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21
An Endoscopic Endonasal Attempt at Pediatric Meningoencephalocele Repair
An Endoscopic Endonasal Attempt at Pediatric Meningoencephalocele Repair
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An Endoscopic Endonasal Attempt at Pediatric Meningoencephalocele Repair

Ear, nose, & throat journal, 2023-09, Vol.102 (9_suppl), p.24S-26S [Peer Reviewed Journal]

The Author(s) 2023 ;ISSN: 0145-5613 ;EISSN: 1942-7522 ;DOI: 10.1177/01455613231187760 ;PMID: 37574852

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22
An Interesting Secondary Airway Lesion in an Infant With Laryngomalacia
An Interesting Secondary Airway Lesion in an Infant With Laryngomalacia
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An Interesting Secondary Airway Lesion in an Infant With Laryngomalacia

Ear, nose, & throat journal, 2021-03, Vol.100 (3), p.NP156-NP157 [Peer Reviewed Journal]

The Author(s) 2019 ;ISSN: 0145-5613 ;EISSN: 1942-7522 ;DOI: 10.1177/0145561319872729 ;PMID: 31550930

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23
Perinatal outcome after selective termination in dichorionic twins discordant for congenital anomalies
Perinatal outcome after selective termination in dichorionic twins discordant for congenital anomalies
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Perinatal outcome after selective termination in dichorionic twins discordant for congenital anomalies

Acta obstetricia et gynecologica Scandinavica, 2021-11, Vol.100 (11), p.2029-2035 [Peer Reviewed Journal]

2021 The Authors. published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG) ;2021. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.14249

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24
Congenital Aural Fistula Developing Between the Third and Fourth Hillocks of the Embryonal Helix and Presenting a Large Temporal Mass: A Case Report
Congenital Aural Fistula Developing Between the Third and Fourth Hillocks of the Embryonal Helix and Presenting a Large Temporal Mass: A Case Report
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Congenital Aural Fistula Developing Between the Third and Fourth Hillocks of the Embryonal Helix and Presenting a Large Temporal Mass: A Case Report

Ear, nose, & throat journal, 2023-06, Vol.102 (6), p.NP265-NP268 [Peer Reviewed Journal]

The Author(s) 2021 ;ISSN: 0145-5613 ;EISSN: 1942-7522 ;DOI: 10.1177/01455613211009150 ;PMID: 33829886

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25
The onset of PI3K‐related vascular malformations occurs during angiogenesis and is prevented by the AKT inhibitor miransertib
The onset of PI3K‐related vascular malformations occurs during angiogenesis and is prevented by the AKT inhibitor miransertib
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The onset of PI3K‐related vascular malformations occurs during angiogenesis and is prevented by the AKT inhibitor miransertib

EMBO molecular medicine, 2022-07, Vol.14 (7), p.e15619-n/a [Peer Reviewed Journal]

2022 The Authors. Published under the terms of the CC BY 4.0 license ;2022 The Authors. Published under the terms of the CC BY 4.0 license. ;2022. 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. ;ISSN: 1757-4676 ;ISSN: 1757-4684 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.202115619 ;PMID: 35695059

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26
The SGLT family—sodium‐glucose transporters with roles beyond glucose and the kidney
The SGLT family—sodium‐glucose transporters with roles beyond glucose and the kidney
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The SGLT family—sodium‐glucose transporters with roles beyond glucose and the kidney

Journal of cellular and molecular medicine, 2024-03, Vol.28 (6), p.e18152-n/a [Peer Reviewed Journal]

2024 The Authors. published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;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. ;ISSN: 1582-1838 ;EISSN: 1582-4934 ;DOI: 10.1111/jcmm.18152 ;PMID: 38445802

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27
Congenital anomalies and maternal age: A systematic review and meta‐analysis of observational studies
Congenital anomalies and maternal age: A systematic review and meta‐analysis of observational studies
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Congenital anomalies and maternal age: A systematic review and meta‐analysis of observational studies

Acta obstetricia et gynecologica Scandinavica, 2022-05, Vol.101 (5), p.484-498 [Peer Reviewed Journal]

2022 The Authors. published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). ;2022 The Authors. Acta Obstetricia et Gynecologica Scandinavica published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). ;2022. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.14339 ;PMID: 35288928

