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Results 21 - 40 of 1,246  for All Library Resources

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21
Risk and time preferences in individuals with lifestyle-related and non-lifestyle-related cardiovascular diseases: a pilot study
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Risk and time preferences in individuals with lifestyle-related and non-lifestyle-related cardiovascular diseases: a pilot study

BMJ open, 2024-05, Vol.14 (5), p.e080867 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. 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. ;ISSN: 2044-6055 ;EISSN: 2044-6055 ;DOI: 10.1136/bmjopen-2023-080867

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22
Disease severity impacts perceived quality of life in congenital diaphragmatic hernia: a prospective observational study
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Disease severity impacts perceived quality of life in congenital diaphragmatic hernia: a prospective observational study

Archives of disease in childhood, 2024-04, p.archdischild-2024-326906 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;2024 Author(s) (or their employer(s)) 2024. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0003-9888 ;EISSN: 1468-2044 ;DOI: 10.1136/archdischild-2024-326906 ;PMID: 38589198

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23
Prenatal phenotype of a homozygous nonsense MPDZ variant in a fetus with severe congenital hydrocephalus
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Prenatal phenotype of a homozygous nonsense MPDZ variant in a fetus with severe congenital hydrocephalus

Prenatal diagnosis, 2024-05, Vol.44 (5), p.657 [Peer Reviewed Journal]

2024 John Wiley & Sons Ltd. ;EISSN: 1097-0223 ;DOI: 10.1002/pd.6546 ;PMID: 38498110

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24
Congenital Haemostasis Disorders and Urology Surgery: Is It Safe?
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Article
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Congenital Haemostasis Disorders and Urology Surgery: Is It Safe?

Journal of clinical medicine, 2024-04, Vol.13 (8), p.2357 [Peer Reviewed Journal]

2024 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 (https://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. ;ISSN: 2077-0383 ;EISSN: 2077-0383 ;DOI: 10.3390/jcm13082357 ;PMID: 38673628

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25
Matching actions to needs: shifting policy responses to the changing health needs of Chinese children and adolescents
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Matching actions to needs: shifting policy responses to the changing health needs of Chinese children and adolescents

The Lancet (British edition), 2024-05, Vol.403 (10438), p.1808-1820 [Peer Reviewed Journal]

2024 Elsevier Ltd ;Copyright © 2024 Elsevier Ltd. All rights reserved, including those for text and data mining, AI training, and similar technologies. ;2024. Elsevier Ltd ;ISSN: 0140-6736 ;EISSN: 1474-547X ;DOI: 10.1016/S0140-6736(23)02894-5 ;PMID: 38643776

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26
PfAgo-Based Zika Virus Detection
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Article
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PfAgo-Based Zika Virus Detection

Viruses, 2024-03, Vol.16 (4), p.539 [Peer Reviewed Journal]

2024 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 (https://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. ;2024 by the authors. 2024 ;EISSN: 1999-4915 ;DOI: 10.3390/v16040539 ;PMID: 38675882

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27
The burden of psychological trauma and post-traumatic stress disorder among adults with congenital heart disease: PTSD in ACHD
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The burden of psychological trauma and post-traumatic stress disorder among adults with congenital heart disease: PTSD in ACHD

The American journal of cardiology, 2024-05, Vol.219, p.9-16 [Peer Reviewed Journal]

2024 ;Copyright © 2024. Published by Elsevier Inc. ;Copyright Elsevier Limited May 15, 2024 ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2024.03.007 ;PMID: 38458583

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28
Hip Joint Stability during and after Femoral Lengthening in Congenital Femoral Deficiency
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Article
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Hip Joint Stability during and after Femoral Lengthening in Congenital Femoral Deficiency

Children (Basel), 2024-04, Vol.11 (4), p.500 [Peer Reviewed Journal]

2024 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 (https://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. ;ISSN: 2227-9067 ;EISSN: 2227-9067 ;DOI: 10.3390/children11040500 ;PMID: 38671717

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29
Editorial: Celebrating Diversity and Advancements in Pediatric Cardiology-A Journey through Specialized Research
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Article
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Editorial: Celebrating Diversity and Advancements in Pediatric Cardiology-A Journey through Specialized Research

Children (Basel), 2024-04, Vol.11 (4), p.455 [Peer Reviewed Journal]

2024 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 (https://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. ;ISSN: 2227-9067 ;EISSN: 2227-9067 ;DOI: 10.3390/children11040455 ;PMID: 38671672

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30
A redeemed strategy for molecular autopsy in unexplained infant deaths
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A redeemed strategy for molecular autopsy in unexplained infant deaths

Journal of translational medicine, 2024-04, Vol.22 (1), p.325-325 [Peer Reviewed Journal]

COPYRIGHT 2024 BioMed Central Ltd. ;2024. This work is licensed 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. ;This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2024 ;ISSN: 1479-5876 ;EISSN: 1479-5876 ;DOI: 10.1186/s12967-024-05130-w ;PMID: 38566140

