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

Results 21 - 40 of 17,683  for All Library Resources

Sorted by: Sorted by: RelevanceOr hit Enter to replace sort method
previous page 1 Results 2 3 4 5 next page
Show only
Refined by: Database: PubMed Central remove
Result Number Material Type Add to My Shelf Action Record Details and Options
21
33 Optimising patient experience within the achd outreach network: a questionnaire based study
33 Optimising patient experience within the achd outreach network: a questionnaire based study
Material Type:
Article 		Add to My Research

33 Optimising patient experience within the achd outreach network: a questionnaire based study

Heart (British Cardiac Society), 2018-02, Vol.104 (Suppl 2), p.A12 [Peer Reviewed Journal]

2018, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;Copyright: 2018 © 2018, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2017-BCCA.33

Full text available

Citations Cited by
22
Self-assembling human heart organoids for the modeling of cardiac development and congenital heart disease
Self-assembling human heart organoids for the modeling of cardiac development and congenital heart disease
Material Type:
Article 		Add to My Research

Self-assembling human heart organoids for the modeling of cardiac development and congenital heart disease

Nature communications, 2021-08, Vol.12 (1), p.5142-5142, Article 5142 [Peer Reviewed Journal]

2021. The Author(s). ;The Author(s) 2021. 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) 2021 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-021-25329-5 ;PMID: 34446706

Full text available

Citations Cited by
23
Clinical Course of Two Children with Congenital Plasminogen Deficiency Type 1
Clinical Course of Two Children with Congenital Plasminogen Deficiency Type 1
Material Type:
Article 		Add to My Research

Clinical Course of Two Children with Congenital Plasminogen Deficiency Type 1

Turkish Thoracic Journal, 2019-09, Vol.20 (1), p.371-371 [Peer Reviewed Journal]

2019. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the associated terms available at https://turkthoracj.org/en/copyright-1014 ;ISSN: 2149-2530 ;EISSN: 1308-5387 ;DOI: 10.5152/TurkThoracJ.2019.371

Full text available

Citations Cited by
24
Systemic AAV Micro-dystrophin Gene Therapy for Duchenne Muscular Dystrophy
Systemic AAV Micro-dystrophin Gene Therapy for Duchenne Muscular Dystrophy
Material Type:
Article 		Add to My Research

Systemic AAV Micro-dystrophin Gene Therapy for Duchenne Muscular Dystrophy

Molecular therapy, 2018-10, Vol.26 (10), p.2337-2356 [Peer Reviewed Journal]

2018 The Author(s) ;Copyright © 2018 The Author(s). Published by Elsevier Inc. All rights reserved. ;2018. The Author(s) ;2018 The Author(s) 2018 ;ISSN: 1525-0016 ;EISSN: 1525-0024 ;DOI: 10.1016/j.ymthe.2018.07.011 ;PMID: 30093306

Full text available

Citations Cited by
25
Responding to comments on “The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy.
Responding to comments on “The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy.
Material Type:
Article 		Add to My Research

Responding to comments on “The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy.

BMC ophthalmology, 2023-09, Vol.23 (1), p.1-371, Article 371 [Peer Reviewed Journal]

COPYRIGHT 2023 BioMed Central Ltd. ;2023. 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. ;BioMed Central Ltd., part of Springer Nature 2023 ;ISSN: 1471-2415 ;EISSN: 1471-2415 ;DOI: 10.1186/s12886-023-03099-6 ;PMID: 37684560

Full text available

Citations Cited by
26
PediTools Electronic Growth Chart Calculators: Applications in Clinical Care, Research, and Quality Improvement
PediTools Electronic Growth Chart Calculators: Applications in Clinical Care, Research, and Quality Improvement
Material Type:
Article 		Add to My Research

PediTools Electronic Growth Chart Calculators: Applications in Clinical Care, Research, and Quality Improvement

Journal of medical Internet research, 2020-01, Vol.22 (1), p.e16204-e16204 [Peer Reviewed Journal]

Joseph H H Chou, Sergei Roumiantsev, Rachana Singh. Originally published in the Journal of Medical Internet Research (http://www.jmir.org), 30.01.2020. ;2020. This work is licensed 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. ;Joseph H H Chou, Sergei Roumiantsev, Rachana Singh. Originally published in the Journal of Medical Internet Research (http://www.jmir.org), 30.01.2020. 2020 ;ISSN: 1438-8871 ;ISSN: 1439-4456 ;EISSN: 1438-8871 ;DOI: 10.2196/16204 ;PMID: 32012066

