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Results 1 - 20 of 11,842  for All Library Resources

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1
Single-cell analysis of developing and azoospermia human testicles reveals central role of Sertoli cells
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Single-cell analysis of developing and azoospermia human testicles reveals central role of Sertoli cells

Nature communications, 2020-11, Vol.11 (1), p.5683-5683, Article 5683 [Peer Reviewed Journal]

The Author(s) 2020. corrected publication 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) 2020, corrected publication 2021 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-020-19414-4 ;PMID: 33173058

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2
Underlying Medical Conditions Associated With Severe COVID-19 Illness Among Children
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Underlying Medical Conditions Associated With Severe COVID-19 Illness Among Children

JAMA Network Open, 2021-06, Vol.4 (6), p.e2111182-e2111182 [Peer Reviewed Journal]

2021. 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 2021 Kompaniyets L et al. . ;ISSN: 2574-3805 ;EISSN: 2574-3805 ;DOI: 10.1001/jamanetworkopen.2021.11182 ;PMID: 34097050

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3
FETAL ECHOCARDIOGRAPHY - THE FIRST OR SKIPPED STEP IN CARDIOLOGY
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FETAL ECHOCARDIOGRAPHY - THE FIRST OR SKIPPED STEP IN CARDIOLOGY

Acta medica Saliniana, 2022-01, Vol.52, p.26-26 [Peer Reviewed Journal]

Copyright University Clinical Center Tuzla 2022 ;ISSN: 0350-364X ;EISSN: 1840-3956

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4
Self-assembling human heart organoids for the modeling of cardiac development and congenital heart disease
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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

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5
Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications
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Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications

Scientific reports, 2021-01, Vol.11 (1), p.1526-1526, Article 1526 [Peer Reviewed Journal]

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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-81093-y ;PMID: 33452396

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6
Clinical Course of Two Children with Congenital Plasminogen Deficiency Type 1
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Article
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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

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7
Responding to comments on “The possible pathogenesis of macular caldera in patients with North Carolina macular dystrophy.
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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

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8
Global epidemiology of Duchenne muscular dystrophy: an updated systematic review and meta-analysis
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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

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9
SCMR Position Paper (2020) on clinical indications for cardiovascular magnetic resonance
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Article
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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

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10
Zika Virus Infection as a Cause of Congenital Brain Abnormalities and Guillain-Barré Syndrome: Systematic Review
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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

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11
In situ immune response and mechanisms of cell damage in central nervous system of fatal cases microcephaly by Zika virus
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In situ immune response and mechanisms of cell damage in central nervous system of fatal cases microcephaly by Zika virus

Scientific reports, 2018-01, Vol.8 (1), p.1-1, Article 1 [Peer Reviewed Journal]

2017. 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) 2017 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-017-17765-5 ;PMID: 29311619

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12
Clinical Features of Varicella-Zoster Virus Infection
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Article
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Clinical Features of Varicella-Zoster Virus Infection

Viruses, 2018-11, Vol.10 (11), p.609 [Peer Reviewed Journal]

2018 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 (http://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. ;2018 by the authors. 2018 ;ISSN: 1999-4915 ;EISSN: 1999-4915 ;DOI: 10.3390/v10110609 ;PMID: 30400213

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13
Describing the Prevalence of Neural Tube Defects Worldwide: A Systematic Literature Review
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Article
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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

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14
Effects of perioperative exercise on cardiorespiratory endurance in children with congenital heart disease in plateau areas after surgical repair
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Article
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Effects of perioperative exercise on cardiorespiratory endurance in children with congenital heart disease in plateau areas after surgical repair

Scientific reports, 2023-10, Vol.13 (1), p.18088-18088, Article 18088 [Peer Reviewed Journal]

The Author(s) 2023. 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. ;Springer Nature Limited 2023 ;ISSN: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-023-45310-0 ;PMID: 37872227

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15
Conformational ensemble of the human TRPV3 ion channel
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Article
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Conformational ensemble of the human TRPV3 ion channel

Nature communications, 2018-11, Vol.9 (1), p.4773-12, Article 4773 [Peer Reviewed Journal]

2018. 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) 2018 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-07117-w ;PMID: 30429472

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16
Ocular manifestations of Sturge-Weber syndrome: pathogenesis, diagnosis, and management
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Article
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Ocular manifestations of Sturge-Weber syndrome: pathogenesis, diagnosis, and management

Clinical ophthalmology (Auckland, N.Z.), 2016-01, Vol.10 (Issue 1), p.871-878 [Peer Reviewed Journal]

COPYRIGHT 2016 Dove Medical Press Limited ;COPYRIGHT 2016 Dove Medical Press Limited ;2016. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2016 Mantelli et al. This work is published and licensed by Dove Medical Press Limited 2016 ;ISSN: 1177-5467 ;ISSN: 1177-5483 ;EISSN: 1177-5483 ;DOI: 10.2147/OPTH.S101963 ;PMID: 27257371

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17
The Role of the Aryl Hydrocarbon Receptor (AHR) in Immune and Inflammatory Diseases
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Article
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The Role of the Aryl Hydrocarbon Receptor (AHR) in Immune and Inflammatory Diseases

International journal of molecular sciences, 2018-12, Vol.19 (12), p.3851 [Peer Reviewed Journal]

2018 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 (http://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. ;2018 by the authors. 2018 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms19123851 ;PMID: 30513921

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18
Poland Syndrome- A Rare Congenital Condition
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Article
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Poland Syndrome- A Rare Congenital Condition

Journal of Bangladesh College of Physicians & Surgeons, 2018-10, Vol.36 (4), p.166-169 [Peer Reviewed Journal]

Copyright Bangladesh College of Physicians & Surgeons 2018 ;ISSN: 1015-0870 ;EISSN: 2309-6365 ;DOI: 10.3329/jbcps.v36i4.38186

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19
Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study
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Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study

BMJ open, 2019-07, Vol.9 (7), p.e028139-e028139 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ. ;2019 Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ. 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)) 2019. Re-use permitted under CC BY. Published by BMJ. 2019 ;ISSN: 2044-6055 ;EISSN: 2044-6055 ;DOI: 10.1136/bmjopen-2018-028139 ;PMID: 31270117

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20
ISSVA Classification of Vascular Anomalies and Molecular Biology
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Article
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ISSVA Classification of Vascular Anomalies and Molecular Biology

International journal of molecular sciences, 2022-02, Vol.23 (4), p.2358 [Peer Reviewed Journal]

2022 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. ;2022 by the authors. 2022 ;ISSN: 1422-0067 ;ISSN: 1661-6596 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms23042358 ;PMID: 35216474

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