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<p>The journey from the first publication in <i>Pädiatrie Pädologie</i> in 1985 to the opening of a&#xa0;national mitochondrial expertise center in 2025 at the University Hospital for Pediatric and Adolescent Medicine in Salzburg is more than just a&#xa0;medical success story in Austria. Especially in the field of congenital metabolic disorders (rare diseases), it serves as an example of what can be achieved through continuous collaboration, international exchange, and tireless dedication—primarily for patient care, but also for research and education.</p>

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Vom ersten Patienten zum nationalen Zentrum

  • 期刊论文

  • 出版模式：

    开放获取

  • 发表日期：

    2025年8月12日

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  • Wolfgang Sperl

摘要

The journey from the first publication in Pädiatrie Pädologie in 1985 to the opening of a national mitochondrial expertise center in 2025 at the University Hospital for Pediatric and Adolescent Medicine in Salzburg is more than just a medical success story in Austria. Especially in the field of congenital metabolic disorders (rare diseases), it serves as an example of what can be achieved through continuous collaboration, international exchange, and tireless dedication—primarily for patient care, but also for research and education.