skip to main content
Language:
Search Limited to: Search Limited to: Resource type Show Results with: Show Results with: Search type Index

Results 1 - 20 of 550  for All Library Resources

Results 1 2 3 4 5 next page
Refined by: New Records: New From Last Month remove New Records: New From Last 3 Month remove
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Congenital Corneal Staphyloma: A Comprehensive Histopathologic Assessment Including Associated Anterior Segment Abnormalities
Material Type:
Article
Add to My Research

Congenital Corneal Staphyloma: A Comprehensive Histopathologic Assessment Including Associated Anterior Segment Abnormalities

Journal of pediatric ophthalmology and strabismus, 2024-05, Vol.61 (3), p.e28-e32 [Peer Reviewed Journal]

Copyright 2024, SLACK Incorporated ;ISSN: 0191-3913 ;EISSN: 1938-2405 ;DOI: 10.3928/01913913-20240403-01

Full text available

2
How Will Artificial Intelligence Shape the Future of Decision-Making in Congenital Heart Disease?
Material Type:
Article
Add to My Research

How Will Artificial Intelligence Shape the Future of Decision-Making in Congenital Heart Disease?

Journal of clinical medicine, 2024-01, Vol.13 (10), p.2996 [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: 2077-0383 ;DOI: 10.3390/jcm13102996

Full text available

3
The prescription of valproate: risk of harm
Material Type:
Article
Add to My Research

The prescription of valproate: risk of harm

Lancet neurology, 2024-06, Vol.23 (6), p.557-558 [Peer Reviewed Journal]

2024. Elsevier Ltd ;ISSN: 1474-4422 ;EISSN: 1474-4465 ;DOI: 10.1016/S1474-4422(24)00141-8 ;PMID: 38760089

Digital Resources/Online E-Resources

4
A Humanized and Viable Animal Model for Congenital Adrenal Hyperplasia–CYP21A2-R484Q Mutant Mouse
Material Type:
Article
Add to My Research

A Humanized and Viable Animal Model for Congenital Adrenal Hyperplasia–CYP21A2-R484Q Mutant Mouse

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5062 [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/ijms25105062

Full text available

5
This Week in the Journal
Material Type:
Article
Add to My Research

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

Full text available

6
B.3 Neuroimaging markers of cerebrovascular disease and cognition in adults with moderate-great complexity congenital heart disease
Material Type:
Article
Add to My Research

B.3 Neuroimaging markers of cerebrovascular disease and cognition in adults with moderate-great complexity congenital heart disease

Canadian journal of neurological sciences, 2024-06, Vol.51 (s1), p.S5-S5 [Peer Reviewed Journal]

The Author(s), 2024. Published by Cambridge University Press on behalf of Canadian Neurological Sciences Federation ;ISSN: 0317-1671 ;EISSN: 2057-0155 ;DOI: 10.1017/cjn.2024.82

Digital Resources/Online E-Resources

7
Oral Health-Related Quality of Life in Rare Disorders of Congenital Facial Weakness
Material Type:
Article
Add to My Research

Oral Health-Related Quality of Life in Rare Disorders of Congenital Facial Weakness

International journal of environmental research and public health, 2024-01, Vol.21 (5), p.615 [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: 1661-7827 ;EISSN: 1660-4601 ;DOI: 10.3390/ijerph21050615

Full text available

8
Unilateral Glaucoma Without Facial Angioma in a Pediatric Patient: A Suspected Sturge-Weber Syndrome Variant
Material Type:
Article
Add to My Research

Unilateral Glaucoma Without Facial Angioma in a Pediatric Patient: A Suspected Sturge-Weber Syndrome Variant

Journal of pediatric ophthalmology and strabismus, 2024-05, Vol.61 (3), p.e19-e22 [Peer Reviewed Journal]

Copyright 2024, SLACK Incorporated ;ISSN: 0191-3913 ;EISSN: 1938-2405 ;DOI: 10.3928/01913913-20240301-01

Full text available

9
Ultrasonic Evaluation of the Achilles Tendon in Patients Treated for Congenital Clubfoot: Comparison between Patients Treated with Plaster Alone, Achilles Tenotomy, and Z-Plasty Lengthening
Material Type:
Article
Add to My Research

