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1
Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
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Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

Nature communications, 2018-04, Vol.9 (1), p.1416-16, Article 1416 [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. ;Distributed under a Creative Commons Attribution 4.0 International License ;The Author(s) 2018 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-018-03672-4 ;PMID: 29650961

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2
Terminal Digit Preference in Pulmonary Hypertension Endpoints
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Terminal Digit Preference in Pulmonary Hypertension Endpoints

American journal of respiratory and critical care medicine, 2022-06, Vol.205 (12), p.1482-1485 [Peer Reviewed Journal]

Copyright American Thoracic Society Jun 15, 2022 ;ISSN: 1073-449X ;EISSN: 1535-4970 ;DOI: 10.1164/rccm.202108-2015LE ;PMID: 35380935

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3
Peripheral microangiopathy in precapillary pulmonary hypertension: a nailfold video capillaroscopy prospective study
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Peripheral microangiopathy in precapillary pulmonary hypertension: a nailfold video capillaroscopy prospective study

Respiratory research, 2021-01, Vol.22 (1), p.27-27, Article 27 [Peer Reviewed Journal]

COPYRIGHT 2021 BioMed Central Ltd. ;2021. 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) 2021 ;ISSN: 1465-993X ;ISSN: 1465-9921 ;EISSN: 1465-993X ;DOI: 10.1186/s12931-021-01622-1 ;PMID: 33478514

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4
Exome Sequencing in Children With Pulmonary Arterial Hypertension Demonstrates Differences Compared With Adults
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Exome Sequencing in Children With Pulmonary Arterial Hypertension Demonstrates Differences Compared With Adults

Circulation. Cardiovascular genetics, 2018-04, Vol.11 (4), p.e001887-e001887 [Peer Reviewed Journal]

2018 American Heart Association, Inc. ;Copyright American Heart Association, Inc. Apr 2018 ;ISSN: 2574-8300 ;ISSN: 1942-325X ;EISSN: 2574-8300 ;EISSN: 1942-3268 ;DOI: 10.1161/CIRCGEN.117.001887 ;PMID: 29631995

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5
Targeting cyclin-dependent kinases for the treatment of pulmonary arterial hypertension
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Targeting cyclin-dependent kinases for the treatment of pulmonary arterial hypertension

Nature communications, 2019-05, Vol.10 (1), p.2204-17, Article 2204 [Peer Reviewed Journal]

The Author(s) 2019. 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) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-10135-x ;PMID: 31101827

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6
Correction to: Eplerenone attenuates pathological pulmonary vascular rather than right ventricular remodeling in pulmonary arterial hypertension
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Correction to: Eplerenone attenuates pathological pulmonary vascular rather than right ventricular remodeling in pulmonary arterial hypertension

BMC pulmonary medicine, 2022-07, Vol.22 (1), p.1-281, Article 281 [Peer Reviewed Journal]

COPYRIGHT 2022 BioMed Central Ltd. ;2022. 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) 2022 ;ISSN: 1471-2466 ;EISSN: 1471-2466 ;DOI: 10.1186/s12890-022-01978-0 ;PMID: 35858940

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7
2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension
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2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension

European heart journal, 2022-10, Vol.43 (38), p.3618-3731 [Peer Reviewed Journal]

ISSN: 0195-668X ;ISSN: 1522-9645 ;EISSN: 1522-9645 ;DOI: 10.1093/eurheartj/ehac237 ;PMID: 36017548

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8
Survival of Japanese Patients with Idiopathic/Heritable Pulmonary Arterial Hypertension
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Survival of Japanese Patients with Idiopathic/Heritable Pulmonary Arterial Hypertension

The American journal of cardiology, 2017-05, Vol.119 (9), p.1479-1484 [Peer Reviewed Journal]

Elsevier Inc. ;2017 Elsevier Inc. ;Copyright © 2017 Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited May 1, 2017 ;ISSN: 0002-9149 ;EISSN: 1879-1913 ;DOI: 10.1016/j.amjcard.2017.01.015 ;PMID: 28267959

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9
33 Cardiac MRI thresholds for improvement in pulmonary arterial hypertension
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33 Cardiac MRI thresholds for improvement in pulmonary arterial hypertension

Heart (British Cardiac Society), 2023-01, Vol.109 (Suppl 1), p.A25-A25 [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-2022-BSCMR.32

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10
Updated Clinical Classification of Pulmonary Hypertension
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Updated Clinical Classification of Pulmonary Hypertension

Journal of the American College of Cardiology, 2013-12, Vol.62 (25), p.D34-D41 [Peer Reviewed Journal]

American College of Cardiology Foundation ;2013 American College of Cardiology Foundation ;2015 INIST-CNRS ;Copyright © 2013 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2013.10.029 ;PMID: 24355639 ;CODEN: JACCDI

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11
Pulmonary Arterial Hypertension: Epidemiology and Registries
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Pulmonary Arterial Hypertension: Epidemiology and Registries