Full text available

Citations Cited by
27
Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysis
Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysis
Material Type:
Article 		Add to My Research

Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysis

Orphanet journal of rare diseases, 2020-06, Vol.15 (1), p.1-141, Article 141 [Peer Reviewed Journal]

COPYRIGHT 2020 BioMed Central Ltd. ;2020. 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. ;Attribution ;The Author(s) 2020 ;ISSN: 1750-1172 ;EISSN: 1750-1172 ;DOI: 10.1186/s13023-020-01430-8 ;PMID: 32503598

Full text available

Citations Cited by
28
SCMR Position Paper (2020) on clinical indications for cardiovascular magnetic resonance
SCMR Position Paper (2020) on clinical indications for cardiovascular magnetic resonance
Material Type:
Article 		Add to My Research

SCMR Position Paper (2020) on clinical indications for cardiovascular magnetic resonance

Journal of cardiovascular magnetic resonance, 2020-11, Vol.22 (1), p.76-76, Article 76 [Peer Reviewed Journal]

COPYRIGHT 2020 BioMed Central Ltd. ;COPYRIGHT 2020 BioMed Central Ltd. ;2020. 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) 2020 ;ISSN: 1532-429X ;ISSN: 1097-6647 ;EISSN: 1532-429X ;DOI: 10.1186/s12968-020-00682-4 ;PMID: 33161900

Full text available

Citations Cited by
29
C Outcomes of a nationwide cardiac screening programme in young individuals
C Outcomes of a nationwide cardiac screening programme in young individuals
Material Type:
Article 		Add to My Research

C Outcomes of a nationwide cardiac screening programme in young individuals

Heart (British Cardiac Society), 2022-06, Vol.108 (Suppl 1), p.A174-A174 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;2022 Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2022-BCS.227

Full text available

Citations Cited by
30
Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
Material Type:
Article 		Add to My Research

Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

American journal of human genetics, 2010-05, Vol.86 (5), p.749-764 [Peer Reviewed Journal]

2010 The American Society of Human Genetics ;2015 INIST-CNRS ;Copyright (c) 2010 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;Copyright University of Chicago, acting through its Press May 14, 2010 ;2010 The American Society of Human Genetics. Published by Elsevier Ltd. All right reserved. 2010 The American Society of Human Genetics ;ISSN: 0002-9297 ;ISSN: 1537-6605 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2010.04.006 ;PMID: 20466091 ;CODEN: AJHGAG

Full text available

Citations Cited by
31
C65 PEDIATRIC CASE REPORTS: BRONCHIECTASIS, CYSTIC FIBROSIS, AND LUNG INFECTIONS: A Case Of Severe, Diffuse Bronchiectasis In A 3 Year Old Female
C65 PEDIATRIC CASE REPORTS: BRONCHIECTASIS, CYSTIC FIBROSIS, AND LUNG INFECTIONS: A Case Of Severe, Diffuse Bronchiectasis In A 3 Year Old Female
Material Type:
Article 		Add to My Research

C65 PEDIATRIC CASE REPORTS: BRONCHIECTASIS, CYSTIC FIBROSIS, AND LUNG INFECTIONS: A Case Of Severe, Diffuse Bronchiectasis In A 3 Year Old Female

American journal of respiratory and critical care medicine, 2017-01, Vol.195 [Peer Reviewed Journal]

Copyright American Thoracic Society 2017 ;ISSN: 1073-449X ;EISSN: 1535-4970

Full text available

Citations Cited by
32
C61 TUBERCULOSIS CASE REPORTS: A Rare Complication Of A Common Disease
C61 TUBERCULOSIS CASE REPORTS: A Rare Complication Of A Common Disease
Material Type:
Article 		Add to My Research

C61 TUBERCULOSIS CASE REPORTS: A Rare Complication Of A Common Disease

American journal of respiratory and critical care medicine, 2017-01, Vol.195 [Peer Reviewed Journal]

