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1
B Genetic and phenotypic architecture of myocardial trabeculation in the left and right ventricles
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B Genetic and phenotypic architecture of myocardial trabeculation in the left and right ventricles

Heart (British Cardiac Society), 2024-06, Vol.110 (Suppl 3), p.A287-A289 [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: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2024-BCS.286

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2
91 Findings and outcomes of patients undergoing ctcoronary angiography
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91 Findings and outcomes of patients undergoing ctcoronary angiography

Heart (British Cardiac Society), 2024-06, Vol.110 (Suppl 3), p.A95-A95 [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: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2024-BCS.91

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3
This Week in the Journal
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This Week in the Journal

The New England journal of medicine, 2024-05, Vol.390 (17), p.1548 [Peer Reviewed Journal]

Copyright © 2024 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMtwj240502

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4
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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5
Identification of novel variations in three cases with rare inherited neuromuscular disorder
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Identification of novel variations in three cases with rare inherited neuromuscular disorder

Experimental and therapeutic medicine, 2024-06, Vol.27 (6)

Copyright Spandidos Publications UK Ltd. 2024 ;Copyright: © 2024 Chen et al. 2024 ;ISSN: 1792-0981 ;EISSN: 1792-1015 ;DOI: 10.3892/etm.2024.12558 ;PMID: 38756899

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6
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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7
Lymphatic malformations: mechanistic insights and evolving therapeutic frontiers
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Lymphatic malformations: mechanistic insights and evolving therapeutic frontiers

The Journal of clinical investigation, 2024-03, Vol.134 (6), p.1-9 [Peer Reviewed Journal]

Copyright American Society for Clinical Investigation Mar 2024 ;ISSN: 0021-9738 ;ISSN: 1558-8238 ;EISSN: 1558-8238 ;DOI: 10.1172/JCI172844

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8
Preconception counselling in women of reproductive age attending cardiology clinics in Scotland
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Preconception counselling in women of reproductive age attending cardiology clinics in Scotland

Heart (British Cardiac Society), 2024-04, p.heartjnl-2023-323666 [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: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2023-323666 ;PMID: 38627021

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9
Test-Retest of the Spot Vision Screener among Children with Ophthalmological Diseases including Strabismus
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Test-Retest of the Spot Vision Screener among Children with Ophthalmological Diseases including Strabismus

Journal of ophthalmology, 2024-05, Vol.2024, p.2173860-2173860 [Peer Reviewed Journal]

Copyright © 2024 Mika Ichimura et al. ;COPYRIGHT 2024 Hindawi Limited ;Copyright © 2024 Mika Ichimura et al. 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. ;Copyright © 2024 Mika Ichimura et al. 2024 ;ISSN: 2090-004X ;EISSN: 2090-0058 ;DOI: 10.1155/2024/2173860 ;PMID: 38741691

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10
Systematic reanalysis of copy number losses of uncertain clinical significance
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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
Discerning clinicopathological features of congenital neutropenia syndromes: an approach to diagnostically challenging differential diagnoses
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Article
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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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12
Bilateral congenital knee dislocation
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Article
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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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13
Newborn Skin: Part I. Common Rashes and Skin Changes
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Newborn Skin: Part I. Common Rashes and Skin Changes

American family physician, 2024-03, Vol.109 (3), p.212-216 [Peer Reviewed Journal]

2024. American Academy of Family Physicians ;ISSN: 0002-838X ;EISSN: 1532-0650 ;PMID: 38574210

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14
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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15
Increased enhancer-promoter interactions during developmental enhancer activation in mammals
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Article
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Increased enhancer-promoter interactions during developmental enhancer activation in mammals

Nature genetics, 2024-04, Vol.56 (4), p.675-3 [Peer Reviewed Journal]

2024. The Author(s), under exclusive licence to Springer Nature America, Inc. ;Copyright Nature Publishing Group Apr 2024 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/s41588-024-01681-2 ;PMID: 38509385

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16
Syphilis Complicating Pregnancy and Congenital Syphilis
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Article
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Syphilis Complicating Pregnancy and Congenital Syphilis

The New England journal of medicine, 2024-04, Vol.390 (13), p.1251-1251 [Peer Reviewed Journal]

Copyright © 2024 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMc2401932 ;PMID: 38598598

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17
A HGF Mutation in the Familial Case of Primary Lymphedema: A Report
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Article
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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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18
37 SMPD4 regulates mitotic nuclear envelope dynamics and its loss causes microcephaly and diabetes
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Article
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37 SMPD4 regulates mitotic nuclear envelope dynamics and its loss causes microcephaly and diabetes

BMJ paediatrics open, 2024-05, Vol.8 (Suppl 4), p.A13-A14 [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. ;EISSN: 2399-9772 ;DOI: 10.1136/bmjpo-2024-ASPED.37

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19
Non-cardiac birth defects and long-term risk of cardiovascular hospitalisation
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Article
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Non-cardiac birth defects and long-term risk of cardiovascular hospitalisation

Heart (British Cardiac Society), 2024-05, p.heartjnl-2023-323632 [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: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2023-323632 ;PMID: 38772572

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20
Chiari I Malformation and Intramedullary Hemorrhage in a female Patient with Klippel Trenaunay Syndrome: A Rare Case Report Study
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Article
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Chiari I Malformation and Intramedullary Hemorrhage in a female Patient with Klippel Trenaunay Syndrome: A Rare Case Report Study

International journal of caring sciences, 2024-04, Vol.17 (1), p.603-609 [Peer Reviewed Journal]

2024. 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: 1791-5201 ;EISSN: 1792-037X

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