Journal of the American College of Cardiology, 2013-12, Vol.62 (25), p.D51-D59 [Peer Reviewed Journal]

2015 INIST-CNRS ;Copyright © 2013 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;ISSN: 0735-1097 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2013.10.023 ;PMID: 24355642 ;CODEN: JACCDI

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12
Prognostic Value of Echocardiographic Variables Prior to and Following Initiation of Parenteral Prostacyclin Therapy
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Prognostic Value of Echocardiographic Variables Prior to and Following Initiation of Parenteral Prostacyclin Therapy

Chest, 2022-09, Vol.162 (3), p.669-683 [Peer Reviewed Journal]

2022 American College of Chest Physicians ;ISSN: 0012-3692 ;EISSN: 1931-3543 ;DOI: 10.1016/j.chest.2022.04.011

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13
A therapeutic antibody targeting osteoprotegerin attenuates severe experimental pulmonary arterial hypertension
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A therapeutic antibody targeting osteoprotegerin attenuates severe experimental pulmonary arterial hypertension

Nature communications, 2019-11, Vol.10 (1), p.5183-18, Article 5183 [Peer Reviewed Journal]

2019. 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) 2019 ;ISSN: 2041-1723 ;EISSN: 2041-1723 ;DOI: 10.1038/s41467-019-13139-9 ;PMID: 31729368

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14
Confusion in connection with pulmonary hypertension due to premature ventricular complexes requires diagnostic work-up
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Confusion in connection with pulmonary hypertension due to premature ventricular complexes requires diagnostic work-up

European heart journal : case reports, 2023-07, Vol.7 (7), p.ytad321 [Peer Reviewed Journal]

COPYRIGHT 2023 Oxford University Press ;ISSN: 2514-2119 ;EISSN: 2514-2119 ;DOI: 10.1093/ehjcr/ytad249 ;PMID: 37501708

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15
Pulmonary Arterial Hypertension and Hereditary Haemorrhagic Telangiectasia
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Pulmonary Arterial Hypertension and Hereditary Haemorrhagic Telangiectasia

International journal of molecular sciences, 2018-10, Vol.19 (10), p.3203 [Peer Reviewed Journal]

2018 by the authors. 2018 ;ISSN: 1422-0067 ;EISSN: 1422-0067 ;DOI: 10.3390/ijms19103203 ;PMID: 30336550

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16
Macitentan and Morbidity and Mortality in Pulmonary Arterial Hypertension
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Macitentan and Morbidity and Mortality in Pulmonary Arterial Hypertension

The New England journal of medicine, 2013-08, Vol.369 (9), p.809-818 [Peer Reviewed Journal]

Copyright © 2013 Massachusetts Medical Society. All rights reserved. ;2014 INIST-CNRS ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1213917 ;PMID: 23984728 ;CODEN: NEJMAG

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17
A68 WOW: PHARMACOLOGICAL TREATMENT OF PULMONARY HYPERTENSION: Transition From Pde-5 Inhibitors To Riociguat In Pulmonary Hypertension
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A68 WOW: PHARMACOLOGICAL TREATMENT OF PULMONARY HYPERTENSION: Transition From Pde-5 Inhibitors To Riociguat In Pulmonary Hypertension

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

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18
A68 WOW: PHARMACOLOGICAL TREATMENT OF PULMONARY HYPERTENSION: Rationale And Design Of The Replace Trial: Riociguat Replacing Phosphodiesterase 5 Inhibitor (pde5i) Therapy Evaluated Against Continued Pde5i Therapy In Patients With Pulmonary Arterial Hypertension (pah)
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A68 WOW: PHARMACOLOGICAL TREATMENT OF PULMONARY HYPERTENSION: Rationale And Design Of The Replace Trial: Riociguat Replacing Phosphodiesterase 5 Inhibitor (pde5i) Therapy Evaluated Against Continued Pde5i Therapy In Patients With Pulmonary Arterial Hypertension (pah)

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

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19
A18 U GOT THE LOOK: DRUGS, TOXINS, GENES AND RISK ASSESSMENT IN PULMONARY HYPERTENSION: Genetic And Molecular Differences Between Combined And Isolated Post-Capillary Pulmonary Hypertension
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A18 U GOT THE LOOK: DRUGS, TOXINS, GENES AND RISK ASSESSMENT IN PULMONARY HYPERTENSION: Genetic And Molecular Differences Between Combined And Isolated Post-Capillary Pulmonary Hypertension

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

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20
S91 Patterns of cytokines and growth factors in pulmonary arterial hypertension patients with BMPR2 mutations and PAH patients without driving mutations and their influence on survival
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S91 Patterns of cytokines and growth factors in pulmonary arterial hypertension patients with BMPR2 mutations and PAH patients without driving mutations and their influence on survival

Thorax, 2021-02, Vol.76 (Suppl 1), p.A55-A56 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0040-6376 ;EISSN: 1468-3296 ;DOI: 10.1136/thorax-2020-BTSabstracts.96

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