OK, now I'll bite
And, Im not a Fellow... Geez. Im not even a doctor.
PAH is not diagnosed by Interventional (not invasive) cardiologists. There are red flags on physical exam, 2D echo, EKG, and chest x-ray that should get anyone thinking about it. And the 2D echo will give you a pretty stinkin' good indication of whats going on... and thats non-invasive. If you want to go for a pulmonary artery cath, a pulmonologist can do that too. The diagnosis can be made by whosoever feels inclined.
I could easily argue that PAH is a pulmonary vascular disease which can have cardiac manifestations. And, there are a number of pulmonary vascular diseases, this is just one of them. Why woud this one go to cardiology? "Cor Pulmonale!" you say? Yes! Pulmonale... Pulmonale.... Pulm... anyway.
As far as clinically... the disease is rare, and academic medical centers pretty much see most of it. Whether the disease is managed by Cardiology or Pulmonology depends on the institution. I gave you six examples of where it happens to be under Pulmonology. Sometimes it changes... It recently moved from Pulm to Cardio at U of MD. Its probably going to be an interdisciplinary approach anyway.
There are articles on PAH everywhere, in the JACC, CHEST, wherever.... Last I checked, whoever wants to study it can do so.
So, thats that.
Different fellowships are different. Some offer experience with transplant, and some dont. Some offer experience with PAH, and some dont. Some have more procedural training than others. Some offer a lot of research experience, and some dont. When the times comes, you'll know whats important to you, and you'll choose your fellowship with that in mind
Similarly, individual clinical departments are different.
Those advanced fellowships you mentioned are post-doc clinical fellowships that are usually for really smart folks who are in academic medicine. They are designed by the institution itself, so they can have whatever curriculum they want. I didnt look into those particular fellowships myself, but heart failure vs. transplant...?
To address you initial questions: Google it.
1. I found a case report of a RVAD being effective in secondary PAH.
2. Depends on what you call a cure. I dont know if extending someones expected 2.5 year survival of PAH, to a 40% 5-year survival in an immunocompromized state post heart-lung transplant is really a cure. Im not saying that it isnt. Im saying I dont know.
I dont have the foggiest idea of what youre talking about in the other two statements.
Youre lucky im on vacation and bored out of my skull. Most individuals dont want to come home from the hospital and do homework.