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  • Deutsch
  • English
  • Home
  • What is PH
    • Diagnostics (non-scientific)
    • Diagnostics (scientific)
      • Indtroduction
      • Definition
      • Pathogenesis
      • Classification
      • NYHA Classification
      • Diagnostics
        • Clinical Symptoms
        • Status
        • Laboratory tests
        • ECG
        • Chest X-Ray
        • Transthoriacic Echocardography (TTE)
        • Ventilation/Perfusion Scintigraphy of the lung (V/Q Scan)
        • Computed Tomography
        • Pulmonary Angiography
        • Right Heart Catheter and Haemodynamic Testing
      • Treatment
      • Surgical Therapies
      • References
  • For Affected
    • Become a member
    • Specialist centres
    • Psychological support
    • Pharmacy service
    • Oxygen supply
    • Social assistance
      • Disability pass
      • Care allowance
  • Events & Projects
    • Zoo Run
    • World PH Day
    • Milestones
    • Newsletter
  • Research Association
    • Research Projects
      • 6 min. test-App
    • Annual Report and Financial Report
    • Statuten & Register
  • About PH Austria
    • Team
      • Medical Advisory Board
    • Annual Report
    • Statues and register of associations
  • Donation
    • Donation to PH Austria – Initiative Lungenhochdruck
    • Donation to Lungenkinder Forschungsverein
    • Vergissmeinnicht Initiative
  • Contact

Research Projects

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Research Projects

Previous research projects

Development of a website and app for the 6-minute walking test for children and adolescents

After a lung transplant on the highest mountain in North Africa

Expanded gene analysis and establishment of a gene bank in children with pulmonary hypertension

New echo parameter 4 DS Train right ventricle in correlation with genetic factors

Expanded gene analysis and establishment of a gene bank in children with pulmonary hypertension (PH)

Effectiveness and tolerability of macitentan in the treatment of childhood pulmonary hypertension / pulmonary hypertensive vasculopathy

Long-term effects of macitentan in childhood pulmonary hypertension / pulmonary hypertensive vasculopathy

Molecular genetic examinations in pulmonary hypertension (PAH)

Interim report Molecular genetic studies in PAH and application Clinical and translational analysis of iron dyshomeostasis in patients with pulmonary arterial hypertension

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PH Austria - Initiative Lungenhochdruck
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  • +43 (0)1/ 402 37 25
  • info@phaustria.org
Patient telephone
  • Eva Otter: +43 (0)664/28 80 888
  • Gerald Fischer: +43 (0)664/ 22 88 888

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PH Austria - Lungenhochdruck

Pulmonary hypertension is a rare disease that can affect anyone at any time and of any age and is not yet curable. Since it is very rare, there is unfortunately hardly any research funding available, which is why personal initiative is very important

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