Luke Stockdale - phaware® interview 560
Feb 18, 2026
From Knee Pain to Gene Discovery: One Family’s Unexpected Diagnosis
What started as routine investigations into hereditary knee problems turned into a life-altering discovery for Luke Stockdale and his family — a TBX4 gene mutation linked to pulmonary arterial hypertension (PAH). In this episode, Luke shares...
Feb 17, 2026
From Knee Pain to Gene Discovery: One Family’s Unexpected Diagnosis
What started as routine investigations into hereditary knee problems turned into a life-altering discovery for Luke Stockdale and his family — a TBX4 gene mutation linked to pulmonary arterial hypertension (PAH). In this episode, Luke shares how...
Drs. Matina Prapa and Olivier Danhaive - phaware® interview 559
Feb 11, 2026
How a Global Team Is Rewriting the
TBX4 Playbook
Rare diseases thrive in isolation. TBX4Life is changing that.
In this episode, Drs. Prapa and Danhaive share how
international collaboration is creating real-time change for
patients. From newborn screening to natural history studies to
rethinking how we talk about...
Feb 10, 2026
How a Global Team Is Rewriting the TBX4
Playbook
Rare diseases thrive in isolation. TBX4Life is changing that.
In this episode, Drs. Prapa and Danhaive share how
international collaboration is creating real-time change for
patients. From newborn screening to natural history studies to
rethinking how we talk about...
Anton Morkin - phaware® interview 558
Feb 4, 2026
One Dad’s Mission to Cure His Son’s Genetic Disease
When Anton Morkin’s son was diagnosed with “idiopathic” pulmonary hypertension, he refused to accept “no known cause” as an answer. What followed was a crash course in genetics, the discovery of a rare mutation, and the formation of a worldwide...