Prof. Dr. Joachim Woelfle

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Pediatric and Adolescent Medicine

  • University Hospital Erlangen
  • location Germany

From the start of his academic career, Prof. Dr. Joachim Woelfle had a major interest in growth disorders. During his residency in Bonn, Prof. Dr. Woelfle started his scientific education as the head of a junior research group, trying to elucidate the role of pulsatile growth hormone release on gene transcription. This was followed by a 3-year postdoc timeout at OHSU in Oregon, where he mainly worked on GH-receptor-induced signalling, which led to the biochemical identification of Stat5b as a main regulator of IGF-1 gene transcription. This was soon followed by the identification of a first patient with GHIS, harbouring a Stat5b mutation, by Vivien Hwa and Ron Rosenfeld. Since then, Prof. Dr. Woelfle’s main clinical and research interests focused on growth disorders, first as head of pediatric endocrinology division at the university of Bonn, Germany; since 2019 as the chair of pediatrics at the university of  Erlangen.

Prof. Dr. Joachim Woelfle has received financial support/sponsorship for research support, consultation, or speaker fees from the following companies:

Programmes developed by Prof. Dr. Joachim Woelfle

podcast Podcast

Episode

1

of 2

episode
Pediatrics Endocrinology Rare diseases 
Short stature: Key challenges in diagnosis and management – Episode 1

Video podcast exploring primary IGF-I deficiency, GH deficiency and other rare growth disorders

Experts
Prof. Dr. Joachim Woelfle, Prof. Philippe Backeljauw
Endorsed by
The Magic Foundation
  • download Downloadable
    Resources
  • clock MIN
  • calendar Dec 2023

Educational programme supported by an Independent Educational Grant from Ipsen.