Copyright American Thoracic Society 2017 ;ISSN: 1073-449X ;EISSN: 1535-4970

Full text available

Citations Cited by
33
A41 LAM AND OTHER CYSTIC LUNG DISEASE: CASE REPORTS: Asymptomatic Adult With Congenital Cystic Adenomatoid Malformation Of The Lungs
A41 LAM AND OTHER CYSTIC LUNG DISEASE: CASE REPORTS: Asymptomatic Adult With Congenital Cystic Adenomatoid Malformation Of The Lungs
Material Type:
Article 		Add to My Research

A41 LAM AND OTHER CYSTIC LUNG DISEASE: CASE REPORTS: Asymptomatic Adult With Congenital Cystic Adenomatoid Malformation Of The Lungs

American journal of respiratory and critical care medicine, 2017-01, Vol.195 [Peer Reviewed Journal]

Copyright American Thoracic Society 2017 ;ISSN: 1073-449X ;EISSN: 1535-4970

Full text available

Citations Cited by
34
C70 CALL MY NAME: CASE REPORTS IN PULMONARY VASCULAR DISEASE: Pulmonary Venous Varix: An Uncommon Pulmonary Vascular Abnormality as A Cause Of ischemic Stroke
C70 CALL MY NAME: CASE REPORTS IN PULMONARY VASCULAR DISEASE: Pulmonary Venous Varix: An Uncommon Pulmonary Vascular Abnormality as A Cause Of ischemic Stroke
Material Type:
Article 		Add to My Research

C70 CALL MY NAME: CASE REPORTS IN PULMONARY VASCULAR DISEASE: Pulmonary Venous Varix: An Uncommon Pulmonary Vascular Abnormality as A Cause Of ischemic Stroke

American journal of respiratory and critical care medicine, 2017-01, Vol.195 [Peer Reviewed Journal]

Copyright American Thoracic Society 2017 ;ISSN: 1073-449X ;EISSN: 1535-4970

Full text available

Citations Cited by
35
Zika Virus Infection as a Cause of Congenital Brain Abnormalities and Guillain-Barré Syndrome: Systematic Review
Zika Virus Infection as a Cause of Congenital Brain Abnormalities and Guillain-Barré Syndrome: Systematic Review
Material Type:
Article 		Add to My Research

Zika Virus Infection as a Cause of Congenital Brain Abnormalities and Guillain-Barré Syndrome: Systematic Review

PLoS medicine, 2017-01, Vol.14 (1), p.e1002203-e1002203 [Peer Reviewed Journal]

2017 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Krauer F, Riesen M, Reveiz L, Oladapo OT, Martínez-Vega R, Porgo TV, et al. (2017) Zika Virus Infection as a Cause of Congenital Brain Abnormalities and Guillain-Barré Syndrome: Systematic Review. PLoS Med 14(1): e1002203. doi:10.1371/journal.pmed.1002203 ;2017 Krauer et al 2017 Krauer et al ;2017 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Krauer F, Riesen M, Reveiz L, Oladapo OT, Martínez-Vega R, Porgo TV, et al. (2017) Zika Virus Infection as a Cause of Congenital Brain Abnormalities and Guillain-Barré Syndrome: Systematic Review. PLoS Med 14(1): e1002203. doi:10.1371/journal.pmed.1002203 ;ISSN: 1549-1676 ;ISSN: 1549-1277 ;EISSN: 1549-1676 ;DOI: 10.1371/journal.pmed.1002203 ;PMID: 28045901

Full text available

Citations Cited by
36
Isolated tricuspid regurgitation: outcomes and therapeutic interventions
Isolated tricuspid regurgitation: outcomes and therapeutic interventions
Material Type:
Article 		Add to My Research

Isolated tricuspid regurgitation: outcomes and therapeutic interventions

Heart (British Cardiac Society), 2018-05, Vol.104 (10), p.798-806 [Peer Reviewed Journal]

Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. ;2018 Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. 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 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. ;Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. 2018 ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2017-311586 ;PMID: 29229649

Full text available

Citations Cited by
37
Zika: the origin and spread of a mosquito-borne virus
Zika: the origin and spread of a mosquito-borne virus
Material Type:
Article 		Add to My Research

Zika: the origin and spread of a mosquito-borne virus

Bulletin of the World Health Organization, 2016-09, Vol.94 (9), p.675-686C [Peer Reviewed Journal]

Copyright World Health Organization Sep 2016 ;(c) 2016 The authors; licensee World Health Organization. 2016 ;ISSN: 0042-9686 ;EISSN: 1564-0604 ;DOI: 10.2471/BLT.16.171082 ;PMID: 27708473 ;CODEN: BWHOA6

