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Results 1 - 20 of 119  for All Library Resources

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Refined by: creation date: 2008 To 2015 remove xxx: xxx remove
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1
Risk Assessment for Continuous Flow Left Ventricular Assist Devices: Does the Destination Therapy Risk Score Work?
Material Type:
Article
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Risk Assessment for Continuous Flow Left Ventricular Assist Devices: Does the Destination Therapy Risk Score Work?

Journal of the American College of Cardiology, 2012-07, Vol.60 (1), p.44-51 [Peer Reviewed Journal]

American College of Cardiology Foundation ;Copyright Elsevier Limited Jul 3, 2012 ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2012.02.032

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2
Arthroprosthetic cobaltism and cardiomyopathy
Material Type:
Article
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Arthroprosthetic cobaltism and cardiomyopathy

Heart, lung & circulation, 2012-11, Vol.21 (11), p.759 [Peer Reviewed Journal]

Copyright © 2012 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ). Published by Elsevier B.V. All rights reserved. ;EISSN: 1444-2892 ;DOI: 10.1016/j.hlc.2012.03.013 ;PMID: 22520206

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3
Rationale and design of the Percutaneous Stem Cell Injection Delivery Effects on Neomyogenesis in Dilated Cardiomyopathy (the POSEIDON-DCM study): a phase I/II, randomized pilot study of the comparative safety and efficacy of transendocardial injection of autologous mesenchymal stem cell vs. allogeneic mesenchymal stem cells in patients with non-ischemic dilated cardiomyopathy
Material Type:
Article
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Rationale and design of the Percutaneous Stem Cell Injection Delivery Effects on Neomyogenesis in Dilated Cardiomyopathy (the POSEIDON-DCM study): a phase I/II, randomized pilot study of the comparative safety and efficacy of transendocardial injection of autologous mesenchymal stem cell vs. allogeneic mesenchymal stem cells in patients with non-ischemic dilated cardiomyopathy

Journal of cardiovascular translational research, 2014-12, Vol.7 (9), p.769 [Peer Reviewed Journal]

EISSN: 1937-5395 ;DOI: 10.1007/s12265-014-9594-0 ;PMID: 25354998

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4
Nav1.5 mutations linked to dilated cardiomyopathy phenotypes: Is the gating pore current the missing link?
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Article
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Nav1.5 mutations linked to dilated cardiomyopathy phenotypes: Is the gating pore current the missing link?

Channels (Austin, Tex.), 2014, Vol.8 (1), p.90-94 [Peer Reviewed Journal]

Copyright © 2014 Landes Bioscience 2014 ;ISSN: 1933-6950 ;EISSN: 1933-6969 ;DOI: 10.4161/chan.27179 ;PMID: 24300601

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5
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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Article
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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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6
Disrupting Virchow's triad: can factor X inhibition reduce risk of adverse outcomes in patients with ischaemic cardiomyopathy?
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Article
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Disrupting Virchow's triad: can factor X inhibition reduce risk of adverse outcomes in patients with ischaemic cardiomyopathy?

European journal of heart failure, 2015-07, Vol.17 (7), p.647-651 [Peer Reviewed Journal]

2015 The Authors. © 2015 European Society of Cardiology ;ISSN: 1388-9842 ;EISSN: 1879-0844 ;DOI: 10.1002/ejhf.296 ;PMID: 26018996

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7
The calcium release-activated calcium channel Orai1 represents a crucial component in hypertrophic compensation and the development of dilated cardiomyopathy
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Article
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The calcium release-activated calcium channel Orai1 represents a crucial component in hypertrophic compensation and the development of dilated cardiomyopathy

Channels (Austin, Tex.), 2014-01, Vol.8 (1), p.35-43 [Peer Reviewed Journal]

Copyright © 2014 Landes Bioscience 2014 ;ISSN: 1933-6950 ;EISSN: 1933-6969 ;DOI: 10.4161/chan.26581 ;PMID: 24135962

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8
Carnitine Uptake Defect (Primary Carnitine Deficiency): Risk in Genotype-Phenotype Correlation
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Article
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Carnitine Uptake Defect (Primary Carnitine Deficiency): Risk in Genotype-Phenotype Correlation

Human mutation, 2013-04, Vol.34 (4), p.655-655 [Peer Reviewed Journal]

2013 Wiley Periodicals, Inc. ;ISSN: 1059-7794 ;EISSN: 1098-1004 ;DOI: 10.1002/humu.22286 ;PMID: 23520115

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9
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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Article
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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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10
A novel variant in plakophilin-2 gene detected in a family with arrhythmogenic right ventricular cardiomyopathy
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Article
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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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11
Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype-phenotype associations for laminopathies
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Article
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Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype-phenotype associations for laminopathies