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28
High maternal blood lipid levels during early pregnancy are associated with increased risk of congenital heart disease in offspring
High maternal blood lipid levels during early pregnancy are associated with increased risk of congenital heart disease in offspring
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High maternal blood lipid levels during early pregnancy are associated with increased risk of congenital heart disease in offspring

Acta obstetricia et gynecologica Scandinavica, 2021-10, Vol.100 (10), p.1806-1813 [Peer Reviewed Journal]

2021 The Authors. published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). ;2021. This article 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: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.14225 ;PMID: 34346055

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29
Hippocampal alterations and functional correlates in adolescents and young adults with congenital heart disease
Hippocampal alterations and functional correlates in adolescents and young adults with congenital heart disease
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Hippocampal alterations and functional correlates in adolescents and young adults with congenital heart disease

Human brain mapping, 2019-08, Vol.40 (12), p.3548-3560 [Peer Reviewed Journal]

2019 Wiley Periodicals, Inc. ;ISSN: 1065-9471 ;EISSN: 1097-0193 ;DOI: 10.1002/hbm.24615 ;PMID: 31070841

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30
A Novel Technique for Reconstruction of a Congenitally Absent Earlobe
A Novel Technique for Reconstruction of a Congenitally Absent Earlobe
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A Novel Technique for Reconstruction of a Congenitally Absent Earlobe

Ear, nose, & throat journal, 2022-09, Vol.101 (8), p.NP358-NP361 [Peer Reviewed Journal]

The Author(s) 2020 ;ISSN: 0145-5613 ;EISSN: 1942-7522 ;DOI: 10.1177/0145561320971930 ;PMID: 33155853

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31
Endoscopic Surgery of Congenital Cholesteatoma in the Anterior Epitympanic Recess: A Case Report of a Rare Location
Endoscopic Surgery of Congenital Cholesteatoma in the Anterior Epitympanic Recess: A Case Report of a Rare Location
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Endoscopic Surgery of Congenital Cholesteatoma in the Anterior Epitympanic Recess: A Case Report of a Rare Location

Ear, nose, & throat journal, 2022-12, Vol.101 (10), p.677-679 [Peer Reviewed Journal]

The Author(s) 2020 ;ISSN: 0145-5613 ;EISSN: 1942-7522 ;DOI: 10.1177/0145561320969249 ;PMID: 33314962

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32
Demyelinating processes in aging and stroke in the central nervous system and the prospect of treatment strategy
Demyelinating processes in aging and stroke in the central nervous system and the prospect of treatment strategy
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Demyelinating processes in aging and stroke in the central nervous system and the prospect of treatment strategy

CNS neuroscience & therapeutics, 2020-12, Vol.26 (12), p.1219-1229 [Peer Reviewed Journal]

2020 The Authors. published by John Wiley & Sons Ltd ;2020 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. ;2020. 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. ;ISSN: 1755-5930 ;EISSN: 1755-5949 ;DOI: 10.1111/cns.13497 ;PMID: 33210839

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33
Prenatal detection of major congenital malformations in a cohort of 19 367 Danish fetuses with a complete follow‐up six months after birth
Prenatal detection of major congenital malformations in a cohort of 19 367 Danish fetuses with a complete follow‐up six months after birth
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Prenatal detection of major congenital malformations in a cohort of 19 367 Danish fetuses with a complete follow‐up six months after birth

Acta obstetricia et gynecologica Scandinavica, 2023-08, Vol.102 (8), p.1115-1124 [Peer Reviewed Journal]

2023 The Authors. published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). ;2023 The Authors. Acta Obstetricia et Gynecologica Scandinavica published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG). ;2023. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;ISSN: 0001-6349 ;EISSN: 1600-0412 ;DOI: 10.1111/aogs.14582 ;PMID: 37270668

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34
Guidance for the prevention and emergency management of adult patients with adrenal insufficiency
Guidance for the prevention and emergency management of adult patients with adrenal insufficiency
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Guidance for the prevention and emergency management of adult patients with adrenal insufficiency

Clinical medicine (London, England), 2020-07, Vol.20 (4), p.371-378 [Peer Reviewed Journal]