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31
Population-based retrospective cohort study on community-acquired pneumonia hospitalization in children with a ventricular septal defect
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Article
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Population-based retrospective cohort study on community-acquired pneumonia hospitalization in children with a ventricular septal defect

Scientific reports, 2024-04, Vol.14 (1), p.9307-9307 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. 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) 2024 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-59510-9 ;PMID: 38654012

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32
Jejunal Diverticulosis: An Atypical Lead Point for Small Bowel Volvulus
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Article
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Jejunal Diverticulosis: An Atypical Lead Point for Small Bowel Volvulus

Curēus (Palo Alto, CA), 2024-03, Vol.16 (3), p.e56125 [Peer Reviewed Journal]

Copyright © 2024, Agarwal et al. ;Copyright © 2024, Agarwal et al. This work is published under https://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: 2168-8184 ;EISSN: 2168-8184 ;DOI: 10.7759/cureus.56125 ;PMID: 38618384

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33
Exploring the Implications of Golgi Apparatus Dysfunction in Bone Diseases
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Article
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Exploring the Implications of Golgi Apparatus Dysfunction in Bone Diseases

Curēus (Palo Alto, CA), 2024-03, Vol.16 (3), p.e56982-e56982 [Peer Reviewed Journal]

Copyright © 2024, Iacobescu et al. ;Copyright © 2024, Iacobescu et al. This work is published under https://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. ;Copyright © 2024, Iacobescu et al. 2024 Iacobescu et al. ;ISSN: 2168-8184 ;EISSN: 2168-8184 ;DOI: 10.7759/cureus.56982 ;PMID: 38665758

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34
The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease
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Article
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The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease

Journal of human genetics, 2024-05, Vol.69 (5), p.215-222 [Peer Reviewed Journal]

2024. The Author(s). ;The Author(s) 2024. corrected publication 2024. 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) 2024, corrected publication 2024 ;ISSN: 1434-5161 ;EISSN: 1435-232X ;DOI: 10.1038/s10038-024-01225-w ;PMID: 38409496

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35
Characteristics, predictors and outcomes of new-onset QT prolongation in sepsis: a multicenter retrospective study
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Characteristics, predictors and outcomes of new-onset QT prolongation in sepsis: a multicenter retrospective study

Critical care (London, England), 2024-04, Vol.28 (1), p.115-115 [Peer Reviewed Journal]

2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;2024. This work is licensed 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) 2024 ;ISSN: 1364-8535 ;EISSN: 1466-609X ;DOI: 10.1186/s13054-024-04879-2 ;PMID: 38594724

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36
The First Korean Case with Cardiac, Facial, and Digital Anomalies with Developmental Delay Caused by De Novo TRAF7 p.Arg655Gln Variant
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The First Korean Case with Cardiac, Facial, and Digital Anomalies with Developmental Delay Caused by De Novo TRAF7 p.Arg655Gln Variant

International journal of molecular sciences, 2024-04, Vol.25 (7), p.3701 [Peer Reviewed Journal]

2024 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 (https://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. ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms25073701 ;PMID: 38612512

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37
Thymic Atrophy and Immune Dysregulation in Infants with Complex Congenital Heart Disease
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Article
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Thymic Atrophy and Immune Dysregulation in Infants with Complex Congenital Heart Disease

Journal of clinical immunology, 2024-03, Vol.44 (3), p.69-69 [Peer Reviewed Journal]

The Author(s) 2024 ;2024. The Author(s). ;The Author(s) 2024. 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: 0271-9142 ;EISSN: 1573-2592 ;DOI: 10.1007/s10875-024-01662-4 ;PMID: 38393459

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38
Identification of a novel de novo mutation in SOX4 for syndromic tooth agenesis
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Article
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Identification of a novel de novo mutation in SOX4 for syndromic tooth agenesis

Clinical oral investigations, 2024-04, Vol.28 (5), p.287-287 [Peer Reviewed Journal]

The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. ;2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature. ;ISSN: 1432-6981 ;EISSN: 1436-3771 ;DOI: 10.1007/s00784-024-05659-6 ;PMID: 38684576

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39
Resilience in patients and family caregivers living with congenital disorders of glycosylation (CDG): a quantitative study using the brief resilience coping scale (BRCS)
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Article
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Resilience in patients and family caregivers living with congenital disorders of glycosylation (CDG): a quantitative study using the brief resilience coping scale (BRCS)

Orphanet journal of rare diseases, 2024-03, Vol.19 (1), p.98-98 [Peer Reviewed Journal]

2024. The Author(s). ;2024. This work is licensed 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) 2024 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-024-03043-x ;PMID: 38439013

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40
Autosomal recessive non‐syndromic hearing loss genes in Pakistan during the previous three decades
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Article
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Autosomal recessive non‐syndromic hearing loss genes in Pakistan during the previous three decades

Journal of cellular and molecular medicine, 2024-04, Vol.28 (8), p.e18119-n/a [Peer Reviewed Journal]

2024 The Authors. published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;2024 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;2024. 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: 1582-1838 ;EISSN: 1582-4934 ;DOI: 10.1111/jcmm.18119 ;PMID: 38534090

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