Proteins, structure, function, and bioinformatics, 2014-06, Vol.82 (6), p.904-915 [Peer Reviewed Journal]

2013 Wiley Periodicals, Inc. ;ISSN: 0887-3585 ;EISSN: 1097-0134 ;DOI: 10.1002/prot.24465 ;PMID: 24375749

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12
ALMS1-deficient fibroblasts over-express extra-cellular matrix components, display cell cycle delay and are resistant to apoptosis
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Article
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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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13
Peptides Derived from the Extracellular Loops of Receptors: Structure, Mechanism of Action, Use in Physiology and Medicine
Material Type:
Article
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Peptides Derived from the Extracellular Loops of Receptors: Structure, Mechanism of Action, Use in Physiology and Medicine

Neuroscience and behavioral physiology, 2013, Vol.43 (1), p.111-121 [Peer Reviewed Journal]

Springer Science+Business Media New York 2012 ;Springer Science+Business Media New York 2013 ;ISSN: 0097-0549 ;EISSN: 1573-899X ;DOI: 10.1007/s11055-012-9700-1

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14
Fetology: diagnosis and management of the fetal patient
Material Type:
Book
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Fetology: diagnosis and management of the fetal patient

ISBN: 0071760873 ;ISBN: 9780071442015 ;ISBN: 9780071760874 ;ISBN: 0071442014 ;EISBN: 9780071760874 ;EISBN: 0071760873

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15
Dystrophinopathies
Material Type:
Book Chapter
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Dystrophinopathies

Neuromuscular Disorders of Infancy, Childhood, and Adolescence, 2015, p.551-592

Copyright © 2015 Elsevier Inc. All rights reserved. ;ISBN: 0124170447 ;ISBN: 9780124170445 ;EISBN: 0124170447 ;EISBN: 9780124170445 ;DOI: 10.1016/B978-0-12-417044-5.00030-5

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16
Adipophilin/perilipin-2 as a lipid droplet-specific marker for metabolically active cells and diseases associated with metabolic dysregulation
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Article
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Adipophilin/perilipin-2 as a lipid droplet-specific marker for metabolically active cells and diseases associated with metabolic dysregulation

Histopathology, 2013-03, Vol.62 (4), p.617-631 [Peer Reviewed Journal]

2012 Blackwell Publishing Ltd ;2012 Blackwell Publishing Ltd. ;Copyright © 2013 Blackwell Publishing Ltd ;ISSN: 0309-0167 ;EISSN: 1365-2559 ;DOI: 10.1111/his.12038 ;PMID: 23347084 ;CODEN: HISTDD

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17
Ferri's Differential Diagnosis: A Practical Guide to the Differential Diagnosis of Symptoms, Signs, and Clinical Disorders
Material Type:
Book
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Ferri's Differential Diagnosis: A Practical Guide to the Differential Diagnosis of Symptoms, Signs, and Clinical Disorders

ISBN: 0323076998 ;ISBN: 9780323076999 ;EISBN: 0323081630 ;EISBN: 9780323081634 ;OCLC: 861539507

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18
Response to Chen et al.: Carnitine Uptake Defect (Primary Carnitine Deficiency): Risk in Genotype-Phenotype Correlation
Material Type:
Article
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Response to Chen et al.: Carnitine Uptake Defect (Primary Carnitine Deficiency): Risk in Genotype-Phenotype Correlation

Human mutation, 2013-04, Vol.34 (4), p.656-656 [Peer Reviewed Journal]

2013 Wiley Periodicals, Inc. ;ISSN: 1059-7794 ;EISSN: 1098-1004 ;DOI: 10.1002/humu.22285 ;PMID: 23520116

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19
Genetics
Material Type:
Book Chapter
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Genetics

Mayo Clinic Internal Medicine Review, 2008, p.383-399

2008 by Taylor & Francis Group, LLC ;EISBN: 9780429142215 ;EISBN: 1420084798 ;EISBN: 9781420084795 ;EISBN: 0429142218 ;DOI: 10.1201/b14434-29

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20
miR-590-3p Is a Novel MicroRNA in Myocarditis by Targeting Nuclear Factor Kappa-B in vivo
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Article
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miR-590-3p Is a Novel MicroRNA in Myocarditis by Targeting Nuclear Factor Kappa-B in vivo

Cardiology, 2015-01, Vol.132 (3), p.182-188 [Peer Reviewed Journal]

2015 S. Karger AG, Basel ;2015 S. Karger AG, Basel. ;ISSN: 0008-6312 ;EISSN: 1421-9751 ;DOI: 10.1159/000433596 ;PMID: 26278103

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