2020 © 2020 THE AUTHORS. Published by Elsevier Limited on behalf of the Royal College of Physicians. ;Royal College of Physicians 2020. All rights reserved. ;Copyright Royal College of Physicians Jul 2020 ;Royal College of Physicians 2020. All rights reserved. 2020 ;ISSN: 1470-2118 ;EISSN: 1473-4893 ;DOI: 10.7861/clinmed.2019-0324 ;PMID: 32675141

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35
KYNU, a novel potential target that underpins CD44‐promoted breast tumour cell invasion
KYNU, a novel potential target that underpins CD44‐promoted breast tumour cell invasion
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KYNU, a novel potential target that underpins CD44‐promoted breast tumour cell invasion

Journal of cellular and molecular medicine, 2021-03, Vol.25 (5), p.2309-2314 [Peer Reviewed Journal]

2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;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. ;ISSN: 1582-1838 ;EISSN: 1582-4934 ;DOI: 10.1111/jcmm.16296 ;PMID: 33486887

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36
Large Congenital Epulis in a Newborn: Diagnosis and Management
Large Congenital Epulis in a Newborn: Diagnosis and Management
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Large Congenital Epulis in a Newborn: Diagnosis and Management

Ear, nose, & throat journal, 2020-08, Vol.99 (7), p.NP79-NP81 [Peer Reviewed Journal]

The Author(s) 2019 ;ISSN: 0145-5613 ;EISSN: 1942-7522 ;DOI: 10.1177/0145561319851498 ;PMID: 31132898

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37
Musculoskeletal defects associated with myosin heavy chain-embryonic loss of function are mediated by the YAP signaling pathway
Musculoskeletal defects associated with myosin heavy chain-embryonic loss of function are mediated by the YAP signaling pathway
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Musculoskeletal defects associated with myosin heavy chain-embryonic loss of function are mediated by the YAP signaling pathway

EMBO molecular medicine, 2023-09, Vol.15 (9), p.e17187-e17187 [Peer Reviewed Journal]

2023 The Authors. Published under the terms of the CC BY 4.0 license. ;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. ;2023 The Authors. Published under the terms of the CC BY 4.0 license ;ISSN: 1757-4676 ;EISSN: 1757-4684 ;DOI: 10.15252/emmm.202217187 ;PMID: 37492882

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38
Clinicopathological‐genetic features of congenital myasthenic syndrome from a Chinese neuromuscular centre
Clinicopathological‐genetic features of congenital myasthenic syndrome from a Chinese neuromuscular centre
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Clinicopathological‐genetic features of congenital myasthenic syndrome from a Chinese neuromuscular centre

Journal of cellular and molecular medicine, 2022-07, Vol.26 (14), p.3828-3836 [Peer Reviewed Journal]

2022 The Authors. published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;2022 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;2022. 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. ;ISSN: 1582-1838 ;EISSN: 1582-4934 ;DOI: 10.1111/jcmm.17417 ;PMID: 35670010

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39
From phenotype to mechanism: Prenatal spectrum of NKAP mutation‐related disorder and its pathogenesis inducing congenital heart disease
From phenotype to mechanism: Prenatal spectrum of NKAP mutation‐related disorder and its pathogenesis inducing congenital heart disease
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From phenotype to mechanism: Prenatal spectrum of NKAP mutation‐related disorder and its pathogenesis inducing congenital heart disease

Journal of cellular and molecular medicine, 2024-04, Vol.28 (8), p.e18305-n/a [Peer Reviewed Journal]

2024 The Authors. published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;2024 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;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. ;ISSN: 1582-1838 ;EISSN: 1582-4934 ;DOI: 10.1111/jcmm.18305 ;PMID: 38647244

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40
Genetic analysis of the CITED2 gene promoter in isolated and sporadic congenital ventricular septal defects
Genetic analysis of the CITED2 gene promoter in isolated and sporadic congenital ventricular septal defects
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Genetic analysis of the CITED2 gene promoter in isolated and sporadic congenital ventricular septal defects

Journal of cellular and molecular medicine, 2021-02, Vol.25 (4), p.2254-2261 [Peer Reviewed Journal]

2021 The Authors. published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. ;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. ;ISSN: 1582-1838 ;EISSN: 1582-4934 ;DOI: 10.1111/jcmm.16218 ;PMID: 33439552

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