Full text available

Citations Cited by
38
Describing the Prevalence of Neural Tube Defects Worldwide: A Systematic Literature Review
Describing the Prevalence of Neural Tube Defects Worldwide: A Systematic Literature Review
Material Type:
Article 		Add to My Research

Describing the Prevalence of Neural Tube Defects Worldwide: A Systematic Literature Review

PloS one, 2016-04, Vol.11 (4), p.e0151586-e0151586 [Peer Reviewed Journal]

COPYRIGHT 2016 Public Library of Science ;COPYRIGHT 2016 Public Library of Science ;This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication: https://creativecommons.org/publicdomain/zero/1.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0151586 ;PMID: 27064786

Full text available

Citations Cited by
39
Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism data
Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism data
Material Type:
Article 		Add to My Research

Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism data

Genetics (Austin), 2011-09, Vol.189 (1), p.237-249 [Peer Reviewed Journal]

Copyright Genetics Society of America Sep 2011 ;Copyright © 2011 by the Genetics Society of America 2011 ;ISSN: 1943-2631 ;ISSN: 0016-6731 ;EISSN: 1943-2631 ;DOI: 10.1534/genetics.111.130922 ;PMID: 21705750 ;CODEN: GENTAE

Full text available

Citations Cited by
40
BS73 T cell responses driving inflammatory mechanisms in paediatric congenital heart disease graft rjection
BS73 T cell responses driving inflammatory mechanisms in paediatric congenital heart disease graft rjection
Material Type:
Article 		Add to My Research

BS73 T cell responses driving inflammatory mechanisms in paediatric congenital heart disease graft rjection

Heart (British Cardiac Society), 2023-06, Vol.109 (Suppl 3), p.A298-A298 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;2023 Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 1355-6037 ;EISSN: 1468-201X ;DOI: 10.1136/heartjnl-2023-BCS.286

Full text available

Citations Cited by

Results 21 - 40 of 17,683  for All Library Resources

Sorted by: Sorted by: RelevanceOr hit Enter to replace sort method
previous page 1 Results 2 3 4 5 next page

Personalize your results

  1. Edit

Refine Search Results

Expand My Results

  1.   

Show only

  1. Peer-reviewed Journals (17,233)

Refine My Results

Creation Date 

From To
Refine
  1. Before 1989  (61)
  2. 1989 To 1997  (206)
  3. 1998 To 2006  (823)
  4. 2007 To 2016  (3,285)
  5. After 2016  (13,309)
  6. More options open sub menu

Resource Type 

  1. Articles  (17,658)
  2. Reviews  (17)
  3. Reports  (5)
  4. Conference Proceedings  (3)
  5. More options open sub menu

Subject 

  1. Congenital Diseases  (17,280)
  2. Science & Technology  (15,146)
  3. Life Sciences & Biomedicine  (13,697)
  4. Humans  (7,511)
  5. Patients  (5,800)
  6. Pediatrics  (4,462)
  7. Female  (4,346)
  8. Mutation  (4,112)
  9. Cardiovascular Disease  (3,978)
  10. Male  (3,591)
  11. General & Internal Medicine  (3,145)
  12. Medicine, General & Internal  (3,108)
  13. Heart  (2,861)
  14. Age  (2,796)
  15. Genetic Disorders  (2,564)
  16. Case Report  (2,500)
  17. Surgery  (2,379)
  18. Pregnancy  (2,340)
  19. Genes  (2,296)
  20. Proteins  (2,257)
  21. More options open sub menu

Language 

  1. English  (17,675)
  2. Japanese  (1,165)
  3. Portuguese  (147)
  4. French  (32)
  5. Turkish  (25)
  6. Norwegian  (13)
  7. German  (6)
  8. Spanish  (6)
  9. Korean  (4)
  10. Chinese  (4)
  11. Russian  (1)
  12. Italian  (1)
  13. More options open sub menu
INSPIRE LIBRARY - TON DUC THANG UNIVERSITY (84-028) 37 755 057 Feedback
19 Nguyen Huu Tho St. Dist.7, HCM thuvien@tdtu.edu.vn

Copyright © 2017 INSPIRE LIBRARY - TON DUC THANG UNIVERSITY

Searching Remote Databases, Please Wait