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1
Procedural elements of the complete examination and screening of the healthy term neonate: a protocol for a scoping review and evidence map
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Procedural elements of the complete examination and screening of the healthy term neonate: a protocol for a scoping review and evidence map

BMJ paediatrics open, 2024-06, Vol.8 (1), p.e002286 [Peer Reviewed Journal]

2024 Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: 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. ;Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ. ;ISSN: 2399-9772 ;EISSN: 2399-9772 ;DOI: 10.1136/bmjpo-2023-002286

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2
Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins
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Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins

International journal of molecular sciences, 2024-06, Vol.25 (11), p.5836 [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/ijms25115836

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3
The Increased Burden of Rare Variants in Four Matrix Metalloproteinase-Related Genes in Childhood Glaucoma Suggests a Complex Genetic Inheritance of the Disease
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The Increased Burden of Rare Variants in Four Matrix Metalloproteinase-Related Genes in Childhood Glaucoma Suggests a Complex Genetic Inheritance of the Disease

International journal of molecular sciences, 2024-06, Vol.25 (11), p.5757 [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/ijms25115757

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4
Endothelial-to-Mesenchymal Transition in an Hereditary Hemorrhagic Telangiectasia-like Pediatric Case of Multiple Pulmonary Arteriovenous Malformations
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Endothelial-to-Mesenchymal Transition in an Hereditary Hemorrhagic Telangiectasia-like Pediatric Case of Multiple Pulmonary Arteriovenous Malformations

International journal of molecular sciences, 2024-06, Vol.25 (11), p.6163 [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/ijms25116163

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5
Phenolic Compounds from Cherries and Berries for Chronic Disease Management and Cardiovascular Risk Reduction
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Phenolic Compounds from Cherries and Berries for Chronic Disease Management and Cardiovascular Risk Reduction

Nutrients, 2024-01, Vol.16 (11), p.1597 [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. ;EISSN: 2072-6643 ;DOI: 10.3390/nu16111597

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6
Top 10 research priorities for congenital diaphragmatic hernia in Australia: James Lind Alliance Priority Setting Partnership
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Top 10 research priorities for congenital diaphragmatic hernia in Australia: James Lind Alliance Priority Setting Partnership

Archives of disease in childhood. Fetal and neonatal edition, 2024-06, p.fetalneonatal-2024-327108 [Peer Reviewed Journal]

2024 Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: 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: 1359-2998 ;EISSN: 1468-2052 ;DOI: 10.1136/archdischild-2024-327108

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7
Severe case of aplasia cutis congenita
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Severe case of aplasia cutis congenita

Archives of disease in childhood. Fetal and neonatal edition, 2024-04, p.fetalneonatal-2024-327067 [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: 1359-2998 ;EISSN: 1468-2052 ;DOI: 10.1136/archdischild-2024-327067 ;PMID: 38604652

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8
Zebrafish Congenital Heart Disease Models: Opportunities and Challenges
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Zebrafish Congenital Heart Disease Models: Opportunities and Challenges

International journal of molecular sciences, 2024-06, Vol.25 (11), p.5943 [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/ijms25115943

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9
Contraction or sequence variant of an intergenic repeat-Alu element leads to inherited thyroid disease
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Contraction or sequence variant of an intergenic repeat-Alu element leads to inherited thyroid disease

Nature genetics, 2024-05, Vol.56 (5), p.738-739 [Peer Reviewed Journal]

Copyright Nature Publishing Group May 2024 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-024-01723-9 ;PMID: 38714867

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10
Systematic reanalysis of copy number losses of uncertain clinical significance
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Article
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Systematic reanalysis of copy number losses of uncertain clinical significance

Journal of medical genetics, 2024-04, p.jmg-2023-109559 [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: 0022-2593 ;EISSN: 1468-6244 ;DOI: 10.1136/jmg-2023-109559 ;PMID: 38604752

