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Pulmonary hypertension and pulmonary arterial hypertension: a clarification is needed

N. Galiè, M. Palazzini, A. Manes
European Respiratory Journal 2010 36: 986-990; DOI: 10.1183/09031936.00038410
N. Galiè
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  • For correspondence: Nazzareno.galie@unibo.it
M. Palazzini
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A. Manes
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Article Information

vol. 36 no. 5 986-990
DOI 
https://doi.org/10.1183/09031936.00038410
PubMed 
21037366

Published By 
European Respiratory Society
Print ISSN 
0903-1936
Online ISSN 
1399-3003
History 
  • Published online October 31, 2010.

Copyright & Usage 
©ERS 2010

Author Information

  1. N. Galiè,
  2. M. Palazzini and
  3. A. Manes
  1. Istituto di Cardiologia, Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy
  1. N. Galiè, Istituto di Cardiologia, Azienda Ospedaliero-Universitaria di Bologna, Via Massarenti 9, 40138-Bologna, Italy. E-mail: Nazzareno.galie{at}unibo.it
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Vol 36 Issue 5 Table of Contents
European Respiratory Journal: 36 (5)
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Pulmonary hypertension and pulmonary arterial hypertension: a clarification is needed
N. Galiè, M. Palazzini, A. Manes
European Respiratory Journal Nov 2010, 36 (5) 986-990; DOI: 10.1183/09031936.00038410

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Pulmonary hypertension and pulmonary arterial hypertension: a clarification is needed
N. Galiè, M. Palazzini, A. Manes
European Respiratory Journal Nov 2010, 36 (5) 986-990; DOI: 10.1183/09031936.00038410
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  • Article
    • PH IS A HAEMODYNAMIC AND PATHOPHYSIOLOGICAL CONDITION
    • DOPPLER ECHOCARDIOGRAPHY CAN PROVIDE AN ESTIMATE OF THE LIKELIHOOD OF PH
    • PH CAN BE FOUND IN AT LEAST 37 SYNDROMES CLASSIFIED INTO SIX CLINICAL GROUPS
    • PAH IS A CLINICAL GROUP OF RARE CONDITIONS
    • THE FINAL CLINICAL DIAGNOSIS IN THE INDIVIDUAL PATIENT WITH PH REQUIRES AN APPROPRIATE DIAGNOSTIC ALGORITHM
    • CONCLUSIONS
    • Footnotes
    • REFERENCES
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  • Pulmonary vascular disease
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