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1
First Results of the DEB-AMI (Drug Eluting Balloon in Acute ST-Segment Elevation Myocardial Infarction) Trial: A Multicenter Randomized Comparison of Drug-Eluting Balloon Plus Bare-Metal Stent Versus Bare-Metal Stent Versus Drug-Eluting Stent in Primary Percutaneous Coronary Intervention With 6-Month Angiographic, Intravascular, Functional, and Clinical Outcomes
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First Results of the DEB-AMI (Drug Eluting Balloon in Acute ST-Segment Elevation Myocardial Infarction) Trial: A Multicenter Randomized Comparison of Drug-Eluting Balloon Plus Bare-Metal Stent Versus Bare-Metal Stent Versus Drug-Eluting Stent in Primary Percutaneous Coronary Intervention With 6-Month Angiographic, Intravascular, Functional, and Clinical Outcomes

Journal of the American College of Cardiology, 2012-06, Vol.59 (25), p.2327-2337 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright © 2012 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2012.02.027 ;PMID: 22503057 ;CODEN: JACCDI

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2
Pre-eclampsia and peripartum cardiomyopathy in molar pregnancy: clinical implication for maternally imprinted genes
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Pre-eclampsia and peripartum cardiomyopathy in molar pregnancy: clinical implication for maternally imprinted genes

Ultrasound in obstetrics & gynecology, 2004-04, Vol.23 (4), p.398 [Peer Reviewed Journal]

Copyright 2004 ISUOG. ;ISSN: 0960-7692 ;EISSN: 1469-0705 ;DOI: 10.1002/uog.1015 ;PMID: 15065193

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3
Machine learning of native T1 mapping radiomics for classification of hypertrophic cardiomyopathy phenotypes
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Machine learning of native T1 mapping radiomics for classification of hypertrophic cardiomyopathy phenotypes

Scientific reports, 2021-12, Vol.11 (1), p.23596-23596, Article 23596 [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: 2045-2322 ;EISSN: 2045-2322 ;DOI: 10.1038/s41598-021-02971-z ;PMID: 34880319

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4
Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study
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Hereditary transthyretin amyloidosis in mainland China: a unicentric retrospective study

Annals of clinical and translational neurology, 2021-04, Vol.8 (4), p.831-841 [Peer Reviewed Journal]

2021 The Authors. published by Wiley Periodicals LLC on behalf of American Neurological Association ;2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. ;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: 2328-9503 ;EISSN: 2328-9503 ;DOI: 10.1002/acn3.51328 ;PMID: 33739616

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5
Identification of cardiovascular and molecular prognostic factors for the medium-term and long-term outcomes of sepsis (ICROS): protocol for a prospective monocentric cohort study
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Identification of cardiovascular and molecular prognostic factors for the medium-term and long-term outcomes of sepsis (ICROS): protocol for a prospective monocentric cohort study

BMJ open, 2020-06, Vol.10 (6), p.e036527-e036527 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. ;2020 Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ 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, appropriate credit is given, any changes made indicated, 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. ;Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. 2020 ;ISSN: 2044-6055 ;EISSN: 2044-6055 ;DOI: 10.1136/bmjopen-2019-036527 ;PMID: 32580988

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6
ALMS1-deficient fibroblasts over-express extra-cellular matrix components, display cell cycle delay and are resistant to apoptosis
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ALMS1-deficient fibroblasts over-express extra-cellular matrix components, display cell cycle delay and are resistant to apoptosis

PloS one, 2011-04, Vol.6 (4), p.e19081-e19081 [Peer Reviewed Journal]

COPYRIGHT 2011 Public Library of Science ;COPYRIGHT 2011 Public Library of Science ;2011 Zulato et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;Zulato et al. 2011 ;ISSN: 1932-6203 ;EISSN: 1932-6203 ;DOI: 10.1371/journal.pone.0019081 ;PMID: 21541333

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7
Clinical characteristics and outcomes of familial and idiopathic dilated cardiomyopathy in Cape Town: a comparative study of 120 cases followed up over 14 years
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Clinical characteristics and outcomes of familial and idiopathic dilated cardiomyopathy in Cape Town: a comparative study of 120 cases followed up over 14 years

South African medical journal, 2011-06, Vol.101 (6), p.399-404 [Peer Reviewed Journal]

COPYRIGHT 2011 Health & Medical Publishing Group ;COPYRIGHT 2011 Health & Medical Publishing Group ;ISSN: 0256-9574 ;PMID: 21920074

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8
New targets for monitoring and therapy in Barth syndrome
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New targets for monitoring and therapy in Barth syndrome

Genetics in medicine, 2016-10, Vol.18 (10), p.1001-1010 [Peer Reviewed Journal]

Copyright Nature Publishing Group Oct 2016 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2015.204 ;PMID: 26845103

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9
A novel variant in plakophilin-2 gene detected in a family with arrhythmogenic right ventricular cardiomyopathy
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A novel variant in plakophilin-2 gene detected in a family with arrhythmogenic right ventricular cardiomyopathy

Journal of interventional cardiac electrophysiology, 2012-06, Vol.34 (1), p.11-18 [Peer Reviewed Journal]

Springer Science+Business Media, LLC 2011 ;Springer Science+Business Media, LLC 2012 ;ISSN: 1383-875X ;ISSN: 1572-8595 ;EISSN: 1572-8595 ;DOI: 10.1007/s10840-011-9643-4 ;PMID: 22170284

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