
The transcription factor GATA 4 promotes myocardial regeneration in neonatal mice
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Article
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The transcription factor GATA 4 promotes myocardial regeneration in neonatal mice

EMBO molecular medicine, 2017-02, Vol.9 (2), p.265-279 [Peer Reviewed Journal]

2017. 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: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.201606602

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10
Grown up congenital heart (GUCH) disease: a half century of change
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Article
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Grown up congenital heart (GUCH) disease: a half century of change

Clinical medicine (London, England), 2008-04, Vol.8 (2), p.169-177 [Peer Reviewed Journal]

2008 © 2008 THE AUTHORS. Published by Elsevier Limited on behalf of the Royal College of Physicians. ;2008 Royal College of Physicians 2008 ;ISSN: 1470-2118 ;EISSN: 1473-4893 ;DOI: 10.7861/clinmedicine.8-2-169 ;PMID: 18478862

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