A review in @FrontMedicine aims to outline the major pathophysiological changes and the underlying mechanisms leading to myocardial remodeling and cardiac functional derangement in DM-CMP.
Read and download the full article ⬇️
Web of Science ha eliminado 82 Journals de su clasificación por comportamientos fraudulentos, de editoriales como MDPI, Hindawi Ltd., etc.
Desde 2017, >5000 artículos provienen de Universidades en España, costando varios millones €.
Las Universidades más (y menos) afectadas ⬇️
Swedish researchers just published the first #POTS symptom score, based on the 12 most common symptoms reported by 1000s of patients in the Big POTS Study, a collaboration between Dysautonomia International, Vanderbilt & Univ of Calgary. This is progress!
https://t.co/bTD5Xlz5HQ
#FridayFacts There are NO FDA approved drugs for POTS and that has to change. Share to help raise awareness! You can help us find more effective treatments for POTS by making a contribution at https://t.co/BJTa6J5szt.
@morganstephensa Looking at the history of post-viral illnesses, they have always been politicized and largely ignored by the government and academia, like post-viral #POTS. The government ignoring the plight of millions of sick people is inherently political. There are just more of us now.
We need more research to truly understand the etiology of #POTS and long #COVID. Mast cell activation may be at least part of that picture. The plots show the similarity in symptoms between #MCAS and long COVID. Treatment with mast cell stabilizers could be helpful. #SUTP
It's #DysautonomiaAwarenessMonth! Call a school nurse in your area and ask if you can send them printouts on POTS and dysautonomia, which they can use for kids and parents in their school. You can download the printouts and other materials here: https://t.co/g7qwG7kvJw.
It's #DysautonomiaAwarenessMonth! Diabetes is the most common cause of autonomic neuropathy, which can be a serious complication of diabetes. Even pre-diabetes can cause autonomic neuropathy. Share to raise awareness!
New research from @OUHSC_research and @VUMChealth finding elevated muscarinic 2 receptor antibody activity in half of #POTS patients, which they suggest increases tachycardia upon standing by exaggerating vagal withdrawal.
https://t.co/1vOHmKOdUD
POTS symptoms vary from mild to severe. This small study found that people with POTS improved their quality of life despite their symptoms remaining relatively stable over time. The journey with chronic illness is long and difficult, but can get better over time. #SUTP#POTS
Each time we share data suggesting gender disparities in healthcare impact women with dysautonomia, some people get angry with us and claim it’s not true. Gender disparities in healthcare are real, and in some cases, lead to the death of women. Read this study.
Our Featured Video of the Week, presented by Dr. Wolfgang Singer and guests, focuses on “Thermoregulatory Sweat Test”. Read more here:
https://t.co/hIVbGvWLbS
#TheDysautonomiaProject#Dysautonomia#Education