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11
Transcatheter Embolization in Congenital Cardiovascular Malformations—Variable Use of Vascular Plugs
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Transcatheter Embolization in Congenital Cardiovascular Malformations—Variable Use of Vascular Plugs

Cardiovascular therapeutics, 2024-05, Vol.2024 [Peer Reviewed Journal]

Copyright © 2024 Jochen Pfeifer et al. ;COPYRIGHT 2024 Hindawi Limited ;Copyright © 2024 Jochen Pfeifer et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0 ;ISSN: 1755-5914 ;EISSN: 1755-5922 ;DOI: 10.1155/2024/4778469

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12
Discerning clinicopathological features of congenital neutropenia syndromes: an approach to diagnostically challenging differential diagnoses
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Discerning clinicopathological features of congenital neutropenia syndromes: an approach to diagnostically challenging differential diagnoses

Journal of clinical pathology, 2024-04, p.jcp-2022-208686 [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: 0021-9746 ;EISSN: 1472-4146 ;DOI: 10.1136/jcp-2022-208686 ;PMID: 38589208

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13
Advanced magnetic resonance imaging detects altered placental development in pregnancies affected by congenital heart disease
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Article
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Advanced magnetic resonance imaging detects altered placental development in pregnancies affected by congenital heart disease

Scientific reports, 2024-05, Vol.14 (1), p.12357-12 [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 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-024-63087-8 ;PMID: 38811636

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14
Bilateral congenital knee dislocation
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Bilateral congenital knee dislocation

Archives of disease in childhood. Fetal and neonatal edition, 2024-04, p.fetalneonatal-2024-327076 [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: 1359-2998 ;EISSN: 1468-2052 ;DOI: 10.1136/archdischild-2024-327076 ;PMID: 38636982

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15
At a glance
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Article
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At a glance

British journal of ophthalmology, 2023-09, Vol.107 (9), p.i-ii [Peer Reviewed Journal]

2023 Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0007-1161 ;EISSN: 1468-2079 ;DOI: 10.1136/bjo-2023-324331

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16
Lumbar Spinal Stenosis: Diagnosis and Management
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Article
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Lumbar Spinal Stenosis: Diagnosis and Management

American family physician, 2024-04, Vol.109 (4), p.350-359 [Peer Reviewed Journal]

2024. American Academy of Family Physicians ;ISSN: 0002-838X ;EISSN: 1532-0650 ;PMID: 38648834

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17
Case Report of Suspected Gonadal Mosaicism in FOXP1-Related Neurodevelopmental Disorder
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Case Report of Suspected Gonadal Mosaicism in FOXP1-Related Neurodevelopmental Disorder

International journal of molecular sciences, 2024-06, Vol.25 (11), p.5709 [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/ijms25115709

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18
A HGF Mutation in the Familial Case of Primary Lymphedema: A Report
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A HGF Mutation in the Familial Case of Primary Lymphedema: A Report

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5464 [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/ijms25105464 ;PMID: 38791500

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19
Non-invasive estimation of pulmonary hypertension and clinical deterioration risk in pediatric congenital heart disease: Development and validation of predictive tools
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Non-invasive estimation of pulmonary hypertension and clinical deterioration risk in pediatric congenital heart disease: Development and validation of predictive tools

Chinese medical journal, 2024-04, Vol.137 (11), p.1384-1386 [Peer Reviewed Journal]

Copyright © 2024 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0366-6999 ;EISSN: 2542-5641 ;DOI: 10.1097/CM9.0000000000003070 ;PMID: 38595105

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20
Benzathine penicillin G stockouts and other barriers to documented syphilis treatment in pregnancy in Zambia
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Benzathine penicillin G stockouts and other barriers to documented syphilis treatment in pregnancy in Zambia

PloS one, 2024-06, Vol.19 (6), p.e0304576-e0304576 [Peer Reviewed Journal]

COPYRIGHT 2024 Public Library of Science ;2024 Jones 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. ;2024 Jones et al 2024 Jones et al ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0304576

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