Ultrasonic Evaluation of the Achilles Tendon in Patients Treated for Congenital Clubfoot: Comparison between Patients Treated with Plaster Alone, Achilles Tenotomy, and Z-Plasty Lengthening

Children (Basel), 2024-01, Vol.11 (5), p.580 [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: 2227-9067 ;DOI: 10.3390/children11050580

Full text available

10
Identification of novel variations in three cases with rare inherited neuromuscular disorder
Material Type:
Article
Add to My Research

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

Full text available

11
Is Cardiac Transplantation Still a Contraindication in Patients with Muscular Dystrophy-Related End-Stage Dilated Cardiomyopathy? A Systematic Review
Material Type:
Article
Add to My Research

Is Cardiac Transplantation Still a Contraindication in Patients with Muscular Dystrophy-Related End-Stage Dilated Cardiomyopathy? A Systematic Review

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5289 [Peer Reviewed Journal]

2024 by the author. 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/ijms25105289

Full text available

12
Macrocephaly and Finger Changes: A Narrative Review
Material Type:
Article
Add to My Research

Macrocephaly and Finger Changes: A Narrative Review

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5567 [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/ijms25105567

Full text available

13
Altered Serum Proteins Suggest Inflammation, Fibrogenesis and Angiogenesis in Adult Patients with a Fontan Circulation
Material Type:
Article
Add to My Research

Altered Serum Proteins Suggest Inflammation, Fibrogenesis and Angiogenesis in Adult Patients with a Fontan Circulation

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5416 [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/ijms25105416

Full text available

14
Normoxic Management during Cardiopulmonary Bypass Does Not Reduce Cerebral Mitochondrial Dysfunction in Neonatal Swine
Material Type:
Article
Add to My Research

Normoxic Management during Cardiopulmonary Bypass Does Not Reduce Cerebral Mitochondrial Dysfunction in Neonatal Swine

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5466 [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/ijms25105466

Full text available

15
Molecular Mechanisms of Fetal and Neonatal Lupus: A Narrative Review of an Autoimmune Disease Transferal across the Placenta
Material Type:
Article
Add to My Research

Molecular Mechanisms of Fetal and Neonatal Lupus: A Narrative Review of an Autoimmune Disease Transferal across the Placenta

International journal of molecular sciences, 2024-05, Vol.25 (10), p.5224 [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/ijms25105224

Full text available

16
Test-Retest of the Spot Vision Screener among Children with Ophthalmological Diseases including Strabismus
Material Type:
Article
Add to My Research

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

Journal of ophthalmology, 2024, 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

Full text available

17
Non-cardiac birth defects and long-term risk of cardiovascular hospitalisation
Material Type:
Article
Add to My Research

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

Full text available

18
Clinical application of paediatric serum troponin T testing
Material Type:
Article
Add to My Research

Clinical application of paediatric serum troponin T testing

Archives of disease in childhood, 2024-05, p.archdischild-2023-326719 [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-2023-326719 ;PMID: 38719347

Full text available

19
Editorial on the Special Issue “Heme Metabolism and Porphyria”
Material Type:
Article
Add to My Research

Editorial on the Special Issue “Heme Metabolism and Porphyria”

Life (Basel, Switzerland), 2024-01, Vol.14 (5), p.581 [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: 2075-1729 ;DOI: 10.3390/life14050581

Full text available

20
Brugada Syndrome and Pulmonary Atresia with Intact Interventricular Septum: Fortuitous Finding or New Genetic Connection?
Material Type:
Article
Add to My Research

Brugada Syndrome and Pulmonary Atresia with Intact Interventricular Septum: Fortuitous Finding or New Genetic Connection?

Genes, 2024-01, Vol.15 (5), p.638 [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: 2073-4425 ;DOI: 10.3390/genes15050638

Full text available

Results 1 - 20 of 550  for All Library Resources

Results 1 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Refine My Results

Creation Date 

From To

New Records 

  1. New From Last Week  (121)
  2. More options open sub menu

Searching Remote Databases, Please Wait